MX2022002832A - Tratamiento del cancer con recombinacion homologa deficiente. - Google Patents
Tratamiento del cancer con recombinacion homologa deficiente.Info
- Publication number
- MX2022002832A MX2022002832A MX2022002832A MX2022002832A MX2022002832A MX 2022002832 A MX2022002832 A MX 2022002832A MX 2022002832 A MX2022002832 A MX 2022002832A MX 2022002832 A MX2022002832 A MX 2022002832A MX 2022002832 A MX2022002832 A MX 2022002832A
- Authority
- MX
- Mexico
- Prior art keywords
- dnph1
- treatment
- inhibition
- hmdu
- finding
- Prior art date
Links
- 230000002950 deficient Effects 0.000 title abstract 4
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 102100033260 2'-deoxynucleoside 5'-phosphate N-hydrolase 1 Human genes 0.000 abstract 4
- 230000006801 homologous recombination Effects 0.000 abstract 4
- 238000002744 homologous recombination Methods 0.000 abstract 4
- 230000005764 inhibitory process Effects 0.000 abstract 4
- 101000927689 Homo sapiens 2'-deoxynucleoside 5'-phosphate N-hydrolase 1 Proteins 0.000 abstract 3
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 abstract 2
- 238000002679 ablation Methods 0.000 abstract 2
- 230000003197 catalytic effect Effects 0.000 abstract 2
- 230000002068 genetic effect Effects 0.000 abstract 2
- 101710089392 2'-deoxynucleoside 5'-phosphate N-hydrolase 1 Proteins 0.000 abstract 1
- IPAVKOYJGUMINP-XLPZGREQSA-N 5-hydroxymethyl-2'-deoxyuridine Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(CO)=C1 IPAVKOYJGUMINP-XLPZGREQSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 231100000225 lethality Toxicity 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
Classifications
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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- A—HUMAN NECESSITIES
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- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
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- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7088—Compounds having three or more nucleosides or nucleotides
- A61K31/713—Double-stranded nucleic acids or oligonucleotides
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- 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
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- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
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- 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
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- 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
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- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
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Abstract
La presente invención se refiere al descubrimiento de que las células deficientes en recombinación homóloga (HR) son sensibles a la inhibición de PARP mediante (i) la inhibición catalítica o la ablación genética de la 2'-desoxinucleósido 5'-fosfato N-hidrolasa 1 (DNPH1) o (ii) la administración de un sustrato de DNPH1, tal como la 5-hidroximetil desoxiuridina (hmdU). La invención también se relaciona con el hallazgo de que la inhibición catalítica o la ablación genética de DNPH1 combinada con la administración de hmdU causa letalidad sintética en células deficientes en HR en ausencia de inhibición de PARP. Se proporcionan métodos y compuestos para usarse en el tratamiento de cáncer deficiente de HR.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1913030.1A GB201913030D0 (en) | 2019-09-10 | 2019-09-10 | Treatment of hr deficient cancer |
PCT/EP2020/075245 WO2021048235A1 (en) | 2019-09-10 | 2020-09-09 | Treatment of hr deficient cancer |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2022002832A true MX2022002832A (es) | 2022-04-06 |
Family
ID=68241178
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2022002832A MX2022002832A (es) | 2019-09-10 | 2020-09-09 | Tratamiento del cancer con recombinacion homologa deficiente. |
Country Status (10)
Country | Link |
---|---|
US (1) | US20220339179A1 (es) |
EP (1) | EP4028009A1 (es) |
JP (1) | JP2022547206A (es) |
KR (1) | KR20220064380A (es) |
AU (1) | AU2020344145A1 (es) |
CA (1) | CA3153692A1 (es) |
GB (1) | GB201913030D0 (es) |
IL (1) | IL291170A (es) |
MX (1) | MX2022002832A (es) |
WO (1) | WO2021048235A1 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2580963B (en) | 2019-02-01 | 2021-03-31 | Hemispherian As | Cancer therapies |
CN112708676B (zh) * | 2020-12-29 | 2024-05-14 | 南京科佰基因科技有限公司 | 一种用于dna同源重组修复基因检测的标准品及其制备方法 |
CN112853502B (zh) * | 2021-01-14 | 2022-07-15 | 中国医学科学院基础医学研究所 | 小鼠表观遗传基因敲除筛选文库及其构建方法 |
US20240238283A1 (en) * | 2021-05-18 | 2024-07-18 | Onconic Therapeutics Inc. | Parp inhibitor-resistant cancer therapeutic agent |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
