JP2011527565A - 乳癌のリスクアセスメントのための遺伝的変異 - Google Patents
乳癌のリスクアセスメントのための遺伝的変異 Download PDFInfo
- Publication number
- JP2011527565A JP2011527565A JP2011517318A JP2011517318A JP2011527565A JP 2011527565 A JP2011527565 A JP 2011527565A JP 2011517318 A JP2011517318 A JP 2011517318A JP 2011517318 A JP2011517318 A JP 2011517318A JP 2011527565 A JP2011527565 A JP 2011527565A
- Authority
- JP
- Japan
- Prior art keywords
- seq
- breast cancer
- allele
- individual
- risk
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 206010006187 Breast cancer Diseases 0.000 title claims abstract description 429
- 208000026310 Breast neoplasm Diseases 0.000 title claims abstract description 427
- 238000012502 risk assessment Methods 0.000 title claims description 25
- 230000007614 genetic variation Effects 0.000 title description 16
- 238000000034 method Methods 0.000 claims abstract description 265
- 230000002068 genetic effect Effects 0.000 claims abstract description 118
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 101
- 201000010099 disease Diseases 0.000 claims abstract description 100
- 230000004044 response Effects 0.000 claims abstract description 26
- 238000004393 prognosis Methods 0.000 claims abstract description 11
- 108700028369 Alleles Proteins 0.000 claims description 357
- 239000003550 marker Substances 0.000 claims description 323
- 102000054766 genetic haplotypes Human genes 0.000 claims description 214
- 239000000523 sample Substances 0.000 claims description 181
- 150000007523 nucleic acids Chemical class 0.000 claims description 175
- 102000039446 nucleic acids Human genes 0.000 claims description 140
- 108020004707 nucleic acids Proteins 0.000 claims description 140
- 108090000623 proteins and genes Proteins 0.000 claims description 136
- 239000002773 nucleotide Substances 0.000 claims description 110
- 125000003729 nucleotide group Chemical group 0.000 claims description 110
- 230000035772 mutation Effects 0.000 claims description 102
- 206010028980 Neoplasm Diseases 0.000 claims description 87
- 238000011282 treatment Methods 0.000 claims description 74
- 108020004414 DNA Proteins 0.000 claims description 69
- 201000011510 cancer Diseases 0.000 claims description 55
- 239000003814 drug Substances 0.000 claims description 49
- 230000035945 sensitivity Effects 0.000 claims description 45
- 108091028043 Nucleic acid sequence Proteins 0.000 claims description 42
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims description 38
- 108091034117 Oligonucleotide Proteins 0.000 claims description 34
- 239000003153 chemical reaction reagent Substances 0.000 claims description 32
- 230000015654 memory Effects 0.000 claims description 28
- 230000000295 complement effect Effects 0.000 claims description 25
- 229940124597 therapeutic agent Drugs 0.000 claims description 25
- 239000012634 fragment Substances 0.000 claims description 24
- 230000002829 reductive effect Effects 0.000 claims description 24
- 102000036365 BRCA1 Human genes 0.000 claims description 23
- 101150072950 BRCA1 gene Proteins 0.000 claims description 23
- 108020005187 Oligonucleotide Probes Proteins 0.000 claims description 23
- 239000002751 oligonucleotide probe Substances 0.000 claims description 23
- 108700020463 BRCA1 Proteins 0.000 claims description 22
- 101150008921 Brca2 gene Proteins 0.000 claims description 21
- 102000052609 BRCA2 Human genes 0.000 claims description 19
- 108700020462 BRCA2 Proteins 0.000 claims description 19
- 238000003745 diagnosis Methods 0.000 claims description 19
- 239000013068 control sample Substances 0.000 claims description 15
- 238000012544 monitoring process Methods 0.000 claims description 10
- 239000012472 biological sample Substances 0.000 claims description 8
- 239000012830 cancer therapeutic Substances 0.000 claims description 6
- 238000005259 measurement Methods 0.000 claims description 6
- 241000282412 Homo Species 0.000 claims description 5
- 108010011536 PTEN Phosphohydrolase Proteins 0.000 claims description 5
- 230000002441 reversible effect Effects 0.000 claims description 5
- 108010078814 Tumor Suppressor Protein p53 Proteins 0.000 claims description 4
- 230000007423 decrease Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000000149 penetrating effect Effects 0.000 claims description 4
- 208000035327 Oestrogen receptor positive breast cancer Diseases 0.000 claims description 3
- 102000014160 PTEN Phosphohydrolase Human genes 0.000 claims description 3
- 238000011325 biochemical measurement Methods 0.000 claims description 3
- 239000000872 buffer Substances 0.000 claims description 3
- 201000007281 estrogen-receptor positive breast cancer Diseases 0.000 claims description 3
- 239000002243 precursor Substances 0.000 claims description 3
- 201000007283 progesterone-receptor positive breast cancer Diseases 0.000 claims description 2
- 102000015098 Tumor Suppressor Protein p53 Human genes 0.000 claims 1
- 230000004043 responsiveness Effects 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 abstract description 4
- 108090000765 processed proteins & peptides Proteins 0.000 description 76
- 102000004196 processed proteins & peptides Human genes 0.000 description 74
- 229920001184 polypeptide Polymers 0.000 description 73
- 230000014509 gene expression Effects 0.000 description 63
- 238000012360 testing method Methods 0.000 description 58
- 238000001514 detection method Methods 0.000 description 51
- 210000000349 chromosome Anatomy 0.000 description 38
- 238000004458 analytical method Methods 0.000 description 36
- 210000004027 cell Anatomy 0.000 description 31
- 238000003556 assay Methods 0.000 description 30
- 102000004169 proteins and genes Human genes 0.000 description 29
- 102100033934 DNA repair protein RAD51 homolog 2 Human genes 0.000 description 28
- 238000009396 hybridization Methods 0.000 description 27
- 238000012216 screening Methods 0.000 description 27
- 229940079593 drug Drugs 0.000 description 25
- 108020004999 messenger RNA Proteins 0.000 description 25
- 102000054765 polymorphisms of proteins Human genes 0.000 description 25
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 23
- 101001132307 Homo sapiens DNA repair protein RAD51 homolog 2 Proteins 0.000 description 22
- 238000003860 storage Methods 0.000 description 22
- 101000890757 Homo sapiens FH1/FH2 domain-containing protein 3 Proteins 0.000 description 21
- 239000000969 carrier Substances 0.000 description 21
- 102100040129 FH1/FH2 domain-containing protein 3 Human genes 0.000 description 20
- 101000633968 Homo sapiens Tubby protein homolog Proteins 0.000 description 20
- NKANXQFJJICGDU-QPLCGJKRSA-N Tamoxifen Chemical compound C=1C=CC=CC=1C(/CC)=C(C=1C=CC(OCCN(C)C)=CC=1)/C1=CC=CC=C1 NKANXQFJJICGDU-QPLCGJKRSA-N 0.000 description 20
- 238000005516 engineering process Methods 0.000 description 20
- 239000002609 medium Substances 0.000 description 20
- 101000836383 Homo sapiens Serpin H1 Proteins 0.000 description 19
- 150000001413 amino acids Chemical group 0.000 description 19
- 239000000203 mixture Substances 0.000 description 19
- 239000013615 primer Substances 0.000 description 19
