WO2013101436A1 - Methods of identifying and using mdm2 inhibitors - Google Patents
Methods of identifying and using mdm2 inhibitors Download PDFInfo
- Publication number
- WO2013101436A1 WO2013101436A1 PCT/US2012/068557 US2012068557W WO2013101436A1 WO 2013101436 A1 WO2013101436 A1 WO 2013101436A1 US 2012068557 W US2012068557 W US 2012068557W WO 2013101436 A1 WO2013101436 A1 WO 2013101436A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cells
- mdm2
- cancer
- inhibitor
- huwel
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 64
- 239000012819 MDM2-Inhibitor Substances 0.000 title claims abstract description 27
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 118
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 claims abstract description 114
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 claims abstract description 114
- 201000011510 cancer Diseases 0.000 claims abstract description 84
- 239000003112 inhibitor Substances 0.000 claims abstract description 64
- 238000011282 treatment Methods 0.000 claims abstract description 45
- 101001056180 Homo sapiens Induced myeloid leukemia cell differentiation protein Mcl-1 Proteins 0.000 claims abstract description 34
- 102100026539 Induced myeloid leukemia cell differentiation protein Mcl-1 Human genes 0.000 claims abstract description 34
- 230000003247 decreasing effect Effects 0.000 claims abstract description 27
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 claims abstract description 16
- 239000005483 tyrosine kinase inhibitor Substances 0.000 claims abstract description 16
- 238000012216 screening Methods 0.000 claims abstract description 7
- 150000004917 tyrosine kinase inhibitor derivatives Chemical class 0.000 claims abstract description 6
- 239000002136 L01XE07 - Lapatinib Substances 0.000 claims description 140
- BCFGMOOMADDAQU-UHFFFAOYSA-N lapatinib Chemical compound O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 BCFGMOOMADDAQU-UHFFFAOYSA-N 0.000 claims description 140
- 229960004891 lapatinib Drugs 0.000 claims description 139
- 102100025064 Cellular tumor antigen p53 Human genes 0.000 claims description 45
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 claims description 42
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 claims description 42
- 101000721661 Homo sapiens Cellular tumor antigen p53 Proteins 0.000 claims description 41
- 230000000694 effects Effects 0.000 claims description 40
- 230000001965 increasing effect Effects 0.000 claims description 27
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- 102100033849 CCHC-type zinc finger nucleic acid binding protein Human genes 0.000 claims description 18
- 101001012157 Homo sapiens Receptor tyrosine-protein kinase erbB-2 Proteins 0.000 claims description 15
- 102100030086 Receptor tyrosine-protein kinase erbB-2 Human genes 0.000 claims description 15
- 229940083338 MDM2 inhibitor Drugs 0.000 claims description 13
- 206010006187 Breast cancer Diseases 0.000 claims description 11
- 208000026310 Breast neoplasm Diseases 0.000 claims description 11
- 102000006275 Ubiquitin-Protein Ligases Human genes 0.000 claims description 8
- 108010083111 Ubiquitin-Protein Ligases Proteins 0.000 claims description 8
- 230000003993 interaction Effects 0.000 claims description 8
- 102000052116 epidermal growth factor receptor activity proteins Human genes 0.000 claims description 7
- 108700015053 epidermal growth factor receptor activity proteins Proteins 0.000 claims description 7
- YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 claims description 7
- -1 small molecule tyrosine kinase inhibitor Chemical class 0.000 claims description 7
- 241000282414 Homo sapiens Species 0.000 claims description 6
- 238000013518 transcription Methods 0.000 claims description 6
- 230000035897 transcription Effects 0.000 claims description 6
- 206010009944 Colon cancer Diseases 0.000 claims description 2
- 208000032612 Glial tumor Diseases 0.000 claims description 2
- 206010018338 Glioma Diseases 0.000 claims description 2
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 2
- 208000029742 colonic neoplasm Diseases 0.000 claims description 2
- 230000007423 decrease Effects 0.000 claims description 2
- 206010017758 gastric cancer Diseases 0.000 claims description 2
- 201000011549 stomach cancer Diseases 0.000 claims description 2
- 238000013519 translation Methods 0.000 claims description 2
- CQARAIRTGMAYMZ-IBGZPJMESA-N (4S)-5-amino-5-oxo-4-[3-[4-(5-phenylthiophen-2-yl)phenyl]propanoylamino]pentanoic acid Chemical compound C1=CC(CCC(=O)N[C@@H](CCC(O)=O)C(=O)N)=CC=C1C1=CC=C(C=2C=CC=CC=2)S1 CQARAIRTGMAYMZ-IBGZPJMESA-N 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- BDUHCSBCVGXTJM-IZLXSDGUSA-N Nutlin-3 Chemical compound CC(C)OC1=CC(OC)=CC=C1C1=N[C@H](C=2C=CC(Cl)=CC=2)[C@H](C=2C=CC(Cl)=CC=2)N1C(=O)N1CC(=O)NCC1 BDUHCSBCVGXTJM-IZLXSDGUSA-N 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 208000020816 lung neoplasm Diseases 0.000 claims 1
- 230000004044 response Effects 0.000 abstract description 11
- 239000012830 cancer therapeutic Substances 0.000 abstract description 4
- 210000004027 cell Anatomy 0.000 description 259
- 108090000623 proteins and genes Proteins 0.000 description 55
- 102000004169 proteins and genes Human genes 0.000 description 52
- 235000018102 proteins Nutrition 0.000 description 49
- 238000003119 immunoblot Methods 0.000 description 37
- BDUHCSBCVGXTJM-WUFINQPMSA-N 4-[[(4S,5R)-4,5-bis(4-chlorophenyl)-2-(4-methoxy-2-propan-2-yloxyphenyl)-4,5-dihydroimidazol-1-yl]-oxomethyl]-2-piperazinone Chemical compound CC(C)OC1=CC(OC)=CC=C1C1=N[C@@H](C=2C=CC(Cl)=CC=2)[C@@H](C=2C=CC(Cl)=CC=2)N1C(=O)N1CC(=O)NCC1 BDUHCSBCVGXTJM-WUFINQPMSA-N 0.000 description 24
- 239000000203 mixture Substances 0.000 description 19
- 102100030497 Cytochrome c Human genes 0.000 description 18
- 108010075031 Cytochromes c Proteins 0.000 description 18
- 230000035772 mutation Effects 0.000 description 17
- 102000007469 Actins Human genes 0.000 description 16
- 108010085238 Actins Proteins 0.000 description 16
- 230000015556 catabolic process Effects 0.000 description 16
- 238000006731 degradation reaction Methods 0.000 description 16
- 239000006166 lysate Substances 0.000 description 16
- 102000044159 Ubiquitin Human genes 0.000 description 13
- 238000001114 immunoprecipitation Methods 0.000 description 13
- 238000010798 ubiquitination Methods 0.000 description 13
- 108091027967 Small hairpin RNA Proteins 0.000 description 12
- 108090000848 Ubiquitin Proteins 0.000 description 12
- 230000014509 gene expression Effects 0.000 description 12
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 10
- 238000000338 in vitro Methods 0.000 description 10
- 239000004055 small Interfering RNA Substances 0.000 description 9
- 230000006907 apoptotic process Effects 0.000 description 8
- 239000013592 cell lysate Substances 0.000 description 8
- 230000005764 inhibitory process Effects 0.000 description 8
- 230000001404 mediated effect Effects 0.000 description 8
- 230000026731 phosphorylation Effects 0.000 description 8
- 238000006366 phosphorylation reaction Methods 0.000 description 8
- 102000004039 Caspase-9 Human genes 0.000 description 7
- 108090000566 Caspase-9 Proteins 0.000 description 7
- 238000012413 Fluorescence activated cell sorting analysis Methods 0.000 description 7
- 201000010099 disease Diseases 0.000 description 7
- 238000003197 gene knockdown Methods 0.000 description 7
- 108090000672 Annexin A5 Proteins 0.000 description 6
- 102000004121 Annexin A5 Human genes 0.000 description 6
- 102000011727 Caspases Human genes 0.000 description 6
- 108010076667 Caspases Proteins 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 241000699666 Mus <mouse, genus> Species 0.000 description 6
- 241000699670 Mus sp. Species 0.000 description 6
- 238000003556 assay Methods 0.000 description 6
- 230000037396 body weight Effects 0.000 description 6
- 230000007547 defect Effects 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 230000006641 stabilisation Effects 0.000 description 6
- 238000011105 stabilization Methods 0.000 description 6
- 210000001519 tissue Anatomy 0.000 description 6
- 108090000397 Caspase 3 Proteins 0.000 description 5
- 102100029855 Caspase-3 Human genes 0.000 description 5
- 230000004913 activation Effects 0.000 description 5
- 230000001640 apoptogenic effect Effects 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 230000002438 mitochondrial effect Effects 0.000 description 5
- 239000013612 plasmid Substances 0.000 description 5
- 239000011535 reaction buffer Substances 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- 150000003384 small molecules Chemical class 0.000 description 5
- 230000004614 tumor growth Effects 0.000 description 5
- 108010016317 ubiquitin-aldehyde Proteins 0.000 description 5
- 230000003442 weekly effect Effects 0.000 description 5
- 229920000936 Agarose Polymers 0.000 description 4
- 108010089941 Apoptosomes Proteins 0.000 description 4
- ZBNZXTGUTAYRHI-UHFFFAOYSA-N Dasatinib Chemical compound C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1Cl ZBNZXTGUTAYRHI-UHFFFAOYSA-N 0.000 description 4
- 239000002067 L01XE06 - Dasatinib Substances 0.000 description 4
- 241000699660 Mus musculus Species 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 101150063416 add gene Proteins 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229960002448 dasatinib Drugs 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 210000003470 mitochondria Anatomy 0.000 description 4
- 230000002018 overexpression Effects 0.000 description 4
- 230000037361 pathway Effects 0.000 description 4
- 102000003998 progesterone receptors Human genes 0.000 description 4
- 108090000468 progesterone receptors Proteins 0.000 description 4
- 230000002441 reversible effect Effects 0.000 description 4
- 230000011664 signaling Effects 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 208000024891 symptom Diseases 0.000 description 4
- 230000008685 targeting Effects 0.000 description 4
- 238000001890 transfection Methods 0.000 description 4
- 229960000575 trastuzumab Drugs 0.000 description 4
- 230000003827 upregulation Effects 0.000 description 4
- 238000001262 western blot Methods 0.000 description 4
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 3
- 229940123169 Caspase inhibitor Drugs 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000007995 HEPES buffer Substances 0.000 description 3
- 101000761737 Homo sapiens Ubiquitin-conjugating enzyme E2 L3 Proteins 0.000 description 3
- 241000124008 Mammalia Species 0.000 description 3
- 108091000080 Phosphotransferase Proteins 0.000 description 3
- 239000012614 Q-Sepharose Substances 0.000 description 3
- 102000001332 SRC Human genes 0.000 description 3
- 108060006706 SRC Proteins 0.000 description 3
- 102100024861 Ubiquitin-conjugating enzyme E2 L3 Human genes 0.000 description 3
- 210000000577 adipose tissue Anatomy 0.000 description 3
- 230000002424 anti-apoptotic effect Effects 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 230000001086 cytosolic effect Effects 0.000 description 3
- SUYVUBYJARFZHO-RRKCRQDMSA-N dATP Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@H]1C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O1 SUYVUBYJARFZHO-RRKCRQDMSA-N 0.000 description 3
- SUYVUBYJARFZHO-UHFFFAOYSA-N dATP Natural products C1=NC=2C(N)=NC=NC=2N1C1CC(O)C(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O1 SUYVUBYJARFZHO-UHFFFAOYSA-N 0.000 description 3
- 208000035475 disorder Diseases 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 238000011580 nude mouse model Methods 0.000 description 3
- 102000020233 phosphotransferase Human genes 0.000 description 3
- 230000001960 triggered effect Effects 0.000 description 3
- 238000011144 upstream manufacturing Methods 0.000 description 3
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 2
- 108010039627 Aprotinin Proteins 0.000 description 2
- 108091023037 Aptamer Proteins 0.000 description 2
- 102000051485 Bcl-2 family Human genes 0.000 description 2
- 108700038897 Bcl-2 family Proteins 0.000 description 2
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 2
- 102000052052 Casein Kinase II Human genes 0.000 description 2
- 108010010919 Casein Kinase II Proteins 0.000 description 2
- 108010091675 Cellular Apoptosis Susceptibility Protein Proteins 0.000 description 2
- 101710163595 Chaperone protein DnaK Proteins 0.000 description 2
- 102100038595 Estrogen receptor Human genes 0.000 description 2
- 102100029091 Exportin-2 Human genes 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 101710178376 Heat shock 70 kDa protein Proteins 0.000 description 2
- 101710152018 Heat shock cognate 70 kDa protein Proteins 0.000 description 2
- GDBQQVLCIARPGH-UHFFFAOYSA-N Leupeptin Natural products CC(C)CC(NC(C)=O)C(=O)NC(CC(C)C)C(=O)NC(C=O)CCCN=C(N)N GDBQQVLCIARPGH-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- DRBBFCLWYRJSJZ-UHFFFAOYSA-N N-phosphocreatine Chemical compound OC(=O)CN(C)C(=N)NP(O)(O)=O DRBBFCLWYRJSJZ-UHFFFAOYSA-N 0.000 description 2
- 229920002684 Sepharose Polymers 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000000692 Student's t-test Methods 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000005557 antagonist Substances 0.000 description 2
- 229960003982 apatinib Drugs 0.000 description 2
- 230000005756 apoptotic signaling Effects 0.000 description 2
- 229960004405 aprotinin Drugs 0.000 description 2
- 230000003190 augmentative effect Effects 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 210000000481 breast Anatomy 0.000 description 2
- 238000004113 cell culture Methods 0.000 description 2
- 230000030833 cell death Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000003292 diminished effect Effects 0.000 description 2
- 231100000673 dose–response relationship Toxicity 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 108010038795 estrogen receptors Proteins 0.000 description 2
- 239000012091 fetal bovine serum Substances 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- 238000001215 fluorescent labelling Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000002523 gelfiltration Methods 0.000 description 2
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 230000009848 hypophosphorylation Effects 0.000 description 2
- 239000012742 immunoprecipitation (IP) buffer Substances 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- ZPNFWUPYTFPOJU-LPYSRVMUSA-N iniprol Chemical compound C([C@H]1C(=O)NCC(=O)NCC(=O)N[C@H]2CSSC[C@H]3C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](C(N[C@H](C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=4C=CC(O)=CC=4)C(=O)N[C@@H](CC=4C=CC=CC=4)C(=O)N[C@@H](CC=4C=CC(O)=CC=4)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC=4C=CC=CC=4)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC2=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H]2N(CCC2)C(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N2[C@@H](CCC2)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N2[C@@H](CCC2)C(=O)N3)C(=O)NCC(=O)NCC(=O)N[C@@H](C)C(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@H](C(=O)N1)C(C)C)[C@@H](C)O)[C@@H](C)CC)=O)[C@@H](C)CC)C1=CC=C(O)C=C1 ZPNFWUPYTFPOJU-LPYSRVMUSA-N 0.000 description 2
- 208000032839 leukemia Diseases 0.000 description 2
- GDBQQVLCIARPGH-ULQDDVLXSA-N leupeptin Chemical compound CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C=O)CCCN=C(N)N GDBQQVLCIARPGH-ULQDDVLXSA-N 0.000 description 2
- 108010052968 leupeptin Proteins 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- WPEWQEMJFLWMLV-UHFFFAOYSA-N n-[4-(1-cyanocyclopentyl)phenyl]-2-(pyridin-4-ylmethylamino)pyridine-3-carboxamide Chemical compound C=1C=CN=C(NCC=2C=CN=CC=2)C=1C(=O)NC(C=C1)=CC=C1C1(C#N)CCCC1 WPEWQEMJFLWMLV-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 238000001543 one-way ANOVA Methods 0.000 description 2
- 238000003305 oral gavage Methods 0.000 description 2
- 230000000861 pro-apoptotic effect Effects 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000007115 recruitment Effects 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000002864 sequence alignment Methods 0.000 description 2
- 238000012353 t test Methods 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- 230000001052 transient effect Effects 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- 230000034512 ubiquitination Effects 0.000 description 2
- GGXRLUDNGFFUKI-ORGXJRBJSA-N (4s)-4-[[(2s)-2-acetamido-3-carboxypropanoyl]amino]-5-[[(2s)-1-[[(2s)-3-carboxy-1-(4-nitroanilino)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-oxopentanoic acid Chemical compound OC(=O)C[C@H](NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)NC1=CC=C([N+]([O-])=O)C=C1 GGXRLUDNGFFUKI-ORGXJRBJSA-N 0.000 description 1
- UMCMPZBLKLEWAF-BCTGSCMUSA-N 3-[(3-cholamidopropyl)dimethylammonio]propane-1-sulfonate Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCC[N+](C)(C)CCCS([O-])(=O)=O)C)[C@@]2(C)[C@@H](O)C1 UMCMPZBLKLEWAF-BCTGSCMUSA-N 0.000 description 1
- WEVYNIUIFUYDGI-UHFFFAOYSA-N 3-[6-[4-(trifluoromethoxy)anilino]-4-pyrimidinyl]benzamide Chemical compound NC(=O)C1=CC=CC(C=2N=CN=C(NC=3C=CC(OC(F)(F)F)=CC=3)C=2)=C1 WEVYNIUIFUYDGI-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 102100022997 Acidic leucine-rich nuclear phosphoprotein 32 family member A Human genes 0.000 description 1
- 241000691306 Actia Species 0.000 description 1
- 101000783817 Agaricus bisporus lectin Proteins 0.000 description 1
- 108020000948 Antisense Oligonucleotides Proteins 0.000 description 1
- 102100021569 Apoptosis regulator Bcl-2 Human genes 0.000 description 1
- MLDQJTXFUGDVEO-UHFFFAOYSA-N BAY-43-9006 Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3C=C(C(Cl)=CC=3)C(F)(F)F)=CC=2)=C1 MLDQJTXFUGDVEO-UHFFFAOYSA-N 0.000 description 1
- 108091007065 BIRCs Proteins 0.000 description 1
- 101150086017 Bcl2l11 gene Proteins 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 102000002164 CARD domains Human genes 0.000 description 1
- 108050009503 CARD domains Proteins 0.000 description 1
- 101100314454 Caenorhabditis elegans tra-1 gene Proteins 0.000 description 1
- 208000005623 Carcinogenesis Diseases 0.000 description 1
- 201000009030 Carcinoma Diseases 0.000 description 1
- 101150008459 Clec4d gene Proteins 0.000 description 1
- 102000004420 Creatine Kinase Human genes 0.000 description 1
- 108010042126 Creatine kinase Proteins 0.000 description 1
- 108010086821 DEVDase Proteins 0.000 description 1
- 101710101803 DNA-binding protein J Proteins 0.000 description 1
- 241000252212 Danio rerio Species 0.000 description 1
- 101100226776 Drosophila melanogaster fax gene Proteins 0.000 description 1
- 206010059866 Drug resistance Diseases 0.000 description 1
- 102100034893 E3 ubiquitin-protein ligase HUWE1 Human genes 0.000 description 1
- 102100032257 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 101710147878 Exportin-2 Proteins 0.000 description 1
- 108091008794 FGF receptors Proteins 0.000 description 1
- 108091006010 FLAG-tagged proteins Proteins 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- 208000017891 HER2 positive breast carcinoma Diseases 0.000 description 1
- 101710113864 Heat shock protein 90 Proteins 0.000 description 1
- 102100034051 Heat shock protein HSP 90-alpha Human genes 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000757200 Homo sapiens Acidic leucine-rich nuclear phosphoprotein 32 family member A Proteins 0.000 description 1
- 101000971171 Homo sapiens Apoptosis regulator Bcl-2 Proteins 0.000 description 1
- 101001019732 Homo sapiens E3 ubiquitin-protein ligase HUWE1 Proteins 0.000 description 1
- 101001015963 Homo sapiens E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 description 1
- 101001034652 Homo sapiens Insulin-like growth factor 1 receptor Proteins 0.000 description 1
- 101000984710 Homo sapiens Lymphocyte-specific protein 1 Proteins 0.000 description 1
- 101000588130 Homo sapiens Microsomal triglyceride transfer protein large subunit Proteins 0.000 description 1
- 101000692455 Homo sapiens Platelet-derived growth factor receptor beta Proteins 0.000 description 1
- 101000823316 Homo sapiens Tyrosine-protein kinase ABL1 Proteins 0.000 description 1
- 102000055031 Inhibitor of Apoptosis Proteins Human genes 0.000 description 1
- 102100039688 Insulin-like growth factor 1 receptor Human genes 0.000 description 1
- 102000015617 Janus Kinases Human genes 0.000 description 1
- 108010024121 Janus Kinases Proteins 0.000 description 1
- 239000005411 L01XE02 - Gefitinib Substances 0.000 description 1
