Epigenetics and Cancer Research Laboratory, Biochemistry and Molecular Biology Group, Department of Life Science, National Institute of Technology, Rourkela, India.
Department of Molecular Biology, ICMR-National Institute for Research in Environmental Health, Bypass Road, Bhauri, Bhopal, 462 030, MP, India.
Cancer Lett. 2024 Apr 10;587:216779. doi: 10.1016/j.canlet.2024.216779. Epub 2024 Mar 6.
Cellular physiology is critically regulated by multiple signaling nexuses, among which cell death mechanisms play crucial roles in controlling the homeostatic landscape at the tissue level within an organism. Apoptosis, also known as programmed cell death, can be induced by external and internal stimuli directing the cells to commit suicide in unfavourable conditions. In contrast, stress conditions like nutrient deprivation, infection and hypoxia trigger autophagy, which is lysosome-mediated processing of damaged cellular organelle for recycling of the degraded products, including amino acids. Apparently, apoptosis and autophagy both are catabolic and tumor-suppressive pathways; apoptosis is essential during development and cancer cell death, while autophagy promotes cell survival under stress. Moreover, autophagy plays dual role during cancer development and progression by facilitating the survival of cancer cells under stressed conditions and inducing death in extreme adversity. Despite having two different molecular mechanisms, both apoptosis and autophagy are interconnected by several crosslinking intermediates. Epigenetic modifications, such as DNA methylation, post-translational modification of histone tails, and miRNA play a pivotal role in regulating genes involved in both autophagy and apoptosis. Both autophagic and apoptotic genes can undergo various epigenetic modifications and promote or inhibit these processes under normal and cancerous conditions. Epigenetic modifiers are uniquely important in controlling the signaling pathways regulating autophagy and apoptosis. Therefore, these epigenetic modifiers of both autophagic and apoptotic genes can act as novel therapeutic targets against cancers. Additionally, liquid-liquid phase separation (LLPS) also modulates the aggregation of misfolded proteins and provokes autophagy in the cytosolic environment. This review deals with the molecular mechanisms of both autophagy and apoptosis including crosstalk between them; emphasizing epigenetic regulation, involvement of LLPS therein, and possible therapeutic approaches against cancers.
细胞生理学受到多种信号枢纽的严格调控,其中细胞死亡机制在控制生物体组织水平的动态平衡方面起着至关重要的作用。细胞凋亡,又称程序性细胞死亡,可以由外部和内部刺激诱导,导致细胞在不利条件下自杀。相比之下,营养缺乏、感染和缺氧等应激条件会触发自噬,这是溶酶体介导的对受损细胞细胞器的处理,用于回收降解产物,包括氨基酸。显然,凋亡和自噬都是分解代谢和肿瘤抑制途径;凋亡在发育和癌细胞死亡中是必要的,而自噬则促进细胞在应激下的存活。此外,自噬在癌症发展和进展中具有双重作用,一方面通过在应激条件下促进癌细胞存活,另一方面通过诱导极端逆境下的细胞死亡。尽管具有两种不同的分子机制,但凋亡和自噬通过几种交联中间体相互关联。表观遗传修饰,如 DNA 甲基化、组蛋白尾部的翻译后修饰和 miRNA,在调节自噬和凋亡相关基因中起着关键作用。自噬和凋亡基因都可以经历各种表观遗传修饰,并在正常和癌变条件下促进或抑制这些过程。表观遗传修饰剂在控制调节自噬和凋亡的信号通路方面具有独特的重要性。因此,自噬和凋亡基因的这些表观遗传修饰剂可以作为针对癌症的新型治疗靶点。此外,液-液相分离 (LLPS) 也调节错误折叠蛋白的聚集,并在细胞质环境中引发自噬。本综述涉及自噬和凋亡的分子机制,包括它们之间的串扰;强调表观遗传调控、LLPS 的参与及其对癌症的可能治疗方法。