解旋酶
癌症研究
生物
计算生物学
癌症
免疫疗法
遗传学
基因
核糖核酸
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2024-08-02
卷期号:14 (8): 1369-1371
标识
DOI:10.1158/2159-8290.cd-24-0771
摘要
In this issue, Picco and colleagues provide further evidence that WRN inhibitors are synthetically lethal in microsatellite instability-high (MSI-H) cancers and function by blocking the helicase domain of select WRN residues. They demonstrate that WRN inhibitors may be even more effective in a subset of MSI-high tumors with (TA)n repeat expansions, which represents a possible strategy in clinical development. See related article by Picco et al., p. 1457 (1).
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