EA036942B1 - Применение amg232 в комбинации с цитарабином или децитабином для лечения острого миелогенного лейкоза - Google Patents
Применение amg232 в комбинации с цитарабином или децитабином для лечения острого миелогенного лейкоза Download PDFInfo
- Publication number
- EA036942B1 EA036942B1 EA201690980A EA201690980A EA036942B1 EA 036942 B1 EA036942 B1 EA 036942B1 EA 201690980 A EA201690980 A EA 201690980A EA 201690980 A EA201690980 A EA 201690980A EA 036942 B1 EA036942 B1 EA 036942B1
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- EA
- Eurasian Patent Office
- Prior art keywords
- chlorophenyl
- compound
- compounds
- treatment
- present
- Prior art date
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
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- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Hematology (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Pulmonology (AREA)
- Gastroenterology & Hepatology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361902717P | 2013-11-11 | 2013-11-11 | |
| PCT/US2014/065034 WO2015070224A2 (en) | 2013-11-11 | 2014-11-11 | Combination therapy including an mdm2 inhibitor and one or more additional pharmaceutically active agents for the treatment of cancers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA201690980A1 EA201690980A1 (ru) | 2016-09-30 |
| EA036942B1 true EA036942B1 (ru) | 2021-01-18 |
Family
ID=52001089
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201690980A EA036942B1 (ru) | 2013-11-11 | 2014-11-11 | Применение amg232 в комбинации с цитарабином или децитабином для лечения острого миелогенного лейкоза |
| EA202092456A EA202092456A3 (ru) | 2013-11-11 | 2014-11-11 | Комбинированная терапия, включающая ингибитор mdm2 и один или более дополнительных фармацевтически активных агентов, для лечения различных видов рака |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA202092456A EA202092456A3 (ru) | 2013-11-11 | 2014-11-11 | Комбинированная терапия, включающая ингибитор mdm2 и один или более дополнительных фармацевтически активных агентов, для лечения различных видов рака |
Country Status (33)
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3159352B1 (en) | 2007-03-28 | 2023-08-02 | President and Fellows of Harvard College | Stitched polypeptides |
| KR102104762B1 (ko) | 2010-08-13 | 2020-04-24 | 에일러론 테라퓨틱스 인코포레이티드 | 펩티도미메틱 거대고리 |
| JP6093770B2 (ja) | 2011-09-27 | 2017-03-08 | アムジエン・インコーポレーテツド | 癌の治療のためのmdm2阻害剤としての複素環化合物 |
| TW201806968A (zh) | 2011-10-18 | 2018-03-01 | 艾利倫治療公司 | 擬肽巨環化合物 |
| BR112015009470A2 (pt) | 2012-11-01 | 2019-12-17 | Aileron Therapeutics Inc | aminoácidos dissubstituídos e seus métodos de preparação e uso |
| US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
| JP6377123B2 (ja) | 2013-03-14 | 2018-08-22 | アムジエン・インコーポレーテツド | 癌の治療のためのmdm2阻害剤としてのヘテロアリール酸モルホリノン化合物 |
