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核因子 κB 在干扰素反应中的作用。

The role of nuclear factor κB in the interferon response.

机构信息

Department of Pathology and Laboratory Medicine and Center for Cancer Research, University of Tennessee Health Science Center, Memphis, Tennessee 38163, USA.

出版信息

J Interferon Cytokine Res. 2011 Jul;31(7):553-9. doi: 10.1089/jir.2011.0028. Epub 2011 Jun 1.

DOI:10.1089/jir.2011.0028
PMID:21631354
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3128784/
Abstract

The nuclear factor κB (NF-κB) transcription factor regulates the expression of genes involved in cell survival and immune responses. We have identified a novel interferon (IFN)-activated signaling pathway that leads to NF-κB activation and demonstrate that a subset of IFN-stimulated genes and microRNAs that play key roles in cellular response to IFN is regulated by NF-κB. This review focuses on the IFN-induced NF-κB activation pathway and the role of NF-κB in the expression of IFN-induced coding and noncoding genes, antiviral activity and apoptosis, and the therapeutic application of IFN in cancer and infectious disease.

摘要

核因子 κB(NF-κB)转录因子调节参与细胞存活和免疫反应的基因的表达。我们已经确定了一种新的干扰素(IFN)激活信号通路,该通路导致 NF-κB 的激活,并证明了 IFN 刺激的基因和 microRNA 的亚组在细胞对 IFN 的反应中发挥关键作用,受 NF-κB 调控。这篇综述重点介绍了 IFN 诱导的 NF-κB 激活途径以及 NF-κB 在 IFN 诱导的编码和非编码基因表达、抗病毒活性和细胞凋亡中的作用,以及 IFN 在癌症和传染病中的治疗应用。

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本文引用的文献

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The specificity of innate immune responses is enforced by repression of interferon response elements by NF-κB p50.先天免疫反应的特异性是通过 NF-κB p50 抑制干扰素反应元件来实现的。
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Differential expression of interferon-induced microRNAs in patients with chronic hepatitis C virus infection treated with pegylated interferon alpha.聚乙二醇干扰素α治疗慢性丙型肝炎病毒感染患者中干扰素诱导的 microRNAs 的差异表达。
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