- 238000005215 recombination Methods 0.000 description 19
- 230000006798 recombination Effects 0.000 description 19
- 210000001519 tissue Anatomy 0.000 description 19
- 102100027287 Serpin H1 Human genes 0.000 description 18
- 102100029249 Tubby protein homolog Human genes 0.000 description 18
- 230000008859 change Effects 0.000 description 18
- 230000000694 effects Effects 0.000 description 18
- 230000000692 anti-sense effect Effects 0.000 description 17
- 102000015694 estrogen receptors Human genes 0.000 description 17
- 108010038795 estrogen receptors Proteins 0.000 description 17
- 239000000047 product Substances 0.000 description 17
- 238000001959 radiotherapy Methods 0.000 description 17
- 101000611194 Homo sapiens Trinucleotide repeat-containing gene 6A protein Proteins 0.000 description 16
- 108010021466 Mutant Proteins Proteins 0.000 description 16
- 102000008300 Mutant Proteins Human genes 0.000 description 16
- 102100037504 Paired box protein Pax-5 Human genes 0.000 description 16
- 239000004055 small Interfering RNA Substances 0.000 description 16
- 230000001225 therapeutic effect Effects 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 15
- 238000011161 development Methods 0.000 description 15
- 108091092878 Microsatellite Proteins 0.000 description 14
- 238000012228 RNA interference-mediated gene silencing Methods 0.000 description 14
- 239000003623 enhancer Substances 0.000 description 14
- 230000006870 function Effects 0.000 description 14
- 230000009368 gene silencing by RNA Effects 0.000 description 14
- 102000003998 progesterone receptors Human genes 0.000 description 14
- 108090000468 progesterone receptors Proteins 0.000 description 14
- 101000601724 Homo sapiens Paired box protein Pax-5 Proteins 0.000 description 13
- 108020004711 Nucleic Acid Probes Proteins 0.000 description 13
- 210000000481 breast Anatomy 0.000 description 13
- 239000002853 nucleic acid probe Substances 0.000 description 13
- 108020004459 Small interfering RNA Proteins 0.000 description 12
- 238000009607 mammography Methods 0.000 description 12
- 238000007726 management method Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 102000004190 Enzymes Human genes 0.000 description 11
- 108090000790 Enzymes Proteins 0.000 description 11
- 230000008901 benefit Effects 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 11
- 229940088598 enzyme Drugs 0.000 description 11
- 238000003752 polymerase chain reaction Methods 0.000 description 11
- 238000001356 surgical procedure Methods 0.000 description 11
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 10
- 238000004891 communication Methods 0.000 description 10
- 239000002131 composite material Substances 0.000 description 10
- 230000000875 corresponding effect Effects 0.000 description 10
- 238000012217 deletion Methods 0.000 description 10
- 230000037430 deletion Effects 0.000 description 10
- 229960001603 tamoxifen Drugs 0.000 description 10
- 238000004422 calculation algorithm Methods 0.000 description 9
- 230000002113 chemopreventative effect Effects 0.000 description 9
- 238000013461 design Methods 0.000 description 9
- 238000009826 distribution Methods 0.000 description 9
- 238000003780 insertion Methods 0.000 description 9
- 230000037431 insertion Effects 0.000 description 9
- 230000037361 pathway Effects 0.000 description 9
- WGZDBVOTUVNQFP-UHFFFAOYSA-N N-(1-phthalazinylamino)carbamic acid ethyl ester Chemical compound C1=CC=C2C(NNC(=O)OCC)=NN=CC2=C1 WGZDBVOTUVNQFP-UHFFFAOYSA-N 0.000 description 8
- 210000004369 blood Anatomy 0.000 description 8
- 239000008280 blood Substances 0.000 description 8
- 238000004364 calculation method Methods 0.000 description 8
- 238000002512 chemotherapy Methods 0.000 description 8
- 230000003247 decreasing effect Effects 0.000 description 8
- 230000003287 optical effect Effects 0.000 description 8
- 239000002987 primer (paints) Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 102000053602 DNA Human genes 0.000 description 7
- 208000034826 Genetic Predisposition to Disease Diseases 0.000 description 7
- 108091093037 Peptide nucleic acid Proteins 0.000 description 7
- 230000003321 amplification Effects 0.000 description 7
- 102220362489 c.10C>A Human genes 0.000 description 7
- 230000001976 improved effect Effects 0.000 description 7
- 239000002679 microRNA Substances 0.000 description 7
- 238000003199 nucleic acid amplification method Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 102200024044 rs1555523872 Human genes 0.000 description 7
- 229940095743 selective estrogen receptor modulator Drugs 0.000 description 7
- 239000000333 selective estrogen receptor modulator Substances 0.000 description 7
- 238000012163 sequencing technique Methods 0.000 description 7
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 6
- 101710018890 RAD51B Proteins 0.000 description 6
- 108091027967 Small hairpin RNA Proteins 0.000 description 6
- 239000000074 antisense oligonucleotide Substances 0.000 description 6
- 238000012230 antisense oligonucleotides Methods 0.000 description 6
- 102220371036 c.22C>A Human genes 0.000 description 6
- 230000002759 chromosomal effect Effects 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000003205 genotyping method Methods 0.000 description 6
- 210000003917 human chromosome Anatomy 0.000 description 6
- 230000000069 prophylactic effect Effects 0.000 description 6
- 230000005855 radiation Effects 0.000 description 6
- 238000010561 standard procedure Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 208000024891 symptom Diseases 0.000 description 6
- 230000014616 translation Effects 0.000 description 6
- 206010067484 Adverse reaction Diseases 0.000 description 5
- 102100025064 Cellular tumor antigen p53 Human genes 0.000 description 5
- 108010042407 Endonucleases Proteins 0.000 description 5
- 208000033640 Hereditary breast cancer Diseases 0.000 description 5
- 108060003951 Immunoglobulin Proteins 0.000 description 5
- 206010027476 Metastases Diseases 0.000 description 5
- 102100040241 Trinucleotide repeat-containing gene 6A protein Human genes 0.000 description 5
- 230000006838 adverse reaction Effects 0.000 description 5
- 239000002299 complementary DNA Substances 0.000 description 5
- 238000012937 correction Methods 0.000 description 5
- 238000002405 diagnostic procedure Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 208000025581 hereditary breast carcinoma Diseases 0.000 description 5
- 102000018358 immunoglobulin Human genes 0.000 description 5
- 238000001727 in vivo Methods 0.000 description 5
- 230000007774 longterm Effects 0.000 description 5
- 238000013507 mapping Methods 0.000 description 5
- 238000012775 microarray technology Methods 0.000 description 5
- 230000002265 prevention Effects 0.000 description 5
- 230000003449 preventive effect Effects 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 230000008439 repair process Effects 0.000 description 5
- 238000012552 review Methods 0.000 description 5
- 230000004083 survival effect Effects 0.000 description 5
- 238000013519 translation Methods 0.000 description 5