| MX378969B (es) * | 2013-11-11 | 2025-03-11 | Amgen Inc | Terapia de combinacion que incluye un inhibidor mdm2 y uno o mas agentes farmaceuticamente activos adicionales para el tratamiento de canceres. |
| MX389354B (es) | 2014-09-24 | 2025-03-20 | Aileron Therapeutics Inc | Macrociclos peptidomimeticos y formulaciones de los mismos. |
| KR20170058424A (ko) | 2014-09-24 | 2017-05-26 | 에일러론 테라퓨틱스 인코포레이티드 | 펩티드모방 거대고리 및 이의 용도 |
| CA2976752C (en) | 2015-02-20 | 2019-12-17 | Daiichi Sankyo Company, Limited | Method for treating cancer by combined use |
| SG11201707750YA (en) | 2015-03-20 | 2017-10-30 | Aileron Therapeutics Inc | Peptidomimetic macrocycles and uses thereof |
| EP3341023A1 (en) * | 2015-08-28 | 2018-07-04 | Novartis AG | Combination therapy using pi3k inhbitor and mdm2 inhibitor |
| AU2016314082B2 (en) * | 2015-08-28 | 2019-07-25 | Novartis Ag | Mdm2 inhibitors and combinations thereof |
| WO2017200826A1 (en) * | 2016-05-16 | 2017-11-23 | Albert Einstein College Of Medicine, Inc. | Assays and compounds for treatment of cancer |
| PL3458101T3 (pl) | 2016-05-20 | 2021-05-31 | F. Hoffmann-La Roche Ag | Koniugaty PROTAC-przeciwciało i sposoby ich stosowania |
| US20190240210A1 (en) * | 2016-10-17 | 2019-08-08 | Daiichi Sankyo Company, Limited | Treatment Method by Combined Use of MDM2 Inhibitor and DNA Methyltransferase Inhibitor |
| WO2018134254A1 (en) | 2017-01-17 | 2018-07-26 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| IL319432A (en) * | 2018-04-30 | 2025-05-01 | Kartos Therapeutics Inc | Methods of treating cancer |
| KR20210043499A (ko) | 2018-05-25 | 2021-04-21 | 카토스 테라퓨틱스, 인크. | 골수증식성 신생물 치료 방법 |
| WO2020023502A1 (en) | 2018-07-23 | 2020-01-30 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
| CN110963958B (zh) * | 2018-09-30 | 2025-10-10 | 上海长森药业有限公司 | 一种mdm2抑制剂,及其制备方法、药物组合物和应用 |
| EP3927344A4 (en) * | 2018-12-11 | 2023-01-18 | Kartos Therapeutics | METHODS AND COMPOSITIONS FOR THE TREATMENT OF AN EYE CONDITION |
| CN111434353A (zh) * | 2019-02-02 | 2020-07-21 | 中国科学院上海营养与健康研究所 | Ras抑制剂筛选及疗效标志物 |
| CN112294965B (zh) | 2019-07-26 | 2023-03-14 | 苏州亚盛药业有限公司 | Mdm2抑制剂的药物组合物及其在预防和/或治疗疾病中的用途 |
| TW202128156A (zh) * | 2019-11-14 | 2021-08-01 | 美商夸格智財控股有限公司 | 用於癌症治療之btk抑制劑及mdm2抑制劑之組合 |
| WO2021254277A1 (en) * | 2020-06-15 | 2021-12-23 | Ascentage Pharma (Suzhou) Co., Ltd. | Microsuspension of an mdm2 inhibitor and therapeutic applications thereof |
| TW202227082A (zh) * | 2020-08-12 | 2022-07-16 | 美商施維雅製藥有限公司 | 用於治療癌症之組合療法 |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| CN115089585A (zh) * | 2022-08-05 | 2022-09-23 | 中国科学院大学宁波华美医院 | Mdm2抑制剂rg7112联合依托泊苷在治疗肺癌中的应用 |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
| WO2024254156A1 (en) * | 2023-06-05 | 2024-12-12 | Kartos Therapeutics, Inc. | Treatment of endometrial cancer with mdm2 inhibitors |
| WO2025098488A1 (zh) * | 2023-11-09 | 2025-05-15 | 深圳艾欣达伟医药科技有限公司 | 上调p53蛋白表达或激活p53功能的药物与DNA烷化剂联用治疗癌症 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110319378A1 (en) * | 2010-06-04 | 2011-12-29 | Amgen Inc. | Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer |
