Targeting vacuolar H+-ATPases as a new strategy against cancer

被引:216
作者
Fais, Stefano
De Milito, Angelo
You, Haiyan
Qin, Wenxin
机构
[1] Ist Super Sanita, Dept Drug Res & Evaluat, Drug Resistance & Expt Therapeut, Pharmacogenet Sect, I-00161 Rome, Italy
[2] Shanghai Jiao Tong Univ, Shanghai Canc Inst, WHO Collaborat Ctr Res Canc, Natl Lab Oncogenes & Related Genes, Shanghai 200030, Peoples R China
关键词
D O I
10.1158/0008-5472.CAN-07-1805
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Growing evidence suggests a key role of tumor acidic microenvironment in cancer development, progression, and metastasis. As a consequence, the need for compounds that specifically target the mechanism(s) responsible for the low pH of tumors is increasing. Among the key regulators of the tumor acidic microenvironment, vacuolar H+-ATPases (V-ATPases) play an important role. These proteins cover a number of functions in a variety of normal as well as tumor cells, in which they pump ions across the membranes. We discuss here some recent results showing that a molecular inhibition of V-ATPases by small interfering RNA in vivo as well as a pharmacologic inhibition through proton pump inhibitors led to tumor cytotoxicity and marked inhibition of human tumor growth in xenograft models. These results propose V-ATPases as a key target for new strategies in cancer treatment.
引用
收藏
页码:10627 / 10630
页数:4
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