癌症研究
聚ADP核糖聚合酶
DNA修复
DNA损伤
聚合酶
突变
核苷酸切除修复
生物
分子生物学
基因
DNA
遗传学
作者
Kasper Fugger,Ilirjana Bajrami,Mariana Silva dos Santos,Sarah Jane Young,Simone Kunzelmann,Geoff Kelly,Graeme Hewitt,Harshil Patel,Robert Goldstone,Thomas Carell,Simon J. Boulton,James I. MacRae,Ian A. Taylor,Stephen C. West
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-04-09
卷期号:372 (6538): 156-165
被引量:74
标识
DOI:10.1126/science.abb4542
摘要
Three strikes to knock cancer out BRCA1 and BRCA2 are tumor-suppressor genes, and patients with mutations in these genes are predisposed to breast, ovarian, and other cancers. Because BRCA1 and BRCA2 mutations affect pathways involved in DNA break repair, these patients' tumors are usually vulnerable to treatments that further damage DNA repair, such as poly(ADP-ribose) polymerase (PARP) inhibitors, but they can acquire resistance to therapy. Using a genome-wide screening approach, Fugger et al. identified a protein called DNPH1 as a “nucleotide sanitizer” that prevents the incorporation of abnormal nucleotides into DNA (see the Perspective by Kriaucionis). The authors examined its mechanism of action and demonstrated how it can be targeted to expedite the killing of BRCA1 -mutant cancer cells in combination with PARP inhibitor treatment. Science , this issue p. 156 ; see also p. 127
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