| US20130245039A1 (en) * | 2012-03-19 | 2013-09-19 | Hoffmann-La Roche Inc. | Combination therapy for proliferative disorders |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL153817A0 (en) | 2000-07-19 | 2003-07-31 | Warner Lambert Co | Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids |
| AU2005295441B2 (en) | 2004-10-18 | 2009-04-23 | Amgen, Inc. | Thiadiazole compounds and methods of use |
| WO2007084391A2 (en) | 2006-01-18 | 2007-07-26 | Amgen Inc. | Thiazole compounds as protein kinase b ( pkb) inhibitors |
| US7705018B2 (en) | 2007-03-23 | 2010-04-27 | Amgen Inc. | Substituted quinolines and their uses in treatment of inflammatory and related conditions |
| US7919498B2 (en) | 2007-03-23 | 2011-04-05 | Amgen Inc. | Substituted pyrazolo[3,4-d]pyrimidines as PI3K inhibitors |
| AU2008231304B2 (en) | 2007-03-23 | 2011-05-12 | Amgen Inc. | Heterocyclic compounds and their uses |
| US7625895B2 (en) | 2007-04-12 | 2009-12-01 | Hoffmann-Le Roche Inc. | Diphenyl-dihydro-imidazopyridinones |
| CA2689092C (en) | 2007-06-07 | 2013-01-15 | Amgen Inc. | Raf kinase modulators and methods of use |
| AU2008276512A1 (en) | 2007-07-17 | 2009-01-22 | Amgen Inc. | Thiadiazole modulators of PKB |
| US7897619B2 (en) | 2007-07-17 | 2011-03-01 | Amgen Inc. | Heterocyclic modulators of PKB |
| TW200911798A (en) | 2007-08-02 | 2009-03-16 | Amgen Inc | PI3 kinase modulators and methods of use |
| US8841312B2 (en) | 2007-12-19 | 2014-09-23 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
| CA2710194C (en) | 2007-12-19 | 2014-04-22 | Amgen Inc. | Inhibitors of p13 kinase |
| JP5530422B2 (ja) | 2008-04-07 | 2014-06-25 | アムジエン・インコーポレーテツド | 細胞周期阻害薬としてのgem−二置換およびスピロ環式アミノピリジン/ピリミジン |
| US8415376B2 (en) | 2008-05-30 | 2013-04-09 | Amgen Inc. | Inhibitors of PI3 kinase |
| US20110263647A1 (en) | 2009-01-15 | 2011-10-27 | Amgen Inc. | Fluoroisoquinoline substituted thiazole compounds and methods of use |
| WO2010096314A1 (en) | 2009-02-18 | 2010-08-26 | Amgen Inc. | INDOLE/BENZIMIDAZOLE COMPOUNDS AS mTOR KINASE INHIBITORS |
| MX2011009796A (es) | 2009-03-20 | 2011-12-14 | Amgen Inc | Inhibidores de la cinasa pi3. |
| UY32582A (es) | 2009-04-28 | 2010-11-30 | Amgen Inc | Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero |
| EP2430013B1 (en) | 2009-05-13 | 2014-10-15 | Amgen Inc. | Heteroaryl compounds as pikk inhibitors |
| EA201270013A1 (ru) | 2009-06-25 | 2012-06-29 | Амген Инк. | Гетероциклические соединения и их применение |
| WO2010151791A1 (en) | 2009-06-25 | 2010-12-29 | Amgen Inc. | Heterocyclic compounds and their uses |
| MX2011013667A (es) | 2009-06-25 | 2012-03-06 | Amgen Inc | Compuestos heterociclicos y sus usos. |
| WO2010151735A2 (en) | 2009-06-25 | 2010-12-29 | Amgen Inc. | Heterocyclic compounds and their uses |
