Dias Nathalie, Bailly Christian
INSERM U-524 et Laboratoire de Pharmacologie Antitumorale du Centre Oscar Lambret, IRCL, 59045 Lille, France.
Biochem Pharmacol. 2005 Jul 1;70(1):1-12. doi: 10.1016/j.bcp.2005.03.021.
Mitochondria, the power houses of the cell, are at the cross-road of many cellular pathways. They play a central role in energy metabolism, regulate calcium flux and are implicated in apoptosis. Mitochondrial dysfunctions have been associated with various physiopathological disorders, especially neurodegenerative diseases and cancer. Structurally diverse pharmacological agents have shown direct effects on mitochondria ultra-structures and functions, either at the DNA level or upon targeting proteins located in the inner or outer mitochondrial membranes. The brief review deals with the molecular targets and mechanisms of action of chemically diverse small molecules acting on specific mitochondrial loci, such as the respiratory chain, DNA biogenesis, potassium channels, the Bcl-2 protein and the permeability transition pores (PTP). Drugs, which specifically compromise the structural and functional integrity of mitochondria, may provide novel opportunities to combat cancer cell proliferation, providing that these molecules can be selectively delivered to tumor sites. Different examples reported here show that mitochondrial insult or failure can rapidly lead to inhibition of cell survival and proliferation. Mitochondrial impairment may be a successful anti-cancer strategy.
线粒体作为细胞的“动力工厂”,处于许多细胞信号通路的交叉点。它们在能量代谢中起核心作用,调节钙通量,并与细胞凋亡相关。线粒体功能障碍与多种生理病理紊乱有关,尤其是神经退行性疾病和癌症。结构多样的药物制剂已显示出对线粒体超微结构和功能有直接影响,无论是在DNA水平,还是作用于位于线粒体内膜或外膜的蛋白质时。本简要综述探讨了作用于特定线粒体位点(如呼吸链、DNA生物合成、钾通道、Bcl-2蛋白和通透性转换孔(PTP))的化学结构各异的小分子的分子靶点和作用机制。专门破坏线粒体结构和功能完整性的药物可能为对抗癌细胞增殖提供新机会,前提是这些分子能够被选择性地输送到肿瘤部位。此处报道的不同实例表明,线粒体损伤或功能衰竭可迅速导致细胞存活和增殖受到抑制。线粒体损伤可能是一种成功的抗癌策略。