Integration of Mitochondrial Targeting for Molecular Cancer Therapeutics

Q3 Biochemistry, Genetics and Molecular Biology International Journal of Cell Biology Pub Date : 2015-12-02 DOI:10.1155/2015/283145
P. Marchetti, P. Guerreschi, L. Mortier, J. Kluza
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引用次数: 26

Abstract

Mitochondrial metabolism greatly influences cancer cell survival, invasion, metastasis, and resistance to many anticancer drugs. Furthermore, molecular-targeted therapies (e.g., oncogenic kinase inhibitors) create a dependence of surviving cells on mitochondrial metabolism. For these reasons, inhibition of mitochondrial metabolism represents promising therapeutic pathways in cancer. This review provides an overview of mitochondrial metabolism in cancer and discusses the limitations of mitochondrial inhibition for cancer treatment. Finally, we present preclinical evidence that mitochondrial inhibition could be associated with oncogenic “drivers” inhibitors, which may lead to innovative drug combinations for improving the efficacy of molecular-targeted therapy.
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线粒体靶向在分子癌症治疗中的整合
线粒体代谢在很大程度上影响着癌细胞的生存、侵袭、转移和对许多抗癌药物的耐药性。此外,分子靶向治疗(例如,致癌激酶抑制剂)使存活细胞依赖于线粒体代谢。由于这些原因,抑制线粒体代谢代表了有希望的癌症治疗途径。本文综述了线粒体代谢在癌症中的作用,并讨论了线粒体抑制在癌症治疗中的局限性。最后,我们提出的临床前证据表明,线粒体抑制可能与致癌“驱动因素”抑制剂有关,这可能会导致创新药物组合,以提高分子靶向治疗的疗效。
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来源期刊
International Journal of Cell Biology
International Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
3.30
自引率
0.00%
发文量
4
审稿时长
20 weeks
期刊最新文献
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