自噬
细胞生物学
细胞凋亡
生物
HMGB1
程序性细胞死亡
溶酶体
癌变
癌细胞
癌症
癌症研究
免疫学
生物化学
遗传学
炎症
酶
作者
Ruochan Chen,Zou Ju,Xiao Yan Zhong,Jie Li,Rui Kang,Daolin Tang
出处
期刊:Cancer Letters
[Elsevier]
日期:2023-11-24
卷期号:581: 216494-216494
被引量:8
标识
DOI:10.1016/j.canlet.2023.216494
摘要
Lysosome-mediated autophagy and caspase-dependent apoptosis are dynamic processes that maintain cellular homeostasis, ensuring cell health and functionality. The intricate interplay and reciprocal regulation between autophagy and apoptosis are implicated in various human diseases, including cancer. High-mobility group box 1 (HMGB1), a nonhistone chromosomal protein, plays a pivotal role in coordinating autophagy and apoptosis levels during tumor initiation, progression, and therapy. The regulation of autophagy machinery and the apoptosis pathway by HMGB1 is influenced by various factors, including the protein's subcellular localization, oxidative state, and interactions with binding partners. In this narrative review, we provide a comprehensive overview of the structure and function of HMGB1, with a specific focus on the interplay between autophagic degradation and apoptotic death in tumorigenesis and cancer therapy. Gaining a comprehensive understanding of the significance of HMGB1 as a biomarker and its potential as a therapeutic target in tumor diseases is crucial for advancing our knowledge of cell survival and cell death.
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