癌症治疗
癌细胞
癌症
氧化磷酸化
体内
癌症研究
癌症治疗
生物能学
对接(动物)
线粒体
化学
磷酸化
计算生物学
娴熟的
小分子
生物化学
细胞
细胞生物学
抗癌药物
生物
转移
生物信息学
酶
体外
癌细胞系
作者
Alaa M.A. Osman,Alya A. Arabi
标识
DOI:10.1016/j.bcp.2026.117695
摘要
Mitochondrial Complexes I-IV in the Electron Transport Chain (ETC) are strategic targets for cancer treatment since they provide the energy and biosynthetic demands of cancer cells. This review covers in silico, in vitro, and in vivo findings related to the inhibition of ETC complexes in order to block cancer cell survival. It also includes computational docking studies that we performed to confirm the binding of literature-reported inhibitors to ETC complexes. This review also covers details about bioenergetic disruption as well as innovative therapeutic strategies based on the Oxidative Phosphorylation (OXPHOS) activity and the ETC dependencies in cancer cells. This review serves as a guide for the development of small molecules that target the ETC for cancer treatment.
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