RIPK1和RIPK3 -癌症中的新靶点?

K. Gurol, Suraj Shah, A. Degterev
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引用次数: 1

摘要

摘要:RIPK1和RIPK3是同源的丝氨酸/苏氨酸激酶,它们在坏死复合体中协同作用,启动一种被称为坏死性坏死的亚型。坏死性上睑下垂已逐渐成为一种与临床高度相关的坏死形式,可以靶向治疗。除了坏死性坏死,RIPK1和RIPK3还参与了其他病理生理相关反应,包括细胞凋亡和炎症的调节。最近,人们发现RIPK1/RIPK3通路在癌症中可能发生系统性改变。这些通路的状态可能提供预后价值,而RIPK1/RIPK3信号的治疗性调节可能代表了一种对抗各种形式人类癌症的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RIPK1 and RIPK3 – emerging targets in cancer?
Abstract: RIPK1 and RIPK3 are homologous Ser/Thr kinases, which act in concert within the necrosome complexes to initiate a sub-type of regulated necrosis, termed necroptosis. Necroptosis has gradually emerged as a highly clinically relevant form of necrosis, which can be targeted therapeutically. Besides necroptosis, RIPK1 and RIPK3 have been implicated in other pathophysiologically-relevant responses, including regulation of apoptosis and inflammation. More recently, it became evident that RIPK1/RIPK3 pathways may be systematically altered in cancers. Status of these pathways may provide a prognostic value, and therapeutic modulation of RIPK1/RIPK3 signaling may represent a new strategy against various forms of human cancer.  
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