- 230000005945 translocation Effects 0.000 description 5
- 238000011277 treatment modality Methods 0.000 description 5
- 102000040650 (ribonucleotides)n+m Human genes 0.000 description 4
- 108020000948 Antisense Oligonucleotides Proteins 0.000 description 4
- 238000002965 ELISA Methods 0.000 description 4
- 102100031780 Endonuclease Human genes 0.000 description 4
- 108020004511 Recombinant DNA Proteins 0.000 description 4
- 238000012300 Sequence Analysis Methods 0.000 description 4
- 102100040244 Trinucleotide repeat-containing gene 6B protein Human genes 0.000 description 4
- 238000011226 adjuvant chemotherapy Methods 0.000 description 4
- 238000013459 approach Methods 0.000 description 4
- 238000003491 array Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000013500 data storage Methods 0.000 description 4
- 230000029087 digestion Effects 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- 238000003197 gene knockdown Methods 0.000 description 4
- 230000030279 gene silencing Effects 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 206010073096 invasive lobular breast carcinoma Diseases 0.000 description 4
- 230000009401 metastasis Effects 0.000 description 4
- 108091070501 miRNA Proteins 0.000 description 4
- 230000008520 organization Effects 0.000 description 4
- 230000002093 peripheral effect Effects 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 230000009862 primary prevention Effects 0.000 description 4
- 229960004622 raloxifene Drugs 0.000 description 4
- GZUITABIAKMVPG-UHFFFAOYSA-N raloxifene Chemical compound C1=CC(O)=CC=C1C1=C(C(=O)C=2C=CC(OCCN3CCCCC3)=CC=2)C2=CC=C(O)C=C2S1 GZUITABIAKMVPG-UHFFFAOYSA-N 0.000 description 4
- 230000001105 regulatory effect Effects 0.000 description 4
- 238000000528 statistical test Methods 0.000 description 4
- 238000013517 stratification Methods 0.000 description 4
- 238000013518 transcription Methods 0.000 description 4
- 230000035897 transcription Effects 0.000 description 4
- 108700010154 BRCA2 Genes Proteins 0.000 description 3
- 108091006146 Channels Proteins 0.000 description 3
- 206010071602 Genetic polymorphism Diseases 0.000 description 3
- 101000611192 Homo sapiens Trinucleotide repeat-containing gene 6B protein Proteins 0.000 description 3
- 108091092919 Minisatellite Proteins 0.000 description 3
- 206010033128 Ovarian cancer Diseases 0.000 description 3
- 206010061535 Ovarian neoplasm Diseases 0.000 description 3
- 101710149067 Paired box protein Pax-5 Proteins 0.000 description 3
- 102000012338 Poly(ADP-ribose) Polymerases Human genes 0.000 description 3
- 108010061844 Poly(ADP-ribose) Polymerases Proteins 0.000 description 3
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 description 3
- 230000002159 abnormal effect Effects 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 239000000427 antigen Substances 0.000 description 3
- 108091007433 antigens Proteins 0.000 description 3
- 102000036639 antigens Human genes 0.000 description 3
- 239000003886 aromatase inhibitor Substances 0.000 description 3
- 238000012098 association analyses Methods 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 229960002685 biotin Drugs 0.000 description 3
- 235000020958 biotin Nutrition 0.000 description 3
- 239000011616 biotin Substances 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 230000037433 frameshift Effects 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 238000012226 gene silencing method Methods 0.000 description 3
- 238000012252 genetic analysis Methods 0.000 description 3
- 230000009395 genetic defect Effects 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 230000003054 hormonal effect Effects 0.000 description 3
- 230000003834 intracellular effect Effects 0.000 description 3
- 238000002372 labelling Methods 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000005055 memory storage Effects 0.000 description 3
- 230000037353 metabolic pathway Effects 0.000 description 3
- 206010061289 metastatic neoplasm Diseases 0.000 description 3
- 210000004940 nucleus Anatomy 0.000 description 3
- 238000002966 oligonucleotide array Methods 0.000 description 3
- 210000000056 organ Anatomy 0.000 description 3
- 238000002823 phage display Methods 0.000 description 3
- 238000007894 restriction fragment length polymorphism technique Methods 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 229940126586 small molecule drug Drugs 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 230000008685 targeting Effects 0.000 description 3
- 238000012384 transportation and delivery Methods 0.000 description 3
- 210000004881 tumor cell Anatomy 0.000 description 3
- 239000013598 vector Substances 0.000 description 3
- 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 2
- 241000722946 Acanthocybium solandri Species 0.000 description 2
- 102100029470 Apolipoprotein E Human genes 0.000 description 2
- 101710095339 Apolipoprotein E Proteins 0.000 description 2
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 description 2
- 108700040618 BRCA1 Genes Proteins 0.000 description 2
- 101150064168 CHEK2 gene Proteins 0.000 description 2
- 108020004705 Codon Proteins 0.000 description 2
- 206010014733 Endometrial cancer Diseases 0.000 description 2
- 206010014759 Endometrial neoplasm Diseases 0.000 description 2
- 101710182389 Fibroblast growth factor receptor 2 Proteins 0.000 description 2
- 238000000729 Fisher's exact test Methods 0.000 description 2
- 206010064571 Gene mutation Diseases 0.000 description 2
- 101100220617 Homo sapiens CHEK2 gene Proteins 0.000 description 2
- 101000721661 Homo sapiens Cellular tumor antigen p53 Proteins 0.000 description 2
- 101000777277 Homo sapiens Serine/threonine-protein kinase Chk2 Proteins 0.000 description 2
- 101100099892 Homo sapiens TNRC6B gene Proteins 0.000 description 2
- 208000037396 Intraductal Noninfiltrating Carcinoma Diseases 0.000 description 2
- 206010073094 Intraductal proliferative breast lesion Diseases 0.000 description 2
- 206010073099 Lobular breast carcinoma in situ Diseases 0.000 description 2
- 108060001084 Luciferase Proteins 0.000 description 2
- 239000005089 Luciferase Substances 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 206010030113 Oedema Diseases 0.000 description 2
- 108700020796 Oncogene Proteins 0.000 description 2
- 108700026244 Open Reading Frames Proteins 0.000 description 2
- 108091000080 Phosphotransferase Proteins 0.000 description 2
- 108010083644 Ribonucleases Proteins 0.000 description 2
- 102000006382 Ribonucleases Human genes 0.000 description 2
- 108020004682 Single-Stranded DNA Proteins 0.000 description 2
- 108010090804 Streptavidin Proteins 0.000 description 2
- 206010047249 Venous thrombosis Diseases 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 210000004381 amniotic fluid Anatomy 0.000 description 2
- 229940046844 aromatase inhibitors Drugs 0.000 description 2
- 239000000090 biomarker Substances 0.000 description 2
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000003759 clinical diagnosis Methods 0.000 description 2
- 230000002596 correlated effect Effects 0.000 description 2
- 210000000805 cytoplasm Anatomy 0.000 description 2
