摘要
坏死性凋亡是不依赖于caspase激活的一种细胞程序性死亡方式,其激活主要依赖于坏死性小体的形成。坏死性凋亡的调控受到多种因素响,RIPK1既可启动坏死性凋亡,也可抑制坏死性凋亡;caspase-8是坏死性凋亡的重要负反馈调节蛋白;CHIP是新发现的坏死性凋亡调控蛋白。坏死性凋亡的触发为对经典凋亡途径抵抗的肿瘤提供了新的治疗策略。
Necroptosis, it is activated by the formation of necrosome, is a way of programmed cell death that independent of the activation of caspase. Necroptosis is regulated by many factors, for example, RIPK1 can initiate necroptosis, but also inhibit necroptosis; caspase-8 is the key negative regulation factor of necroptosis; CHIP is a new regulation protein of necroptosis. Triggering necroptosis is a promising strategy to overcome apoptosis resistance in cancer .
出处
《基础医学与临床》
CSCD
2017年第7期1051-1054,共4页
Basic and Clinical Medicine
基金
国家自然基金(30801088
81201488
81571572)