上睑下垂
甲戊酸途径
癌症研究
ARID1A型
生物
细胞凋亡
还原酶
程序性细胞死亡
酶
生物化学
突变
基因
作者
Wei Zhou,Heng Liu,Zhe Yuan,Joseph A. Zundell,Martina Towers,Jianhuang Lin,Simona Lombardi,Hao Nie,Brennah Murphy,Tyler T. Yang,Chen Wang,Liping Liang,Aaron R. Goldman,Toshitha Kannan,Andrew V. Kossenkov,Ronny Drapkin,Luis J. Montaner,Daniel T. Claiborne,Nan Zhang,Shuai Wu,Rugang Zhang
出处
期刊:Cancer Cell
[Elsevier]
日期:2023-04-01
卷期号:41 (4): 740-756.e10
被引量:18
标识
DOI:10.1016/j.ccell.2023.03.002
摘要
ARID1A, encoding a subunit of the SWI/SNF complex, is mutated in ∼50% of clear cell ovarian carcinoma (OCCC) cases. Here we show that inhibition of the mevalonate pathway synergizes with immune checkpoint blockade (ICB) by driving inflammasome-regulated immunomodulating pyroptosis in ARID1A-inactivated OCCCs. SWI/SNF inactivation downregulates the rate-limiting enzymes in the mevalonate pathway such as HMGCR and HMGCS1, which creates a dependence on the residual activity of the pathway in ARID1A-inactivated cells. Inhibitors of the mevalonate pathway such as simvastatin suppresses the growth of ARID1A mutant, but not wild-type, OCCCs. In addition, simvastatin synergizes with anti-PD-L1 antibody in a genetic OCCC mouse model driven by conditional Arid1a inactivation and in a humanized immunocompetent ARID1A mutant patient-derived OCCC mouse model. Our data indicate that inhibition of the mevalonate pathway simultaneously suppresses tumor cell growth and boosts antitumor immunity by promoting pyroptosis, which synergizes with ICB in suppressing ARID1A-mutated cancers.
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