自噬
mTORC1型
溶酶体
PI3K/AKT/mTOR通路
细胞生物学
氯喹
生物
分解代谢
雷帕霉素的作用靶点
化学
生物化学
信号转导
新陈代谢
免疫学
细胞凋亡
疟疾
酶
作者
Vito W. Rebecca,Michael C. Nicastri,Noel P. McLaughlin,Colin Fennelly,Quentin McAfee,Amruta Ronghe,Michel Nofal,Chun-Yan Lim,Eric S. Witze,Cynthia I. Chude,Gao Zhang,Gretchen M. Alicea,Shengfu Piao,Sengottuvelan Murugan,Rani Ojha,Samuel M. Levi,Zhi Wei,Julie S. Barber-Rotenberg,Maureen E. Murphy,Gordon B. Mills
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2017-09-13
卷期号:7 (11): 1266-1283
被引量:178
标识
DOI:10.1158/2159-8290.cd-17-0741
摘要
Lysosomes serve dual roles in cancer metabolism, executing catabolic programs (i.e., autophagy and macropinocytosis) while promoting mTORC1-dependent anabolism. Antimalarial compounds such as chloroquine or quinacrine have been used as lysosomal inhibitors, but fail to inhibit mTOR signaling. Further, the molecular target of these agents has not been identified. We report a screen of novel dimeric antimalarials that identifies dimeric quinacrines (DQ) as potent anticancer compounds, which concurrently inhibit mTOR and autophagy. Central nitrogen methylation of the DQ linker enhances lysosomal localization and potency. An
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