奥拉帕尼
IDH2型
IDH1
PARP抑制剂
髓系白血病
癌症研究
突变体
异柠檬酸脱氢酶
同源重组
聚ADP核糖聚合酶
生物
合成致死
突变
分子生物学
遗传学
基因
酶
聚合酶
生物化学
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2017-04-01
卷期号:7 (4): OF4-OF4
被引量:6
标识
DOI:10.1158/2159-8290.cd-nb2017-026
摘要
Abstract Several cancers, including glioma and acute myeloid leukemia, carry mutations in IDH1 or IDH2. Researchers have found that these mutations impair homologous recombination, making the tumors sensitive to PARP inhibition. They showed that one such inhibitor, olaparib, killed IDH1/2-mutant cancer cells in culture and slowed tumor growth in mice.
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