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LRG1通过调节上皮-间质转化抑制食管鳞状细胞癌的迁移和侵袭。

LRG1 Suppresses Migration and Invasion of Esophageal Squamous Cell Carcinoma by Modulating Epithelial to Mesenchymal Transition.

作者信息

Zhang Ninggang, Ren Yaqiong, Wang Yusheng, Zhao Lei, Wang Bin, Ma Nina, Gao Zhengxing, Cao Bangwei

机构信息

Cancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.

Shanxi Cancer Hospital Affiliated to Shanxi Medical University, No. 3 of Zhigong Xincun Street, Xinghualing District, Taiyuan, Shanxi 030013, China.

出版信息

J Cancer. 2020 Jan 14;11(6):1486-1494. doi: 10.7150/jca.36189. eCollection 2020.

Abstract

: Esophageal squamous cell carcinoma (ESCC) is a common cancer with poor prognosis. The molecular pathogenesis underlying ESCC remains to be explored. Leucine-rich ɑ-2-glycoprotein 1 (LRG1) has been implicated in the pathogenesis of various cancer types, however its role in ESCC is unknown. : Data from the public database was analyzed to address the expression of LRG1 in ESCC. Gain-of-function studies were performed in select ESCC cell lines by over-expression or addition of recombinant LRG1, while loss-of-function studies achieved by small interfering RNA mediated knockdown. Wound healing and transwell assays were conducted to investigate ESCC cell migration and invasion upon manipulating LRG1 levels. Western blot and Immunofluorescence staining were used to examine the changes in epithelial to mesenchymal transition (EMT) and TGFβ signaling pathway. : LRG1 mRNA levels were found to be significantly down-regulated in patients with ESCC as well as in several ESCC cell lines. Silencing of LRG1 promoted, while overexpression of LRG1 inhibited ESCC cell migration and invasion. In line with this, Silencing of LRG1 enhanced, while overexpression of LRG1 reduced TGFβ signaling and EMT of ESCC cells. : LRG1 suppresses ESCC cell migration and invasion via negative modulation of TGFβ signaling and EMT. Down-regulation of LRG1 in ESCC patients may favor tumor metastasis and disease progression.

摘要

食管鳞状细胞癌(ESCC)是一种常见的预后较差的癌症。ESCC潜在的分子发病机制仍有待探索。富含亮氨酸的α-2-糖蛋白1(LRG1)已被证明与多种癌症类型的发病机制有关,然而其在ESCC中的作用尚不清楚。

分析公共数据库中的数据以研究LRG1在ESCC中的表达。通过过表达或添加重组LRG1在选定的ESCC细胞系中进行功能获得性研究,而通过小干扰RNA介导的敲低来实现功能丧失性研究。进行伤口愈合和transwell实验以研究在调控LRG1水平后ESCC细胞的迁移和侵袭情况。使用蛋白质免疫印迹法和免疫荧光染色来检测上皮-间质转化(EMT)和TGFβ信号通路的变化。

研究发现,ESCC患者以及几种ESCC细胞系中LRG1 mRNA水平显著下调。沉默LRG1可促进ESCC细胞迁移和侵袭,而LRG1过表达则抑制其迁移和侵袭。与此一致的是,沉默LRG1增强了ESCC细胞的TGFβ信号传导和EMT,而LRG1过表达则降低了这些过程。

LRG1通过对TGFβ信号传导和EMT的负调控抑制ESCC细胞迁移和侵袭。ESCC患者中LRG1的下调可能有利于肿瘤转移和疾病进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c44/6995366/faffaaa06d04/jcav11p1486g001.jpg

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