- 239000005551 L01XE03 - Erlotinib Substances 0.000 description 1
- 239000005511 L01XE05 - Sorafenib Substances 0.000 description 1
- 239000012098 Lipofectamine RNAiMAX Substances 0.000 description 1
- 241001599018 Melanogaster Species 0.000 description 1
- 240000000233 Melia azedarach Species 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101000931108 Mus musculus DNA (cytosine-5)-methyltransferase 1 Proteins 0.000 description 1
- 108091034117 Oligonucleotide Proteins 0.000 description 1
- 108700020796 Oncogene Proteins 0.000 description 1
- 229930012538 Paclitaxel Natural products 0.000 description 1
- 206010034133 Pathogen resistance Diseases 0.000 description 1
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 description 1
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 description 1
- 102100026547 Platelet-derived growth factor receptor beta Human genes 0.000 description 1
- 108010090931 Proto-Oncogene Proteins c-bcl-2 Proteins 0.000 description 1
- 102000013535 Proto-Oncogene Proteins c-bcl-2 Human genes 0.000 description 1
- 206010037211 Psychomotor hyperactivity Diseases 0.000 description 1
- 239000012979 RPMI medium Substances 0.000 description 1
- 238000011529 RT qPCR Methods 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 102100029981 Receptor tyrosine-protein kinase erbB-4 Human genes 0.000 description 1
- 101710100963 Receptor tyrosine-protein kinase erbB-4 Proteins 0.000 description 1
- 239000012722 SDS sample buffer Substances 0.000 description 1
- 101100071632 Schizosaccharomyces pombe (strain 972 / ATCC 24843) hsp9 gene Proteins 0.000 description 1
- 238000012300 Sequence Analysis Methods 0.000 description 1
- 102220497176 Small vasohibin-binding protein_T47D_mutation Human genes 0.000 description 1
- 229940122924 Src inhibitor Drugs 0.000 description 1
- 239000012505 Superdex™ Substances 0.000 description 1
- 108010065917 TOR Serine-Threonine Kinases Proteins 0.000 description 1
- 102000013530 TOR Serine-Threonine Kinases Human genes 0.000 description 1
- 108090000190 Thrombin Proteins 0.000 description 1
- 241000254113 Tribolium castaneum Species 0.000 description 1
- 108010091356 Tumor Protein p73 Proteins 0.000 description 1
- 102000018252 Tumor Protein p73 Human genes 0.000 description 1
- 102100022596 Tyrosine-protein kinase ABL1 Human genes 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 108010038407 acetyl-aspartyl-glutamyl-valyl-aspartic acid p-nitroanilide Proteins 0.000 description 1
- 208000009956 adenocarcinoma Diseases 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 239000000611 antibody drug conjugate Substances 0.000 description 1
- 229940049595 antibody-drug conjugate Drugs 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 239000000074 antisense oligonucleotide Substances 0.000 description 1
- 238000012230 antisense oligonucleotides Methods 0.000 description 1
- 230000005775 apoptotic pathway Effects 0.000 description 1
- 108010078837 aspartyl-glutamyl-valyl-aspartyl-p-nitroanilide Proteins 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 230000003305 autocrine Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000004611 cancer cell death Effects 0.000 description 1
- 230000005880 cancer cell killing Effects 0.000 description 1
- 230000036952 cancer formation Effects 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000011097 chromatography purification Methods 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000011284 combination treatment Methods 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 229940127089 cytotoxic agent Drugs 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000003413 degradative effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 1
- 230000003828 downregulation Effects 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 229960001433 erlotinib Drugs 0.000 description 1
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 description 1
- DEFVIWRASFVYLL-UHFFFAOYSA-N ethylene glycol bis(2-aminoethyl)tetraacetic acid Chemical compound OC(=O)CN(CC(O)=O)CCOCCOCCN(CC(O)=O)CC(O)=O DEFVIWRASFVYLL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 210000002950 fibroblast Anatomy 0.000 description 1
- 102000052178 fibroblast growth factor receptor activity proteins Human genes 0.000 description 1
- 238000001943 fluorescence-activated cell sorting Methods 0.000 description 1
- 108020001507 fusion proteins Proteins 0.000 description 1
- 102000037865 fusion proteins Human genes 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 229960002584 gefitinib Drugs 0.000 description 1
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical compound C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 description 1
- 229960003180 glutathione Drugs 0.000 description 1
- 229940022353 herceptin Drugs 0.000 description 1
- 102000051793 human LSP1 Human genes 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229960003685 imatinib mesylate Drugs 0.000 description 1
- YLMAHDNUQAMNNX-UHFFFAOYSA-N imatinib methanesulfonate Chemical compound CS(O)(=O)=O.C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 YLMAHDNUQAMNNX-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001361 intraarterial administration Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 206010073095 invasive ductal breast carcinoma Diseases 0.000 description 1
- 201000010985 invasive ductal carcinoma Diseases 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 101150042836 mcl gene Proteins 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 239000002773 nucleotide Substances 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- 229940127084 other anti-cancer agent Drugs 0.000 description 1
- 229960001592 paclitaxel Drugs 0.000 description 1
- 230000003076 paracrine Effects 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000011340 peptidyl-tyrosine autophosphorylation Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 230000023603 positive regulation of transcription initiation, DNA-dependent Effects 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000001686 pro-survival effect Effects 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 108010008361 protein phosphatase 5 Proteins 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- 238000000163 radioactive labelling Methods 0.000 description 1
- 108700015182 recombinant rCAS Proteins 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 231100000004 severe toxicity Toxicity 0.000 description 1
- 238000009097 single-agent therapy Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 229960003787 sorafenib Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 102000009076 src-Family Kinases Human genes 0.000 description 1
- 108010087686 src-Family Kinases Proteins 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229960004072 thrombin Drugs 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- 238000010361 transduction Methods 0.000 description 1
- 230000026683 transduction Effects 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- 230000001875 tumorinhibitory effect Effects 0.000 description 1
- 229940094060 tykerb Drugs 0.000 description 1
- 150000003668 tyrosines Chemical class 0.000 description 1
- WQAJKOXBERTWBK-UHFFFAOYSA-N verdine Natural products CC1CNC2C(C1)OC3(CCC4C5CCC6(O)CC(O)CC(O)C6(C)C5C(=O)C4=C3C)C2C WQAJKOXBERTWBK-UHFFFAOYSA-N 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/32—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against translation products of oncogenes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
- C12N15/1135—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against oncogenes or tumor suppressor genes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
- C12N15/1137—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y603/00—Ligases forming carbon-nitrogen bonds (6.3)
- C12Y603/02—Acid—amino-acid ligases (peptide synthases)(6.3.2)
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/5011—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing antineoplastic activity
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/10—Type of nucleic acid
- C12N2310/14—Type of nucleic acid interfering N.A.
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/50—Physical structure
- C12N2310/53—Physical structure partially self-complementary or closed
- C12N2310/531—Stem-loop; Hairpin
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/52—Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
Definitions
- tumorigenesis is driven by activated tyrosine kinases that promote pro-survival/anti ⁇ apoptotic signaling. n these tumors, targeted kinase inhibition triggers apoptosis and tumor regression.
- acquired resistance to these inhibitors is a significant clinical problem. This resistance often results from mutations in the tyrosine kinase itself (e.g., imaiinib-resistance stemming from mutation of Bcr-Abl in chronic myelogenous .leukemias), but tills is not always the case.
- HER2 kinase Overexpression of HER2 kinase in 20-30% of breast cancers is associated with poor clinical outcomes.
- HER2-directed therapeutics have been approved or are in clinical trials, including trastuzuraab (Herceptin),. a monoclonal antibody directed against the extraceliuiar domain of HER2 kinase and Iapatinib (Tykerb), a small molecule able to inhibit HER2 and EGFR kinase activities.
- trastuzuraab Herceptin
- Tykerb Iapatinib
- a breast cancer patient undergoes Iapatinib treatment after progressing on trastuzumab.
- the anti-tumor effects of Iapatinib mono- therapy are generally short-lived, with cancer cells developing resistance to this drag over time.
- apoptotie inhibitors whose expression levels are specifically upregulated in lapatinib resistant cells, including X-iinked inhibitor of apoptosis protein (XIAP), and Mcl-l, an anti-apoptotic Bcl-2 family member (seen in iapatinib-resistant colon cancer cells).
- XIAP X-iinked inhibitor of apoptosis protein
- Mcl-l an anti-apoptotic Bcl-2 family member (seen in iapatinib-resistant colon cancer cells).
- cancers that may be treated using the methods described herein include those thai are or may become resistant to treatment with tyrosine kinase inhibitors or have elevated levels of Mcl-l or PP5 or decreased levels of Huwel or CAS, regardless of p53 status (mutant or wild-type).
- methods of treating a subject with a cancer having resistance to an inhibitor of tyrosine kinase activity by administering an inhibitor of tyrosine kinase activity and an inhibitor of E3 ubiquitin Hgase MDM2 to the subject are provided.
- methods of treating a subject with a cancer lacking wi ld-type p53 include administering an MDM2 inhibitor in an effective amount to a subject with cancer lacking wild-type p53 to treat the cancer.
- methods of treating a subject with a cancer having cells comprising increased levels of MDM2, Mcl-l or PP5 or decreased levels of CAS or Huwel are provided.
- the methods include administering an MDM2 inhibitor In an effective amount to the subject to treat the cancer.
- the metliods include coiiiaciing ceils with increased levels of Mcl- ⁇ or PP5 or decreased levels of CAS or Huwel as compared to a control cell with an agent and deiermlning the level of at least one of Mcl-l, PP5, CAS or Huwel in the cancer cell after contact with the agent.
- Agents capable of decreasing the level of Mcl-l or PP5 or increasing the level of CAS or Huwel in the cells after contact with the agent as compared to the level in a control untreated cell are candidate inhibitors of MDM2 and may be effective cancer therapeutics,
- methods of developing a treatment plan for an individual with cancer are provided.
- the methods include obtaining a sample comprising cancer cells from a subject and assaying the cells to determine the level of at least one of p53, MDM2, Mcl ⁇ l, PP5. CAS or Huwel in the cancer cells as compared to the level in control cells.
- a MD 2 inhibitor is administered to the subject if the cancer cells lack wild-type p53, have increased levels of
- MDM2 Mci-1 or PP5 or have decreased levels of CAS or Huwel as compared to control cells.
- Figure 1 is a photograph of a Western blot showing the level of p53 (top band) and actin (bottom band) expression in the cell lines used in the study. Three of the four cell lines have wild-type p53.
- Figure 2 is a set of graphs showing the percentage of cells undergoing apoptotic cell death for each of the four cell lines and their matched resistant cell line in the presence or absence of lapatinib and/or an MDM2 inhibitor, ⁇ -21 , as measured by FACS analysis for Annexin V. Results are expressed as mean / ⁇ SEM of Annexm V positive ceils.
- Graph A shows the results for BT474 and rBT474.
- Graph B shows the results tor SK.BR3 and rSKBR.3.
- Graph C shows the results for AU565 and rAU565.
- Graph D shows the results for SUM! 0 and rSUM190.
- Figure 3 is a set of photographs showing that Mcl-1 is stabilized in lapatinib-resistant cells.
- Figure 3A is a photomicrograph of lapatinib-sensitive and resistant BT474 cells (BT474 and rBT474, respectively) treated with 1 ⁇ lapatinib for 48 hours.
- Figure 3B is a set of immunoblots showing the levels of HER2 and phospho-HER2. in untreated cells and cells treated with lapatinib. Ceils were treated with or without lapatinib (1 ⁇ ) for 24 hours in the presence of the caspase inhibitor z-VAD (50 ⁇ ). The cells were harvested and cell, lysates were immunobiotted using antibodies against phospho ⁇ H£R2 (Y877) and total HER2.
- Figure 3C is an immunobiot for phospho-A T (T308) and total ART.
- BT474 and rBT474 cells were treated with 1 ⁇ lapatinib in the presence of 50 uM z-VAD. At the indicated time points, the cells were harvested and immunobiotted.
- Figure 3D is an immunobiot for phospho- Eril 2(T202/Y204) and total Erkl/2.
- BT474 and rBT474 cells were treated with l ⁇ lapatinib in the presence of 50 ⁇ z-VAD. At the indicated time points, the cells were harvested and immunobiotted.
- Figure 3E is an immunobiot for Mcl-1, Bim, and Actin.
- BT474 and rBT474 cells left or SKBR3 and rS B 3 cells (right) were treated with ! ⁇ lapatinib. The ceils were harvested at the indicated time points and immunoblotted.
- Figure 3F is an autoradiograph showing the ",5 [S
- Figure 3G is an autograph showing the 3i [S] ⁇ labeled Mcl-1 to monitor Mcl-1 stability over time, The ⁇ [Sj-iabeled Mcl-1 was incubated in lysates prepared from rBT474 cells treated with or without 1 ⁇ lapatinib.
- Figure 3H is an immunoblot for HA. S BR3 or rS B 3 cells were co-transfected with FLAG-Mcl-1 and HA- Ubiquitin (Ub). Cells were treated with l ⁇ lapatinib for 24 hours in the presence of z-VAD.
- FIG. 4 is a photograph of a Western blot for cytochrome c and actin in cytosolic lysates lacking mitochondria.
- BT474 and rBT474 cells were treated with 1 ⁇ lapatinib or without any drug for 24 hours.
- the rBT474 ceils prevent mitochondrial cytochrome c release in response to treatment with lapatinib.
- Figure 5 is an autoradiograph showing the stability of 3 [S]-labeled Mcl-1 in rBT474 cell lysates alter the cells were treated with or without 1 ⁇ lapatinib and 5 uM ubiquitin aldehyde (UB-Aldehyde) and incubated for 30 minutes,
- Figure 6 is a photograph of an immunoblot for Apaf-1 , Hsp90p or actin in ceil lysates of
- Figure 7 is a set of photographs and graphs showing PP5 stability and post-cytochrome c protection in !apatinib-resistant cells.
- Figure 7A is an immunoblot for caspase-9 (cleaved and non-cleaved) and cleaved caspase-3 (C9 and C3, respectively) showing rBT474 cells cultured in the absence or presence of 1 ⁇ lapatinib for one week, as compared to BT474 cells which were rnalntained without lapatinib. Cytosolic lysates prepared from BT474 or rBT474 were incubated with 1 raM dATP and various amounts of cytochrome c (CC).
- caspase-9 cleaved and non-cleaved
- C9 and C3 cleaved caspase-3
- Figure 7B is a set of graphs showing Caspase 3 activity in the indicated cell lysates over time. Caspase-3 activity was assayed by measuring cleavage of DEVD-pNA following incubation of the cell lysates with 1 mM dATP and various concentrations of cytochrome c.
- Figure 7C is an autoradiograph of """P and an imrriunoblot showing the percentage of the protein phosphorylated. In the presence of [ ⁇ - j2 P]ATP, recombinant His-tagged HSP90p proteins (wild type and the indicated mutants) on nickel heads were incubated with the HSP90P-iargeted kinase casein kinase 2.
- Figure 7D is an autoradio graph and corresponding immunoblot showing BT474 or rBT474 cells after being cultured in the absence or presence of I ⁇ lapatinib for 24 hours in the presence of z-VAD. Recombinant His-tagged HSP90P protein on nickel beads was incubated with the cell iysates in the presence of Py- j2 P]ATP.
- Figure 7E is an immunoblot for phospho-Hsp90P (Ser226) and total HSP9 p at various time points. BT474 or rBT474 cells were treated with 1 ⁇ lapatinib for the indicated amount of time.
- Figure 7F is a set of graphs showing FACS analysis for the phosphorylation status of Msp90p (Ser255).
- BT474 or rBT474 cells cultured in the presence of 1 ⁇ lapatinib for 24 hours were fixed with formaldehyde and incubated with phospho-Hsp90P (Ser255) antibody followed by an AIexa488-conjugated secondary antibody.
- Figure 7G is an immunoblot for PP5 and actia at the indicated time points.
- BT474 and rBT474 (left) or AU565 and rAU565 cells (right) were treated with 1 ⁇ lapatinib.
- Figure 7H is an autoradiograph of immunopredpiiated FLAG-PP5 using an anti-FLAG agarose.
- BT474 or rBT474 cells were transfected with FLAG-PP5 and subsequently labeled by the addition of J ⁇ [S]-Met. Cells were cultured in the presence of lapatinib and harvested at various time points after addition of lapatinib.
- Figure 71 is an immunoblot for HA or PP5 after immunoprecipitation using anti- FLAG agarose.
- BT474 or rBT474 cells were co-transfected with FLAG-PP5 and HA-Ub. Cells were cultured in the presence or absence of 1 ⁇ lapatinib for 24 hours. Ceils were lian'ested after treatment with ⁇ MGI32 for 8 hours (* IgG heavy chain).
- Figure 8 is a set of graphs showing FACS analysis for phosphorylation of ⁇ 90 ⁇ in MEFs derived from wild-type (PPS " "1" ) or PP5 deficient (FP5 '! ) mice after incubation with either a phospho ⁇ S226 or a phospho ⁇ S255 ⁇ $ ⁇ 90 ⁇ antibody followed by an Alexa488 conjugated secondary antibody.
- Figure 9 is an autoradiograph (top) for ubiquitinylated PP5 or a photograph of an immunoblot (bottom) for Huwe! showing biochemical purification of the PP5-targeted E3 ligase.
- Cell-free Iysates (SI 00) prepared from S BR3 cells were fractionated over a Q- sepharose column.
- Flow-through (FTQ) as well as bound proteins e!uting at 100, 250, 500, 750, and .1000 mM NaCl (Q10, Q25, Q50, Q75, and Q1.00, respectively) were collected and dialyzed overnight Ubiquity!
- tion of PP5 was reconstituted in vitro by incubating 35 S-methionine labeled PP5 (3 ⁇ ) with, each Q-sepharose fraction (25 ⁇ ) supplemented with 1.5 ng ⁇ El, 10 ng/ul
- Figure 10 is a set of photographs showing that Huwel is a PP5 ubiquitin Hgase.
- Figure 10A is an immunoblot for HA or PP5 after immunoprecipitation with HA.
- BT474 cells were transfected with empty vector or HA -tagged Huwel encoding residues 2473-4374 or the full- length protein and harvested after 24 hours.
- Figure 10B is an immunoblot for Huwel .
- BT474 cells were transfected with GFP- or Huwel -specific siRNA (100 nM) and harvested after 72 hours.
- Figure IOC is an immunoblot for PP5, Mcl-i, and Actin.
- FIG. 10D is an immunoblot for PP5 IJbiquitylation of PP5 was reconstituted in vitro by incubating recombinant PP5 protein with El, UbcH7 (E2), ubiquitin (lib), and recombinant Huwel protein (wild type (wt) or Huwel (C/S)) in reaction buffer at37*C for 3 hours.
- Figure 10E is a set of immunobiots for PP5 and Huwel after immunoprecipitation with FLAG antibodies.
- BT474 or rBT474 ceils were transfected with FLAG-PP5 and the cells were treated with 1 ⁇ , ⁇ lapatinib in the presence of z-VAD for 24 hours. Cells were harvested after treatment with 30 ⁇ MG132 for 8 hours (* IgG heavy chain).
- Figure 7F is an immunoblot for Apaf-1 and caspase-9. Cell lysates prepared from ⁇ 474 or rBT474 cells were incubated with or without 1 mM dATP and 10 ng ⁇ cytochrome c, After incubation (30 rain), lysates were subjected to gel filtration (Superdex 200 column). Shown by asterisks is thai a portion of Apaf-1 in the lapatinib-treaied resistant cell lysate formed higher- order oligomers In response to cytochrome c.