- 231100000433 cytotoxic Toxicity 0.000 description 2
- 230000001472 cytotoxic effect Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 238000002716 delivery method Methods 0.000 description 2
- 238000007876 drug discovery Methods 0.000 description 2
- 208000028715 ductal breast carcinoma in situ Diseases 0.000 description 2
- 238000013399 early diagnosis Methods 0.000 description 2
- 238000001962 electrophoresis Methods 0.000 description 2
- 210000003754 fetus Anatomy 0.000 description 2
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 238000003209 gene knockout Methods 0.000 description 2
- 238000001794 hormone therapy Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound 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 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 description 2
- 230000003053 immunization Effects 0.000 description 2
- 230000002163 immunogen Effects 0.000 description 2
- 230000002055 immunohistochemical effect Effects 0.000 description 2
- 238000001114 immunoprecipitation Methods 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 208000030776 invasive breast carcinoma Diseases 0.000 description 2
- 230000003447 ipsilateral effect Effects 0.000 description 2
- 230000003902 lesion Effects 0.000 description 2
- 210000004698 lymphocyte Anatomy 0.000 description 2
- 239000002207 metabolite Substances 0.000 description 2
- 230000001394 metastastic effect Effects 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000003990 molecular pathway Effects 0.000 description 2
- 210000004877 mucosa Anatomy 0.000 description 2
- 210000003205 muscle Anatomy 0.000 description 2
- 238000011275 oncology therapy Methods 0.000 description 2
- 238000009806 oophorectomy Methods 0.000 description 2
- 230000002974 pharmacogenomic effect Effects 0.000 description 2
- 102000020233 phosphotransferase Human genes 0.000 description 2
- 210000002826 placenta Anatomy 0.000 description 2
- 238000013439 planning Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000011321 prophylaxis Methods 0.000 description 2
- 238000012175 pyrosequencing Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000012857 radioactive material Substances 0.000 description 2
- 238000003753 real-time PCR Methods 0.000 description 2
- 102000027426 receptor tyrosine kinases Human genes 0.000 description 2
- 108091008598 receptor tyrosine kinases Proteins 0.000 description 2
- 230000000306 recurrent effect Effects 0.000 description 2
- 108091008146 restriction endonucleases Proteins 0.000 description 2
- 230000019491 signal transduction Effects 0.000 description 2
- 238000011895 specific detection Methods 0.000 description 2
- 238000007619 statistical method Methods 0.000 description 2
- 230000004960 subcellular localization Effects 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- 208000011580 syndromic disease Diseases 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000011269 treatment regimen Methods 0.000 description 2
- 108700026220 vif Genes Proteins 0.000 description 2
- 230000003612 virological effect Effects 0.000 description 2
- CDFKCKUONRRKJD-UHFFFAOYSA-N 1-(3-chlorophenoxy)-3-[2-[[3-(3-chlorophenoxy)-2-hydroxypropyl]amino]ethylamino]propan-2-ol;methanesulfonic acid Chemical compound CS(O)(=O)=O.CS(O)(=O)=O.C=1C=CC(Cl)=CC=1OCC(O)CNCCNCC(O)COC1=CC=CC(Cl)=C1 CDFKCKUONRRKJD-UHFFFAOYSA-N 0.000 description 1
- RNAMYOYQYRYFQY-UHFFFAOYSA-N 2-(4,4-difluoropiperidin-1-yl)-6-methoxy-n-(1-propan-2-ylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine Chemical compound N1=C(N2CCC(F)(F)CC2)N=C2C=C(OCCCN3CCCC3)C(OC)=CC2=C1NC1CCN(C(C)C)CC1 RNAMYOYQYRYFQY-UHFFFAOYSA-N 0.000 description 1
- 102100027962 2-5A-dependent ribonuclease Human genes 0.000 description 1
- 108010000834 2-5A-dependent ribonuclease Proteins 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- 101150090724 3 gene Proteins 0.000 description 1
- 102100024420 39S ribosomal protein S30, mitochondrial Human genes 0.000 description 1
- CJIJXIFQYOPWTF-UHFFFAOYSA-N 7-hydroxycoumarin Natural products O1C(=O)C=CC2=CC(O)=CC=C21 CJIJXIFQYOPWTF-UHFFFAOYSA-N 0.000 description 1
- 102000000872 ATM Human genes 0.000 description 1
- 108010022752 Acetylcholinesterase Proteins 0.000 description 1
- 102100033639 Acetylcholinesterase Human genes 0.000 description 1
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
- 108010000239 Aequorin Proteins 0.000 description 1
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 1
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 1
- 208000024827 Alzheimer disease Diseases 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 108091023037 Aptamer Proteins 0.000 description 1
- 229940122815 Aromatase inhibitor Drugs 0.000 description 1
- 108010004586 Ataxia Telangiectasia Mutated Proteins Proteins 0.000 description 1
- 108090001008 Avidin Proteins 0.000 description 1
- 231100000699 Bacterial toxin Toxicity 0.000 description 1
- 102100026189 Beta-galactosidase Human genes 0.000 description 1
- 208000005623 Carcinogenesis Diseases 0.000 description 1
- 108090000994 Catalytic RNA Proteins 0.000 description 1
- 102000053642 Catalytic RNA Human genes 0.000 description 1
- 208000002177 Cataract Diseases 0.000 description 1
- 208000010833 Chronic myeloid leukaemia Diseases 0.000 description 1
- 108091026890 Coding region Proteins 0.000 description 1
- 108091033380 Coding strand Proteins 0.000 description 1
- 108020004635 Complementary DNA Proteins 0.000 description 1
- 206010010356 Congenital anomaly Diseases 0.000 description 1
- 208000036493 Contralateral breast cancer Diseases 0.000 description 1
- 208000012609 Cowden disease Diseases 0.000 description 1
- 201000002847 Cowden syndrome Diseases 0.000 description 1
- 101710112752 Cytotoxin Proteins 0.000 description 1
- IGXWBGJHJZYPQS-SSDOTTSWSA-N D-Luciferin Chemical compound OC(=O)[C@H]1CSC(C=2SC3=CC=C(O)C=C3N=2)=N1 IGXWBGJHJZYPQS-SSDOTTSWSA-N 0.000 description 1
- 108020003215 DNA Probes Proteins 0.000 description 1
- 230000005778 DNA damage Effects 0.000 description 1
- 231100000277 DNA damage Toxicity 0.000 description 1
- 239000003155 DNA primer Substances 0.000 description 1
- 239000003298 DNA probe Substances 0.000 description 1
- 230000033616 DNA repair Effects 0.000 description 1
- 102000016928 DNA-directed DNA polymerase Human genes 0.000 description 1
- 108010014303 DNA-directed DNA polymerase Proteins 0.000 description 1
- XPDXVDYUQZHFPV-UHFFFAOYSA-N Dansyl Chloride Chemical compound C1=CC=C2C(N(C)C)=CC=CC2=C1S(Cl)(=O)=O XPDXVDYUQZHFPV-UHFFFAOYSA-N 0.000 description 1
- 206010051055 Deep vein thrombosis Diseases 0.000 description 1
- CYCGRDQQIOGCKX-UHFFFAOYSA-N Dehydro-luciferin Natural products OC(=O)C1=CSC(C=2SC3=CC(O)=CC=C3N=2)=N1 CYCGRDQQIOGCKX-UHFFFAOYSA-N 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- 108010036364 Deoxyribonuclease IV (Phage T4-Induced) Proteins 0.000 description 1
- 241000702421 Dependoparvovirus Species 0.000 description 1
- 206010061818 Disease progression Diseases 0.000 description 1
- 206010061819 Disease recurrence Diseases 0.000 description 1