| HRP20150104T1 (xx) | 2009-09-11 | 2015-03-13 | Amgen, Inc. | N-(4-((3-(2-amino-4-pirimidinil)-2-piridinil)oksi)fenil)-4-(4-metil-2-thienil)-1-ftalazinamin za primjenu u tretmanu kancera rezistentnog na antimitotiäśke agense |
| KR20120031734A (ko) * | 2010-09-27 | 2012-04-04 | 삼성전자주식회사 | 급성 골수성 백혈병 환자의 시타라빈 민감성을 예측하기 위한 키트 및 방법 |
| EP2670396A1 (en) * | 2011-01-31 | 2013-12-11 | Celgene Corporation | Pharmaceutical compositions of cytidine analogs and methods of use thereof |
| JP6093770B2 (ja) | 2011-09-27 | 2017-03-08 | アムジエン・インコーポレーテツド | 癌の治療のためのmdm2阻害剤としての複素環化合物 |
| WO2013144923A1 (en) | 2012-03-30 | 2013-10-03 | Takeda Pharmaceutical Company Limited | Administration of a raf inhibitor and a mek inhibitor in the treatment of melanoma |
| CA2901696C (en) | 2013-02-19 | 2021-04-13 | Amgen Inc. | Cis-morpholinone and other compounds as mdm2 inhibitors for the treatment of cancer |
| AU2014223547B2 (en) | 2013-02-28 | 2017-11-16 | Amgen Inc. | A benzoic acid derivative MDM2 inhibitor for the treatment of cancer |
| JP6377123B2 (ja) | 2013-03-14 | 2018-08-22 | アムジエン・インコーポレーテツド | 癌の治療のためのmdm2阻害剤としてのヘテロアリール酸モルホリノン化合物 |
| JOP20200296A1 (ar) * | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
| US20150031642A1 (en) | 2013-07-26 | 2015-01-29 | Boehringer Ingelheim International Gmbh | Combination treatment of acute myeloid leukemia and myelodysplastic syndrome i |
| MX378969B (es) * | 2013-11-11 | 2025-03-11 | Amgen Inc | Terapia de combinacion que incluye un inhibidor mdm2 y uno o mas agentes farmaceuticamente activos adicionales para el tratamiento de canceres. |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110319378A1 (en) * | 2010-06-04 | 2011-12-29 | Amgen Inc. | Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer |
| US20130245039A1 (en) * | 2012-03-19 | 2013-09-19 | Hoffmann-La Roche Inc. | Combination therapy for proliferative disorders |
Non-Patent Citations (24)
| Title |
|---|
| BOSE P, GRANT S: "Mcl-1 as a therapeutic target in acute myelogenous leukemia (AML)", LEUKEMIA RESEARCH REPORTS, ELSEVIER LTD., GB, vol. 2, no. 1, 1 January 2013 (2013-01-01), GB, pages 12 - 14, XP002740451, ISSN: 2213-0489, DOI: 10.1016/j.lrr.2012.11.006 * |
| CHITHRA D. PALANI; JAMES F. BECK; JÜRGEN SONNEMANN: "Histone deacetylase inhibitors enhance the anticancer activity of nutlin-3 and induce p53 hyperacetylation and downregulation of MDM2 and MDM4 gene expression", INVESTIGATIONAL NEW DRUGS, KLUWER ACADEMIC PUBLISHERS, BO, vol. 30, no. 1, 3 August 2010 (2010-08-03), Bo, pages 25 - 36, XP035000732, ISSN: 1573-0646, DOI: 10.1007/s10637-010-9510-7 * |
| FALCHOOK G S, LEWIS K D, INFANTE J R, GORDON M S, VOGELZANG N J, DEMARINI D J, SUN P, MOY C, SZABO S A, ROADCAP L T, PEDDAREDDIGAR: "Activity of the oral MEK inhibitor trametinib in patients with advanced melanoma: a phase 1 dose-escalation trial.", THE LANCET ONCOLOGY, ELSEVIER, AMSTERDAM, NL, vol. 13, no. 8, 1 August 2012 (2012-08-01), AMSTERDAM, NL, pages 782 - 789, XP002727794, ISSN: 1470-2045, DOI: 10.1016/S1470-2045(12)70269-3 * |
