Regulation of anoikis by extrinsic death receptor pathways

被引:38
作者
Han, Ying-Hao [1 ]
Wang, Yuan [1 ]
Lee, Seung-Jae [2 ,3 ]
Jin, Mei-Hua [1 ]
Sun, Hu-Nan [1 ]
Kwon, Taeho [4 ,5 ]
机构
[1] Heilongjiang Bayi Agr Univ, Coll Life Sci & Biotechnol, Daqing 163319, Peoples R China
[2] Korea Res Inst Biosci Biotechnol KRIBB, Funct Biomat Res Ctr, Jeonbuk 56212, South Korea
[3] Univ Sci & Technol, KRIBB Sch Biotechnol, Dept Appl Biol Engn, Daejeon 34113, South Korea
[4] Korea Res Inst Biosci & Biotechnol KRIBB, Primate Resources Ctr, Jeonbuk 56216, South Korea
[5] Univ Sci & Technol, KRIBB Sch Biosci, Dept Funct Genom, Daejeon 34141, South Korea
关键词
Aanoikis; Death receptor pathway; Fas; TNFR1/TNFR2; DR4/DR5; Cancer metastasis; ANCHORAGE-INDEPENDENT GROWTH; NECROSIS-FACTOR RECEPTOR; MEDIATED APOPTOSIS; FAS LIGAND; DOWN-REGULATION; CANCER; CELLS; RESISTANCE; ACTIVATION; PROTEIN;
D O I
10.1186/s12964-023-01247-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Metastatic cancer cells can develop anoikis resistance in the absence of substrate attachment and survive to fight tumors. Anoikis is mediated by endogenous mitochondria-dependent and exogenous death receptor pathways, and studies have shown that caspase-8-dependent external pathways appear to be more important than the activity of the intrinsic pathways. This paper reviews the regulation of anoikis by external pathways mediated by death receptors. Different death receptors bind to different ligands to activate downstream caspases. The possible mechanisms of Fas-associated death domain (FADD) recruitment by Fas and TNF receptor 1 associated-death domain (TRADD) recruitment by tumor necrosis factor receptor 1 (TNFR1), and DR4- and DR5-associated FADD to induce downstream caspase activation and regulate anoikis were reviewed. This review highlights the possible mechanism of the death receptor pathway mediation of anoikis and provides new insights and research directions for studying tumor metastasis mechanisms.9w_3dtXFY6CUXRSJ-7gGifVideo Abstract
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页数:14
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