3-Bromopyruvate: A New Targeted Antiglycolytic Agent and a Promise for Cancer Therapy

被引:106
作者
Ganapathy-Kanniappan, S. [1 ]
Vali, M. [1 ]
Kunjithapatham, R. [1 ]
Buijs, M. [1 ]
Syed, L. H. [1 ]
Rao, P. P. [1 ]
Ota, S. [1 ]
Kwak, B. K. [1 ]
Loffroy, R. [1 ]
Geschwind, J. F. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21287 USA
关键词
Alkylating agent; glycolysis; 3-bromopyruvate; anti-metabolite; GAPDH; ENDOPLASMIC-RETICULUM STRESS; MATURE BOAR SPERMATOZOA; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; CELL-DEATH; ALDEHYDE DEHYDROGENASE; PYRUVATE-KINASE; BROMOPYRUVATE INACTIVATION; HEPATOCELLULAR-CARCINOMA; ESCHERICHIA-COLI; SUBSTRATE ANALOG;
D O I
10.2174/138920110791591427
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pyruvate analog, 3-bromopyruvate, is an alkylating agent and a potent inhibitor of glycolysis. This antiglycolytic property of 3-bromopyruvate has recently been exploited to target cancer cells, as most tumors depend on glycolysis for their energy requirements. The anticancer effect of 3-bromopyruvate is achieved by depleting intracellular energy (ATP) resulting in tumor cell death. In this review, we will discuss the principal mechanism of action and primary targets of 3-bromopyruvate, and report the impressive antitumor effects of 3-bromopyruvate in multiple animal tumor models. We describe that the primary mechanism of 3-bromopyruvate is via preferential alkylation of GAPDH and that 3-bromopyruvate mediated cell death is linked to generation of free radicals. Research in our laboratory also revealed that 3-bromopyruvate induces endoplasmic reticulum stress, inhibits global protein synthesis further contributing to cancer cell death. Therefore, these and other studies reveal the tremendous potential of 3-bromopyruvate as an anticancer agent.
引用
收藏
页码:510 / 517
页数:8
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