- Figure 11 is a set of photographs of immunobiots showing CAS degradation in lapatinib- resistant ceils.
- Figure 1 i A is an immunoblot for CAS and Actin.
- BT474 and rBT474 left or AU565 and rAU565 cells (right) cultured in the absence of lapatinib for one week were treated with 1 ⁇ lapatinib and the cells were harvested at various time points.
- Figure ⁇ is an immmunoblot for CAS and Actin.
- rBT474 cells were maintained in the presence of 1 ⁇ lapatinib and the cells were harvested at various time points following removal of lapatinib.
- Figure HC is an immunoblot for FLAG and actin
- BT474 and rBT474 cells were transiently transfected with FLAG-tagged CAS and subsequently treated with 50 pg/ml cycloheximide (CHX) and 1 ⁇ lapatinib and the celis were harvested at various time points
- Figure 1 I D is an immunoblot using HA to analyze ubiquitination of CAS.
- BT474 and rBT474 left or SKBR3 and rS B 3 cells (right) were co-transfected with FLAG-CAS and HA-Ub, Cells were treated with 1 ⁇ lapatinib for 24 hours in the presence of z-VAD, After treatment with 10 ⁇ MG 132 for 8 hours, cells were harvested and FLAG-CAS was retrieved by immunoprecipitation.
- Figure I IE is an immunoblot for FLAG-tagged proteins retrieved by imimrnoprecipitation and association with MDM2.
- Figure 1 I F is an immunoblot for CAs after Immunoprecipitation for FLAG.
- B I299 cells were transfected. with empty vector, FLAG-CA8 WI27A , or FLAG-CAS wild type. Cells were treated with 10 ⁇ MG132 for 3 hours.
- Figure 1 1 G is a set of immimoblots for MDM2, CAS and acti . SKBR3 cells were transfected with increasing amounts of MDM2. After 48 hours, cells were harvested and immunoblotted (* non-specific band).
- Figure i lH is an immunoblot for CAS, Ubiquitylation of CAS was reconstituted in vitro by incubating recombinant CAS protein with EI, UbcH ' 5 (£2), ubiquitin (Ub), and recombinant MDM2 protein (wild type (wt) or a eaialytlcally inactive mutant (C/A)) in reaction buffer incubated at 37°C for 3 hours and analyzed by immunoblotting for CAS.
- Figure 1 11 is an immunoblot for MDM2 or CAs after immunoprecipitation with FLAG.
- BT474 and rBT474 cells were transfected with FLAG-CAS.
- Figure 12 A is a schematic diagram of CAS/CSE1L protein sequence. The M.DM2 binding motif is highlighted.
- Figure 12B is a schematic diagram of Huwel protein showing the MDM2 binding region,
- Figure 13 is a set of immunoblots showing MDM2 -mediated ubiquitylation and degradation of Huwel in lapatinib-resistant cells.
- Figure 13 A. is a set of immunoblots for Huwel. MDM2, and Actin. Cells treated with 1 ⁇ lapatinib were harvested at various time points and immunoblotted. MDM2 shows greater stability in the resistant cell lines in the presence of lapatinib.
- Figure 13B is an immunoblot for HA and actin. BT474 and rBT474 cells were transiently transfected with HA-tagged Huwel and subsequently treated with 50 pg/ml cyeloheximide (CHX) and 1 ⁇ lapatinib.
- CHX pg/ml cyeloheximide
- Figure 13C is an immunoblot for Huwel and DM2. Immunoprecipitation was carried out using HI 299 cell iysates and anti-Huwel antibody (or control IgG).
- Figure 1.3D is an immunoblot for HA or MDM2 after immunoprecipitation with HA. BT474 cells were transfected with HA-tagged Huwel encoding the full-length protein, residues 1 -2474, or residues 2473-4374.
- Figure 13E is a set of immunoblots for Huwel or MDM2 after immunoprecipitation with HA. HI 299 cells were transfected with empty vector, HA-Huwel , or HA-Huwel wild type.
- Figure 13 F is an immimoblot for Huwel and Actin.
- FIG. 13G is an immimoblot for Huwel, MDM2. and actin. SUM 190 cells were transfected with Scrambled or MDM2-specific siR A (100 nM) and harvested after 72 hours.
- Figure 13 H is an immunobiot for Huwel. Ubiquitylation of Huwel was reconstituted in vitro by incubating recombinant Huwel protein (Huwel 1"2474 ) with El, UbeH5 (E2), ubiquitin ( lib), and recombinant MDM2 protein in reaction buffer at 37°C for 3 hours.
- Figure 131 is a set of immunoblots for HA and actin.
- rBT474 cells were transfected with scrambled or MDM2-- specific siRNA (50 nM), Twenty-four hours later, the ceils were replated and further transfected with. HA-tagged Huwel (wild type), Forty-eight hours after siRNA transfection, the cells were treated with 1 ⁇ lapatinib. After 24 hours of lapatinib treatment, 50 ,u.g/mi cyeloheximide (CHX) was added to the culture medium and cells were harvested at various time points for immunofaiotting.
- CHX ,u.g/mi cyeloheximide
- Figure 14 shows that MDM2 inhibition can reverse lapatinib resistance.
- Figure 14A is an immunoblot and associated graph, The immimoblot shows that the siRNA treatment was effective and the graph shows the MDM2 inhibitor can increase apoptosis in response to treatment with lapatinib.
- rBT474 cells were transfected with scrambled or MDM2 ⁇ specific siRNA (20 nM). Forty-eight hours after siRNA transfection, cells were treated with 1 ⁇ lapatinib for 48 hours, and cells were harvested and subjected to Annexin V staining. The percentage of Annexin V-positive ceils was analyzed by FACS. Results are expressed as a mean percentage ⁇ SEM and analyzed by t-test (* ⁇ 0.05).
- Figure 14B is an immunoblot showing reduction in MDM2 by the shRNAs and a graph showing the effectiveness of shRNA targeting MDM2 to reduce tumor volume in a mouse.
- rBT474 cells stably expressing control or MDM2- specific shRNA (#1 or #2) were injected into the mammary fat pad of female nude mice.
- the oral administration of lapatinib 100 mg/kg, twice daily by oral gavage
- results are expressed as a mean percentage ⁇ SEM.
- the statistical difference in tumor volume was analyzed by one-way ANOVA (P-0.000) followed by pairwise comparisons using the Bonferroni correction for multiple comparisons.
- Figure 14C is a set of immunoblots for MDM2, H.uwel and aciin. HI 299 ceils were transfected with HA-Huwel (C/S). Twenty-four hours post-transfection, cells were treated with 10 ⁇ Nutih 3a for 6 hours. HA-Huwel (C/S) was retrieved by immunoprecipltation and association of MDM2 was analyzed by mimunoblotting.
- Figure 14D is a set of immunoblots for Huwel , CAS, DM2, PPS, Mel-1 , and Actin.
- FIG. 14E is a set of graphs comparing the effectiveness of treatment with an MDM2 .nhibitor,mitlin-3 a, alone or in combination with lapatinib to treat a tumor in a mouse.
- BT474 and r.BT474 cells were injected into the mammary fad pad of each mouse.
- mice When tumors developed to a size of 200 mm " ', the mice were randomly assigned to receive vehicle, lapatinib (100 mg kg), Nutlin-3 (100 mg/kg), or Lapatinib + Nutlin-3 and treated twice daily by oral gavage. Results are expressed as a mean percentage ⁇ SEM. The statistical difference in tumor volume was analyzed by one-way ANOVA (p-0.003 and P-0.000 for BT474 and rBT474 xenografts, respectively) followed by pairwise comparisons using the Bonferroni correction for multiple comparisons.
- rAU565 cells stably expressing control or p53-specific shRNA were treated with DMSO or 10 ⁇ Nutlin-3a in the presence of absence of 1 ⁇ lapatinib for 48 hours. Percentage of apoptotie cell death was measured by FACS analysis using Annexin V, Results are expressed as a mean percentage ⁇ SEM of Annexin V-positive cells (*P ⁇ 0.05 by t-test).
- Figure 14G is a model for coordinate control of multiple apoptotie regulators by the MDM2 and Huwel .
- Figure 15 is a set of graphs similar to those presented above in Figure ME but using AU565 and rAU565 as the cells.
- Figure 16 is a set of immunoblots for total SRC and phosphor-SRC (Y416) in the cell lines used in this study. Cells were treated with DM SO or lapatinib (1 ⁇ ) for 24 hours in the presence of caspase inhibitor z ⁇ VAD.
- Figure 17 is a set of immunoblots for MDM2, pY41 s SRC and actin in two of the resistant ceil lines after pre-treatment with DMSO or 1 ⁇ dasatinib lor 24 hours followed by treatment of the cells with 1 u lapatinib and harvested at the indicated time points.
- DM2 inhibitors are known and were developed for use in cancer patients with wild-type p53. See e.g., U.S. Patent Nos. 7,834,016 and 7,759,383 and U.S. Patent Publication Nos. US2010/0216770; US2011/0130418, US2010/0168163 and US2010/0240637, each of which is incorporated herein by reference in its entirety. As demonstrated in the Examples, a new and unexpected mechanism of action for MD 2 inhibitors is disclosed herein and establishes the usefulness of DM2 inhibitors to treat distinct cancers, i .e. those lacking wild-type p53 or comprising a p53 mutation, and to be used in distinct combinations with oilier chemotherapeutic agents than previously contemplated.
- the Examples reveal an unexpected signaling network in which the MDM2 ubiquitin ligase could trans-ubiqiutyiate another E3 ligase, Huwel , to control its substrates, cl-1 and protein phosphatase 5 (PP5), an indirect apoptosome regulator. As shown in the Examples, Huwel transmits a signal from MDM2 to control apoptotic events both upstream and
- MDM2 could ubiquitylate CAS, the requisite ATP exchange factor for Apaf-1.
- MDSVi2-dependent pathways were subverted in lapatinib- resistant cells, and inhibition of MDM2 could rectify all apoptotic defects, overcoming drug resistance, regardless of cellular p53 status.
- Resistance to tyrosine kinase inhibitors, like lapatinib. often develops during treatment of cancer and although we have currently only demonstrated that this pathway is responsible for lapatinib resistance, it is likely a general resistance pathway and experiments are ongoing to demonstrate as much.
- treatment of a subject (a mouse) with cancer or a cancer cell with both lapatinib and an M DM2 inhibitor blocked the development of resistance and resulted in tumor regression or cancer cell death in either lapatinib resistant or sensitive cancer cells.
- the cancer is generally a cancer with a mutation in a tyrosine kinase, overexpression of a tyrosine kinase or uncontrolled activity of a tyrosine kinase by autocrine paracrine stimulation such thai the tyrosine kinase is more active than that of a control non-cancerous cell derived from the same or similar tissue as the cancer.
- the cancer may be a breast, lung, colon, gastric cancer or a glioma or leukemia.
- the cancer does not have a wild-type p53.
- the cancer has wild- type p53.
- the subjects include mammals, including domesticated animals, mice, rats and hum ns.
- Treating cancer includes, but is not limited to, reducing the number of cancer cells or the size of a tumor in the subject, reducing progression of a cancer to a more aggressive form, reducing proliferation of cancer cells or reducing the speed of tumor growth, killing of cancer cells, inducing apopiosis of cancer cells, reducing metastasis of cancer cells or reducing the likelihood of recurrence of a cancer in a subject.
- Treating a subject as used herein refers to any type of treatment that imparts a benefit to a subject afflicted with a disease or at risk of developing the disease, including impro vement in the condition of the subject (e.g., in one or more symptoms), delay in the progression of the disease, delay the onset of symptoms or slowing the progression of symptoms, etc.
- the cancer is a cancer overexpressing a tyrosine kinase or with, a mutation in a tyrosine kinase, such as HER2 or EGFR, and the cancer is resistant or likely to develop resistance to at least one inhibitor of tyrosine kinase activity.
- Resistance to an inhibitor of tyrosine kinase activity includes cancers and ceils comprising a mutation in the targeted tyrosine kinase or a related gene such that the cells are able to survive and or continue to grow in the presence of an inhibitor of the tyrosine kinase and also includes cancers or cells that are at risk of developing resistance to the inhibitors.
- the subject may be treated by administering the inhibitor of tyrosine kinase activity and administering an inhibitor of E3 ubiquitin Hgase, MDM2 (also called HDM2 in humans) to the subject.
- tyrosine kinases whose overactivity is associated with cancer include, but are not limited to EGFR, IGFR, PDGFR, FGFR, SRC, mTOR, ABL, FAX, and Janus kinase.
- the tyrosine kinase is a member of the HER or EGFR class of tyrosine kinases which includes EGFR, HER 2, HERS and HER4.
- the kinase is HER2 or EGFR.
- the cancer may also be resistant to treatment with an antibody specific for the tyrosine kinase.
- a HER2+ cancer may be resistant to treatment with trastuzumab.
- the inhibitor of tyrosine kinase activity may be any inhibitor that targets the activity of the tyrosine kinase.
- the inhibitors include small molecule tyrosine kinase inhibitors, antibodies, antibody-drug conjugates, antisense oligonucleotides, aptamers, peptides and peptide mimetics.
- Tyrosine kinase inhibitors include fiavoperidol, imatinib mesylate, erlotinib, gefitinib, dasatinib, Iapatinib, iapatinib ditos late, sorafenib, suniiinib, sunitmib maieate, temsiroiimus.
- the inhibitor is an inhibitor of ATP binding to the tyrosine kinase.
- the inhibitor of tyrosine kinase activity is Iapatinib.
- the inhibitor is an inhibitor of HER.2 such as trastuzumab.
- Other anti-cancer agents may also be used in combination with M DM2 inhibitors.
- the cells of the cancer being treated using the methods described herein may have increased MDM2, Mcl-l or PP5 or decreased Huwel or CAS as compared to control cells.
- the cells may only have this differential expression after contact with a tyrosine kinase inhibitor.
- the control cells may be cancer cells that are not resistant to treatment with an inhibitor of tyrosine kinase activity, such as Iapatinib, or non-cancerous ceils of the same cel.! type as the cancer cells, i.e. derived from the same tissue.
- the cancer ceils may only demonstrate the increased Mcl-l or PP5 or decreased Huwel or CAS when in the presence of the inhibitor of tyrosine kinase activity.
- the transcription levels of Mcl-l or PP5 or Huwel or CAS may be unchanged and the difference in levels of these markers in the cancer ceil is due to increased stability of the proteins or decreased degradation of the proteins.
- the levels of these proteins in cancer cells may be measured via methods available to those of skill in the art.
- the level of MDM2, Mcl-l, PP5, CAS or Huwel in the cells may be determined by methods including but not limited to Western blot, FACs analysis, imraunoprecipitation, radioiabeling, fluorescence labeling or other antibody based-detection assay.
- the level of these markers being determined is the protein level, not the ieve! of transcription.
- the stability of these proteins may also be determined rather than the level at any point in time. Stability of the proteins may be assessed using methods available to those skilled in the art, such as pulse-chase experiments followed by one of the above methods to separate the proteins from the cell.
- the MDM2 inhibitors include any inhibitors capable of blocking the interaction of MD 2 with a target molecule such as p53, Huwel and CAS, capable of inhibiting the ubiquitin iigase activity of MDM2, an inhibitor of MDM2 transcription or translation or a molecule capable of decreasing the half-life of MDM2 in the cell.
- the M.DM2 inhibitors may be small molecule pharmaceuticals, RNA-based molecules such as an shRNA or giRNA, an aptamer or antibody or any other class of inhibitory molecule.
- RNA-based molecules such as an shRNA or giRNA, an aptamer or antibody or any other class of inhibitory molecule.
- Methods of treating a subject with a. cancer overexpressing or having a mutation in a tyrosine kinase, such as HER2, by administering an inhibitor of tyrosine kinase activity and administering an inhibitor of MDM2 to the subject are provided.
- the inhibitor of tyrosine kinase activity and the inhibitor of MDM2 may be administered in any order, at the same time or as part, of a unitary composition.
- the two inhibitors may be administered such thai one inhibitor is administered before the other with a difference in administration time of 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 16 hours, 20 hours, 1 day, 2 days, 4 days, 7 days, 2 weeks, 4 weeks or more, in another embodiment, methods of treating a subject with a cancer in which at least some of the cells of the cancer lack wild-type p53 or have a p53 mutation and optionally comprise a mutation in or overexpression of a tyrosine kinase are provided.
- an MDM2 inhibitor is administered in an effective amount to treat a subject with a cancer lacking wild-type p53 or having a p53 mutation.
- the p53 status of the cancer may be determined prior to treating the subject with the MDM2 inhibitor.
- control ceils may be cancerous cells sensitive to tyrosine kinase inhibitors, such as lapatinib or non-cancerous cells, in these methods, an MDM2 inhibitor is administered to a subject in an amount effective to treat the cancer.
- an inhibitor of tyrosine kinase activity may also be administered to the subject to treat the cancer.
- the two inhibitors may be provided separately, at the same time or even within the same composition.
- the protein expression levels of at least one of MDM2, cH , PP5, Huwel or CAS may be determined prior to initiating treatment. Those of skill in the art will appreciate that several methods exist to assess the level of each of these proteins within the cell, some of which are discussed aove.
- an effective amount or a therapeutically effective amount as used herein means the amount of a compound that, when administered to a subject for treating a state, disorder or condition is sufficient to effect a treatment (as defined above).
- the therapeutically effective amount will vary depending on the compound, formulation or composition, the disease and its severity and the age, weight, physical condition and responsiveness of the subject to be treated.
- compositions comprising the inhibitors described herein may be administered by any means known to those skilled in the art, including, but. not limited to, oral, topical, intranasal, intraperitoneal, parenteral, intravenous, intraarterial, intramuscular, sublingual, or subcutaneous.
- the compositions may be formulated as an ingestabie, injectable, topical or suppository formulation.
- the compositions may also be delivered with in a liposomal or time-release vehicle.
- Administration of the compositions to a subj ect in accordance with the invention appears to exhibit beneficial effects in a dose-dependent manner. Thus, within broad limits, administration of larger quantities of the compositions is expected to achieve increased beneficial biological effects than administration of a smaller amount. Moreover, efficacy is also contemplated at dosages below the level at which severe toxicity is seen.
- the specific dosage administered in any given case will be adjusted in. accordance with the compositions being administered, the disease to be treated or inhibited, the condition of the subject, and other relevant medical factors that may modify the activity of the compositions or the response of the subject, as is well known by those skilled in the art.
- the specific dose for a particular subject depends on age, body weight, general state of health, diet, the timing and mode of administration, the rate of excretion, medicaments used in combination and the severity of the particular disorder to which the therapy is applied. Dosages for a given patient can be determined using conventional considerations, e.g., by customary comparison of the differential activities of the compositions such as by means of an appropriate conventional pharmacological or prophylactic protocol.
- the maximal dosage for a subject is the highest dosage that does not cause undesirable or intolerable side effects,
- the number of variables in regard to an individual treatment regimen is large, and a considerable range of doses is expected.
- the route of administration will also impact the dosage requirements. It is anticipated thai dosages of the composition will reduce growth of the cancer by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90 or 100% compared to a cancer left untreated. It is specifically contemplated that pharmaceutical preparations and compositions may palliate or alleviate symptoms of the disease without providing a cure, or, in some embodiments, may be used to cure the disease or disorder.
- Suitable effective dosage amounts for administering the compositions may be determined by those of skill in the art, but typically range from about 1 microgram to about 10.000 micrograms per kilogram of body weight weekly, al though they are typically about 1,000 micrograms or less per kilogram of body weight weekly. In some embodiments, the effective dosage amount ranges from about 10 to about 10,000 micrograms per kilogram of body weight weekly. In another embodiment, the effective dosage amount ranges from about 50 to about 5,000 micrograms per kilogram of body weight weekly, in another embodiment, the effective dosage amoun t ranges from about 75 to about 1,000 micrograms per kilogram of body weight weekly.
