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线粒体自噬在癌症和癌症治疗中的新兴多方面作用。

The emerging, multifaceted role of mitophagy in cancer and cancer therapeutics.

机构信息

Cancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Odisha, India.

Cancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Odisha, India.

出版信息

Semin Cancer Biol. 2020 Nov;66:45-58. doi: 10.1016/j.semcancer.2019.07.015. Epub 2019 Jul 24.

Abstract

Mitophagy is an evolutionarily conserved cellular process which selectively eliminates dysfunctional mitochondria by targeting them to the autophagosome for degradation. Dysregulated mitophagy results in the accumulation of damaged mitochondria, which plays an important role in carcinogenesis and tumor progression. The role of mitophagy receptors and adaptors including PINK1, Parkin, BNIP3, BNIP3L/NIX, and p62/SQSTM1, and the signaling pathways that govern mitophagy are impaired in cancer. Furthermore, the contribution of mitophagy in regulating the metabolic switch may establish a balance between aerobic glycolysis and oxidative phosphorylation for cancer cell survival. Moreover, ROS-driven mitophagy achieves different goals depending on the stage of tumorigenesis. Mitophagy promotes plasticity in the cancer stem cell through the metabolic reconfiguration for better adaption to the tumor microenvironment. In addition, the present review sheds some light on the role of mitophagy in stemness and differentiation during the transition of cell's fate, which could have a crucial role in cancer progression and metastasis. In conclusion, this review deals with the detailed molecular mechanisms underlying mitophagy, along with highlighting the dual role of mitophagy in different aspects of cancer, suggesting it as a possible target in the mitophagy-modulated cancer therapy.

摘要

自噬是一种进化上保守的细胞过程,通过将功能失调的线粒体靶向自噬体进行降解来选择性地消除它们。自噬失调导致受损线粒体的积累,这在致癌作用和肿瘤进展中起着重要作用。自噬受体和衔接蛋白(如 PINK1、Parkin、BNIP3、BNIP3L/NIX 和 p62/SQSTM1)以及调控自噬的信号通路在癌症中受损。此外,自噬在调节代谢转换中的作用可能在有氧糖酵解和氧化磷酸化之间建立平衡,以维持癌细胞的存活。此外,ROS 驱动的自噬通过代谢重配置来实现不同的目标,以促进癌细胞的可塑性,从而更好地适应肿瘤微环境。此外,本综述还探讨了自噬在细胞命运转变过程中的干性和分化中的作用,这可能在癌症进展和转移中起着关键作用。总之,本综述涉及自噬的详细分子机制,并强调了自噬在癌症不同方面的双重作用,表明它可能成为自噬调节癌症治疗的一个潜在靶点。

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