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纤维连接蛋白-3抑制Wnt/β-连环蛋白信号通路及肺癌侵袭。

Fibulin-3 suppresses Wnt/β-catenin signaling and lung cancer invasion.

作者信息

Chen Xiaojun, Meng Jie, Yue Wen, Yu Jian, Yang Jie, Yao Zhi, Zhang Lin

机构信息

Department of Immunology, Tianjin Key Laboratory of Cellular and Molecular Immunology, Key Laboratory of Immuno Microenvironment and Disease of the Educational Ministry, Tianjin Medical University, Tianjin 300070, China and Departments of Pharmacology and Chemical Biology and Pathology, University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.

Department of Immunology, Tianjin Key Laboratory of Cellular and Molecular Immunology, Key Laboratory of Immuno Microenvironment and Disease of the Educational Ministry, Tianjin Medical University, Tianjin 300070, China and.

出版信息

Carcinogenesis. 2014 Aug;35(8):1707-16. doi: 10.1093/carcin/bgu023. Epub 2014 Jan 30.

Abstract

The 5 year survival rate of lung cancer is <20%, with most patients dying from distant metastasis. However, the molecular mechanisms underlying lung cancer invasion and metastasis have not been fully characterized. In this study, we found that fibulin-3, a fibulin family extracellular matrix protein, functions as a suppressor of lung cancer invasion and metastasis. Fibulin-3 was downregulated in large fractions of lung tumors and cell lines, and inhibited lung cancer cell invasion and the expression of matrix metalloproteinase-7 (MMP-7), a promoter of lung cancer invasion. The expression levels of fibulin-3 and MMP-7 were inversely correlated in lung tumors. Fibulin-3 inhibited extracellular signal-regulated kinase (ERK) to activate glycogen synthase kinase 3β and suppress Wnt/β-catenin signaling, which induces MMP-7 expression in lung cancer cells. Furthermore, fibulin-3 expression impeded the growth and metastasis of lung tumors in mice. Collectively, these results suggest that downregulation of fibulin-3 contributes to lung cancer invasion and metastasis by activating Wnt/β-catenin signaling and MMP-7 expression.

摘要

肺癌的5年生存率低于20%,大多数患者死于远处转移。然而,肺癌侵袭和转移的分子机制尚未完全明确。在本研究中,我们发现纤连蛋白-3(一种纤连蛋白家族的细胞外基质蛋白)发挥着肺癌侵袭和转移抑制因子的作用。在大部分肺癌肿瘤和细胞系中,纤连蛋白-3表达下调,它可抑制肺癌细胞侵袭以及基质金属蛋白酶-7(MMP-7,一种肺癌侵袭促进因子)的表达。在肺癌肿瘤中,纤连蛋白-3和MMP-7的表达水平呈负相关。纤连蛋白-3抑制细胞外信号调节激酶(ERK),从而激活糖原合酶激酶3β并抑制Wnt/β-连环蛋白信号传导,而该信号传导可诱导肺癌细胞中MMP-7的表达。此外,纤连蛋白-3的表达可阻碍小鼠肺癌肿瘤的生长和转移。总体而言,这些结果表明纤连蛋白-3的下调通过激活Wnt/β-连环蛋白信号传导和MMP-7表达促进肺癌的侵袭和转移。

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