Department of Medicinal Chemistry, College of Pharmacy, Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan 48109, United States.
J Med Chem. 2020 Dec 10;63(23):14276-14307. doi: 10.1021/acs.jmedchem.0c01013. Epub 2020 Oct 26.
Certain subtypes of cancer cells require oxidative phosphorylation (OXPHOS) to survive. Increased OXPHOS dependency is frequently a hallmark of cancer stem cells and cells resistant to chemotherapy and targeted therapies. Suppressing the OXPHOS function might also influence the tumor microenvironment by alleviating hypoxia and improving the antitumor immune response. Thus, targeting OXPHOS is a promising strategy to treat various cancers. A growing arsenal of therapeutic agents is under development to inhibit this biological process. This Perspective provides an overview of the structure and function of OXPHOS complexes, their biological functions in cancer, relevant research tools and models, as well as the limitations of OXPHOS as drug targets. We also focus on the current development status of OXPHOS inhibitors and potential therapeutic strategies to strengthen their clinical applications.
某些癌症细胞亚型需要氧化磷酸化(OXPHOS)才能存活。OXPHOS 依赖性增加通常是癌症干细胞和对化疗和靶向治疗有抵抗力的细胞的标志。抑制 OXPHOS 功能还可以通过减轻缺氧和改善抗肿瘤免疫反应来影响肿瘤微环境。因此,靶向 OXPHOS 是治疗各种癌症的一种有前途的策略。越来越多的治疗剂正在开发中以抑制这一生物过程。本观点概述了 OXPHOS 复合物的结构和功能、它们在癌症中的生物学功能、相关的研究工具和模型,以及 OXPHOS 作为药物靶点的局限性。我们还重点介绍了 OXPHOS 抑制剂的当前开发状况和潜在的治疗策略,以加强它们的临床应用。