Department of Oncohaematology and Cellular and Gene Therapy, IRCSS Bambino Gesù Children's Hospital, 00165, Rome, Italy.
Department of Biology, University of Tor Vergata, 00133, Rome, Italy.
Cell Death Differ. 2019 Mar;26(4):690-702. doi: 10.1038/s41418-019-0292-y. Epub 2019 Feb 6.
Autophagy and mitophagy act in cancer as bimodal processes, whose differential functions strictly depend on cancer ontogenesis, progression, and type. For instance, they can act to promote cancer progression by helping cancer cells survive stress or, instead, when mutated or abnormal, to induce carcinogenesis by influencing cell signaling or promoting intracellular toxicity. For this reason, the study of autophagy in cancer is the main focus of many researchers and several clinical trials are already ongoing to manipulate autophagy and by this way determine the outcome of disease therapy. Since the establishment of the cancer stem cell (CSC) theory and the discovery of CSCs in individual cancer types, autophagy and mitophagy have been proposed as key mechanisms in their homeostasis, dismissal or spread, even though we still miss a comprehensive view of how and by which regulatory molecules these two processes drive cell fate. In this review, we will dive into the deep water of autophagy, mitophagy, and CSCs and offer novel viewpoints on possible therapeutic strategies, based on the modulation of these degradative systems.
自噬和线粒体自噬在癌症中作为双模态过程发挥作用,其差异功能严格取决于癌症的发生、进展和类型。例如,它们可以通过帮助癌细胞在压力下存活来促进癌症进展,或者在发生突变或异常时,通过影响细胞信号转导或促进细胞内毒性来诱导癌变。出于这个原因,对癌症中的自噬的研究是许多研究人员的主要关注点,并且已经有几项临床试验正在进行,以操纵自噬,并通过这种方式确定疾病治疗的结果。自从癌症干细胞 (CSC) 理论的建立和在个别癌症类型中发现 CSCs 以来,自噬和线粒体自噬已被提出作为它们的动态平衡、排除或传播的关键机制,尽管我们仍然缺乏对这两个过程如何以及通过哪些调节分子驱动细胞命运的全面了解。在这篇综述中,我们将深入探讨自噬、线粒体自噬和 CSCs,并基于这些降解系统的调节提供新的治疗策略观点。