Mitochondria-targeted magnolol inhibits OXPHOS, proliferation, and tumor growth via modulation of energetics and autophagy in melanoma cells.
Cancer treatment and research communications（2020）
摘要
These findings have implications in the treatment of melanomas with enhanced OXPHOS status due to metabolic reprogramming or drug resistance.
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关键词
Bioenergetic metabolism,Melanoma,Mitochondria-targeted agents,Mitophagy,Oxidative phosphorylation
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