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肿瘤坏死因子信号传导及其他方面的分子机制。

Molecular mechanism of TNF signaling and beyond.

作者信息

Liu Zheng Gang

机构信息

Cell and Cancer Biology Branch, Center for Cancer Research, National Cancer Institute, NIH, 9000 Rockville Pike Bethesda, MD 20892, USA.

出版信息

Cell Res. 2005 Jan;15(1):24-7. doi: 10.1038/sj.cr.7290259.

Abstract

Tumor necrosis factor (TNF) is a proinflammatory cytokine that plays a critical role in diverse cellular events, including cell proliferation, differentiation and apoptosis. TNF is also involved in many types of diseases. In recent years, the molecular mechanisms of TNF functions have been intensively investigated. Studies from many laboratories have demonstrated that the TNF-mediated diverse biological responses are achieved through activating multiple signaling pathways. Especially the activation of transcription factors NF-kB and AP-1 plays a critical role in mediating these cellular responses. Several proteins, including FADD, the death domain kinase RIP and the TNF receptor associated factor TRAF2 have been identified as the key effectors of TNF signaling. Recently, we found that the effector molecules of TNF signaling, such as RIP and TRAF2, are also involved in other cellular responses. These finding suggests that RIP and TRAF2 serve a broader role than as just an effector of TNF signaling.

摘要

肿瘤坏死因子(TNF)是一种促炎细胞因子,在多种细胞事件中发挥关键作用,包括细胞增殖、分化和凋亡。TNF还与多种疾病有关。近年来,TNF功能的分子机制得到了深入研究。许多实验室的研究表明,TNF介导的多种生物学反应是通过激活多条信号通路实现的。特别是转录因子NF-κB和AP-1的激活在介导这些细胞反应中起关键作用。包括FADD、死亡结构域激酶RIP和TNF受体相关因子TRAF2在内的几种蛋白质已被确定为TNF信号传导的关键效应分子。最近,我们发现TNF信号传导的效应分子,如RIP和TRAF2,也参与其他细胞反应。这些发现表明,RIP和TRAF2的作用比仅仅作为TNF信号传导的效应分子更为广泛。

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