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PARP抑制剂与合成致死 被引量:3

Poly(ADP-ribose) polymerase inhibitors and synthetic lethality
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摘要 随着人们对恶性肿瘤生物学认识的加深,一些新的抗肿瘤策略不断出现。例如之前已有基于肿瘤中的癌基因依赖现象的分子靶向疗法成功用于临床,而合成致死成为当下抗肿瘤药物发展的又一新的方向。研究表明,PARP-1与BRCA1/2之间为合成致死的关系。本文对PARP-1抑制与BRCA1/2缺陷如何构成其合成致死作用以及此作用在抗肿瘤中的潜在应用价值进行综述。 In recent years,some new anticancer strategies have been found with a growing understanding of the underlying biology of cancer.For example,molecular targeting cancer therapy,which is based on the oncogene addiction phenomenon,had proved to be a successful strategy in some specific cancer types.A more recent example came from synthetic lethality which is now showing great promise as a new direction of anticancer drug discovery.Previous research has shown that PARP-1 and BRCA have a relationship of synthetic lethality.We herein describe the rationale of this synthetic lethality and the potential applications of this interaction in anticancer therapy.
作者 赵娜 孙宏斌
出处 《中国药科大学学报》 CAS CSCD 北大核心 2012年第2期107-112,共6页 Journal of China Pharmaceutical University
关键词 PARP抑制剂 合成致死 BRCA 同源重组 分子靶向疗法 肿瘤 poly(ADP-ribose) polymerase inhibitors synthetic lethality BRCA homologous recombination molecular targeting therapy tumor
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参考文献42

  • 1Chan DA,Giaccia AJ.Harnessing synthetic lethal interactions inanticancer drug discovery[J].Nat Rev Drug Discov,2011,10(5):351-364.
  • 2Hanahan D,Weinberg RA.The hallmarks of cancer[J].Cell,2000,100(1):57-70.
  • 3Brough R,Frankum JR,Costa-Cabral S,et al.Searching for syn-thetic lethality in cancer[J].Curr Opin Genet Dev,2011,21(1):34-41.
  • 4Weinstein IB.Addiction to oncogenes—the Achilles heal of cancer[J].Science,2002,297(5 578):63-64.
  • 5Sharma SV,Settleman J.Oncogene addiction:setting the stage formolecularly targeted cancer therapy[J].Genes Dev,2007,21(24):3 214-3 231.
  • 6Brody LC.Treating cancer by targeting a weakness[J].N Engl JMed,2005,353(9):949-950.
  • 7Mizuarai S,Kotani H.Synthetic lethal interactions for the deve-lopment of cancer therapeutics:biological and methodologicaladvancements[J].Hum Genet,2010,128(6):567-575.
  • 8Iglehart JD,Silver DP.Synthetic lethality—a new direction incancer-drug development[J].N Engl J Med,2009,361(2):189-191.
  • 9Lucchesi JC.Synthetic lethality and semi-lethality among func-tionally related mutants of Drosophila melanogaster[J].Genetics,1968,59(1):37-44.
  • 10Dobzhansky T.Genetics of natural populations.Xiii.Recombina-tion and variability in populations of Drosophila pseudoobscura[J].Genetics,1946,31(3):269-290.

同被引文献39

  • 1Drew Y, Plummer R. PARP inhibitors in cancer therapy: two modes of attack on the cancer cell widening the clinical applications [ J ]. Drug Resist Updat, 2009, 12 ( 6 ) : 153-156.
  • 2Durkacz B W,Omidiji O,Gray D A,et al. (ADP-ribose)n participates in DNA excision repair[ J]. Nature,1980,283 ( 5747 ) : 593-596.
  • 3Plummer R, Jones C, Middleton M, et al. Phase I study of the poly(ADP-ribose) polymerase inhibitor, AG014699, in combination with temozolomide in patients with advanced solid tumors [ J ]. Clin Cancer Res, 2008, 14 (23) :7917-7923.
  • 4Sodhi R K, Singh N, Jaggi A S. Poly (ADP-ribose) poly- merase-1 (PARP-1) and its therapeutic implications E J ].Vascul Pharmacol, 201 O, 53 ( 3/4 ) :77- 87.
  • 5Tutt A, Ashworth A. The relationship between the roles of BRCA genes in DNA repair and cancer predisposition [ J ]. Trends Mol Med,2002,8 ( 12 ) :571-576.
  • 6Xu J, Wang B, Zhang Y, et al. Clinical implications for BRCA gene mutation in breast cancer[J]. Mol Biol Rep, 2012,39 (3) :3097-3102.
  • 7Farmer H, McCabe N, Lord C J. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy [ J]. Nature,2005,434 (7035) :917-921.
  • 8Sandhu S K,Yap T A, de Bono J S. The emerging role of poly(ADP-ribose) polymerase inhibitors in cancer treat- ment[ I]. Curt Drug Targets ,2011,12(14) :2034-2044.
  • 9Bryant H E,Schuhz N,Thomas H D,et al. Specific killing of BRCA2-deficient tumors with inhibitors of poly ( ADP- ribose) polymerase [ J ]. Nature, 2005, 434 ( 7035 ) : 913-917.
  • 10Iglehart J D, Silver D P. Synthetic lethality-- direction in cancer-drug development[ J ]. N Engl J Med, 2009,361(2) :189-191.

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