雷达51
PARP1
同源重组
DNA修复
BRCA2蛋白
PARP抑制剂
聚ADP核糖聚合酶
奥拉帕尼
癌症研究
软膜
分子生物学
基底切除修复术
聚合酶
DNA损伤
突变
合成致死
生物
DNA
遗传学
基因
种系突变
作者
Helen E. Bryant,Niklas Schultz,Huw D. Thomas,Kayan M. Parker,Dan Flower,Elena López,Suzanne Kyle,Mark Meuth,Nicola J. Curtin,Thomas Helleday
出处
期刊:Nature
[Springer Nature]
日期:2005-04-14
卷期号:434 (7035): 913-917
被引量:4399
摘要
Poly(ADP-ribose) polymerase (PARP1) facilitates DNA repair by binding to DNA breaks and attracting DNA repair proteins to the site of damage. Nevertheless, PARP1-/- mice are viable, fertile and do not develop early onset tumours. Here, we show that PARP inhibitors trigger gamma-H2AX and RAD51 foci formation. We propose that, in the absence of PARP1, spontaneous single-strand breaks collapse replication forks and trigger homologous recombination for repair. Furthermore, we show that BRCA2-deficient cells, as a result of their deficiency in homologous recombination, are acutely sensitive to PARP inhibitors, presumably because resultant collapsed replication forks are no longer repaired. Thus, PARP1 activity is essential in homologous recombination-deficient BRCA2 mutant cells. We exploit this requirement in order to kill BRCA2-deficient tumours by PARP inhibition alone. Treatment with PARP inhibitors is likely to be highly tumour specific, because only the tumours (which are BRCA2-/-) in BRCA2+/- patients are defective in homologous recombination. The use of an inhibitor of a DNA repair enzyme alone to selectively kill a tumour, in the absence of an exogenous DNA-damaging agent, represents a new concept in cancer treatment.
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