| FENG J, TAMASKOVIC R, YANG Z, BRAZIL D P, MERLO A, HESS D, HEMMINGS B A: "Stabilization of Mdm2 via decreased ubiquitination is mediated by protein kinase B/Akt-dependent phosphorylation.", JOURNAL OF BIOLOGICAL CHEMISTRY, AMERICAN SOCIETY FOR BIOCHEMISTRY AND MOLECULAR BIOLOGY, vol. 279, no. 34, 20 August 2004 (2004-08-20), pages 35510 - 35517, XP002740653, ISSN: 0021-9258, DOI: 10.1074/jbc.M404936200 * |
| FLAHERTY KEITH T, ET AL: "Combined BRAF and MEK Inhibition in Melanoma with BRAF V600 Mutations", THE NEW ENGLAND JOURNAL OF MEDICINE, MASSACHUSETTS MEDICAL SOCIETY, US, vol. 367, no. 18, 1 November 2012 (2012-11-01), US, pages 1694 - 1703, XP002725869, ISSN: 0028-4793, DOI: 10.1056/NEJMoa1210093 * |
| GILES FRANCIS; CORTES JORGE; BERGSTROM DONALD A; XIAO ALAN; BRISTOW PENNY; JONES DAN; VERSTOVSEK SRDAN; THOMAS DEBORAH; KANTARJIAN: "MK-0457, a novel aurora kinase and BCR-ABL inhibitor, is active against BCR-ABL T315I mutant chronic myelogenous leukemia (CML)", BLOOD, AMERICAN SOCIETY OF HEMATOLOGY, US, vol. 108, no. 11, Part 1, 1 November 2006 (2006-11-01), US, pages 52a, XP009124755, ISSN: 0006-4971 * |
| J. G. GREGER, S. D. EASTMAN, V. ZHANG, M. R. BLEAM, A. M. HUGHES, K. N. SMITHEMAN, S. H. DICKERSON, S. G. LAQUERRE, L. LIU, T. M. : "Combinations of BRAF, MEK, and PI3K/mTOR Inhibitors Overcome Acquired Resistance to the BRAF Inhibitor GSK2118436 Dabrafenib, Mediated by NRAS or MEK Mutations", MOLECULAR CANCER THERAPEUTICS, AMERICAN ASSOCIATION FOR CANCER RESEARCH, INC., vol. 11, no. 4, 1 April 2012 (2012-04-01), pages 909 - 920, XP055057160, ISSN: 15357163, DOI: 10.1158/1535-7163.MCT-11-0989 * |
| J. M. GOZGIT, WONG M. J., WARDWELL S., TYNER J. W., LORIAUX M. M., MOHEMMAD Q. K., NARASIMHAN N. I., SHAKESPEARE W. C., WANG F., D: "Potent Activity of Ponatinib (AP24534) in Models of FLT3-Driven Acute Myeloid Leukemia and Other Hematologic Malignancies", MOLECULAR CANCER THERAPEUTICS, AMERICAN ASSOCIATION FOR CANCER RESEARCH, INC., vol. 10, no. 6, 1 June 2011 (2011-06-01), pages 1028 - 1035, XP055056925, ISSN: 15357163, DOI: 10.1158/1535-7163.MCT-10-1044 * |
| JI Z, KUMAR R, TAYLOR M, RAJADURAI A, MARZUKA-ALCALÁ A, CHEN Y E, NJAUW C N, FLAHERTY K, JÖNSSON G, TSAO H.: "Vemurafenib synergizes with nutlin-3 to deplete survivin and suppresses melanoma viability and tumor growth.", CLINICAL CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 19, no. 16, 15 August 2013 (2013-08-15), US, pages 4383 - 4391, XP002734225, ISSN: 1078-0432, DOI: 10.1158/1078-0432.CCR-13-0074 * |
| JI Z, NJAUW C N, TAYLOR M, NEEL V, FLAHERTY K T, TSAO H: "p53 rescue through HDM2 antagonism suppresses melanoma growth and potentiates MEK inhibition.", JOURNAL OF INVESTIGATIVE DERMATOLOGY, NATURE PUBLISHING GROUP, US, vol. 132, no. 2, 1 February 2012 (2012-02-01), US, pages 356 - 364, XP002694638, ISSN: 1523-1747, DOI: 10.1038/jid.2011.313. * |
