Therapeutic potential of ASK1 activators in cancer treatment: Current insights and future directions

被引:7
作者
Wang, Bo [1 ]
Ma, Ying [1 ]
Zhang, Yue [1 ]
Yin, Xunzhe [1 ,2 ]
机构
[1] Jilin Canc Hosp, Dept Integrated Chinese & Western Med, 1066 Jinhu Rd, Changchun 130103, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, 5625 Ren Min St, Changchun 130022, Peoples R China
关键词
ASK1; Apoptosis; Cancer; MAP3K; JNK signaling pathway; P38 MAPK signaling pathway; REGULATING KINASE 1; APOPTOSIS; PROTEIN; PATHWAY; CELLS; NANOPARTICLES; TUMOR; PHOSPHORYLATION; DEGRADATION; INDUCTION;
D O I
10.1016/j.biopha.2024.117214
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Apoptosis signal-regulated kinase 1 (ASK1) is a member of the mitogen-activated protein kinase kinase (MAP3K) family, whose activation and regulation are intricately associated with apoptosis. ASK1 is activated in response to oxidative stress, among other stimuli, subsequently triggering downstream JNK, p38 MAPK, and mitochondria-dependent apoptotic signaling, which participate in the initiation of tumor cell apoptosis induced by various stimuli. Research has shown that ASK1 plays a crucial role in the apoptosis of lung cancer, breast cancer, and liver cancer cells. Currently, the investigation of effective ASK1 activators is a hot topic in research on tumor cell apoptosis. Synthetic compounds such as human beta-defensin, triazolothiazide derivatives and heat shock protein 27 inhibitors; natural compounds such as quercetin, Laminarina japonica polysaccharide-1 peptide and theabrownin; and nanomedicines such as cerium oxide nanoparticles, magnetite FeO nanoparticles and silver nanoparticles can activate ASK1 and induce apoptosis in various tumor cells. This review extensively investigates the roles and activation mechanisms of ASK1, explores its impact on a variety of apoptotic signaling pathways, and discusses the potential therapeutic applications of various ASK1 activators in cancer treatment. In addition, this paper provides an in-depth discussion of the future development of this field and proposes a promising method for further research and clinical progress.
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页数:10
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