The Warburg effect and mitochondrial stability in cancer cells

被引:164
|
作者
Gogvadze, Vladimir [1 ]
Zhivotovsky, Boris [1 ]
Orrenius, Sten [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Toxicol, SE-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
The Warburg effect; Apoptosis; Mitochondria; Cancer; PERMEABILITY TRANSITION-PORE; CYTOCHROME-C RELEASE; HYPOXIA-INDUCIBLE FACTOR-1; ADENINE-NUCLEOTIDE TRANSLOCATOR; SUCCINATE INDUCES APOPTOSIS; EHRLICH ASCITES TUMOR; CYCLOPHILIN-D; OXIDATIVE STRESS; AEROBIC GLYCOLYSIS; ENERGY-METABOLISM;
D O I
10.1016/j.mam.2009.12.004
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 last decade has witnessed a renaissance of Otto Warburg's fundamental hypothesis, which he put forward more than 80 years ago, that mitochondrial malfunction and subsequent stimulation of cellular glucose utilization lead to the development of cancer. Since most tumor cells demonstrate a remarkable resistance to drugs that kill non-malignant cells, the question has arisen whether such resistance might be a consequence of the abnormalities in tumor mitochondria predicted by Warburg. The present review discusses potential mechanisms underlying the upregulation of glycolysis and silencing of mitochondrial activity in cancer cells, and how pharmaceutical intervention in cellular energy metabolism might make tumor cells more susceptible to anti-cancer treatment. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:60 / 74
页数:15
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