| KAO C L, HSU H S, CHEN H W, CHENG T H: "Rapamycin increases the p53/MDM2 protein ratio and p53-dependent apoptosis by translational inhibition of mdm2 in cancer cells.", CANCER LETTERS, NEW YORK, NY, US, vol. 286, no. 2, 28 December 2009 (2009-12-28), US, pages 250 - 259, XP002740446, ISSN: 0304-3835, DOI: 10.1016/j.canlet.2009.05.031 * |
| KENSUKE KOJIMA, KONOPLEVA MARINA, MCQUEEN TERESA, BRIEN SUSAN O ', PLUNKETT WILLIAM, ANDREEFF MICHAEL: "Mdm2 inhibitor Nutlin-3a induces p53-mediated apoptosis by transcription- dependent and transcription-independent mechanisms and may overcome Atm-mediated resistance to fludarabine in chronic lymphocytic leukemia", BLOOD, vol. 108, no. 3, 1 August 2006 (2006-08-01), pages 993 - 1000, XP055140017, DOI: 10.1182/blood-2005-12-5148 * |
| KHOURY H J, CORTES J E, KANTARJIAN H M, GAMBACORTI-PASSERINI C, BACCARANI M, KIM D W, ZARITSKEY A, COUNTOURIOTIS A, BESSON N, LEIP: "Bosutinib is active in chronic phase chronic myeloid leukemia after imatinib and dasatinib and/or nilotinib therapy failure", BLOOD, AMERICAN SOCIETY OF HEMATOLOGY NLD, US, vol. 119, no. 15, 12 April 2012 (2012-04-12), US, pages 3403 - 3412, XP002740449, ISSN: 1528-0020, DOI: 10.1182/blood-2011-11-390120 * |
| KOJIMA K, KONOPLEVA M, SAMUDIO I J, RUVOLO V, ANDREEFF M.: "Mitogen-activated protein kinase kinase inhibition enhances nuclear proapoptotic function of p53 in acute myelogenous leukemia cells", CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 67, no. 7, 1 April 2007 (2007-04-01), US, pages 3210 - 3219, XP002740444, ISSN: 0008-5472, DOI: 10.1158/0008-5472.CAN-06-2712 * |
| KOJIMA K, KONOPLEVA M, SAMUDIO I J, SCHOBER W D, BORNMANN W G, ANDREEFF M.: "Concomitant inhibition of MDM2 and Bcl-2 protein function synergistically induce mitochondrial apoptosis in AML.", CELL CYCLE, LANDES BIOSCIENCE, US, vol. 5, no. 23, 1 December 2006 (2006-12-01), US, pages 2778 - 2786, XP002740450, ISSN: 1551-4005, DOI: 10.4161/cc.5.23.3520 * |
| LIU D, XING M.: "Potent inhibition of thyroid cancer cells by the MEK inhibitor PD0325901 and its potentiation by suppression of the PI3K and NF-kappaB pathways.", THYROID., MARY ANN LIEBERT, NEW YORK, NY., US, vol. 18, no. 8, 1 August 2008 (2008-08-01), US, pages 853 - 864, XP002740459, ISSN: 1050-7256, DOI: 10.1089/thy.2007.0357 * |
| LONG J, PARKIN B, OUILLETTE P, BIXBY D, SHEDDEN K, ERBA H, WANG S, MALEK S N: "Multiple distinct molecular mechanisms influence sensitivity and resistance to MDM2 inhibitors in adult acute myelogenous leukemia.", BLOOD, AMERICAN SOCIETY OF HEMATOLOGY NLD, US, vol. 116, no. 1, 8 July 2010 (2010-07-08), US, pages 71 - 80, XP002740447, ISSN: 1528-0020, DOI: 10.1182/blood-2010-01-261628 * |
| LU WENGE ET AL: "Activation of p53 by roscovitine-mediated suppression of MDM2 expression", ONCOGENE, NATURE PUBLISHING GROUP UK, LONDON, vol. 20, no. 25, 31 May 2001 (2001-05-31), London, pages 3206 - 3216, XP002292792, ISSN: 0950-9232, DOI: 10.1038/sj.onc.1204412 * |