- the effective dosage amounts described herein refer to total amounts administered, that is, if more than one composi tion is administered, the effective dosage amounts correspond to the total amount administered.
- compositions can be administered as a single dose or as divided doses.
- the composition may be administered two or more times separated by 4 hours, 6 hours, 8 hours, 12 hours, a day, two days, three days, four days, one week, two weeks, or by three or more weeks.
- Methods of screening for MDM2 inhibitors capable of being used as cancer therapeutic agents are also provided herein.
- the methods include contacting a cancer cell with an agent and determining the protein expression level of at least one of MDM2, el-1, PP5, CAS or Huwe! in the contacted cancer cell.
- the cancer cells have higher than normal levels of MDM2, Mel-l or PP5 or lower than normal levels of CAS or Huwel as compared to control cells, in particular after the cells are contacted with an inhibitor of tyrosine kinase activity, such as lapatinib.
- the cancer cells may overexpress or comprise a mutation in a tyrosine kinase such as HER2 or EGFR and may be resistant to lapatinib or other tyrosine kinase inhibitors,
- An agent capable of decreasing the levels of MDM2, Mc!-I or PP5 or of increasing the level of Huwel or CAS in the cells after contact with the agent as compared to the level in a control cell is a candidate MDM2 inhibitor.
- Control cells may be cancer cells that are not resistant to the tyrosine kinase inhibitor or non-cancerous cells.
- Untreated cells are cancer cells prior to treatment with the agent. In the methods of screening, the cells may be contacted with lapatinib prior to or at the same time as the cells are contacted with the agent.
- Cells may he contacted with the agent directly or indirectly in vivo, in vitro, or ex vivo.
- Contacting encompasses administration to a ceil, tissue, mammal, patient, or human. Further, contacting a ceil includes adding an agent to a cell culture.
- Other suitable methods may include introducing or administering an agent to a cell, tissue, mammal or patient using appropriate procedures and routes of administration as defined above.
- the level of MDM2, Mcl-i, PP5, CAS or Huwel in the cells may be determined by any method known to those of skill in. the art, including but not limited to Western blot, FACs analysis, imrnunoprecipitation. radio labeling, fluorescence labeling.
- the level of these markers being determined is the protein level, not the level of transcription.
- the stability of these proteins may also be determined rather than the level at any point in time.
- the treatment plans are meant to avoid allowing the cancer to become resistant to tyrosine kinase inhibitors and/or to allow treatment of a cancer that is resistant to treatment with a tyrosine kinase inhibitor.
- the methods include obtaining a sample comprising cancer cells from a subject and assaying the cells to determine the level of at least one of MDM2, Mcl-1, PP5, CAS or Huwel in the cancer cells as compared to the level in control cells.
- the control cells are non-cancerous cells from a similar or from the same tissue or cell-type.
- the treatment plan for the subject includes administration of a MD 2 inhibitor to the subject.
- the level of more than one of MDM2, Mcl-i , PP5, CAS and Huwel are assayed.
- the level of all of MDM2, Mcl-i, PP5, CAS and Huwel are assayed.
- the treatment plan may also include administering a tyrosine kinase inhibitor to the subject.
- rBT474, rS BR2, rSUM190 5 and rAU565 did not die in response to lapatlnib treatment (Fig. 2 and Fig. 3 A).
- IDC invasive ductal carcinoma
- inf - inflammatory carcinoma PR - progesterone receptor
- Mcl-l protein was equally ubiquitylated in S BR3 and rS BR3 cells (Fig. 3H)
- Lapatinib treatment enhanced Mcl-l ubiquityiation in SKBR.3 cells; but diminished Mcl-l. ubiquityiation in rSKBR3 cells (Fig. 3H).
- HSP90P binds directl to the Apaf-1 CARD domain to block caspase-9 recruitment.
- HSP90p hypophosphorylation at residues Ser226 and Ser.255 led to tighter interaction between Apaf-1 and ⁇ 8 ⁇ 90 ⁇ .
- HSP9Gp phosphorylation at both Ser226 and Ser255 was also markedly- decreased in iapati b-treated resistant cells compared to sensitive cells (Figs. 7C-7F),
- Httwel is an E3 Hgase responsible for the degradation of both Mcl-1 and PP5
- PP5 stabilization could result from a defect in an E3 ligase activity responsible for PP5 ubiquitylation in lapatinib-resistant ceils.
- E3 ligase activity responsible for PP5 ubiquitylation in lapatinib-resistant ceils.
- Cytosolic lysates prepared from SK.BR.3 cells were fractionated on a Q-sepharose column and ubquityiation of ⁇ [S]-PP5 by each fraction (supplemented with El, E2, AT and ubiquitin) was analyzed by SDS-PAGE, Most of the PP5- ubiquitinating activity was eiuted with 500 niM NaCI (Fig.
- HSP90p hypophosphorylation downstream of PP5 stabilization might explain apopiosoroe inhibition in the lapatinib-treated resistant cells, but when vve resolved cell lysates by gel filtration, we saw not onl a failure to recruit caspase-9 to Apaf-1 (which could be explained if ⁇ 5 ⁇ 90 ⁇ blocked caspase 9 recruitment), but also a failure of the majority of Apaf-1 to oiigomerize (Fig. 10F).
- cytochrome c to resistant cell lysates, we detected a small percentage of Apaf-I and caspase-9 in very large (1.000-1400 kD) fractions. previously described as iucon'eciiy assembled inactive complexes (Fig. 10F; shown by asterisks). Kim, Jiang, Du, & Wang, Mol. Cell 30, 239-247 (2008).
- cytochrome c induces Apaf-1 to form non-functional aggregates.
- PFIAP1, HSP70, and CAS also known as CSE1L or Exportin-2
- CAS protein levels were markedly decreased in resistant cells compared with parental cells, most notably in the presence of lapatinib (see Fig. 1 1 A).
- CAS protein levels declined over time following lapatinib addition to resistant cells, but. lapatinib removal allowed return of CAS to levels comparable to the parental cells (Figs. 1 A and 1.
- sequence alignment includes p53, p73, p63, CAS (H. sapiens), and CAS homologs (CSE1) from D. melanogaster and 5. cerevisiae (bottom).
- MDM2 is a H «wel-directed E3 ligase
- Huwel protein half-life became significantly shorter, compared to that in BT474 cells (Fig. 13B).
- Huwel and MDM2 are p53-targeting E3 iigases (and DM2 expression can also be modulated in a feedback loop by p53-induced transcription)
- three of the four cell lines (BT474, SKBR3, and SUM 190) express mutant p53 (Table I and Fig. 1), suggesting that the observed changes in Huwel and MDM2 protein levels are independent of the transcriptional activity of p53.
- .Huwel contained a putative MDM2 ⁇ bisding motif at residues 1 198-1205 (Fig. 12B and Table 3): the interaction of these two E3 iigases was confirmed by immunoprecipitation of endogenous proteins (Fig. 13C).
- the sequence alignment includes human p53, Huwel homologs from If. sapiens, M. musculus, B. taurus, D. rerio, T. castaneum., and TO 1 from S. cerevisiae. i»Mt) 0is of MDM2 m® reverse lapatinib resistance
- a hydrophobic pocket in the MDM2 N-terminus binds the transactivation domain of p53. If MDM2 bound Huwel in the same fashion, the MDM2 antagonist Nutlin-3a, that disrupts the p53-MDM2 complex, might also be expected to interfere with Huwel -MDM2 binding. Vassiiev, et al. Science 303, 844-848 (2004). To exclude the possibility that any effects of Nutlin-3a might be mediated by the p53-MDM2 interaction, we employed HI 299 cells. Catalytically inactive Huwel (Huwel (C/S)) bound to endogenous MDM2 and this binding was significantly reduced by Nutlin-3a (Fig. I 4C).
- Nutlh 3a also prevented lapatinib- induced degradation of Huwel (Fig, 14D), suggesting that Nutlin-3a stabilizes Huwel by disrupting Huwel -MDM2 binding. Consequently, Nutlin ⁇ 3a also suppressed lapatmib-mduced upregulation of Mcl-1 and PP5 (Fig. 14D). MDM2 and CAS binding, as well as CAS degradation, was also significantly inhibited by Nutlin-3a (Fig. 14D).
- mice bearing BT474 or rBT474 xenografts were randomly assigned to vehicle, lapatinib.
- Nutlin-3 (a racemic mixture of the enantiomers Nutlin-3 a and Nutlin-3 b), or lapatinib and NutHn-3.
- Lapatinib alone or a combination of lapatinib and Nutlin-3 significantly suppressed growth of BT474-derived tumors, whereas Nutlin-3 alone only modestly inhibited tumor growth (Fig. 1 E).
- Neither lapatinib nor Nutlin-3 inhibited rBT474-derivecl tumor growth as a single agent (Fig. 14E).
- BT474, SKBR3, and AU565 cells were obtained from ATCC.
- SUM 190 cells were obtained from Asterand, Inc.
- Ail cell lines were cultured in RPMI medium containing 10% fetal bovine serum (FBS).
- Lapatinib-resistant cells (rBT474, rS BR3, rAU565, and rSUM ' 190) were established as previously described' 4 . Cobleigh, et at J. Clin. Oncol 17, 2639-2648 (1999). Lapatinib-resistant cells were grown in the presence of 1 ⁇ lapatinib unless otherwise stated.
- Lapatinib and dasatinib were purchased from LC Laboratories. G132 and z-VAD were purchased from Enzo Life Sciences, El, E2, ubiquitin, and Ub- Aldehyde were purchased from Boston Biochem. Nutlm ⁇ 3a and racemate Nutliri-3 were synthesized and purified at the Duke Small Molecule Synthesis Facility, Nutlin ⁇ 3a and N'utlin-3 were also purchased from Cayman Chemical. Cycloheximide and purified cytochrome c was purchased from Sigma.
- anti-HER2 antibody anti-phospho-HER2 (Y877) antibody, anti ⁇ phospho-HER2 (Y1221/Y 1222) antibody, anti-Akt. antibody, anti-phospho-Akt (T308) antibody, anti-caspase-9 antibody, atiti-cleaved easpase-3 antibody, anti-Bcl2 antibody, anti-Bci-xL antibody, anti-ERKl 2 antibody, anti-phospho-ERK.1/2 antibody (T202/Y204), anti- phospho-SRC (Y 16) antibody, anti-SRC antibody, anti-FLAG antibody (Ceil Signaling), ami- Apaf-1 antibody (2E12: Enzo Life Sceinces).
- anti-HSP90p antibody (5E12), anti-MD 2 antibody (2A1 G: Calbiochem), anti-HSP90p antibody (Millipore), ami-pb.ospho-H5P90$ antibody (S226), anti-phospiio-HSP90p antibody (S255) (Abeam), anti-Actm antibody, anti- MDM2 antibody (SMP14), anti-HA antibody (F-7) (Santa Cruz Biotechnology) , , anti-FLAG M2 antibody (Sigma), anti-Bim antibody, anti-cleaved caspase-3 antibody, anti-Mcl-l antibody, anti- PP5 antibody.
- anti-CAS antibody anti-HSP70 antibody (BD Transduction Laboratories), anti- Mcl-1 antibody (BioLegend), anti-Huwel antibody (Bethyi Laboratories), anti- ⁇ antibody (ProSci).
- HA-Huwei constructs in pCMV were generous gifts from Kristian Helm (University of Copenhagen).
- Hu el in pENTR was generous gifts from Jeanette Gowen Cook (University of North Carolina, Chapel Hill).
- Huwel in pENTR was recombined with the destination vector pDESTIO (Invitrogen) for production of His-taggcd protein.
- FLAG-PP5 in pcD A3 and FLAG-CAS in p3XFLAG-CMV10 were kind gifts from Xiao-Fan Wang ⁇ Duke University) and Carol Prives (Columbia University), respectively.
- CAS was also cloned into pENTR and, subsequently, into pDESTIO for bacu!oviral protein expression.
- PP5 was cloned into pGEX-KG for production of GST fusion protein.
- Mcl-1 with the N-terminal FLAG tag was generated from human Mcl-I (a gift from Jeffrey Rathmeil, Duke University) and cloned into pcDNA3.
- the plasmids encoding GST- MDM2, GST-MDM ' 2 C464A , and HA-ubtquitin were obtained from Addgene (Addgene plasmids 1 1 92, 1 1493, and 17608). Fang, et al. J. Biol.
- MDM2 was also cloned into pcDNA3 with an N-terminal FLAG tag. All point mutations (BA-Huwel 1"2474 , HA «Huwel WJ202A , His ⁇ Huwel C434!S , FLAG- CAS* 127' ) were generated with the QuikChange mutagenesis kit (Stratagene),
- siRNA oligos targeting Huwel or GFP were previously described. Hall et at. Mot. Biol. Cell 18, 3340-3350 (2007).
- an shRNA construct in the ientivirai vector pLKO. l- puro (sh D 2 #1) was purchased from Open Biosystems (sense: 5' ⁇ GATTCCAGAGAGTCATGTGTT-S'; SEQ ID NO: 15).
- An additional MD 2 shRNA construct (sh.
- DM2 2 sense: S ' -TTGAAGTTATTAAAGT ' CTGTT-S 5 ; SEQ ID NO: 16) and control shRNA construct (sense: 5 '-CTGTGCTGTAGGTGA AACTGT-3 ' ; SEQ ID NO: 1.7) were also created in the vector pL OJ -puro according to Addgene's pLK.0, 1 protocol (http://www.addgene.org/plko). Stable knockdown of p53 was performed using the vector shp53-pL O. i-puro (Addgene plasmid 191 19), Godar et al. Cell 134, 62-73 (2008). Mouse xenograft experiments
- mice Six week-old female nude mice were purchased from NCI Frederic. Xenograft tumors were produced by injection into the mammary fat pad with ceils (10 x 10 6 ), Tumor volumes were calculated every 3-4 days based on caliper measurements of the short (a) and long (b) tumor diameters (volume - a2b/2). Lapatinib and Nutlin-3 were formulated in vehicle (water with 0.5% Hydroxypropyl methylceilulose and 0, 1% Tween). Mice were dosed orally with vehicle alone, lapatinib ( 100 mg/kg), Nutlin-3 (100 mg/kg), or combination of both twice daily by gavage.
- Cells were transiently transfected with the indicated plasmid by FuGene6 (Roche) based on manufacturer's instruction. Cells were harvested and lysed with co-IP buffer (10 mM. HEPES [pH 7.4], 150 mM KCI, 0.5% NP-40, 1 mM phenylroethyls lfonyl fluoride, 5 ⁇ ⁇ leupeptin, and 5 pg/ml aprotinin). Cell Iysate was incubated with anti-FLAG M2 agarose (Sigma) or anti- AH affinity matrix (Roche) at 4°C for 2-3 hours. The bead pellet was washed three times with co-IP buffer and then incubated with SDS- sample buffer.
- co-IP buffer 10 mM. HEPES [pH 7.4], 150 mM KCI, 0.5% NP-40, 1 mM phenylroethyls lfonyl fluoride, 5 ⁇
- Cell iysates for apoptotic assays were prepared as described previously using buffer A (20 mM HEPES [pH 7.4], 10 mM KCI, 1 .5 m MgCJ2, 1 mM EDTA, 1 mM EGTA, 1 mM dithiothreitol, 1 mM phenyimethylsulfbnyl fluoride, 5 ,ug/mi leupeptin, and 5 ⁇ / ⁇ aprotinin). Kurokawa, Zhao, Reya, & Korabluth. MoL Cell. Biol, 28, 5494-5506 (2008).
- Cell Iysate (10 jig .ul) was incubated in the presence or absence of 1 mM dATP and various concentrations of cytochrome c at 37°C for 30 min, and subjected to gel filtration, caspase assays, or western blotting.
- Coiorimetric caspase assays were performed by incubating cell Iysate (3 ⁇ ) in 90 ⁇ DEVDase buffer (50 mM HEPES [pH 7.5], lOOmMNaCl, 0.1% CHAPS, I OmMDTT, 1 mMEDTA, 10% glycerol) containing the peptide substrate, Ac-DEVD-pNA (200 mM final concentration; BIOMOL Research Labs). Reactions were incubated at 37°C for 30 min. Absorbance of the coiorimetric product was measured at 405 am using a Bio-Rad microplate reader. In vitro uhiquitylalion assays
- Recombinant human PP5 and MDM2 proteins were bacteriaily expressed with a GST tag. After purification by glutathione sepharose 4B (GE Healthcare), the GST tag was cleaved off by thrombin. Recombinant human Huwel wild type, C4341 S mutant (Huwel C/S), and Huwel S"2 M were expressed in the bacuiovirus system and purified from Sf9 cells.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- General Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Analytical Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Cell Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Food Science & Technology (AREA)
- Mycology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Abstract
Methods of treating subjects with cancer and screening for MDM2 inhibitors that may be effective cancer therapeutics are provided herein. The cancers that may be treated using SV1DM2 inhibitors using the methods described herein include those that are or may become resistant to treatment with tyrosine kinase inhibitors. Methods of treating subjects with cancers that have, or develop in response to treatment with tyrosine kinase inhibitors, elevated levels of MDM2, Mcl- 1 or PP5 or decreased levels of Huwel or CAS using MDM2 inhibitors are provided herein. The MDM2 inhibitors may be effective at treating these cancers alone or in combination with a tyrosine kinase inhibitor regardless of p53 states (mutant or wild-type) of the cancer.
Description
METHODS OF IDENTIFYING AND USING M DM2 INHIBITORS
CROSS-REFERENCE TO RELATED APPLICATIONS This patent application claims the benefit of priority of United States Provisional Patent Application No, 61/567,944, filed December 7, 201 1 , which is incorporated herein by reference in its entirety.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH
This invention was made with United States government support awarded by the National institutes of Health grant number ROl CA102707 and K99 CA 140948. The United States may have certain rights in this invention.
SEQUENCE LISTING A Sequence Listing accompanies this application and is incorporated herein by reference in its entirety. The Sequence Listing was filed with the application as a text file.
INTRODUCTION
In a subset of cancers, tumorigenesis is driven by activated tyrosine kinases that promote pro-survival/anti~apoptotic signaling. n these tumors, targeted kinase inhibition triggers apoptosis and tumor regression. However, acquired resistance to these inhibitors is a significant clinical problem. This resistance often results from mutations in the tyrosine kinase itself (e.g., imaiinib-resistance stemming from mutation of Bcr-Abl in chronic myelogenous .leukemias), but tills is not always the case.
Overexpression of HER2 kinase in 20-30% of breast cancers is associated with poor clinical outcomes. Several HER2-directed therapeutics have been approved or are in clinical trials, including trastuzuraab (Herceptin),. a monoclonal antibody directed against the extraceliuiar domain of HER2 kinase and Iapatinib (Tykerb), a small molecule able to inhibit HER2 and EGFR kinase activities. Typically, a breast cancer patient undergoes Iapatinib treatment after progressing on trastuzumab. However, the anti-tumor effects of Iapatinib mono- therapy are generally short-lived, with cancer cells developing resistance to this drag over time.
Mechanisms underlying acquired lapatinib resistance are poorly understood particularly because mutations within HER2 itself are not typically seen in acquired lapatinib resistance. Several studies have identified apoptotie inhibitors whose expression levels are specifically upregulated in lapatinib resistant cells, including X-iinked inhibitor of apoptosis protein (XIAP), and Mcl-l, an anti-apoptotic Bcl-2 family member (seen in iapatinib-resistant colon cancer cells).
SUMMARY
Provided herein are methods of treating subj ects with cancer and screening for MDM2 inhibitors that may be effective cancer therapeutics. The cancers that may be treated using the methods described herein include those thai are or may become resistant to treatment with tyrosine kinase inhibitors or have elevated levels of Mcl-l or PP5 or decreased levels of Huwel or CAS, regardless of p53 status (mutant or wild-type).
In one aspect, methods of treating a subject with a cancer having resistance to an inhibitor of tyrosine kinase activity by administering an inhibitor of tyrosine kinase activity and an inhibitor of E3 ubiquitin Hgase MDM2 to the subject are provided.
In another aspect, methods of treating a subject with a cancer lacking wi ld-type p53 are provided. The methods include administering an MDM2 inhibitor in an effective amount to a subject with cancer lacking wild-type p53 to treat the cancer.