- 208000030453 Drug-Related Side Effects and Adverse reaction Diseases 0.000 description 1
- 101150029707 ERBB2 gene Proteins 0.000 description 1
- 102000004533 Endonucleases Human genes 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 108700024394 Exon Proteins 0.000 description 1
- 102100028412 Fibroblast growth factor 10 Human genes 0.000 description 1
- 102100023600 Fibroblast growth factor receptor 2 Human genes 0.000 description 1
- 206010016654 Fibrosis Diseases 0.000 description 1
- BJGNCJDXODQBOB-UHFFFAOYSA-N Fivefly Luciferin Natural products OC(=O)C1CSC(C=2SC3=CC(O)=CC=C3N=2)=N1 BJGNCJDXODQBOB-UHFFFAOYSA-N 0.000 description 1
- 240000005702 Galium aparine Species 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- 108700039691 Genetic Promoter Regions Proteins 0.000 description 1
- 208000034951 Genetic Translocation Diseases 0.000 description 1
- 208000010412 Glaucoma Diseases 0.000 description 1
- 206010018364 Glomerulonephritis Diseases 0.000 description 1
- 208000031886 HIV Infections Diseases 0.000 description 1
- 108091027305 Heteroduplex Proteins 0.000 description 1
- 101000689854 Homo sapiens 39S ribosomal protein S30, mitochondrial Proteins 0.000 description 1
- 101100227106 Homo sapiens FHOD3 gene Proteins 0.000 description 1
- 101000917237 Homo sapiens Fibroblast growth factor 10 Proteins 0.000 description 1
- 101000984710 Homo sapiens Lymphocyte-specific protein 1 Proteins 0.000 description 1
- 101100351019 Homo sapiens PAX5 gene Proteins 0.000 description 1
- 101001009074 Homo sapiens Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 Proteins 0.000 description 1
- 101000679548 Homo sapiens TOX high mobility group box family member 3 Proteins 0.000 description 1
- 108010001336 Horseradish Peroxidase Proteins 0.000 description 1
- 102000008394 Immunoglobulin Fragments Human genes 0.000 description 1
- 108010021625 Immunoglobulin Fragments Proteins 0.000 description 1
- 102100034343 Integrase Human genes 0.000 description 1
- 101710203526 Integrase Proteins 0.000 description 1
- 239000005517 L01XE01 - Imatinib Substances 0.000 description 1
- 241000713666 Lentivirus Species 0.000 description 1
- 238000003657 Likelihood-ratio test Methods 0.000 description 1
- DDWFXDSYGUXRAY-UHFFFAOYSA-N Luciferin Natural products CCc1c(C)c(CC2NC(=O)C(=C2C=C)C)[nH]c1Cc3[nH]c4C(=C5/NC(CC(=O)O)C(C)C5CC(=O)O)CC(=O)c4c3C DDWFXDSYGUXRAY-UHFFFAOYSA-N 0.000 description 1
- 108010075654 MAP Kinase Kinase Kinase 1 Proteins 0.000 description 1
- 208000004059 Male Breast Neoplasms Diseases 0.000 description 1
- 238000007476 Maximum Likelihood Methods 0.000 description 1
- 102100033115 Mitogen-activated protein kinase kinase kinase 1 Human genes 0.000 description 1
- 208000008770 Multiple Hamartoma Syndrome Diseases 0.000 description 1
- 102000010645 MutS Proteins Human genes 0.000 description 1
- 108010038272 MutS Proteins Proteins 0.000 description 1
- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 description 1
- 102400000058 Neuregulin-1 Human genes 0.000 description 1
- 108090000556 Neuregulin-1 Proteins 0.000 description 1
- 108020004485 Nonsense Codon Proteins 0.000 description 1
- 238000000636 Northern blotting Methods 0.000 description 1
- 101710163270 Nuclease Proteins 0.000 description 1
- 101150017484 PAX5 gene Proteins 0.000 description 1
- 235000011464 Pachycereus pringlei Nutrition 0.000 description 1
- 240000006939 Pachycereus weberi Species 0.000 description 1
- 235000011466 Pachycereus weberi Nutrition 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 108010010677 Phosphodiesterase I Proteins 0.000 description 1
- 108010004729 Phycoerythrin Proteins 0.000 description 1
- 231100000742 Plant toxin Toxicity 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- 241000276498 Pollachius virens Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 102100027376 Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 Human genes 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 208000010378 Pulmonary Embolism Diseases 0.000 description 1
- 108020004518 RNA Probes Proteins 0.000 description 1
- 239000003391 RNA probe Substances 0.000 description 1
- 108091030071 RNAI Proteins 0.000 description 1
- 208000035977 Rare disease Diseases 0.000 description 1
- 208000033722 Rare malignant breast tumor Diseases 0.000 description 1
- 108700008625 Reporter Genes Proteins 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- 108010039491 Ricin Proteins 0.000 description 1
- 108091081021 Sense strand Proteins 0.000 description 1
- 102100031075 Serine/threonine-protein kinase Chk2 Human genes 0.000 description 1
- 206010040844 Skin exfoliation Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 102100022608 TOX high mobility group box family member 3 Human genes 0.000 description 1
- 206010043189 Telangiectasia Diseases 0.000 description 1
- 108091036066 Three prime untranslated region Proteins 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 206010070863 Toxicity to various agents Diseases 0.000 description 1
- 206010066901 Treatment failure Diseases 0.000 description 1
- 101710087261 Trinucleotide repeat-containing gene 6B protein Proteins 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 101150003160 X gene Proteins 0.000 description 1
- DUDJTRNGXIUJEB-UHFFFAOYSA-N [N].NCC(O)=O Chemical group [N].NCC(O)=O DUDJTRNGXIUJEB-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229940022698 acetylcholinesterase Drugs 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 238000009098 adjuvant therapy Methods 0.000 description 1
- 238000001042 affinity chromatography Methods 0.000 description 1
- 238000007844 allele-specific PCR Methods 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- VREFGVBLTWBCJP-UHFFFAOYSA-N alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 description 1
- 238000002669 amniocentesis Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 229940046836 anti-estrogen Drugs 0.000 description 1
- 230000001833 anti-estrogenic effect Effects 0.000 description 1
- 210000000628 antibody-producing cell Anatomy 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 230000003190 augmentative effect Effects 0.000 description 1
- 210000003719 b-lymphocyte Anatomy 0.000 description 1
- 239000000688 bacterial toxin Substances 0.000 description 1
- 108010005774 beta-Galactosidase Proteins 0.000 description 1
- 230000002146 bilateral effect Effects 0.000 description 1
- 230000008827 biological function Effects 0.000 description 1
- 238000001574 biopsy Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000003560 cancer drug Substances 0.000 description 1
- 230000036952 cancer formation Effects 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 210000005056 cell body Anatomy 0.000 description 1
- 230000032823 cell division Effects 0.000 description 1
- 230000007910 cell fusion Effects 0.000 description 1
- 239000013592 cell lysate Substances 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 210000004671 cell-free system Anatomy 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000036755 cellular response Effects 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000012707 chemical precursor Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000009223 counseling Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000000287 crude extract Substances 0.000 description 1
