HMGB1 in the interplay between autophagy and apoptosis in cancer

被引:31
作者
Chen, Ruochan [1 ,2 ]
Zhu, Ju [1 ,2 ]
Zhong, Xiao [1 ,2 ]
Li, Jie [1 ,2 ]
Kang, Rui [3 ]
Tang, Daolin [3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Infect Dis, Hunan Key Lab Viral Hepatitis, Changsha 410008, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Hunan, Peoples R China
[3] UT Southwestern Med Ctr, Dept Surg, Dallas, TX 75390 USA
关键词
HMGB1; Autophagy; Apoptosis; Tumorigenesis; Cancer therapy; IMMUNOGENIC CELL-DEATH; GROUP BOX 1; CHROMATIN PROTEIN HMGB1; BREAST-CANCER; BLADDER-CANCER; UP-REGULATION; HMGB1-INDUCED AUTOPHAGY; TAMOXIFEN RESISTANCE; MALIGNANT PHENOTYPE; ANTITUMOR-ACTIVITY;
D O I
10.1016/j.canlet.2023.216494
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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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页数:19
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