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Necroptosis信号通路与靶向治疗的研究进展 被引量:4

Recent advances in signal pathway of necroptosis and necroptosis targeted therapies
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摘要 Necroptosis是一种可调控的细胞程序性坏死途径,它具有与不可调控性细胞坏死相同的形态学特征。Necroptosis是caspase非依赖的。当细胞凋亡被阻断时,necroptosis信号通路由死亡结构域激活启动,其中RIP1的活化是necroptosis的关键步骤,该步骤可被necrostatin-1特异性抑制。近期研究表明,necroptosis在缺血性损伤、神经退行性疾病、恶性肿瘤、病毒感染和免疫性疾病等多种疾病的病理生理过程中起重要作用,有望作为药物开发的新靶点。对necroptosis的发现历程、信号通路及其在疾病病理生理机制中的作用和靶向necroptosis的治疗等四个方面进行综述。 Necroptosis is a specialized pathway of programmed necrosis induced by the activation of death domain (DD) under conditions when apoptosis execution is prevented. Necroptosis is caspase-independent, mediated by receptor-interacting protein 1 (RIP1) activity and inhibited by necrostatin-1 (Nec-1). Although it occurs under regulated conditions, necroptosis is characterized by the same morphological features as unregulated necrosis. In recent years, necroptosis has been found playing a significant role in multiple pathophysiologic processes. Targeting necroptosis pathway provides a new strategy for treatment of multiple human diseases involving ischemic injury, neurodegeneration disease, malignant tumor, virus infection and autoimmune disease. This review includes four parts: the discovery of necroptosis; the mechanism and signal pathway of necroptosis; the role that necroptosis plays in pathophysiologic processes of several diseases; the necroptosis targeted therapies.
作者 陈牧 黄雷
出处 《生命科学》 CSCD 2012年第7期666-673,共8页 Chinese Bulletin of Life Sciences
基金 国家自然科学基金项目(81071666) 上海市科学技术委员会项目(11140902600)
关键词 NECROPTOSIS 信号通路 病理生理机制 靶向治疗 necroptosis signal pathway pathophysiologic mechanism targeted therapy
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  • 1Lavrik I, Golks A, Krammer PH. Death receptor signaling. J Cell Sci, 2005, 118(Pt 2): 265-7. 被引量:1
  • 2Wang ZB, Liu YQ, Cui YF. Pathways to caspase activa- tion. Cell Biol Int, 2005, 29(7): 489-96. 被引量:1
  • 3Vercammen D, Vandenabeele P, Beyaert R, et al. Tumour necrosis factor-induced necrosis versus anti-Fas-induced apoptosis in L929 cells. Cytokine, 1997, 9(1l): 801-8. 被引量:1
  • 4Kawahara A, Ohsawa Y, Matsumura H, et al. Caspase-in- dependent cell killing by Fas-associated protein with death domain. J Cell Biol, 1998, 143(5): 1353-60. 被引量:1
  • 5Degterev A, Huang Z, Boyce M, et al. Chemical inhibitor of non-apoptotic cell death with therapeutic potential forischemic brain injury. Nat Chem Biol, 2005, 1(2): 112-9. 被引量:1
  • 6Hitomi J, Christofferson DE, Ng A, et al. Identification of a molecular signaling network that regulates a cellular ne- crotic cell death pathway. Cell, 2008, 135(7): 1311-23. 被引量:1
  • 7Vandenabeele P, Galluzzi L, Vanden Berghe T, et al. Mo- lecular mechanisms of necroptosis: an ordered cellular ex- plosion. Nat Rev Mol Cell Biol, 2010, 11(10): 700-14. 被引量:1
  • 8Kim YS, Morgan M J, Choksi S, et al. TNF-induced acti- vation of the Noxl NADPH oxidase and its role in the in- duction of necrotic cell death. Mol Cell, 2007, 26(5): 675- 87. 被引量:1
  • 9Kaiser WJ, Upton JW, Long AB, et al. RIP3 mediates the embryonic lethality of caspase-8-deficient mice. Nature, 2011, 471(7338): 368-72. 被引量:1
  • 10Ermolaeva MA, Michallet MC, Papadopoulou N, et al Function of TRADD in tumor necrosis factor receptor 1 signaling and in TRIF-dependent inflammatory responses Nat Immunol, 2008, 9(9): 1037-46. 被引量:1

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