- 239000012228 culture supernatant Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- 231100000599 cytotoxic agent Toxicity 0.000 description 1
- 239000002619 cytotoxin Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000003936 denaturing gel electrophoresis Methods 0.000 description 1
- 238000003935 denaturing gradient gel electrophoresis Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000035618 desquamation Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000003748 differential diagnosis Methods 0.000 description 1
- 206010013023 diphtheria Diseases 0.000 description 1
- 230000005750 disease progression Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000005782 double-strand break Effects 0.000 description 1
- 230000012361 double-strand break repair Effects 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 239000003596 drug target Substances 0.000 description 1
- 238000002651 drug therapy Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 230000001819 effect on gene Effects 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 238000009585 enzyme analysis Methods 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 239000000328 estrogen antagonist Substances 0.000 description 1
- 201000007280 estrogen-receptor negative breast cancer Diseases 0.000 description 1
- 238000010195 expression analysis Methods 0.000 description 1
- 201000007741 female breast cancer Diseases 0.000 description 1
- 201000002276 female breast carcinoma Diseases 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 101150088071 fgfr2 gene Proteins 0.000 description 1
- 230000004761 fibrosis Effects 0.000 description 1
- MHMNJMPURVTYEJ-UHFFFAOYSA-N fluorescein-5-isothiocyanate Chemical compound O1C(=O)C2=CC(N=C=S)=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 MHMNJMPURVTYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000001502 gel electrophoresis Methods 0.000 description 1
- 101150046383 gene 5 gene Proteins 0.000 description 1
- 238000003633 gene expression assay Methods 0.000 description 1
- 238000013412 genome amplification Methods 0.000 description 1
- 229940080856 gleevec Drugs 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 229940022353 herceptin Drugs 0.000 description 1
- 208000016356 hereditary diffuse gastric adenocarcinoma Diseases 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000010562 histological examination Methods 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- 210000004408 hybridoma Anatomy 0.000 description 1
- 230000003463 hyperproliferative effect Effects 0.000 description 1
- 229960002411 imatinib Drugs 0.000 description 1
- 238000002649 immunization Methods 0.000 description 1
- 238000003018 immunoassay Methods 0.000 description 1
- 238000003119 immunoblot Methods 0.000 description 1
- 238000010166 immunofluorescence Methods 0.000 description 1
- 238000007901 in situ hybridization Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- 210000002490 intestinal epithelial cell Anatomy 0.000 description 1
- 206010073095 invasive ductal breast carcinoma Diseases 0.000 description 1
- 201000010985 invasive ductal carcinoma Diseases 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 238000001155 isoelectric focusing Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 230000000366 juvenile effect Effects 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 238000011454 long-term hormonal therapy Methods 0.000 description 1
- 238000011866 long-term treatment Methods 0.000 description 1
- HWYHZTIRURJOHG-UHFFFAOYSA-N luminol Chemical compound O=C1NNC(=O)C2=C1C(N)=CC=C2 HWYHZTIRURJOHG-UHFFFAOYSA-N 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 238000002595 magnetic resonance imaging Methods 0.000 description 1
- 201000003175 male breast cancer Diseases 0.000 description 1
- 208000010907 male breast carcinoma Diseases 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000008774 maternal effect Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 1
- 238000002493 microarray Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000001823 molecular biology technique Methods 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 238000000491 multivariate analysis Methods 0.000 description 1
- 201000000050 myeloid neoplasm Diseases 0.000 description 1
- ZTLGJPIZUOVDMT-UHFFFAOYSA-N n,n-dichlorotriazin-4-amine Chemical compound ClN(Cl)C1=CC=NN=N1 ZTLGJPIZUOVDMT-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 238000007857 nested PCR Methods 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 230000001818 nuclear effect Effects 0.000 description 1
- 238000007826 nucleic acid assay Methods 0.000 description 1
- 238000007899 nucleic acid hybridization Methods 0.000 description 1
- -1 nucleic acid lipid Chemical class 0.000 description 1
- 238000002515 oligonucleotide synthesis Methods 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 102000045222 parkin Human genes 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000008775 paternal effect Effects 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 230000006320 pegylation Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 210000004214 philadelphia chromosome Anatomy 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 239000003123 plant toxin Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000002264 polyacrylamide gel electrophoresis Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000003234 polygenic effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 235000019419 proteases Nutrition 0.000 description 1
- 230000004853 protein function Effects 0.000 description 1
- 238000000734 protein sequencing Methods 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 208000005069 pulmonary fibrosis Diseases 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 238000010188 recombinant method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000006335 response to radiation Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 125000000548 ribosyl group Chemical group C1([C@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 108091092562 ribozyme Proteins 0.000 description 1
- 238000013058 risk prediction model Methods 0.000 description 1
- 102220381126 rs17001943 Human genes 0.000 description 1
- 102220381284 rs17001977 Human genes 0.000 description 1
- 102220438908 rs17002069 Human genes 0.000 description 1
- 102200081254 rs28997576 Human genes 0.000 description 1
- 102210056307 rs9607721 Human genes 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000007480 sanger sequencing Methods 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 210000003765 sex chromosome Anatomy 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000000392 somatic effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 210000004988 splenocyte Anatomy 0.000 description 1
- 238000013179 statistical model Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000008093 supporting effect Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 208000009056 telangiectasis Diseases 0.000 description 1
