Targeting necroptosis in anticancer therapy: mechanisms and modulators

被引:73
作者
Wu, Ying [1 ]
Dong, Guoqiang [1 ]
Sheng, Chunquan [1 ,2 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
[2] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Cell death; Necroptosis; Inducers; Inhibitors; Anticancer therapy; PROGRAMMED CELL-DEATH; TUMOR NECROSIS FACTOR; DOMAIN-LIKE PROTEIN; TNF-ALPHA; RIP1; KINASE; DEPENDENT NECROPTOSIS; CANCER-CELLS; HIGHLY POTENT; A549; CELLS; ER STRESS;
D O I
10.1016/j.apsb.2020.01.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Necroptosis, a genetically programmed form of necrotic cell death, serves as an important pathway in human diseases. As a critical cell-killing mechanism, necroptosis is associated with cancer progression, metastasis, and immunosurveillance. Targeting necroptosis pathway by small molecule modulators is emerging as an effective approach in cancer therapy, which has the advantage to bypass the apoptosis-resistance and maintain antitumor immunity. Therefore, a better understanding of the mechanism of necroptosis and necroptosis modulators is necessary to develop novel strategies for cancer therapy. This review will summarize recent progress of the mechanisms and detecting methods of necroptosis. In particular, the relationship between necroptosis and cancer therapy and medicinal chemistry of necroptosis modulators will be focused on. (C) 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:1601 / 1618
页数:18
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