Li Renzeng, Wang Limin
Department of Othopedics, The First Affiliated Hospital of Zhengzhou University, No.1 Jianshe Road, Zhengzhou, 450000 Henan, PR China; Department of Orthopaedics, The No.3 People's Hospital of Anyang City, Anyang 455000, PR China.
Department of Othopedics, The First Affiliated Hospital of Zhengzhou University, No.1 Jianshe Road, Zhengzhou, 450000 Henan, PR China.
Biochem Biophys Res Commun. 2016 Jun 10;474(4):730-735. doi: 10.1016/j.bbrc.2016.05.018. Epub 2016 May 5.
Fibulin-4, an extracellular glycoprotein implicated in connective tissue development and elastic fiber formation, draws increasing focuses in cancer research. However, little is known about the underlying oncogenic roles of Fibulin-4 in human osteosarcoma (OS). In this study, by immunohistochemical analysis, upregulated expression of Fibulin-4 was found in the OS clinical specimens and cell lines compared to their normal counterparts. Fibulin-4 was positively correlated with the T stage of OS patients, and the proliferation index Ki67. Based on informatics analysis and functional verification, microRNA-137 was identified as a potential upstream regulator of Fibulin-4. Knockdown of Fibulin-4 or introduction of microRNA-137 inhibited cell proliferation and promoted cell apoptosis, and adverse effects were observed by overexpression of Fibulin-4. Furthermore, the tumor-suppressive functions of microRNA-137 were markedly abolished by restoration of Fibulin-4 expression in OS cells. Mechanistically, Fibulin-4 activated Wnt/β-Catenin pathway and promoted the expression of its downstream targets, including CCND2, c-Myc and VEGF. Taken together, Fibulin-4 plays critical neoplastic roles in tumor growth of human OS by activating Wnt/β-Catenin signaling and may represent a potential therapeutic target.
纤连蛋白-4是一种参与结缔组织发育和弹性纤维形成的细胞外糖蛋白,在癌症研究中越来越受到关注。然而,关于纤连蛋白-4在人类骨肉瘤(OS)中的潜在致癌作用知之甚少。在本研究中,通过免疫组化分析发现,与正常对照相比,OS临床标本和细胞系中纤连蛋白-4的表达上调。纤连蛋白-4与OS患者的T分期以及增殖指数Ki67呈正相关。基于信息学分析和功能验证,确定microRNA-137是纤连蛋白-4的潜在上游调节因子。敲低纤连蛋白-4或导入microRNA-137可抑制细胞增殖并促进细胞凋亡,而纤连蛋白-4的过表达则产生相反的效果。此外,在OS细胞中恢复纤连蛋白-4的表达可明显消除microRNA-137的肿瘤抑制功能。机制上,纤连蛋白-4激活Wnt/β-连环蛋白通路并促进其下游靶标的表达,包括CCND2、c-Myc和VEGF。综上所述,纤连蛋白-4通过激活Wnt/β-连环蛋白信号在人类OS肿瘤生长中发挥关键的肿瘤作用,可能是一个潜在的治疗靶点。