乳腺癌
PI3K/AKT/mTOR通路
癌症研究
突变
生物
P110α
临床试验
基因
遗传学
医学
癌症
生物信息学
信号转导
作者
Neil Vasan,Pedram Razavi,Jared L. Johnson,Hong Shao,Hardik Shah,Alesia Antoine,Erik Ladewig,Alexander N. Gorelick,Ting-Yu Lin,Eneda Toska,Guotai Xu,Abiha Kazmi,Matthew T. Chang,Barry S. Taylor,Maura N. Dickler,Komal Jhaveri,Sarat Chandarlapaty,Raúl Rabadán,Ed Reznik,Melissa Smith
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-11-08
卷期号:366 (6466): 714-723
被引量:255
标识
DOI:10.1126/science.aaw9032
摘要
Seeing double can be a good thing Many human breast cancers harbor activating mutations in PIK3CA , the gene coding for the catalytic subunit of phosphoinositide 3-kinase (PI3K). Clinical trials are underway to evaluate the efficacy of PI3K inhibitors in cancer patients. Vasan et al. found unexpectedly that a subset of breast cancers harbor not one—but two— PIK3CA mutations, and the mutations occur on the same allele (see the Perspective by Toker). In model systems, the double mutations hyperactivate PI3K signaling and enhance tumor growth. Preliminary analysis of clinical trial data suggests that breast cancers with double mutations are more responsive to PI3K inhibitors than those with a single mutation. PIK3CA mutational status could help identify the breast cancer patients most likely to benefit from these drugs. Science , this issue p. 714 ; see also p. 685
科研通智能强力驱动
Strongly Powered by AbleSci AI