In yet another aspect, methods of treating a subject with a cancer having cells comprising increased levels of MDM2, Mcl-l or PP5 or decreased levels of CAS or Huwel are provided. The methods include administering an MDM2 inhibitor In an effective amount to the subject to treat the cancer.
In a still further aspect, methods of screening for MDM2 inhibitors are pro vided. The metliods include coiiiaciing ceils with increased levels of Mcl-ί or PP5 or decreased levels of CAS or Huwel as compared to a control cell with an agent and deiermlning the level of at least one of Mcl-l, PP5, CAS or Huwel in the cancer cell after contact with the agent. Agents capable of decreasing the level of Mcl-l or PP5 or increasing the level of CAS or Huwel in the cells after contact with the agent as compared to the level in a control untreated cell are candidate inhibitors of MDM2 and may be effective cancer therapeutics,
In yet another aspect, methods of developing a treatment plan for an individual with cancer are provided. The methods include obtaining a sample comprising cancer cells from a subject and assaying the cells to determine the level of at least one of p53, MDM2, Mcl~l, PP5. CAS or Huwel in the cancer cells as compared to the level in control cells. A MD 2 inhibitor is administered to the subject if the cancer cells lack wild-type p53, have increased levels of
MDM2, Mci-1 or PP5 or have decreased levels of CAS or Huwel as compared to control cells.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a photograph of a Western blot showing the level of p53 (top band) and actin (bottom band) expression in the cell lines used in the study. Three of the four cell lines have wild-type p53.
Figure 2 is a set of graphs showing the percentage of cells undergoing apoptotic cell death for each of the four cell lines and their matched resistant cell line in the presence or absence of lapatinib and/or an MDM2 inhibitor, ΜΪ-21 , as measured by FACS analysis for Annexin V. Results are expressed as mean /~ SEM of Annexm V positive ceils. Graph A shows the results for BT474 and rBT474. Graph B shows the results tor SK.BR3 and rSKBR.3. Graph C shows the results for AU565 and rAU565. Graph D shows the results for SUM! 0 and rSUM190.
Figure 3 is a set of photographs showing that Mcl-1 is stabilized in lapatinib-resistant cells. Figure 3A is a photomicrograph of lapatinib-sensitive and resistant BT474 cells (BT474 and rBT474, respectively) treated with 1 μΜ lapatinib for 48 hours. Figure 3B is a set of immunoblots showing the levels of HER2 and phospho-HER2. in untreated cells and cells treated with lapatinib. Ceils were treated with or without lapatinib (1 μΜ) for 24 hours in the presence of the caspase inhibitor z-VAD (50 μΜ). The cells were harvested and cell, lysates were immunobiotted using antibodies against phospho~H£R2 (Y877) and total HER2. Figure 3C is an immunobiot for phospho-A T (T308) and total ART. BT474 and rBT474 cells were treated with 1 μΜ lapatinib in the presence of 50 uM z-VAD. At the indicated time points, the cells were harvested and immunobiotted. Figure 3D is an immunobiot for phospho- Eril 2(T202/Y204) and total Erkl/2. BT474 and rBT474 cells were treated with l μΜ lapatinib in the presence of 50 μΜ z-VAD. At the indicated time points, the cells were harvested and immunobiotted. Figure 3E is an immunobiot for Mcl-1, Bim, and Actin. BT474 and rBT474
cells (left) or SKBR3 and rS B 3 cells (right) were treated with ! μΜ lapatinib. The ceils were harvested at the indicated time points and immunoblotted. Figure 3F is an autoradiograph showing the ",5[S| radioactivity in lysates containing 35[S]-Mcl-1 at the indicated time points. "[S]-labeled Mcl-1 protein was incubated in cell-free lysates prepared from BT474 and rBT474 cells (top) or SF BR3 and rS BR.3 cells (bottom). Figure 3G is an autograph showing the 3i[S]~ labeled Mcl-1 to monitor Mcl-1 stability over time, The ^[Sj-iabeled Mcl-1 was incubated in lysates prepared from rBT474 cells treated with or without 1 μΜ lapatinib. Figure 3H is an immunoblot for HA. S BR3 or rS B 3 cells were co-transfected with FLAG-Mcl-1 and HA- Ubiquitin (Ub). Cells were treated with l μΜ lapatinib for 24 hours in the presence of z-VAD. Cells were harvested after treatment with ΙΟμΜ MG132 for 4 hours, FLAG-Mcl-1 was retrieved by immunoprecipitation using anti-flag agarose, and Mcl-1 ubiquitylaiio.il was analyzed by iinmunoblotiing for HA ('* non-specific band, ** IgG heavy chain).
Figure 4 is a photograph of a Western blot for cytochrome c and actin in cytosolic lysates lacking mitochondria. BT474 and rBT474 cells were treated with 1 μΜ lapatinib or without any drug for 24 hours. The rBT474 ceils prevent mitochondrial cytochrome c release in response to treatment with lapatinib.
Figure 5 is an autoradiograph showing the stability of 3 [S]-labeled Mcl-1 in rBT474 cell lysates alter the cells were treated with or without 1 μΜ lapatinib and 5 uM ubiquitin aldehyde (UB-Aldehyde) and incubated for 30 minutes,
Figure 6 is a photograph of an immunoblot for Apaf-1 , Hsp90p or actin in ceil lysates of
BT474 and rBT474 cells after treatment with no drug o 1 μΜ lapatinib for 24 hours in the presence of the caspase inhibitor z-VAD (50 μΜ) showing expression was not altered.
Figure 7 is a set of photographs and graphs showing PP5 stability and post-cytochrome c protection in !apatinib-resistant cells. Figure 7A is an immunoblot for caspase-9 (cleaved and non-cleaved) and cleaved caspase-3 (C9 and C3, respectively) showing rBT474 cells cultured in the absence or presence of 1 μΜ lapatinib for one week, as compared to BT474 cells which were rnalntained without lapatinib. Cytosolic lysates prepared from BT474 or rBT474 were incubated with 1 raM dATP and various amounts of cytochrome c (CC). Figure 7B is a set of graphs showing Caspase 3 activity in the indicated cell lysates over time. Caspase-3 activity was assayed by measuring cleavage of DEVD-pNA following incubation of the cell lysates with 1 mM dATP and various concentrations of cytochrome c. Figure 7C is an autoradiograph of """P
and an imrriunoblot showing the percentage of the protein phosphorylated. In the presence of [γ- j2P]ATP, recombinant His-tagged HSP90p proteins (wild type and the indicated mutants) on nickel heads were incubated with the HSP90P-iargeted kinase casein kinase 2. Figure 7D is an autoradio graph and corresponding immunoblot showing BT474 or rBT474 cells after being cultured in the absence or presence of I μΜ lapatinib for 24 hours in the presence of z-VAD. Recombinant His-tagged HSP90P protein on nickel beads was incubated with the cell iysates in the presence of Py-j2P]ATP. Figure 7E is an immunoblot for phospho-Hsp90P (Ser226) and total HSP9 p at various time points. BT474 or rBT474 cells were treated with 1 μΜ lapatinib for the indicated amount of time. Figure 7F is a set of graphs showing FACS analysis for the phosphorylation status of Msp90p (Ser255). BT474 or rBT474 cells cultured in the presence of 1 μΜ lapatinib for 24 hours were fixed with formaldehyde and incubated with phospho-Hsp90P (Ser255) antibody followed by an AIexa488-conjugated secondary antibody. Figure 7G is an immunoblot for PP5 and actia at the indicated time points. BT474 and rBT474 (left) or AU565 and rAU565 cells (right) were treated with 1 μΜ lapatinib. Figure 7H is an autoradiograph of immunopredpiiated FLAG-PP5 using an anti-FLAG agarose. BT474 or rBT474 cells were transfected with FLAG-PP5 and subsequently labeled by the addition of J~ [S]-Met. Cells were cultured in the presence of lapatinib and harvested at various time points after addition of lapatinib. Figure 71 is an immunoblot for HA or PP5 after immunoprecipitation using anti- FLAG agarose. BT474 or rBT474 cells were co-transfected with FLAG-PP5 and HA-Ub. Cells were cultured in the presence or absence of 1 μΜ lapatinib for 24 hours. Ceils were lian'ested after treatment with ΙΟμΜ MGI32 for 8 hours (* IgG heavy chain).
Figure 8 is a set of graphs showing FACS analysis for phosphorylation of Ηκρ90β in MEFs derived from wild-type (PPS ""1") or PP5 deficient (FP5'!") mice after incubation with either a phospho~S226 or a phospho~S255 Η$ρ90β antibody followed by an Alexa488 conjugated secondary antibody.
Figure 9 is an autoradiograph (top) for ubiquitinylated PP5 or a photograph of an immunoblot (bottom) for Huwe! showing biochemical purification of the PP5-targeted E3 ligase. Cell-free Iysates (SI 00) prepared from S BR3 cells were fractionated over a Q- sepharose column. Flow-through (FTQ) as well as bound proteins e!uting at 100, 250, 500, 750, and .1000 mM NaCl (Q10, Q25, Q50, Q75, and Q1.00, respectively) were collected and dialyzed overnight Ubiquity! tion of PP5 was reconstituted in vitro by incubating 35S-methionine labeled
PP5 (3 μΐ) with, each Q-sepharose fraction (25 μΐ) supplemented with 1.5 ng μΙ El, 10 ng/ul
UbcH7, 2.5 μ μΐ ubiquitin (lib),, and an A TP-regenerating system in reaction buffer (50 aiM Tris. ρίϊ 7.6, 5 mM MgCb, 5 mMATP, 10 siM creatine phosphate, 3,5 U/ml creatine kinase; total reaction volume 40 μί). The reactions were incubated for 2 hours at 37°C prior to analysis.
Figure 10 is a set of photographs showing that Huwel is a PP5 ubiquitin Hgase. Figure 10A is an immunoblot for HA or PP5 after immunoprecipitation with HA. BT474 cells were transfected with empty vector or HA -tagged Huwel encoding residues 2473-4374 or the full- length protein and harvested after 24 hours. Figure 10B is an immunoblot for Huwel . PP5, Mcll and actin. BT474 cells were transfected with GFP- or Huwel -specific siRNA (100 nM) and harvested after 72 hours. Figure IOC is an immunoblot for PP5, Mcl-i, and Actin. BT474 cells were transfected with increasing amounts of wild type Huwel or its catalyticaliy inactive mutant (Huwel (C/S)} and the cells were harvested after 48 hours. Figure 10D is an immunoblot for PP5 IJbiquitylation of PP5 was reconstituted in vitro by incubating recombinant PP5 protein with El, UbcH7 (E2), ubiquitin (lib), and recombinant Huwel protein (wild type (wt) or Huwel (C/S)) in reaction buffer at37*C for 3 hours. Figure 10E is a set of immunobiots for PP5 and Huwel after immunoprecipitation with FLAG antibodies. BT474 or rBT474 ceils were transfected with FLAG-PP5 and the cells were treated with 1 μ,Μ lapatinib in the presence of z-VAD for 24 hours. Cells were harvested after treatment with 30 μΜ MG132 for 8 hours (* IgG heavy chain). Figure 7F is an immunoblot for Apaf-1 and caspase-9. Cell lysates prepared from ΒΪ474 or rBT474 cells were incubated with or without 1 mM dATP and 10 ng μΐ cytochrome c, After incubation (30 rain), lysates were subjected to gel filtration (Superdex 200 column). Shown by asterisks is thai a portion of Apaf-1 in the lapatinib-treaied resistant cell lysate formed higher- order oligomers In response to cytochrome c.
Figure 11 is a set of photographs of immunobiots showing CAS degradation in lapatinib- resistant ceils. Figure 1 i A is an immunoblot for CAS and Actin. BT474 and rBT474 (left) or AU565 and rAU565 cells (right) cultured in the absence of lapatinib for one week were treated with 1 μΜ lapatinib and the cells were harvested at various time points. Figure ΠΒ is an immmunoblot for CAS and Actin. rBT474 cells were maintained in the presence of 1 μΜ lapatinib and the cells were harvested at various time points following removal of lapatinib. Figure HC is an immunoblot for FLAG and actin, BT474 and rBT474 cells were transiently transfected with FLAG-tagged CAS and subsequently treated with 50 pg/ml cycloheximide
(CHX) and 1 μΜ lapatinib and the celis were harvested at various time points, Figure 1 I D is an immunoblot using HA to analyze ubiquitination of CAS. BT474 and rBT474 (left) or SKBR3 and rS B 3 cells (right) were co-transfected with FLAG-CAS and HA-Ub, Cells were treated with 1 μΜ lapatinib for 24 hours in the presence of z-VAD, After treatment with 10 μΜ MG 132 for 8 hours, cells were harvested and FLAG-CAS was retrieved by immunoprecipitation. Figure I IE is an immunoblot for FLAG-tagged proteins retrieved by imimrnoprecipitation and association with MDM2. i l 299 ceils were transfected with empty vector, FLAG-CASWI27A, or FLAG-CAS wild type, Figure 1 I F is an immunoblot for CAs after Immunoprecipitation for FLAG. B I299 cells were transfected. with empty vector, FLAG-CA8WI27A, or FLAG-CAS wild type. Cells were treated with 10 μΜ MG132 for 3 hours. Figure 1 1 G is a set of immimoblots for MDM2, CAS and acti . SKBR3 cells were transfected with increasing amounts of MDM2. After 48 hours, cells were harvested and immunoblotted (* non-specific band). Figure i lH is an immunoblot for CAS, Ubiquitylation of CAS was reconstituted in vitro by incubating recombinant CAS protein with EI, UbcH'5 (£2), ubiquitin (Ub), and recombinant MDM2 protein (wild type (wt) or a eaialytlcally inactive mutant (C/A)) in reaction buffer incubated at 37°C for 3 hours and analyzed by immunoblotting for CAS. Figure 1 11 is an immunoblot for MDM2 or CAs after immunoprecipitation with FLAG. BT474 and rBT474 cells were transfected with FLAG-CAS. Cells were treated with l μΜ lapatinib for 24 hours in the presence of z-VAD. After treatment with 10 μ MG132 for 5 hours, FLAG-CAS was retrieved by immunoprecipitation and association of endogenous DM2 was analyzed by immunoblotting.
Figure 12 A is a schematic diagram of CAS/CSE1L protein sequence. The M.DM2 binding motif is highlighted. Figure 12B is a schematic diagram of Huwel protein showing the MDM2 binding region,
Figure 13 is a set of immunoblots showing MDM2 -mediated ubiquitylation and degradation of Huwel in lapatinib-resistant cells. Figure 13 A. is a set of immunoblots for Huwel. MDM2, and Actin. Cells treated with 1 μΜ lapatinib were harvested at various time points and immunoblotted. MDM2 shows greater stability in the resistant cell lines in the presence of lapatinib. Figure 13B is an immunoblot for HA and actin. BT474 and rBT474 cells were transiently transfected with HA-tagged Huwel and subsequently treated with 50 pg/ml cyeloheximide (CHX) and 1 Μ lapatinib. Figure 13C is an immunoblot for Huwel and DM2. Immunoprecipitation was carried out using HI 299 cell iysates and anti-Huwel antibody
(or control IgG). Figure 1.3D is an immunoblot for HA or MDM2 after immunoprecipitation with HA. BT474 cells were transfected with HA-tagged Huwel encoding the full-length protein, residues 1 -2474, or residues 2473-4374. Figure 13E is a set of immunoblots for Huwel or MDM2 after immunoprecipitation with HA. HI 299 cells were transfected with empty vector, HA-Huwel , or HA-Huwel wild type. Figure 13 F is an immimoblot for Huwel and Actin. BT474 cells were transfected with increasing amounts of MDM2 and harvested after 48 hours. Figure 13G is an immimoblot for Huwel, MDM2. and actin. SUM 190 cells were transfected with Scrambled or MDM2-specific siR A (100 nM) and harvested after 72 hours. Figure 13 H is an immunobiot for Huwel. Ubiquitylation of Huwel was reconstituted in vitro by incubating recombinant Huwel protein (Huwel 1"2474) with El, UbeH5 (E2), ubiquitin ( lib), and recombinant MDM2 protein in reaction buffer at 37°C for 3 hours. Figure 131 is a set of immunoblots for HA and actin. rBT474 cells were transfected with scrambled or MDM2-- specific siRNA (50 nM), Twenty-four hours later, the ceils were replated and further transfected with. HA-tagged Huwel (wild type), Forty-eight hours after siRNA transfection, the cells were treated with 1 μΜ lapatinib. After 24 hours of lapatinib treatment, 50 ,u.g/mi cyeloheximide (CHX) was added to the culture medium and cells were harvested at various time points for immunofaiotting.
Figure 14 shows that MDM2 inhibition can reverse lapatinib resistance. Figure 14A is an immunoblot and associated graph, The immimoblot shows that the siRNA treatment was effective and the graph shows the MDM2 inhibitor can increase apoptosis in response to treatment with lapatinib. rBT474 cells were transfected with scrambled or MDM2~specific siRNA (20 nM). Forty-eight hours after siRNA transfection, cells were treated with 1 μΜ lapatinib for 48 hours, and cells were harvested and subjected to Annexin V staining. The percentage of Annexin V-positive ceils was analyzed by FACS. Results are expressed as a mean percentage ± SEM and analyzed by t-test (*Ρ<0.05). Figure 14B is an immunoblot showing reduction in MDM2 by the shRNAs and a graph showing the effectiveness of shRNA targeting MDM2 to reduce tumor volume in a mouse. rBT474 cells stably expressing control or MDM2- specific shRNA (#1 or #2) were injected into the mammary fat pad of female nude mice. The oral administration of lapatinib (100 mg/kg, twice daily by oral gavage) began when the average tumor volume surpassed 300 mm3. Results are expressed as a mean percentage ± SEM. The statistical difference in tumor volume was analyzed by one-way ANOVA (P-0.000) followed by
pairwise comparisons using the Bonferroni correction for multiple comparisons. *P<0.05 between control and shMDM2#l , and between control and shMD 2#2. Figure 14C is a set of immunoblots for MDM2, H.uwel and aciin. HI 299 ceils were transfected with HA-Huwel (C/S). Twenty-four hours post-transfection, cells were treated with 10 μΜ Nutih 3a for 6 hours. HA-Huwel (C/S) was retrieved by immunoprecipltation and association of MDM2 was analyzed by mimunoblotting. Figure 14D is a set of immunoblots for Huwel , CAS, DM2, PPS, Mel-1 , and Actin. rS BRS cells were cultured in the presence or absence of l μΜ lapatinib for a week, and then treated with 10 μΜ Nutiin-3a in the presence of z-VAD. After 36 hours, cells were harvested and immunoblotted. Figure 14E is a set of graphs comparing the effectiveness of treatment with an MDM2 .nhibitor,mitlin-3 a, alone or in combination with lapatinib to treat a tumor in a mouse. BT474 and r.BT474 cells were injected into the mammary fad pad of each mouse. When tumors developed to a size of 200 mm"', the mice were randomly assigned to receive vehicle, lapatinib (100 mg kg), Nutlin-3 (100 mg/kg), or Lapatinib + Nutlin-3 and treated twice daily by oral gavage. Results are expressed as a mean percentage ± SEM. The statistical difference in tumor volume was analyzed by one-way ANOVA (p-0.003 and P-0.000 for BT474 and rBT474 xenografts, respectively) followed by pairwise comparisons using the Bonferroni correction for multiple comparisons. (Top) *P<0.05 between, control and lapatinib, and between control and japatinib+Nutlin-3, whereas the difference was not significant between control and Nutlin-3 in BT474 xenografts. (Bottom) */*<0.05 between conirol and !apatinib+Nuilin-3 whereas there was no significant difference between control, and Nutlin-3, and between control and lapatinib in rBT474 xenografts. Figure 14F is an immunobiot showing that the shRNA targeting p53 is effective and a graph showing the results of a FACS analysis for Annexin V. rAU565 cells stably expressing control or p53-specific shRNA were treated with DMSO or 10 μΜ Nutlin-3a in the presence of absence of 1 μΜ lapatinib for 48 hours. Percentage of apoptotie cell death was measured by FACS analysis using Annexin V, Results are expressed as a mean percentage ± SEM of Annexin V-positive cells (*P<0.05 by t-test). Figure 14G is a model for coordinate control of multiple apoptotie regulators by the MDM2 and Huwel . In sensitive cells, lapatinib promotes DM2 degradation, which leads to elevations in Huwel , This results in more PP5 and Mcl-1 degradation (loss of MDM2 also leads to less CAS degradation). In !apatmib-resistant ceils, DM2 promotes decreased CAS levels, decreased
Huwel levels and consequently increased. PP5 and Mel- 1. In aggregate, these changes render the cells resistant to lapatinib-induced apoptosis.