| MARTINELLI E, TROIANI T, D'AIUTO E, MORGILLO F, VITAGLIANO D, CAPASSO A, COSTANTINO S, CIUFFREDA L P, MEROLLA F, VECCHIONE L, DE V: "Antitumor activity of pimasertib, a selective MEK 1/2 inhibitor, in combination with PI3K/mTOR inhibitors or with multi-targeted kinase inhibitors in pimasertib-resistant human lung and colorectal cancer cells.", INTERNATIONAL JOURNAL OF CANCER, JOHN WILEY & SONS, INC., US, vol. 133, no. 9, 1 November 2013 (2013-11-01), US, pages 2089 - 2101, XP002740445, ISSN: 0020-7136, DOI: 10.1002/ijc.28236 * |
| NAGMA KHAN, MICHAEL JEFFERS, SAMPATH KUMAR, CRAIG HACKETT, FERENC BOLDOG, NICHOLAI KHRAMTSOV, XIAOZHONG QIAN, EVAN MILLS, STANNY�C: "Determination of the class and isoform selectivity of small-molecule histone deacetylase inhibitors", BIOCHEMICAL JOURNAL, PUBLISHED BY PORTLAND PRESS ON BEHALF OF THE BIOCHEMICAL SOCIETY., vol. 409, no. 2, 15 January 2008 (2008-01-15), pages 581, XP055074060, ISSN: 02646021, DOI: 10.1042/BJ20070779 * |
| TIANJUN ZHOU, COMMODORE LOIS, HUANG WEI-SHENG, WANG YIHAN, THOMAS MATHEW, KEATS JEFF, XU QIHONG, RIVERA VICTOR M., SHAKESPEARE WIL: "Structural Mechanism of the Pan-BCR-ABL Inhibitor Ponatinib (AP24534): Lessons for Overcoming Kinase Inhibitor Resistance", CHEMICAL BIOLOGY & DRUG DESIGN, BLACKWELL MUNKSGAARD, vol. 77, no. 1, 1 January 2011 (2011-01-01), pages 1 - 11, XP055065379, ISSN: 17470277, DOI: 10.1111/j.1747-0285.2010.01054.x * |
| WANG, D. BOERNER, S.A. WINKLER, J.D. LORUSSO, P.M.: "Clinical experience of MEK inhibitors in cancer therapy", BIOCHIMICA ET BIOPHYSICA ACTA (BBA) - MOLECULAR CELL RESEARCH, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM., NL, vol. 1773, no. 8, 1 August 2007 (2007-08-01), NL, pages 1248 - 1255, XP022181677, ISSN: 0167-4889, DOI: 10.1016/j.bbamcr.2006.11.009 * |
| WEIGUO ZHANG, MARINA KONOPLEVA, JARED K. BURKS, KAREN C. DYWER, WENDY D. SCHOBER, JER-YEN YANG, TERESA J. MCQUEEN, MIEN-CHIE HU: "Blockade of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase and murine double minute synergistically induces Apoptosis in acute myeloid leukemia via BH3-only proteins Puma and Bim", CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 70, no. 6, 15 March 2010 (2010-03-15), US, pages 2424 - 2434, XP002740443, ISSN: 1538-7445, DOI: 10.1158/0008-5472.CAN-09-0878 * |
| ZAULI G, VOLTAN R, BOSCO R, MELLONI E, MARMIROLI S, RIGOLIN G M, CUNEO A, SECCHIERO P.: "Dasatinib plus Nutlin-3 shows synergistic antileukemic activity in both p53 wild-type and p53 mutated B chronic lymphocytic leukemias by inhibiting the Akt pathway.", CLINICAL CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 17, no. 4, 15 February 2011 (2011-02-15), US, pages 762 - 770, XP002740448, ISSN: 1078-0432, DOI: 10.1158/1078-0432.CCR-10-2572 * |
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