- 238000005382 thermal cycling Methods 0.000 description 1
- 230000000451 tissue damage Effects 0.000 description 1
- 231100000827 tissue damage Toxicity 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000007723 transport mechanism Effects 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
- HFTAFOQKODTIJY-UHFFFAOYSA-N umbelliferone Natural products Cc1cc2C=CC(=O)Oc2cc1OCC=CC(C)(C)O HFTAFOQKODTIJY-UHFFFAOYSA-N 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- 239000013603 viral vector Substances 0.000 description 1
- 238000001262 western blot Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B35/00—ICT specially adapted for in silico combinatorial libraries of nucleic acids, proteins or peptides
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B99/00—Subject matter not provided for in other groups of this subclass
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16C—COMPUTATIONAL CHEMISTRY; CHEMOINFORMATICS; COMPUTATIONAL MATERIALS SCIENCE
- G16C20/00—Chemoinformatics, i.e. ICT specially adapted for the handling of physicochemical or structural data of chemical particles, elements, compounds or mixtures
- G16C20/60—In silico combinatorial chemistry
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/106—Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/136—Screening for pharmacological compounds
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/172—Haplotypes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A90/00—Technologies having an indirect contribution to adaptation to climate change
- Y02A90/10—Information and communication technologies [ICT] supporting adaptation to climate change, e.g. for weather forecasting or climate simulation
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Genetics & Genomics (AREA)
- Pathology (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- General Engineering & Computer Science (AREA)
- Hospice & Palliative Care (AREA)
- Oncology (AREA)
- Microbiology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Theoretical Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Evolutionary Biology (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Library & Information Science (AREA)
- Computing Systems (AREA)
- Crystallography & Structural Chemistry (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IS8746 | 2008-07-07 | ||
| IS8746 | 2008-07-07 | ||
| PCT/IS2009/000008 WO2010004591A2 (en) | 2008-07-07 | 2009-07-03 | Genetic variants for breast cancer risk assessment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011527565A true JP2011527565A (ja) | 2011-11-04 |
| JP2011527565A5 JP2011527565A5 (enExample) | 2012-08-16 |
Family
ID=41110719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011517318A Pending JP2011527565A (ja) | 2008-07-07 | 2009-07-03 | 乳癌のリスクアセスメントのための遺伝的変異 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8951735B2 (enExample) |
| EP (1) | EP2313525A2 (enExample) |
| JP (1) | JP2011527565A (enExample) |
| KR (1) | KR20110036608A (enExample) |
| CN (1) | CN102144036B (enExample) |
| AU (1) | AU2009269542A1 (enExample) |
| CA (1) | CA2729934A1 (enExample) |
| IL (1) | IL210504A0 (enExample) |
| NZ (1) | NZ590833A (enExample) |
| WO (1) | WO2010004591A2 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011095999A1 (en) * | 2010-02-05 | 2011-08-11 | Decode Genetics Ehf | Genetic variants for predicting risk of breast cancer |
| EP2721180A4 (en) * | 2011-06-16 | 2015-09-02 | Decode Genetics Ehf | GENETIC VARIANTS FOR PREDICTING THE RISK OF BREAST CANCER |
| CN102643905B (zh) * | 2012-04-01 | 2014-06-11 | 周宏灏 | 焦磷酸测序法检测他莫昔芬个体化用药基因多态性的试剂盒及方法 |
| KR101770962B1 (ko) * | 2013-02-01 | 2017-08-24 | 에스케이텔레콤 주식회사 | 유전자 서열 기반 개인 마커에 관한 정보를 제공하는 방법 및 이를 이용한 장치 |
| WO2014119914A1 (ko) * | 2013-02-01 | 2014-08-07 | 에스케이텔레콤 주식회사 | 유전자 서열 기반 개인 마커에 관한 정보를 제공하는 방법 및 이를 이용한 장치 |
| WO2014145705A2 (en) | 2013-03-15 | 2014-09-18 | Battelle Memorial Institute | Progression analytics system |
| CN103981273B (zh) * | 2014-05-30 | 2017-01-18 | 复旦大学附属肿瘤医院 | 一组评估乳腺癌风险的突变基因群及其检测试剂盒 |
| US10395759B2 (en) | 2015-05-18 | 2019-08-27 | Regeneron Pharmaceuticals, Inc. | Methods and systems for copy number variant detection |
| CN105069322B (zh) * | 2015-07-24 | 2018-01-12 | 上海尔云信息科技有限公司 | 疾病易感风险预测装置 |
| CN109074426B (zh) | 2016-02-12 | 2022-07-26 | 瑞泽恩制药公司 | 用于检测异常核型的方法和系统 |
| CN105586427B (zh) * | 2016-03-10 | 2020-06-19 | 厦门艾德生物医药科技股份有限公司 | 检测人类brca1和brca2基因突变的引物、试剂盒及方法 |
| US11332530B2 (en) | 2016-09-23 | 2022-05-17 | Memorial Sloan Kettering Cancer Center | Determinants of cancer response to immunotherapy |
| CN106676169B (zh) * | 2016-11-15 | 2021-01-12 | 上海派森诺医学检验所有限公司 | 一种用于乳腺癌易感基因brca1和brca2突变检测的杂交捕获试剂盒及其方法 |
| CA3051488A1 (en) * | 2017-01-24 | 2018-08-02 | Genetic Technologies Limited | Improved methods for assessing risk of developing breast cancer |
| CN107341347A (zh) * | 2017-06-27 | 2017-11-10 | 天方创新(北京)信息技术有限公司 | 基于评分模型对乳腺癌进行风险评分的方法及装置 |
| EP3814521A4 (en) * | 2018-06-29 | 2022-07-27 | The Jackson Laboratory | SPLICING VARIANTS FOR BREAST CANCER |
| CN108676890B (zh) * | 2018-07-12 | 2022-01-28 | 吉林大学 | 一种女性乳腺恶性肿瘤易感性预测试剂盒及系统 |
| US20230170045A1 (en) * | 2020-04-20 | 2023-06-01 | Myriad Genetics, Inc. | Comprehensive polygenic risk prediction for breast cancer |
| WO2024085660A1 (ko) * | 2022-10-18 | 2024-04-25 | 제노플랜 인크 | 질병 발생 위험도 예측 장치 및 방법 |
| WO2024148280A1 (en) | 2023-01-06 | 2024-07-11 | Ideaya Biosciences, Inc. | Treatment of er+ breast cancer comprising homologous recombination deficiency using parc inhibitor |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040009481A1 (en) * | 2001-06-11 | 2004-01-15 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of human prostate cancer |
| WO2008050356A1 (en) * | 2006-10-27 | 2008-05-02 | Decode Genetics | Cancer susceptibility variants on chr8q24.21 |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4376110A (en) | 1980-08-04 | 1983-03-08 | Hybritech, Incorporated | Immunometric assays using monoclonal antibodies |
| GB8810400D0 (en) | 1988-05-03 | 1988-06-08 | Southern E | Analysing polynucleotide sequences |
| US5700637A (en) | 1988-05-03 | 1997-12-23 | Isis Innovation Limited | Apparatus and method for analyzing polynucleotide sequences and method of generating oligonucleotide arrays |
| US6054270A (en) | 1988-05-03 | 2000-04-25 | Oxford Gene Technology Limited | Analying polynucleotide sequences |
| EP1997891A1 (en) | 1988-09-02 | 2008-12-03 | Dyax Corporation | Generation and selection of recombinant varied binding proteins |
| US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
| US5143854A (en) | 1989-06-07 | 1992-09-01 | Affymax Technologies N.V. | Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof |
| US5744101A (en) | 1989-06-07 | 1998-04-28 | Affymax Technologies N.V. | Photolabile nucleoside protecting groups |
| US5288644A (en) | 1990-04-04 | 1994-02-22 | The Rockefeller University | Instrument and method for the sequencing of genome |
| US5427908A (en) | 1990-05-01 | 1995-06-27 | Affymax Technologies N.V. | Recombinant library screening methods |
