雷达51
范卡
聚ADP核糖聚合酶
同源重组
FANCD2
DNA修复
DNA损伤
奥拉帕尼
聚合酶
生物
BRCA2蛋白
综合征如奈梅亨破损综合症
癌症研究
范科尼贫血
PALB2
突变
分子生物学
遗传学
DNA
种系突变
共济失调毛细血管扩张
基因
作者
Nuala McCabe,Nicholas C. Turner,Christopher J. Lord,Katarzyna Kluzek,Aneta Białkowska,Sally Swift,Sabrina Giavara,Mark J. O’Connor,Andrew N.J. Tutt,Małgorzata Z. Zdzienicka,Graeme C.M. Smith,Alan Ashworth
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2006-08-15
卷期号:66 (16): 8109-8115
被引量:1315
标识
DOI:10.1158/0008-5472.can-06-0140
摘要
Deficiency in either of the breast cancer susceptibility proteins BRCA1 or BRCA2 induces profound cellular sensitivity to the inhibition of poly(ADP-ribose) polymerase (PARP) activity. We hypothesized that the critical role of BRCA1 and BRCA2 in the repair of double-strand breaks by homologous recombination (HR) was the underlying reason for this sensitivity. Here, we examine the effects of deficiency of several proteins involved in HR on sensitivity to PARP inhibition. We show that deficiency of RAD51, RAD54, DSS1, RPA1, NBS1, ATR, ATM, CHK1, CHK2, FANCD2, FANCA, or FANCC induces such sensitivity. This suggests that BRCA-deficient cells are, at least in part, sensitive to PARP inhibition because of HR deficiency. These results indicate that PARP inhibition might be a useful therapeutic strategy not only for the treatment of BRCA mutation-associated tumors but also for the treatment of a wider range of tumors bearing a variety of deficiencies in the HR pathway or displaying properties of 'BRCAness.'
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