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靶向呼吸链复合体I以预防瓦伯格效应。

Targeting respiratory complex I to prevent the Warburg effect.

作者信息

Vatrinet Renaud, Iommarini Luisa, Kurelac Ivana, De Luise Monica, Gasparre Giuseppe, Porcelli Anna Maria

机构信息

Dipartimento di Farmacia e Biotecnologie (FABIT), Università di Bologna, via Irnerio 42, 40126 Bologna, Italy; Dipartimento di Scienze Mediche e Chirurgiche (DIMEC), U.O. Genetica Medica, Pol. Universitario S. Orsola-Malpighi, Università di Bologna, via Massarenti 9, 40138 Bologna, Italy.

Dipartimento di Farmacia e Biotecnologie (FABIT), Università di Bologna, via Irnerio 42, 40126 Bologna, Italy.

出版信息

Int J Biochem Cell Biol. 2015 Jun;63:41-5. doi: 10.1016/j.biocel.2015.01.017. Epub 2015 Feb 7.

DOI:10.1016/j.biocel.2015.01.017
PMID:25668477
Abstract

In the last 10 years, studies of energetic metabolism in different tumors clearly indicate that the definition of Warburg effect, i.e. the glycolytic shift cells undergo upon transformation, ought to be revisited considering the metabolic plasticity of cancer cells. In fact, recent findings show that the shift from glycolysis to re-established oxidative metabolism is required for certain steps of tumor progression, suggesting that mitochondrial function and, in particular, respiratory complex I are crucial for metabolic and hypoxic adaptation. Based on these evidences, complex I can be considered a lethality target for potential anticancer strategies. In conclusion, in this mini review we summarize and discuss why it is not paradoxical to develop pharmacological and genome editing approaches to target complex I as novel adjuvant therapies for cancer treatment. This article is part of a Directed Issue entitled: Energy Metabolism Disorders and Therapies.

摘要

在过去十年中,对不同肿瘤能量代谢的研究清楚地表明,鉴于癌细胞的代谢可塑性,瓦伯格效应(即细胞在转化时经历的糖酵解转变)的定义应该重新审视。事实上,最近的研究结果表明,从糖酵解转变为重新建立的氧化代谢是肿瘤进展某些步骤所必需的,这表明线粒体功能,特别是呼吸链复合体I对于代谢和缺氧适应至关重要。基于这些证据,复合体I可被视为潜在抗癌策略的致死靶点。总之,在本综述中,我们总结并讨论了为何开发针对复合体I的药理学和基因组编辑方法作为癌症治疗的新型辅助疗法并非自相矛盾。本文是名为“能量代谢紊乱与疗法”的特刊的一部分。

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