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在溃疡性结肠炎中 CXCL8 趋化因子。

CXCL8 chemokine in ulcerative colitis.

机构信息

College of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan 250355, PR China.

Department of Oncology, The Fifth People's Hospital of Jinan, Jinan 250022, PR China.

出版信息

Biomed Pharmacother. 2021 Jun;138:111427. doi: 10.1016/j.biopha.2021.111427. Epub 2021 Mar 8.

Abstract

Ulcerative colitis (UC) is a major type of inflammatory bowel disease (IBD), which is characterized by diffuse inflammation of the mucosa of the colon and rectum. Abdominal pain, diarrhea, and hematochezia are UC's main clinical manifestations. Pathogenesis of UC has not yet been clearly elucidated, but it is considered to result from dysregulated expressions of molecules engaged in proinflammatory and anti-inflammatory processes. CXCL8 is one of the most important proinflammatory factors which play a vital role in many inflammatory diseases including UC. The CXCL8-CXCR1/2 axis participates in the pathogenesis of UC through multiple signaling pathways, including PI3k/Akt, MAPKs and NF-κB signaling pathways. Meanwhile, more and more studies in recent years have shown that UC patients have specific non-coding RNA (ncRNA) expression profiles, which may be involved in the occurrence and development of inflammation. In this article, we analyzed the CXCL8-CXCR1/2 axis related signaling pathways and ncRNAs in UC, as well as recent advances in our understanding of the CXCL8-CXCR1/2 axis inhibition as a therapeutic strategy against UC.

摘要

溃疡性结肠炎(UC)是一种主要的炎症性肠病(IBD),其特征为结肠和直肠黏膜的弥漫性炎症。腹痛、腹泻和血便为 UC 的主要临床表现。UC 的发病机制尚未明确,但被认为是与参与促炎和抗炎过程的分子的失调表达有关。CXCL8 是最重要的促炎因子之一,在包括 UC 在内的许多炎症性疾病中发挥着重要作用。CXCL8-CXCR1/2 轴通过多种信号通路(包括 PI3k/Akt、MAPKs 和 NF-κB 信号通路)参与 UC 的发病机制。同时,近年来越来越多的研究表明,UC 患者具有特定的非编码 RNA(ncRNA)表达谱,可能参与炎症的发生和发展。本文分析了 UC 中与 CXCL8-CXCR1/2 轴相关的信号通路和 ncRNA,并概述了我们对抑制 CXCL8-CXCR1/2 轴作为治疗 UC 策略的理解的最新进展。

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