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US5587384A (en) | 1994-02-04 | 1996-12-24 | The Johns Hopkins University | Inhibitors of poly(ADP-ribose) synthetase and use thereof to treat NMDA neurotoxicity |
GB9404485D0 (en) | 1994-03-09 | 1994-04-20 | Cancer Res Campaign Tech | Benzamide analogues |
US6635642B1 (en) | 1997-09-03 | 2003-10-21 | Guilford Pharmaceuticals Inc. | PARP inhibitors, pharmaceutical compositions comprising same, and methods of using same |
US6514983B1 (en) | 1997-09-03 | 2003-02-04 | Guilford Pharmaceuticals Inc. | Compounds, methods and pharmaceutical compositions for treating neural or cardiovascular tissue damage |
US6426415B1 (en) | 1997-09-03 | 2002-07-30 | Guilford Pharmaceuticals Inc. | Alkoxy-substituted compounds, methods and compositions for inhibiting parp activity |
US6506559B1 (en) | 1997-12-23 | 2003-01-14 | Carnegie Institute Of Washington | Genetic inhibition by double-stranded RNA |
US6465448B1 (en) | 1999-08-13 | 2002-10-15 | Case Western Reserve University | Methoxyamine potentiation of temozolomide anti-cancer activity |
ECSP003637A (es) | 1999-08-31 | 2002-03-25 | Agouron Pharma | Inhibidores triciclicos de poli (adp-ribosa) polimerasas |
AU7314200A (en) | 1999-09-17 | 2001-04-24 | Yamanouchi Pharmaceutical Co., Ltd. | Benzimidazole derivatives |
TR200101499T1 (tr) | 1999-09-28 | 2002-09-23 | Basf Aktiengesellschaft | Azepinoindol türevleri, hazırlanmaları ve kullanımları. |
WO2001029058A1 (en) | 1999-10-15 | 2001-04-26 | University Of Massachusetts | Rna interference pathway genes as tools for targeted genetic interference |
US6476048B1 (en) | 1999-12-07 | 2002-11-05 | Inotek Pharamaceuticals Corporation | Substituted phenanthridinones and methods of use thereof |
DE50112961D1 (de) | 2000-02-01 | 2007-10-18 | Abbott Gmbh & Co Kg | Heterozyklische verbindungen und deren anwendung als parp-inhibitoren |
WO2001079184A1 (fr) | 2000-04-18 | 2001-10-25 | Sumitomo Pharmaceuticals Company, Limited | Composes de piperazine substitues |
US7122679B2 (en) | 2000-05-09 | 2006-10-17 | Cephalon, Inc. | Multicyclic compounds and the use thereof |
DE10022925A1 (de) | 2000-05-11 | 2001-11-15 | Basf Ag | Substituierte Indole als PARP-Inhibitoren |
US6723733B2 (en) | 2000-05-19 | 2004-04-20 | Guilford Pharmaceuticals, Inc. | Sulfonamide and carbamide derivatives of 6(5H)phenanthridinones and their uses |
NZ525138A (en) | 2000-10-30 | 2004-03-26 | Kudos Pharm Ltd | Phthalazinone derivatives for use as PARP inhibitors |
JPWO2002068407A1 (ja) | 2001-02-28 | 2004-06-24 | 山之内製薬株式会社 | ベンゾイミダゾール化合物 |
WO2002094790A1 (fr) | 2001-05-23 | 2002-11-28 | Mitsubishi Pharma Corporation | Compose heterocyclique condense et son utilisation medicale |
WO2003007959A1 (en) | 2001-07-16 | 2003-01-30 | Fujisawa Pharmaceutical Co., Ltd. | Quinoxaline derivatives which have parp inhibitory action |
AU2002358650A1 (en) | 2001-12-14 | 2003-06-30 | Altana Pharma Ag | Known and novel 4,5-dihydro-imidazo(4,5,1-ij)quinolin-6-ones useful as poly(adp-ribose)polymerase inhibitors |
AUPR975601A0 (en) | 2001-12-24 | 2002-01-31 | Fujisawa Pharmaceutical Co., Ltd. | Quinazolinone derivatives |
US7157452B2 (en) | 2001-12-31 | 2007-01-02 | Mgi Gp, Inc. | Substituted 4,9-dihydrocyclopenta{imn}phenanthridine-5-ones derivatives thereof and their uses |
WO2003070707A1 (fr) | 2002-02-19 | 2003-08-28 | Ono Pharmaceutical Co., Ltd. | Composes condenses derives de la pyridazine et medicaments contenant lesdits composes comme ingredients actifs |
AUPS137402A0 (en) | 2002-03-26 | 2002-05-09 | Fujisawa Pharmaceutical Co., Ltd. | Novel tricyclic compounds |
SG150548A1 (en) * | 2003-12-01 | 2009-03-30 | Kudos Pharm Ltd | Dna damage repair inhibitors for treatment of cancer |
WO2019133697A1 (en) * | 2017-12-27 | 2019-07-04 | Tesaro, Inc. | Methods of treating cancer |
-
2019
- 2019-09-10 GB GBGB1913030.1A patent/GB201913030D0/en not_active Ceased
-
2020
- 2020-09-09 WO PCT/EP2020/075245 patent/WO2021048235A1/en unknown
- 2020-09-09 AU AU2020344145A patent/AU2020344145A1/en active Pending
- 2020-09-09 CA CA3153692A patent/CA3153692A1/en active Pending
- 2020-09-09 US US17/640,706 patent/US20220339179A1/en active Pending
- 2020-09-09 MX MX2022002832A patent/MX2022002832A/es unknown
- 2020-09-09 JP JP2022515655A patent/JP2022547206A/ja active Pending
- 2020-09-09 EP EP20775209.8A patent/EP4028009A1/en active Pending
- 2020-09-09 KR KR1020227011550A patent/KR20220064380A/ko unknown
-
2022
- 2022-03-07 IL IL291170A patent/IL291170A/en unknown
Also Published As
Publication number | Publication date |
---|---|
IL291170A (en) | 2022-05-01 |
KR20220064380A (ko) | 2022-05-18 |
WO2021048235A1 (en) | 2021-03-18 |
CA3153692A1 (en) | 2021-03-18 |
AU2020344145A1 (en) | 2022-03-31 |
EP4028009A1 (en) | 2022-07-20 |
US20220339179A1 (en) | 2022-10-27 |
GB201913030D0 (en) | 2019-10-23 |
JP2022547206A (ja) | 2022-11-10 |
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