Figure 15 is a set of graphs similar to those presented above in Figure ME but using AU565 and rAU565 as the cells. (Top) *P<0.05 between control and lapatinib, between control and NutIin-3 and between control and lapatinib+Nutiin-3. (Bottom) *P<0.05 between control and lapatinib+Nutlin-3 whereas there was no significant difference between control and Nutli«~3, and between control and lapatinib.
Figure 16 is a set of immunoblots for total SRC and phosphor-SRC (Y416) in the cell lines used in this study. Cells were treated with DM SO or lapatinib (1 μΜ) for 24 hours in the presence of caspase inhibitor z~ VAD.
Figure 17 is a set of immunoblots for MDM2, pY41 s SRC and actin in two of the resistant ceil lines after pre-treatment with DMSO or 1 μΜ dasatinib lor 24 hours followed by treatment of the cells with 1 u lapatinib and harvested at the indicated time points. DETAILED DESCRIPTION
Methods of identifying or screening for MDM2 inhibitors and methods of treating subjects with cancer using MDM2 inhibitors, alone or in combination with other
chemotherapeutics, are provided herein. DM2 inhibitors are known and were developed for use in cancer patients with wild-type p53. See e.g., U.S. Patent Nos. 7,834,016 and 7,759,383 and U.S. Patent Publication Nos. US2010/0216770; US2011/0130418, US2010/0168163 and US2010/0240637, each of which is incorporated herein by reference in its entirety. As demonstrated in the Examples, a new and unexpected mechanism of action for MD 2 inhibitors is disclosed herein and establishes the usefulness of DM2 inhibitors to treat distinct cancers, i .e. those lacking wild-type p53 or comprising a p53 mutation, and to be used in distinct combinations with oilier chemotherapeutic agents than previously contemplated.
The Examples reveal an unexpected signaling network in which the MDM2 ubiquitin ligase could trans-ubiqiutyiate another E3 ligase, Huwel , to control its substrates, cl-1 and protein phosphatase 5 (PP5), an indirect apoptosome regulator. As shown in the Examples, Huwel transmits a signal from MDM2 to control apoptotic events both upstream and
downstream of mitochondria. Furthermore, MDM2 could ubiquitylate CAS, the requisite ATP exchange factor for Apaf-1. These MDSVi2-dependent pathways were subverted in lapatinib-
resistant cells, and inhibition of MDM2 could rectify all apoptotic defects, overcoming drug resistance, regardless of cellular p53 status. Resistance to tyrosine kinase inhibitors, like lapatinib., often develops during treatment of cancer and although we have currently only demonstrated that this pathway is responsible for lapatinib resistance, it is likely a general resistance pathway and experiments are ongoing to demonstrate as much. As demonstrated below, treatment of a subject (a mouse) with cancer or a cancer cell with both lapatinib and an M DM2 inhibitor blocked the development of resistance and resulted in tumor regression or cancer cell death in either lapatinib resistant or sensitive cancer cells.
Therefore provided herein are methods of treating subjects with cancer. The cancer is generally a cancer with a mutation in a tyrosine kinase, overexpression of a tyrosine kinase or uncontrolled activity of a tyrosine kinase by autocrine paracrine stimulation such thai the tyrosine kinase is more active than that of a control non-cancerous cell derived from the same or similar tissue as the cancer. The cancer may be a breast, lung, colon, gastric cancer or a glioma or leukemia. Suitably, the cancer does not have a wild-type p53. Suitably the cancer has wild- type p53. The subjects include mammals, including domesticated animals, mice, rats and hum ns.
Treating cancer includes, but is not limited to, reducing the number of cancer cells or the size of a tumor in the subject, reducing progression of a cancer to a more aggressive form, reducing proliferation of cancer cells or reducing the speed of tumor growth, killing of cancer cells, inducing apopiosis of cancer cells, reducing metastasis of cancer cells or reducing the likelihood of recurrence of a cancer in a subject. Treating a subject as used herein refers to any type of treatment that imparts a benefit to a subject afflicted with a disease or at risk of developing the disease, including impro vement in the condition of the subject (e.g., in one or more symptoms), delay in the progression of the disease, delay the onset of symptoms or slowing the progression of symptoms, etc.
In one embodiment, the cancer is a cancer overexpressing a tyrosine kinase or with, a mutation in a tyrosine kinase, such as HER2 or EGFR, and the cancer is resistant or likely to develop resistance to at least one inhibitor of tyrosine kinase activity. Resistance to an inhibitor of tyrosine kinase activity includes cancers and ceils comprising a mutation in the targeted tyrosine kinase or a related gene such that the cells are able to survive and or continue to grow in the presence of an inhibitor of the tyrosine kinase and also includes cancers or cells that are at
risk of developing resistance to the inhibitors. The subject may be treated by administering the inhibitor of tyrosine kinase activity and administering an inhibitor of E3 ubiquitin Hgase, MDM2 (also called HDM2 in humans) to the subject.
Cancers overexpressing or having mutations in tyrosine kinases are well known in the art, The cancers often have an overactive tyrosine kinase. For example, tyrosine kinases whose overactivity is associated with cancer include, but are not limited to EGFR, IGFR, PDGFR, FGFR, SRC, mTOR, ABL, FAX, and Janus kinase. Suitably, the tyrosine kinase is a member of the HER or EGFR class of tyrosine kinases which includes EGFR, HER 2, HERS and HER4.
Suitably, the kinase is HER2 or EGFR. The cancer may also be resistant to treatment with an antibody specific for the tyrosine kinase. For example, a HER2+ cancer may be resistant to treatment with trastuzumab.
The inhibitor of tyrosine kinase activity may be any inhibitor that targets the activity of the tyrosine kinase. The inhibitors include small molecule tyrosine kinase inhibitors, antibodies, antibody-drug conjugates, antisense oligonucleotides, aptamers, peptides and peptide mimetics. Tyrosine kinase inhibitors include fiavoperidol, imatinib mesylate, erlotinib, gefitinib, dasatinib, Iapatinib, iapatinib ditos late, sorafenib, suniiinib, sunitmib maieate, temsiroiimus. Suitably the inhibitor is an inhibitor of ATP binding to the tyrosine kinase. Suitably, the inhibitor of tyrosine kinase activity is Iapatinib. Suitably, the inhibitor is an inhibitor of HER.2 such as trastuzumab. Other anti-cancer agents may also be used in combination with M DM2 inhibitors.
The cells of the cancer being treated using the methods described herein may have increased MDM2, Mcl-l or PP5 or decreased Huwel or CAS as compared to control cells. The cells may only have this differential expression after contact with a tyrosine kinase inhibitor. The control cells may be cancer cells that are not resistant to treatment with an inhibitor of tyrosine kinase activity, such as Iapatinib, or non-cancerous ceils of the same cel.! type as the cancer cells, i.e. derived from the same tissue. The cancer ceils may only demonstrate the increased Mcl-l or PP5 or decreased Huwel or CAS when in the presence of the inhibitor of tyrosine kinase activity. The transcription levels of Mcl-l or PP5 or Huwel or CAS may be unchanged and the difference in levels of these markers in the cancer ceil is due to increased stability of the proteins or decreased degradation of the proteins.
The levels of these proteins in cancer cells may be measured via methods available to those of skill in the art. For example, the level of MDM2, Mcl-l, PP5, CAS or Huwel in the
cells may be determined by methods including but not limited to Western blot, FACs analysis, imraunoprecipitation, radioiabeling, fluorescence labeling or other antibody based-detection assay. The level of these markers being determined is the protein level, not the ieve! of transcription. The stability of these proteins may also be determined rather than the level at any point in time. Stability of the proteins may be assessed using methods available to those skilled in the art, such as pulse-chase experiments followed by one of the above methods to separate the proteins from the cell.
The MDM2 inhibitors include any inhibitors capable of blocking the interaction of MD 2 with a target molecule such as p53, Huwel and CAS, capable of inhibiting the ubiquitin iigase activity of MDM2, an inhibitor of MDM2 transcription or translation or a molecule capable of decreasing the half-life of MDM2 in the cell. The M.DM2 inhibitors may be small molecule pharmaceuticals, RNA-based molecules such as an shRNA or giRNA, an aptamer or antibody or any other class of inhibitory molecule. Several MDM2 inhibitors have bee previously described as noted above. Two small molecule inhibitors used in the Examples are nutlin~3a and MI-219, a spiro-oxindoie, A siRNA and an shRNA that target MDM2 were also found to be effective inhibitors in the Examples.
Methods of treating a subject with a. cancer overexpressing or having a mutation in a tyrosine kinase, such as HER2, by administering an inhibitor of tyrosine kinase activity and administering an inhibitor of MDM2 to the subject are provided. The inhibitor of tyrosine kinase activity and the inhibitor of MDM2 may be administered in any order, at the same time or as part, of a unitary composition. The two inhibitors may be administered such thai one inhibitor is administered before the other with a difference in administration time of 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 16 hours, 20 hours, 1 day, 2 days, 4 days, 7 days, 2 weeks, 4 weeks or more, in another embodiment, methods of treating a subject with a cancer in which at least some of the cells of the cancer lack wild-type p53 or have a p53 mutation and optionally comprise a mutation in or overexpression of a tyrosine kinase are provided. In these methods, an MDM2 inhibitor is administered in an effective amount to treat a subject with a cancer lacking wild-type p53 or having a p53 mutation. In these methods, the p53 status of the cancer may be determined prior to treating the subject with the MDM2 inhibitor.
In another embodiment, methods of treating subjects with cancers in which at least some of the cancer cells have increased levels of Mcl-1 or PP5 or decreased levels of CAS or Huwe l
as compared to the levels of these markers in control cells. As noted above, control ceils may be cancerous cells sensitive to tyrosine kinase inhibitors, such as lapatinib or non-cancerous cells, in these methods, an MDM2 inhibitor is administered to a subject in an amount effective to treat the cancer. In these methods, an inhibitor of tyrosine kinase activity may also be administered to the subject to treat the cancer. A noted above, the two inhibitors may be provided separately, at the same time or even within the same composition. The protein expression levels of at least one of MDM2, cH , PP5, Huwel or CAS may be determined prior to initiating treatment. Those of skill in the art will appreciate that several methods exist to assess the level of each of these proteins within the cell, some of which are discussed aove.
An effective amount or a therapeutically effective amount as used herein means the amount of a compound that, when administered to a subject for treating a state, disorder or condition is sufficient to effect a treatment (as defined above). The therapeutically effective amount will vary depending on the compound, formulation or composition, the disease and its severity and the age, weight, physical condition and responsiveness of the subject to be treated.
Compositions comprising the inhibitors described herein may be administered by any means known to those skilled in the art, including, but. not limited to, oral, topical, intranasal, intraperitoneal, parenteral, intravenous, intraarterial, intramuscular, sublingual, or subcutaneous. Thus the compositions may be formulated as an ingestabie, injectable, topical or suppository formulation. The compositions may also be delivered with in a liposomal or time-release vehicle. Administration of the compositions to a subj ect in accordance with the invention appears to exhibit beneficial effects in a dose-dependent manner. Thus, within broad limits, administration of larger quantities of the compositions is expected to achieve increased beneficial biological effects than administration of a smaller amount. Moreover, efficacy is also contemplated at dosages below the level at which severe toxicity is seen.
It will be appreciated that the specific dosage administered in any given case will be adjusted in. accordance with the compositions being administered, the disease to be treated or inhibited, the condition of the subject, and other relevant medical factors that may modify the activity of the compositions or the response of the subject, as is well known by those skilled in the art. For example, the specific dose for a particular subject, depends on age, body weight, general state of health, diet, the timing and mode of administration, the rate of excretion, medicaments used in combination and the severity of the particular disorder to which the therapy
is applied. Dosages for a given patient can be determined using conventional considerations, e.g., by customary comparison of the differential activities of the compositions such as by means of an appropriate conventional pharmacological or prophylactic protocol.
The maximal dosage for a subject is the highest dosage that does not cause undesirable or intolerable side effects, The number of variables in regard to an individual treatment regimen is large, and a considerable range of doses is expected. The route of administration will also impact the dosage requirements. It is anticipated thai dosages of the composition will reduce growth of the cancer by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90 or 100% compared to a cancer left untreated. It is specifically contemplated that pharmaceutical preparations and compositions may palliate or alleviate symptoms of the disease without providing a cure, or, in some embodiments, may be used to cure the disease or disorder.
Suitable effective dosage amounts for administering the compositions may be determined by those of skill in the art, but typically range from about 1 microgram to about 10.000 micrograms per kilogram of body weight weekly, al though they are typically about 1,000 micrograms or less per kilogram of body weight weekly. In some embodiments, the effective dosage amount ranges from about 10 to about 10,000 micrograms per kilogram of body weight weekly. In another embodiment, the effective dosage amount ranges from about 50 to about 5,000 micrograms per kilogram of body weight weekly, in another embodiment, the effective dosage amoun t ranges from about 75 to about 1,000 micrograms per kilogram of body weight weekly. The effective dosage amounts described herein refer to total amounts administered, that is, if more than one composi tion is administered, the effective dosage amounts correspond to the total amount administered. The compositions can be administered as a single dose or as divided doses. For example, the composition may be administered two or more times separated by 4 hours, 6 hours, 8 hours, 12 hours, a day, two days, three days, four days, one week, two weeks, or by three or more weeks.
Methods of screening for MDM2 inhibitors capable of being used as cancer therapeutic agents are also provided herein. The methods include contacting a cancer cell with an agent and determining the protein expression level of at least one of MDM2, el-1, PP5, CAS or Huwe! in the contacted cancer cell. The cancer cells have higher than normal levels of MDM2, Mel-l or PP5 or lower than normal levels of CAS or Huwel as compared to control cells, in particular after the cells are contacted with an inhibitor of tyrosine kinase activity, such as lapatinib.
Notably, the cancer cells may overexpress or comprise a mutation in a tyrosine kinase such as HER2 or EGFR and may be resistant to lapatinib or other tyrosine kinase inhibitors, An agent capable of decreasing the levels of MDM2, Mc!-I or PP5 or of increasing the level of Huwel or CAS in the cells after contact with the agent as compared to the level in a control cell is a candidate MDM2 inhibitor. Control cells may be cancer cells that are not resistant to the tyrosine kinase inhibitor or non-cancerous cells. Untreated cells are cancer cells prior to treatment with the agent. In the methods of screening, the cells may be contacted with lapatinib prior to or at the same time as the cells are contacted with the agent.
Cells may he contacted with the agent directly or indirectly in vivo, in vitro, or ex vivo. Contacting encompasses administration to a ceil, tissue, mammal, patient, or human. Further, contacting a ceil includes adding an agent to a cell culture. Other suitable methods may include introducing or administering an agent to a cell, tissue, mammal or patient using appropriate procedures and routes of administration as defined above.
The level of MDM2, Mcl-i, PP5, CAS or Huwel in the cells may be determined by any method known to those of skill in. the art, including but not limited to Western blot, FACs analysis, imrnunoprecipitation. radio labeling, fluorescence labeling. The level of these markers being determined is the protein level, not the level of transcription. The stability of these proteins may also be determined rather than the level at any point in time.
Methods of developing treatment plans for individuals with cancer are also provided, The treatment plans are meant to avoid allowing the cancer to become resistant to tyrosine kinase inhibitors and/or to allow treatment of a cancer that is resistant to treatment with a tyrosine kinase inhibitor. The methods include obtaining a sample comprising cancer cells from a subject and assaying the cells to determine the level of at least one of MDM2, Mcl-1, PP5, CAS or Huwel in the cancer cells as compared to the level in control cells. Suitably the control cells are non-cancerous cells from a similar or from the same tissue or cell-type. If the cancer cells have increased levels of MDM2, Mcl-1 or PP5 or has decreased levels of CAS or Huwel as compared to the control cells, then the treatment plan for the subject includes administration of a MD 2 inhibitor to the subject. In one embodiment the level of more than one of MDM2, Mcl-i , PP5, CAS and Huwel are assayed. In another embodiment, the level of all of MDM2, Mcl-i, PP5, CAS and Huwel are assayed. The treatment plan may also include administering a tyrosine kinase inhibitor to the subject.
The following examples are meant only to be iilustrative and are not meant as limitations on the scope of the invention or of the appended claims. All references cited herein are hereby incorporated by reference in their entireties. EXAMPLES
Md- 1 stabilization in lapatinsb-resistant breast cancer cells
To analyze molecular .mechanisms underlying lapatinib-resistance, four independent lapatinib-resistant HER2 -positive breast cancer cell iines were derived by continuous culture of BT474, SKBR2, SUM 190 and AU565 cells in the presence of lapatmib. Xia, W> e( al. Proc. Natl. Acad, ScL USA 103, 7795-7800 (2006). Regardless of estrogen receptor (BR), progesterone receptor (PR), or p53 status, all four parental sensitive cell lines died from apoptosis in response to lapatmib. See Figure 1 and Table 1. Ail four resistant lines (hereafter referred to as rBT474, rS BR2, rSUM1905 and rAU565) did not die in response to lapatlnib treatment (Fig. 2 and Fig. 3 A). Lapatinib inhibited HER2 tyrosine autophosphorylation eve in resistant cells (Fig. 3B). Furthermore, phosphorylation of both Akt and Erkl/2, two primary downstream effectors in HER2-oyerexpressing breast cancer, were also attenuated in sensitive and resistant cells treated with lapatmib (Figs, 3C and 3D). Akt inhibition was unable to reverse lapadnib resistance.
Table 1
Pathological features of breast cancer cell Maes used m this study
Abbreviations: AC - adenocarcinoma; ER ==· estrogen receptor; IDC ;;;; invasive ductal carcinoma; inf - inflammatory carcinoma; PR - progesterone receptor
♦from the
Since lapatinib promotes tumor regression at least in part by inducing apoptosis, we speculated that resistant cells might have altered apoptotic signaling. Indeed, lapatinib induced mitochondrial cytochrome c release in parental BT474 cells, bat not rBT474 ceils (Fig. 4), suggesting that pro- and anti -apoptotic Bcl-2 family proteins that govern the mitochondrial outer membrane permeability might be modulated in the lapatinib-treated resistant ceils. While we observed no significant difference in expression of multiple Bcl-2 family members (e.g. "Sim, Fig. 3E) between sensitive and resistant cells, the anti-apoptotic Bcl-2 member Mcl-l was significantly upregulated in the resistant breast cancer cells treated with lapatinib (Fig. 3E). in the sensitive cells, Mel- J protein levels decreased upon treatment with lapatinib, whereas Mcl- l protein levels increased in the resistant cells in the presence of lapatinib (Fig. 3E).
