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CCN1 对于酸诱导的食管上皮细胞转化至关重要。

CCN1 is critical for acid-induced esophageal epithelial cell transformation.

机构信息

VA Long Beach Healthcare System, 5901 E. Seventh Street, Long Beach, CA 90822, USA.

出版信息

Biochem Biophys Res Commun. 2010 Feb 19;392(4):533-7. doi: 10.1016/j.bbrc.2010.01.057. Epub 2010 Jan 25.

Abstract

CCN1 is a matricellular protein involved in both wound healing and cancer cell invasion. Increased CCN1 expression has been associated with the development of Barrett's esophagus and the increased risk of progression to esophageal adenocarcinoma. In both cases, acid reflux is a major contributor. Low pH has been shown to induce CCN1 gene expression in esophageal epithelial cells. Here we demonstrated that both CCN1 and low pH could cause esophageal epithelial cell transformation, including loss of E-cadherin, disruption of cell-cell junctions, and expression of mesenchymal markers. Furthermore, knockdown of CCN1 through RNA interference sufficiently attenuated acid-driven cell phenotypic changes, while over-expression of CCN1 exacerbated these effects, indicating a critical role of CCN1 in acid-induced esophageal epithelial cell transformation. Given the pivotal role of low pH in gastro-esophageal reflux disease and its progression towards esophageal adenocarcinoma, our study identified CCN1 as a key molecule mediating this process.

摘要

CCN1 是一种基质细胞蛋白,参与伤口愈合和癌细胞侵袭。CCN1 表达增加与 Barrett 食管的发展和食管腺癌进展的风险增加有关。在这两种情况下,胃酸反流是主要诱因。已经表明,低 pH 值可诱导食管上皮细胞中 CCN1 基因的表达。在这里,我们证明了 CCN1 和低 pH 值都可以导致食管上皮细胞转化,包括 E-钙黏蛋白的丢失、细胞-细胞连接的破坏以及间充质标记物的表达。此外,通过 RNA 干扰敲低 CCN1 足以减弱酸驱动的细胞表型变化,而过表达 CCN1 则加剧了这些效应,表明 CCN1 在酸诱导的食管上皮细胞转化中起关键作用。鉴于低 pH 值在胃食管反流病及其向食管腺癌进展中的关键作用,我们的研究确定 CCN1 是介导这一过程的关键分子。

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