甲戊酸途径
他汀类
重新调整用途
咖啡因
癌症
预酸化
医学
药理学
HMG-CoA还原酶
胆固醇
限制
洛伐他汀
药物重新定位
还原酶
癌症研究
酶
药品
化学
生物
内科学
生物化学
生态学
工程类
机械工程
作者
Derek W. Stouth,Paul Lebeau,Richard C. Austin
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2023-07-05
卷期号:83 (13): 2091-2092
被引量:1
标识
DOI:10.1158/0008-5472.can-23-1066
摘要
Abstract Statins are a class of cholesterol-lowering drugs that inhibit 3-hydroxy-3-methylglutaryl-CoA reductase, the rate-limiting enzyme of the mevalonate pathway. Evidence suggests that certain cancers depend on the mevalonate pathway for growth and survival, and thus blocking the mevalonate pathway with statins may offer a viable therapeutic approach for treating cancer, or at least enhance the efficacy of existing cancer drugs. In this issue of Cancer Research, Tran and colleagues showed that caffeine works jointly with FOXM1 inhibition to enhance the antitumor activity of statins in neuroblastoma cells. They found that caffeine synergizes with statins by suppressing statin-induced feedback activation of the mevalonate pathway. Here, we reflect on the potential of combining caffeine and statin drugs as a strategy for potentiating anticancer activity. See related article by Tran et al., p. 2248
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