Melatonin, mitochondria, and the cancer cell

被引:45
|
作者
Proietti, Sara [1 ]
Cucina, Alessandra [1 ]
Minini, Mirko [1 ]
Bizzarri, Mariano [2 ]
机构
[1] Pietro Valdoni Sapienza Univ Rome, Dept Surg, Via Antonio Scarpa 14, I-00161 Rome, Italy
[2] Sapienza Univ Rome, Dept Expt Med, Viale Regina Elena 324, I-00161 Rome, Italy
关键词
Melatonin; Warburg effect; Mitochondria; Cancer; FATTY-ACID SYNTHASE; T-BUTYL HYDROPEROXIDE; OXIDATIVE STRESS; TUMOR-CELLS; RAT-BRAIN; IN-VITRO; LIVER-MITOCHONDRIA; OXYGEN-CONSUMPTION; AEROBIC GLYCOLYSIS; GENE-EXPRESSION;
D O I
10.1007/s00018-017-2612-z
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 long-recognized fact that oxidative stress within mitochondria is a hallmark of mitochondrial dysfunction has stimulated the development of mitochondria-targeted antioxidant therapies. Melatonin should be included among the pharmacological agents able to modulate mitochondrial functions in cancer, given that a number of relevant melatonin-dependent effects are triggered by targeting mitochondrial functions. Indeed, melatonin may modulate the mitochondrial respiratory chain, thus antagonizing the cancer highly glycolytic bioenergetic pathway of cancer cells. Modulation of the mitochondrial respiratory chain, together with Ca2+ release and mitochondrial apoptotic effectors, may enhance the spontaneous or drug-induced apoptotic processes. Given that melatonin may efficiently counteract the Warburg effect while stimulating mitochondrial differentiation and mitochondrial-based apoptosis, it is argued that the pineal neurohormone could represent a promising new perspective in cancer treatment strategy.
引用
收藏
页码:4015 / 4025
页数:11
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