| AU665190B2 (en) | 1990-07-10 | 1995-12-21 | Cambridge Antibody Technology Limited | Methods for producing members of specific binding pairs |
| GB9015198D0 (en) | 1990-07-10 | 1990-08-29 | Brien Caroline J O | Binding substance |
| WO1992009690A2 (en) | 1990-12-03 | 1992-06-11 | Genentech, Inc. | Enrichment method for variant proteins with altered binding properties |
| ATE439435T1 (de) | 1991-03-01 | 2009-08-15 | Dyax Corp | Chimäres protein mit mikroprotein mit zwei oder mehr disulfidbindungen und ausgestaltungen davon |
| DE69233750D1 (de) | 1991-04-10 | 2009-01-02 | Scripps Research Inst | Bibliotheken heterodimerer Rezeptoren mittels Phagemiden |
| DE4122599C2 (de) | 1991-07-08 | 1993-11-11 | Deutsches Krebsforsch | Phagemid zum Screenen von Antikörpern |
| US6287850B1 (en) | 1995-06-07 | 2001-09-11 | Affymetrix, Inc. | Bioarray chip reaction apparatus and its manufacture |
| EP0695941B1 (en) | 1994-06-08 | 2002-07-31 | Affymetrix, Inc. | Method and apparatus for packaging a chip |
| US6300063B1 (en) | 1995-11-29 | 2001-10-09 | Affymetrix, Inc. | Polymorphism detection |
| EP2369007B1 (en) | 1996-05-29 | 2015-07-29 | Cornell Research Foundation, Inc. | Detection of nucleic acid sequence differences using coupled ligase detection and polymerase chain reactions |
| US6429027B1 (en) | 1998-12-28 | 2002-08-06 | Illumina, Inc. | Composite arrays utilizing microspheres |
| DE10228081A1 (de) * | 2002-06-18 | 2004-01-08 | InViTek Gesellschaft für Biotechnik & Biodesign mbH | Verfahren zum Nachweis einer gesteigerten Tumorsuszeptibilität |
| KR100763902B1 (ko) * | 2004-02-20 | 2007-10-05 | 삼성전자주식회사 | 유방암 특이적 단백질, 그를 코딩하는 유전자, 및 상기단백질 또는 유전자를 이용한 유방암의 진단 방법 |
| WO2006063285A2 (en) * | 2004-12-10 | 2006-06-15 | Sequenom, Inc. | Methods for identifying risk of breast cancer or prostate cancer and treatments thereof |
| CN101037690B (zh) * | 2006-03-16 | 2011-07-20 | 国家人口计生委科学技术研究所 | 具有新的单核苷酸多态性的brca1基因变体和其编码的蛋白质变体 |
| CN101874120B (zh) | 2007-03-26 | 2015-01-14 | 解码遗传学私营有限责任公司 | 作为用于乳腺癌风险评估、诊断、预后和治疗的标记的chr2和chr16的遗传性变型 |
| EP2164984A2 (en) | 2007-05-25 | 2010-03-24 | Decode Genetics EHF. | Genetic variants on chr 5pl2 and 10q26 as markers for use in breast cancer risk assessment, diagnosis, prognosis and treatment |
-
2009
- 2009-07-03 AU AU2009269542A patent/AU2009269542A1/en not_active Abandoned
- 2009-07-03 JP JP2011517318A patent/JP2011527565A/ja active Pending
- 2009-07-03 KR KR1020117002889A patent/KR20110036608A/ko not_active Ceased
- 2009-07-03 EP EP09787620A patent/EP2313525A2/en not_active Withdrawn
- 2009-07-03 WO PCT/IS2009/000008 patent/WO2010004591A2/en not_active Ceased
- 2009-07-03 CA CA2729934A patent/CA2729934A1/en not_active Abandoned
- 2009-07-03 CN CN200980134453.0A patent/CN102144036B/zh not_active Expired - Fee Related
- 2009-07-03 NZ NZ590833A patent/NZ590833A/xx not_active IP Right Cessation
- 2009-07-03 US US13/002,619 patent/US8951735B2/en not_active Expired - Fee Related
-
2011
- 2011-01-06 IL IL210504A patent/IL210504A0/en unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040009481A1 (en) * | 2001-06-11 | 2004-01-15 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of human prostate cancer |
| WO2008050356A1 (en) * | 2006-10-27 | 2008-05-02 | Decode Genetics | Cancer susceptibility variants on chr8q24.21 |
Non-Patent Citations (9)
| Title |
|---|
| GOLD BERT ET AL: "GENOME-WIDE ASSOCIATION STUDY PROVIDES EVIDENCE FOR A BREAST CANCER RISK LOCUS AT 6Q22.33", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF USA, vol. 105, no. 11, JPN5011006575, 1 March 2008 (2008-03-01), US, pages 4340 - 4345, XP002527419, ISSN: 0002728398, DOI: 10.1073/PNAS.0800441105 * |
| HOYAL CAROLYN R ET AL: "GENETIC POLYMORPHISMS IN DPF3 ASSOCIATED WITH RISK OF BREAST CANCER AND LYMPH NODE METASTASES", JOURNAL OF CARCINOGENESIS, vol. 4, no. 1, JPN5011006573, 19 August 2005 (2005-08-19), GB, XP021008706, ISSN: 0002728396, DOI: 10.1186/1477-3163-4-13 * |
| INGRAHAM ET AL, CANCER GENET CYTOGENET, vol. 115, JPN6014001916, 1999, pages 56 - 61, ISSN: 0002728401 * |
| PENG ET AL, GENOMICS, vol. 54, JPN6014001912, 1998, pages 529 - 541, ISSN: 0002728400 * |
| SHLIEN ET AL, PNAS, vol. 105, no. 32, JPN6014001918, 12 August 2008 (2008-08-12), pages 11264 - 11269, ISSN: 0002728402 * |
| STACEY SIMON N ET AL, NATURE GENETICS, vol. 39, no. 7, JPN5011006576, 1 July 2007 (2007-07-01), US, pages 865 - 869, ISSN: 0002728399 * |
| STACEY SIMON N ET AL: "COMMON VARIANTS ON CHROMOSOME 5P12 CONFER SUSCEPTIBILITY TO ESTROGEN RECEPTOR-POSITIVE BREAST CANCER", NATURE GENETICS, vol. 40, no. 6, JPN5011006574, 1 June 2008 (2008-06-01), US, pages 703 - 706, XP002491374, ISSN: 0002728397, DOI: 10.1038/ng.131 * |
| STEEMERS FRANK J ET AL: "WHOLE GENOME GENOTYPING TECHNOLOGIES ON THE BEADARRAY PLATFORM", BIOTECHNOLOGY JOURNAL, vol. 2, no. 1, JPN5011006571, January 2007 (2007-01-01), pages 41 - 49, XP002548190, ISSN: 0002728394, DOI: 10.1002/BIOT.200600213 * |
| THOMAS GILLES ET AL, NATURE GENETICS, vol. 41, no. 5, JPN5011006572, May 2009 (2009-05-01), pages 579 - 584, ISSN: 0002728395 * |
Also Published As
| Publication number | Publication date |
|---|---|
| IL210504A0 (en) | 2011-03-31 |
| EP2313525A2 (en) | 2011-04-27 |
| AU2009269542A1 (en) | 2010-01-14 |
| US20110294673A1 (en) | 2011-12-01 |
| WO2010004591A2 (en) | 2010-01-14 |
| WO2010004591A3 (en) | 2010-03-18 |
| CA2729934A1 (en) | 2010-01-14 |
| CN102144036A (zh) | 2011-08-03 |
| KR20110036608A (ko) | 2011-04-07 |
| CN102144036B (zh) | 2014-07-16 |
| NZ590833A (en) | 2013-01-25 |
| US8951735B2 (en) | 2015-02-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5676245B2 (ja) | 乳癌のリスクアセスメント、診断、予後診断および治療における使用のためのマーカーとしてのchr2およびchr16の遺伝的変異 | |
| CN102144036B (zh) | 用于乳腺癌风险评估的遗传变型 | |
| JP5631000B2 (ja) | Chr8q24.21上の癌感受性変異体 | |
| US8580501B2 (en) | Genetic variants on chr 5p12 and 10q26 as markers for use in breast cancer risk assessment, diagnosis, prognosis and treatment | |
| CN102177252B (zh) | 用于甲状腺癌症的风险评估的遗传变型 | |
| US8865400B2 (en) | Genetic variants contributing to risk of prostate cancer | |
| WO2013035114A1 (en) | Tp53 genetic variants predictive of cancer | |
| CN102137937A (zh) | 作为用于膀胱癌风险评估、诊断、预后和治疗的标志的遗传变型 | |
| US20110020320A1 (en) | Genetic Variants Contributing to Risk of Prostate Cancer | |
| WO2013065072A1 (en) | Risk variants of prostate cancer | |
| EP2681337B1 (en) | Brip1 variants associated with risk for cancer | |
| WO2010131268A1 (en) | Genetic variants for basal cell carcinoma, squamous cell carcinoma and cutaneous melanoma | |
| WO2011095999A1 (en) | Genetic variants for predicting risk of breast cancer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120628 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20120628 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140121 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140414 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140421 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140716 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150127 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150630 |