SMARCA4型
医学
肺癌
肿瘤科
内科学
肺
癌症
生物
病理
基因
表观遗传学
遗传学
染色质重塑
作者
Adam J. Schoenfeld,Chai Bandlamudi,Jessica A. Lavery,Joseph Montecalvo,Azadeh Namakydoust,Hira Rizvi,Jacklynn V. Egger,Carla P. Concepcion,Sonal Paul,Maria E. Arcila,Yahya Daneshbod,Jason C. Chang,Jennifer L. Sauter,Amanda Beras,Marc Ladanyi,Tyler Jacks,Charles M. Rudin,Barry S. Taylor,Mark T.A. Donoghue,Glenn Heller
标识
DOI:10.1158/1078-0432.ccr-20-1825
摘要
SMARCA4 alterations can be divided into two clinically relevant genomic classes associated with differential protein expression as well as distinct prognostic and treatment implications. Both classes co-occur with KEAP1, STK11, and KRAS mutations, but individually represent independent predictors of poor prognosis. Despite association with poor outcomes, SMARCA4-mutant lung cancers may be more sensitive to immunotherapy.
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