Rapid degradation of J" [S]-Mcl- i was observed in ceil-free lysates prepared from sensitive cells, while this degradation was blocked in resistant lysates (Fig. 3F). These results indicate that the observed differences in Mcl-l abundance stemmed from differences in Mcl-l stability. A similar stabilization was observed in the presence of the proieasome inhibitor, MGI32, importantly, although the Mci-1 protein half-life was prolonged in resistant cell lysates, this was only observed in lysates from cells treated with lapatinib (e.g., lapatinib-treated rBT474 cells, Fig. 3G). Addition of ubiquitin aldehyde, a deubiquit l se inhibitor, to the lysates did not prevent the failure to degrade 35[S]-Mcl-1 in resistant ceils (Fig. 5), suggesting that Mcl-l stabilization might be secondary to a defect in Mcl-l ubiquityiation, rather than enhanced deubiquityiation. To examine Mcl-l ubiquityiation directly, we co-transfected FLAG-tagged Mcl-l together with HA-tagged ubiquitin, and examined Mcl-l ubiquityiation by anti-HA antibody following imrnunoprecipitation of FLAG-Mcl-1. In the absence of lapatinib, Mcl-l protein was equally ubiquitylated in S BR3 and rS BR3 cells (Fig. 3H), Lapatinib treatment enhanced Mcl-l ubiquityiation in SKBR.3 cells; but diminished Mcl-l. ubiquityiation in rSKBR3 cells (Fig. 3H). These data suggest that upregulation of Mci-1 protein in the iapatinib-resi slant ceils might result from a lapatinib -dependent defect in the Mcl-l ubiquityiation machinery.
lacorrect apopiosome assembly in lapatlBib-reslstaHt cells
In analyzing the mechanism of lapatinib resistance, we noted that the resistant cells failed to activate caspases when purified cytochrome c was added directly to lysates. Cytochrome c induced robust caspase activation in parental cells, though Apaf-1 , caspase-9 and caspase-3 levels were similar in resistant and sensitive cells (Fig. 6 and Fig, 7 A). As we observed for Mcl- 1 protein stability, the failure of cytochrome c to induce caspase activation in lapatinib-resistant cells was "lapatinib-dependen " When resistant cells were cultured in the presence of lapatinib, the lysates exhibited strong defects in caspase activation. When lapatinib was removed from the culture medium, lysates could respond to cytochrome c (Figs. 7 A. and 7B).
PPS stabilization i¾ lapatimh-restsia breast cancer ceils
HSP90P binds directl to the Apaf-1 CARD domain to block caspase-9 recruitment. We found that this inhibition was significantly increased in leukemic cells where HSP90p hypophosphorylation at residues Ser226 and Ser.255 led to tighter interaction between Apaf-1 and Η8Ρ90β. urokawa, M, Zhao, C, Reya, T, & Kornbluth, S. Mol. Cell Biol 28» 5494-5506 (2008), interestingly, HSP9Gp phosphorylation at both Ser226 and Ser255 was also markedly- decreased in iapati b-treated resistant cells compared to sensitive cells (Figs. 7C-7F),
Since lapatinib did not prevent HSP90P phosphorylation in normal BT474 cells (Fig. 7D), lapatinib was unlikely to inhibit an HSP90p~d.irected kinase (e.g., casein kinase 2). These data suggest that an HSP90P-direcied phosphatase might be modulated in response to lapatinib. PPS regulates the phosphorylation of HSP90 in other settings, Wandinger, S.K,, Suhre, M.H., Wegele, E. & Buchner, X EMBO J. 25, 367-376 (2006). We confirmed that the phosphorylation of Ser226 and Ser255 was significantly increased in PP5"'" mouse embryonic fibroblasts (MEFs) when compared with phosphorylation at these sites in wild type MEFs (Fig. 8). Therefore, we hypothesized tha hypophosphoryiation of HSP90p in lapatinib-resistant ceils might result from upregulation of HSP90P-directed PP5 activity. We found that lapatinib treatment triggered a gradual decrease in PPS levels in sensitive cells, whereas levels were unaltered in resistant cells (Fig. 7G), Indeed, the protein half-life of PPS -was significantly longer in resistant cells than in the parental cells (Fig. 7H), Accordingly, PPS was much more highly ubiquity! ated in sensitive than resistant cells (Fig. 71). Taken together, these results suggest that hypophosphoryiation of HSP90P in resistant ceils may be attributable to enhanced PPS stability.
Httwel is an E3 Hgase responsible for the degradation of both Mcl-1 and PP5
PP5 stabilization could result from a defect in an E3 ligase activity responsible for PP5 ubiquitylation in lapatinib-resistant ceils. Hence, we sought to identify a PP5-direeted E3 ligase through chromatographic purification. Cytosolic lysates prepared from SK.BR.3 cells were fractionated on a Q-sepharose column and ubquityiation of ~ [S]-PP5 by each fraction (supplemented with El, E2, AT and ubiquitin) was analyzed by SDS-PAGE, Most of the PP5- ubiquitinating activity was eiuted with 500 niM NaCI (Fig. 9), Given that we had already found changes in Mcl-1 stability in response to lapatinih, we speculated that a known Mcl-1 -directed E3 ubiquitin ligase might also regulate PP5 stability, indeed, immunoblotting of Q-sepharose fractions revealed that Huwel (also known as Mule, ARF-BPL HectH9), an HECT-domain E3 ligase known to target Mcl-1 for degradation, was also eiuted with 500 mM NaCI, corresponding to the fraction with the PP5-ubiquitylaiing activity (Fig. 9).
In agreement with these observations, we found that HA -Huwel co-immunoprecipitated with endogenous PP5 (Fig, I OA). Moreover, knockdown of Huwel using siRNA increased both PP5 and Mcl-1 levels in BT474 ceils (Fig. lOB). Conversely, overexpressi n of MA-Huwel, but not catalytieally inactive HA-Huwel(C/S), reduced PP5 and Mcl- 1 protein levels (Fig. IOC). We obtained the same results in HeLa cells and the p53-null H 1299 cells. As shown in Fig 10D, in the presence of both El and E2, wild type recombinant Huwel protein, but not Huwel (C/S), ubiquitylated recombinant PP5 in vitro (Fig, 10D). These results suggested that the enhanced protein stability of PP5 and Mcl-1 observed in the resistant cells was due to a defect in protein ubiquitylation mediated by Huwe l (see further in Fig. 13, below).
Downregu!ation of CAS in tapatissib-resistaiit cells
HSP90p hypophosphorylation downstream of PP5 stabilization might explain apopiosoroe inhibition in the lapatinib-treated resistant cells, but when vve resolved cell lysates by gel filtration, we saw not onl a failure to recruit caspase-9 to Apaf-1 (which could be explained if Η5Ρ90β blocked caspase 9 recruitment), but also a failure of the majority of Apaf-1 to oiigomerize (Fig. 10F). Moreover, upon addition of cytochrome c to resistant cell lysates, we detected a small percentage of Apaf-I and caspase-9 in very large (1.000-1400 kD) fractions.
previously described as iucon'eciiy assembled inactive complexes (Fig. 10F; shown by asterisks). Kim, Jiang, Du, & Wang, Mol. Cell 30, 239-247 (2008).
Without nucleotide exchange, cytochrome c induces Apaf-1 to form non-functional aggregates. Accordingly, we examined protein levels of PFIAP1, HSP70, and CAS (also known as CSE1L or Exportin-2), essential components of the nucleotide exchange factor required for loading Apaf-1 with d.ATP. Whereas PHAPI and HSP70 levels did not differ between parental and resistant cells, CAS protein levels were markedly decreased in resistant cells compared with parental cells, most notably in the presence of lapatinib (see Fig. 1 1 A). CAS protein levels declined over time following lapatinib addition to resistant cells, but. lapatinib removal allowed return of CAS to levels comparable to the parental cells (Figs. 1 A and 1. IB), Treatment of parental cells with lapatinib did not affect CAS protein levels (Fig. 1 1 A). In addition, in breast cance cell lines that are non-responsive to lapatinib due to low expression of HER2 (e.g., T47D cells), lapatinib treatment did not alter CAS protein levels. Quantitative real-time PCR demonstrated that lapatinib did not cause a reduction in CAS m NA levels in either sensitive or resistant cells. However, CAS protein was stabilized in sensitive cells, but destabilized in lapatinib-treated resistant cells (Fig. 1 1C). Accordingly, ubiquitylation. of CAS was nearly undetectable in sensitive ceils even in the presence of MGI 32, while CAS ubiquityiated species were readily detected in resistant cells and more prominent in the presence of lapatinib (Fig. 1 1 D). These data suggest that CAS downregulation in lapatimb-resistant cells results from augmented CAS protein, ubiquitylation.
To determine the mode of CAS degradation, we analyzed the CAS protein sequence and identified a potential binding motif for the RING-finger ubiquitin ligase MDM2 (Fig, 12A and Table 2). Kussie, et al Science 274, 948-953 (1996) and Uesugi & Verdine Proc, Natl Acad, Sci. USA 96, 14801-14806 (1 99). MDM2 co-imm noprecipitated with CAS in BT474 and HeLa cells. In addition to MDM2, CAS has also been shown to interact with p53. Tanaka, Ohkubo, Taisuno & Prives. Cell 130, 638-650 (.2007). However, the eo-immiinoprecipitation of MDM2 and CAS in p53-null H1299 cells suggests direct binding of the two proteins, an interaction that was enhanced in the presence of MG132. Importantly, when Tr l27} a conserved residue in the MDM2 binding motif, was replaced with Ala, binding of CAS to MDM2 was diminished (Fig. 1 IE).
Table 2
The sequence alignment is shown that includes p53, p73, p63, CAS (H. sapiens), and CAS homologs (CSE1) from D. melanogaster and 5. cerevisiae (bottom).
Moreover, when expressed in H 1299 cells, ubiquitylation of CAS with the W127A mutation (CAS% ,27A) was significantly suppressed compared with that of wild 'type CAS (Fig. 1 I F). Transient overexpression of MDM2 decreased endogenous CAS protein (Fig. 11 G). Finally, recombinant MDM2, but not its Ring-finger domain mutant (MDM2 64A), promoted in vitro ubiquitylation of CAS (Fig. l lFi). Together, these results indicate that CAS is an MDM2 target, interestingly, in BT474 cells, the CAS-MD 2 interaction decreased in the presence of lapatinib, whereas binding was enhanced in rBT474 cells under the same conditions (Fig. 1 11). These data are consistent with the idea that augmented ubiquitylation and subsequent degradation of CAS protein in lapatinib-resisiant cells is mediated by MDM2.
MDM2 is a H«wel-directed E3 ligase
High Huwel and low MDM2 activities in sensitive cells resulted in reduction of Mcl-l and PP5 and sustained CAS levels, respectively, rendering the sensitive eelis prone to apoptosis. In parental cells. Huwel protein levels remained stable in. the presence of lapatinib, whereas MDM2 rapidly decreased (Fig. 13 A). Conversely, when resistant cells were treated with lapatinib, Huwel levels significantly decreased, whereas MD 2 levels were maintained (Fig. 13 A). Most importantly, reduction of Huwel in resistant cells appeared to be due to lapatinib- induced protein degradation. As shown in Fig. 13B, without lapatinib, Huwel was stable in both BT474 and rBT474 cells. However, in lapatinib-treated rBT474 cells, Huwel protein half-life became significantly shorter, compared to that in BT474 cells (Fig. 13B). Although both Huwel and MDM2 are p53-targeting E3 iigases (and DM2 expression can also be modulated in a
feedback loop by p53-induced transcription), three of the four cell lines (BT474, SKBR3, and SUM 190) express mutant p53 (Table I and Fig. 1), suggesting that the observed changes in Huwel and MDM2 protein levels are independent of the transcriptional activity of p53.
Through protein sequence analysis, we determined that .Huwel contained a putative MDM2~bisding motif at residues 1 198-1205 (Fig. 12B and Table 3): the interaction of these two E3 iigases was confirmed by immunoprecipitation of endogenous proteins (Fig. 13C). The N- terminai portion of Huwel protein (aal -2474) as well as the full-length protein interacted with MDM2 (Fig. I3D), Moreover, replacement of the conserved Trpl202 with Ala (Huwel wl202A) significantly reduced binding between the two proteins (Fig. 13E). importantly, the Huwel - MDM2 interaction was also evident, in HeLa cells and H 1.299 cells, again indicating that their binding is neither specific for breast cancer cells nor mediated by p53. To determine whether MDM2 is a Huwel -directed E3 ligase9. we overexpressed MDM2 in HI 299 cells. As shown, in Fig, 13F, MDM2 expression reduced Huwel protein levels in a dose-dependent manner. In contrast, siRNA knockdown of MDM2 increased Huwel. protein levels (Fig. 130). Using a truncated mutant of Huwel (Huwel ), to allow visualization of an electrophoretic mobility shift, we confirmed that, in the presence of both E l and E2, MDM2 could ubiquity! ate Huwel in vitro (Fig. 13H). Moreover, lapatinib treatment triggered degradation of Huwel in resistant ceils treated with control siRNA, but when these celis were treated with MDM2 siRNA, Huwel stability was markedly increased, even in the presence of lapatinib, consistent with MDM2 acting as a Huwel -directed iigase (Fig. 131).
Table 3
The sequence alignment includes human p53, Huwel homologs from If. sapiens, M. musculus, B. taurus, D. rerio, T. castaneum., and TO 1 from S. cerevisiae.
i»Mt) 0is of MDM2 m® reverse lapatinib resistance
The findings above raised the interesting possibility that the observed changes in Met- 1 , PP5, and CAS in iapatimb-resistant ceils could all be traced to high MDM2 activity in the resistant cells. Accordingly, when resistant cells were co-treated with lapatinib, MDM2 knockdown induced significant apopiotic cell death (Fig, 14A). To evaluate this further, we implanted xenografts of rBT474 cells stably expressing control or MDM2 shRNAs into the mammary fat pads of female nude mice (Fig. 14B). Tumors developed similarly for all tumors. Nevertheless, oral lapatinib administration induced regression of xenografted tumors expressing MDM2 shRNAs, while control tumors continued to grow (Fig. 14B). Moreover, by the end of treatment period, six out of ten mice i the MDM2 knock-down group had tumors smaller than 50 mm3.
A hydrophobic pocket in the MDM2 N-terminus binds the transactivation domain of p53. If MDM2 bound Huwel in the same fashion, the MDM2 antagonist Nutlin-3a, that disrupts the p53-MDM2 complex, might also be expected to interfere with Huwel -MDM2 binding. Vassiiev, et al. Science 303, 844-848 (2004). To exclude the possibility that any effects of Nutlin-3a might be mediated by the p53-MDM2 interaction, we employed HI 299 cells. Catalytically inactive Huwel (Huwel (C/S)) bound to endogenous MDM2 and this binding was significantly reduced by Nutlin-3a (Fig. I 4C). Importantly, Nutlh 3a also prevented lapatinib- induced degradation of Huwel (Fig, 14D), suggesting that Nutlin-3a stabilizes Huwel by disrupting Huwel -MDM2 binding. Consequently, Nutlin~3a also suppressed lapatmib-mduced upregulation of Mcl-1 and PP5 (Fig. 14D). MDM2 and CAS binding, as well as CAS degradation, was also significantly inhibited by Nutlin-3a (Fig. 14D).
To examine the effect of Nutlin-3 a in vivo, mice bearing BT474 or rBT474 xenografts were randomly assigned to vehicle, lapatinib. Nutlin-3 (a racemic mixture of the enantiomers Nutlin-3 a and Nutlin-3 b), or lapatinib and NutHn-3. Lapatinib alone or a combination of lapatinib and Nutlin-3 significantly suppressed growth of BT474-derived tumors, whereas Nutlin-3 alone only modestly inhibited tumor growth (Fig. 1 E). Neither lapatinib nor Nutlin-3 inhibited rBT474-derivecl tumor growth as a single agent (Fig. 14E). Nevertheless, combination treatment of lapatinib and Nutlin-3 significantly suppressed tumor growth, resulting in ^50% reduction in tumor volume (Fig, 14E). These experiments were repeated using p53-positive AU565 and rAU565 ceils. Lapatinib substantially inhibited AU565, but not rAU565-derived
tumor growth. (Fig, 15). Nutlin-3 treatment alone had moderate tumor inhibitory effects on these p53-positive cells, but combination lapatinib/nutlin-3 treatment reduced tumor volume by ""50% by the end of evaluation period (Fig. 15). Tissue culture experiments conducted in parallel with all four sensitive/resistant cell line pairs using the MDM2 antagonist Mi-2.19, sugges that similar effects are likely to be obtained with other MDM2 inhibitors (Fig. 2). Importantly, the ability of the MDM2 inhibitors to re-sensitize resistant cells to lapatinib was not compromised by RNAi- mediated knock-down of p53 in rAU565 cells (Fig. 14F). Taken together, these results demonstrate that regardless of p53 status, an MDM2 inhibitor, such as Nutlin-Sa, can reverse lapatinib resistance, potentially by stabilizing CAS and Huwel, thereby promoting loss of PP5 and Mcl-1 (Fig. 14G).
We have demonstrated that multiple changes m the levels of apoptotie regulators, both upstream and downstream of mitochondrial cytochrome c release, cause resistance to lapatinib. Furthermore, these changes could be attributed to a previously unsuspected network of MDM2 (and Huwel ) substrates. Failure to degrade DM2 in response to lapatinib in ail four independently-derived lapatinib-resistant cell lines was the key factor in apregulating the anti- apoptotie .machinery in these cells (see Model, Fig. 14G).
We identified changes in mitochondrial cytochrome c release following lapatinib treatment but also have found that the apoptosome is refractory to cytochrome c-induced activation in the resistant cells. There is some debate as to the significance of apoptosome inhibition in cancers which already have a block to mitochondria) c^ochrome c release. However, we postulate that the block is more profound when several loci in the apoptotie pathway are affected: even if small amounts of cytochrome c were released in response to lapatinib in the resistant cells, efficient caspase activation would be inhibited at the level of the apoptosome. Since PP5 and Mcl-1 are both controlled by Huwel, apoptotie inhibition both upstream and downstream of the mitochondria could be controlled coordinately.
We also determined that CAS was downreguiated through MDM2 -mediated ubiquitylation. Interestingly, CAS was identified as a gene which, when knocked down, renders breast cancer cells resistant to apoptosis. CAS also binds to a subset of p53 target genes to regulate p53-mediated gene expression, in this regard, our results raise the interesting possibility that, in addition to ubiquitylation of p53, MDM2 might also modulate the p53 signaling pathwa by targeting CAS for degradation. Alteration of multiple apoptotie regulators in lapatinib-
resistant cells also increased their resistance to other pro-apoptotic stimuli (e.g. other potential therapeutics such as taxol and other apoptotic inducers such as staurospaurine) in the presence of lapatinib. These data raise the significant concern that modulation of apoptotic pathways in lapatinib-resistant cells might confer cross-resistance to multiple ehemotherapeutie agents.
The basis for the difference in MDM2 levels in resistant and sensitive cells is not clear.
In BT474/rBT474 cells, -we have seen marked differences in MD 2 half-life as well as changes in MDM2 R A levels. Note that we did not detect consistent upregulation of SRC kinase activity (Fig. 16), recently implicated in acquired resistance to trastuzumab or lapatinib in HER2{+) breast cancer, Zhang, et l. Nat. Med. 17, 461-469 (201 1) and exer et at. Oncogene 30(4O):4163-74 (201 1). The SRC inhibitor dasatinib also did not affect MD 2 protein levels or apoptotic resistance in lapatinib-resistant cells (Fig. 17). it is possible that a mutation, modification, or novel binding, partner renders MD 2 unable to auto-ubiquitylate, but still able to ubiquitylate substrates in trans. Finally, failure to degrade MDM2 in the resistant cells could result from mutation i MDM2 itself, rendering it insensitive to degradative signals triggered by lapatinib in sensitive ceils. Answering these questions will provide a stepping-stone from MD 2 to the relevant signaling factor(s) primarily responsible for the lapatinib resistance, while revealing additional nodes in the MDM2/Huwe.l regulatory network.
METHODS
Cell Culture
BT474, SKBR3, and AU565 cells were obtained from ATCC. SUM 190 cells were obtained from Asterand, Inc. Ail cell lines were cultured in RPMI medium containing 10% fetal bovine serum (FBS). Lapatinib-resistant cells (rBT474, rS BR3, rAU565, and rSUM'190) were established as previously described'4. Cobleigh, et at J. Clin. Oncol 17, 2639-2648 (1999). Lapatinib-resistant cells were grown in the presence of 1 μΜ lapatinib unless otherwise stated.
Reagents and antibodies
Lapatinib and dasatinib were purchased from LC Laboratories. G132 and z-VAD were purchased from Enzo Life Sciences, El, E2, ubiquitin, and Ub- Aldehyde were purchased from Boston Biochem. Nutlm~3a and racemate Nutliri-3 were synthesized and purified at the Duke
Small Molecule Synthesis Facility, Nutlin~3a and N'utlin-3 were also purchased from Cayman Chemical. Cycloheximide and purified cytochrome c was purchased from Sigma.
The following antibodies were used: anti-HER2 antibody, anti-phospho-HER2 (Y877) antibody, anti~phospho-HER2 (Y1221/Y 1222) antibody, anti-Akt. antibody, anti-phospho-Akt (T308) antibody, anti-caspase-9 antibody, atiti-cleaved easpase-3 antibody, anti-Bcl2 antibody, anti-Bci-xL antibody, anti-ERKl 2 antibody, anti-phospho-ERK.1/2 antibody (T202/Y204), anti- phospho-SRC (Y 16) antibody, anti-SRC antibody, anti-FLAG antibody (Ceil Signaling), ami- Apaf-1 antibody (2E12: Enzo Life Sceinces). anti-HSP90p antibody (5E12), anti-MD 2 antibody (2A1 G: Calbiochem), anti-HSP90p antibody (Millipore), ami-pb.ospho-H5P90$ antibody (S226), anti-phospiio-HSP90p antibody (S255) (Abeam), anti-Actm antibody, anti- MDM2 antibody (SMP14), anti-HA antibody (F-7) (Santa Cruz Biotechnology),, anti-FLAG M2 antibody (Sigma), anti-Bim antibody, anti-cleaved caspase-3 antibody, anti-Mcl-l antibody, anti- PP5 antibody. anti-CAS antibody, anti-HSP70 antibody (BD Transduction Laboratories), anti- Mcl-1 antibody (BioLegend), anti-Huwel antibody (Bethyi Laboratories), anti-ΡΗΑΡΪ antibody (ProSci).
Plasmids
HA-Huwei constructs in pCMV (wild type, C4341 S mutant, and aa 2473-4374 mntant) were generous gifts from Kristian Helm (University of Copenhagen). Hu el in pENTR was generous gifts from Jeanette Gowen Cook (University of North Carolina, Chapel Hill). Huwel in pENTR was recombined with the destination vector pDESTIO (Invitrogen) for production of His-taggcd protein. FLAG-PP5 in pcD A3 and FLAG-CAS in p3XFLAG-CMV10 were kind gifts from Xiao-Fan Wang {Duke University) and Carol Prives (Columbia University), respectively. CAS was also cloned into pENTR and, subsequently, into pDESTIO for bacu!oviral protein expression. PP5 was cloned into pGEX-KG for production of GST fusion protein. Mcl-1 with the N-terminal FLAG tag was generated from human Mcl-I (a gift from Jeffrey Rathmeil, Duke University) and cloned into pcDNA3. The plasmids encoding GST- MDM2, GST-MDM'2C464A, and HA-ubtquitin were obtained from Addgene (Addgene plasmids 1 1 92, 1 1493, and 17608). Fang, et al. J. Biol. Chem, 275, 8945-8951 (2000) and Lim. el al. J. NeuroscL 25, 2002-2009 (2005). MDM2 was also cloned into pcDNA3 with an N-terminal
FLAG tag. All point mutations (BA-Huwel 1"2474, HA«HuwelWJ202A, His~Huwel C434!S, FLAG- CAS*127' ) were generated with the QuikChange mutagenesis kit (Stratagene),
RNA' i
Transient siRNA transfections were performed using Lipofectamine RNAiMAX
(invitrogen) according to manufacturer's instruction. MDM2-specif!c siRNA (sense: 5'- CACCUCACAGAUUCCAGCUUCGGAA-3'; SEQ ID NO: 13) and its scrambled siRNA control (sense: 5 '-CACACACUUAGGA.CCCUUCGUCGAA-3 ' ; SEQ ID NO: 14) were designed and synthesized by Invitrogen, siRNA oligos targeting Huwel or GFP were previously described. Hall et at. Mot. Biol. Cell 18, 3340-3350 (2007).
For stable knockdown of MDM2, an shRNA construct in the ientivirai vector pLKO. l- puro (sh D 2 #1) was purchased from Open Biosystems (sense: 5'~ GATTCCAGAGAGTCATGTGTT-S'; SEQ ID NO: 15). An additional MD 2 shRNA construct (sh. DM2 2 sense: S'-TTGAAGTTATTAAAGT'CTGTT-S5; SEQ ID NO: 16) and control shRNA construct (sense: 5 '-CTGTGCTGTAGGTGA AACTGT-3 ' ; SEQ ID NO: 1.7) were also created in the vector pL OJ -puro according to Addgene's pLK.0, 1 protocol (http://www.addgene.org/plko). Stable knockdown of p53 was performed using the vector shp53-pL O. i-puro (Addgene plasmid 191 19), Godar et al. Cell 134, 62-73 (2008). Mouse xenograft experiments
Six week-old female nude mice were purchased from NCI Frederic. Xenograft tumors were produced by injection into the mammary fat pad with ceils (10 x 106), Tumor volumes were calculated every 3-4 days based on caliper measurements of the short (a) and long (b) tumor diameters (volume - a2b/2). Lapatinib and Nutlin-3 were formulated in vehicle (water with 0.5% Hydroxypropyl methylceilulose and 0, 1% Tween). Mice were dosed orally with vehicle alone, lapatinib ( 100 mg/kg), Nutlin-3 (100 mg/kg), or combination of both twice daily by gavage.
Immunoprecipitation
Cells were transiently transfected with the indicated plasmid by FuGene6 (Roche) based on manufacturer's instruction. Cells were harvested and lysed with co-IP buffer (10 mM. HEPES
[pH 7.4], 150 mM KCI, 0.5% NP-40, 1 mM phenylroethyls lfonyl fluoride, 5 μ τύ leupeptin, and 5 pg/ml aprotinin). Cell Iysate was incubated with anti-FLAG M2 agarose (Sigma) or anti- AH affinity matrix (Roche) at 4°C for 2-3 hours. The bead pellet was washed three times with co-IP buffer and then incubated with SDS- sample buffer.
A popiosis assays
Cell iysates for apoptotic assays were prepared as described previously using buffer A (20 mM HEPES [pH 7.4], 10 mM KCI, 1 .5 m MgCJ2, 1 mM EDTA, 1 mM EGTA, 1 mM dithiothreitol, 1 mM phenyimethylsulfbnyl fluoride, 5 ,ug/mi leupeptin, and 5 μ§/ιηΙ aprotinin). Kurokawa, Zhao, Reya, & Korabluth. MoL Cell. Biol, 28, 5494-5506 (2008). Cell Iysate (10 jig .ul) was incubated in the presence or absence of 1 mM dATP and various concentrations of cytochrome c at 37°C for 30 min, and subjected to gel filtration, caspase assays, or western blotting.
Gel filtration was performed as previously described. Spector, Xia, El-Hariry, Yarden, & Bacus. Breast Cancer Res, 9, 205-212 (2007). After incubation with cytochrome c, the ceil Iysate (in a volume of 250 μ.1) was loaded onto a Superdex 200 column at a. flow rate of 0.3 ml/mm.
Coiorimetric caspase assays were performed by incubating cell Iysate (3 μΐ) in 90 μΐ DEVDase buffer (50 mM HEPES [pH 7.5], lOOmMNaCl, 0.1% CHAPS, I OmMDTT, 1 mMEDTA, 10% glycerol) containing the peptide substrate, Ac-DEVD-pNA (200 mM final concentration; BIOMOL Research Labs). Reactions were incubated at 37°C for 30 min. Absorbance of the coiorimetric product was measured at 405 am using a Bio-Rad microplate reader. In vitro uhiquitylalion assays
Recombinant human PP5 and MDM2 proteins were bacteriaily expressed with a GST tag. After purification by glutathione sepharose 4B (GE Healthcare), the GST tag was cleaved off by thrombin. Recombinant human Huwel wild type, C4341 S mutant (Huwel C/S), and Huwel S"2 M were expressed in the bacuiovirus system and purified from Sf9 cells.
For in vitro ubiquity lation assays, 100 ng of purified recombinant PP5 or Huwe l '"i474 was incubated with 10 ng El, 100 ng E2 (UbcHSb or UbcH7), 100 μ$ ubiquitin, and 0.5 g of a
purified E3 enzyme (Huwel wild type, Huwel C/S. or MD 2) in 40 μΐ of reaction buffer (50 raM Tris, pH 7.5, 5 mM MgCl2, 2 mU ATP, 2 mM DTT). After incubation at 30°C for 3 hours, the reaction was terminated by addition of SDS-sampJe buffer.
Statistics
The statistical analysis was carried out using GraphPad Prism software version 4,0c (GraphPad software inc.).
Claims
1. A method of treating a subject with a cancer having resistance to an inhibitor of tyrosine kinase activity comprising administering an inhibitor of tyrosine kinase activity to the subject and administering an inhibitor of the E3 ubiquitin ligase MDM2 to the subject.
2. A method of treating a subject with a cancer that lacks wild-type p53, comprising
administering an MDM2 inhibitor in an effective amount to the subject with the cancer lacking wild-type p53,
3. A m ethod of treating a subject with a cancer having cells comprising increased levels of MDM2, Mcl-I or PP5 or decreased levels of CAS or Huwel as compared to control cells, comprising administering an DM2 inhibitor in an effective amount to the subject.
4. The method of any one of claims 2-3, further comprising administering an inhibitor of tyrosine kinase activity,
5. The method of claim I or 4, wherein the inhibiior of tyrosine kinase activity is a small molecule tyrosine kinase inhibitor.
6. The method of claim 1 or 4, wherein the inhibitor of tyrosine kinase activity is an
inhibitor of ATP binding to the tyrosine kinase.
7. The method of claim .1 or 4, wherein the inhibitor of tyrosine kinase activity is an
inhibitor of HER2 and/or EGFR.
8. The method of claim 3 or 4, wherein the inhibitor is lapatinib.
9. The method of any one of claims 1-8, wherein the subject is resistant to treatment with an antibody specific for the tyrosine kinase.
10. The. method of claim 9, wherein the antibody is rrastuzumab.
1 L The method of any one of claims 1-10, wherein the cancer is breast cancer, lung cancer, colon cancer, gastric cancer or glioma.
12. The method of any one of claims 1-11, wherein cells from the cancer have increased
MDlvl.2, Mcl-l or PP5 as compared to control ceils.
13. The method of any one of claims 1 -12, wherein cells from the cancer have decreased
Huwel or CAS as compared to control cells.
14. The method of any one of claims 1-13, wherein the DM2 inhibiior is an inhibitor of the interaction of DM2 with a target, an inhibitor of ubiquitin ligase activity, an inhibitor of MD 2 transcription or translation or a molecule that decreases the half-life of MDM2 in a cell.
15. The method of claim 14, wherein the inhibitor of MDM2 is nutlin-3 or nuthn~3a.
16,. The method of claim 14, wherein the inhibitor of MDM2 is a spiro-oxindole.
17. The method of any one of claims 1- 16, wherein the subject is a human.
18. The method any one of claims 1 -17, further comprising determining the cancer lacks wild-type p53 prior to administering the MDM2 inhibitor,
19. The method of any one of claims 1 -18 , further comprising determining the level of at least one of MDM2. Mcl-1, PP5, CAS and Huwel in cells of the cancer prior to administering the MDM2 inhibitor.
20. A .method of screening for MDM2 inhibitors comprising contacting a cell with an agent, wherein the cell has increased levels of Mcl-1 or PP5 or decreased levels of CAS or Huwel as compared to a control cel l, and determining the level of at least one of Mcl-1, PP5, CAS or Huwel in the cancer cell after contact with the agent, wherein an agent capable of decreasing the level of Mcl-1 or PP5 or increasing the level of C AS or Huwel in the cells after contact with the agent as compared to the level in a control untreated cell is a candidate inhibitor of MDM2.
21. The method of claim 20, further comprising contacting the cell with iapatinib prior to or concomitant with contacting the cell with the agent.
22. The method of claim 20 or 21, further comprising determining the level of Mcl-1 , PP5, CAS and Huwel in the cancer cell,
23. A method of developing a treatment plan for an individual with cancer comprising
obtaining a sample comprising cancer cells from, a subject; assaying the cells to determine the level of at least one of p53, MDM2, Mcl-1 , PP5, CAS or Huwel in the cancer cells as compared to the level in control cells and. administering a MDM2 inhibitor to the subject if the cancer cells lack wild-type p53, have increased levels of MDM2, Mcl-1 or PP5 or has decreased levels of CAS or Huwel as compared to control cells.
24. The method of claim 23, wherein the l evel of p53, MDM2, Mcl-1 , PP5, CAS and Huwel are all assayed.
25. The method of claim 23 or 24, further comprising administering a tyrosine kinase
inhibitor.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2858565A CA2858565A1 (en) | 2011-12-07 | 2012-12-07 | Methods of identifying and using mdm2 inhibitors |
EP12861144.9A EP2788004B1 (en) | 2011-12-07 | 2012-12-07 | Methods of identifying and using mdm2 inhibitors |
US14/363,346 US9937178B2 (en) | 2011-12-07 | 2012-12-07 | Methods of identifying and using MDM2 inhibitors |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161567944P | 2011-12-07 | 2011-12-07 | |
US61/567,944 | 2011-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013101436A1 true WO2013101436A1 (en) | 2013-07-04 |
Family
ID=48698510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2012/068557 WO2013101436A1 (en) | 2011-12-07 | 2012-12-07 | Methods of identifying and using mdm2 inhibitors |
Country Status (4)
Country | Link |
---|---|
US (1) | US9937178B2 (en) |
EP (1) | EP2788004B1 (en) |
CA (1) | CA2858565A1 (en) |
WO (1) | WO2013101436A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015168108A3 (en) * | 2014-04-28 | 2015-12-17 | Rxi Pharmaceuticals Corporation | Methods for treating cancer using nucleic targeting mdm2 or mycn |
US10240149B2 (en) | 2010-03-24 | 2019-03-26 | Phio Pharmaceuticals Corp. | Reduced size self-delivering RNAi compounds |
US10934550B2 (en) | 2013-12-02 | 2021-03-02 | Phio Pharmaceuticals Corp. | Immunotherapy of cancer |
CN112891354A (en) * | 2021-03-18 | 2021-06-04 | 新乡医学院 | Application of MDM2 inhibitor Nutlin-3a in preparation of medicine for activating endoplasmic reticulum stress-induced cancer cell apoptosis |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20180064540A (en) * | 2015-10-23 | 2018-06-14 | 다이이찌 산쿄 가부시키가이샤 | MDM2 Inhibitor Therapy for Cancer Treatment |
WO2019031637A1 (en) * | 2017-08-11 | 2019-02-14 | 전남대학교산학협력단 | Cancer marker genes for p53-non mutational cancer, and therapeutic agent screening method |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110112052A1 (en) * | 2009-11-12 | 2011-05-12 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2307822T3 (en) * | 2001-12-18 | 2008-12-01 | F. Hoffmann-La Roche Ag | CIS-IMIDAZOLINS AS INHIBITORS OF MDM2. |
EP2596366A4 (en) | 2010-07-21 | 2014-04-16 | Joseph P Errico | Combination therapy with mdm2 and efgr inhibitors |
-
2012
- 2012-12-07 US US14/363,346 patent/US9937178B2/en not_active Expired - Fee Related
- 2012-12-07 WO PCT/US2012/068557 patent/WO2013101436A1/en active Application Filing
- 2012-12-07 EP EP12861144.9A patent/EP2788004B1/en not_active Not-in-force
- 2012-12-07 CA CA2858565A patent/CA2858565A1/en not_active Abandoned
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110112052A1 (en) * | 2009-11-12 | 2011-05-12 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
Non-Patent Citations (7)
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10240149B2 (en) | 2010-03-24 | 2019-03-26 | Phio Pharmaceuticals Corp. | Reduced size self-delivering RNAi compounds |
US11118178B2 (en) | 2010-03-24 | 2021-09-14 | Phio Pharmaceuticals Corp. | Reduced size self-delivering RNAI compounds |
US10934550B2 (en) | 2013-12-02 | 2021-03-02 | Phio Pharmaceuticals Corp. | Immunotherapy of cancer |
WO2015168108A3 (en) * | 2014-04-28 | 2015-12-17 | Rxi Pharmaceuticals Corporation | Methods for treating cancer using nucleic targeting mdm2 or mycn |
US11279934B2 (en) | 2014-04-28 | 2022-03-22 | Phio Pharmaceuticals Corp. | Methods for treating cancer using nucleic acids targeting MDM2 or MYCN |
CN112891354A (en) * | 2021-03-18 | 2021-06-04 | 新乡医学院 | Application of MDM2 inhibitor Nutlin-3a in preparation of medicine for activating endoplasmic reticulum stress-induced cancer cell apoptosis |
Also Published As
Publication number | Publication date |
---|---|
EP2788004A4 (en) | 2015-12-30 |
EP2788004A1 (en) | 2014-10-15 |
US9937178B2 (en) | 2018-04-10 |
CA2858565A1 (en) | 2013-07-04 |
EP2788004B1 (en) | 2019-07-03 |
US20140336202A1 (en) | 2014-11-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Ge et al. | FBXO22 degrades nuclear PTEN to promote tumorigenesis | |
Kim et al. | Methylation-dependent regulation of HIF-1α stability restricts retinal and tumour angiogenesis | |
Lee et al. | NEDD4L downregulates autophagy and cell growth by modulating ULK1 and a glutamine transporter | |
Hong et al. | Targeting posttranslational modifications of RIOK1 inhibits the progression of colorectal and gastric cancers | |
Yuan et al. | Deubiquitylase OTUD3 regulates PTEN stability and suppresses tumorigenesis | |
Han et al. | ERK-mediated phosphorylation regulates SOX10 sumoylation and targets expression in mutant BRAF melanoma | |
Che et al. | Pathogenetic, prognostic, and therapeutic role of fatty acid synthase in human hepatocellular carcinoma | |
Hu et al. | The USP10-HDAC6 axis confers cisplatin resistance in non-small cell lung cancer lacking wild-type p53 | |
Borroni et al. | Smurf2 regulates stability and the autophagic–lysosomal turnover of lamin A and its disease‐associated form progerin | |
Xie et al. | FAF1 phosphorylation by AKT accumulates TGF-β type II receptor and drives breast cancer metastasis | |
US9937178B2 (en) | Methods of identifying and using MDM2 inhibitors | |
Lin et al. | Induction of Cbl‐dependent epidermal growth factor receptor degradation in Ling Zhi‐8 suppressed lung cancer | |
Zhang et al. | The deubiquitylase USP2 maintains ErbB2 abundance via counteracting endocytic degradation and represents a therapeutic target in ErbB2-positive breast cancer | |
Li et al. | RNF167 activates mTORC1 and promotes tumorigenesis by targeting CASTOR1 for ubiquitination and degradation | |
Wu et al. | A novel mechanism of indole-3-carbinol effects on breast carcinogenesis involves induction of Cdc25A degradation | |
Huang et al. | The NEDD4‐1 E3 ubiquitin ligase: A potential molecular target for bortezomib sensitivity in multiple myeloma | |
Huang et al. | IRTKS is correlated with progression and survival time of patients with gastric cancer | |
Lauter et al. | Targeting of the AXL receptor tyrosine kinase by small molecule inhibitor leads to AXL cell surface accumulation by impairing the ubiquitin-dependent receptor degradation | |
Cheng et al. | Cigarette smoke-induced LKB1/AMPK pathway deficiency reduces EGFR TKI sensitivity in NSCLC | |
Zhou et al. | Induction of NEDD8-conjugating enzyme E2 UBE2F by platinum protects lung cancer cells from apoptosis and confers to platinum-insensitivity | |
Zhao et al. | Systematic identification of CDC34 that functions to stabilize EGFR and promote lung carcinogenesis | |
Zhang et al. | The regulation of CPNE1 ubiquitination by the NEDD4L is involved in the pathogenesis of non-small cell lung cancer | |
Li et al. | A low-molecular-weight compound exerts anticancer activity against breast and lung cancers by disrupting EGFR/Eps8 complex formation | |
Nikonova et al. | Opposing effects of inhibitors of Aurora-A and EGFR in autosomal-dominant polycystic kidney disease | |
Chen et al. | TRABID inhibition activates cGAS/STING-mediated anti-tumor immunity through mitosis and autophagy dysregulation |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12861144 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2858565 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14363346 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012861144 Country of ref document: EP |