Hu Xiao, Feng Yujie, Sun Lin, Qu Linlin, Sun Chuandong
Department of Hepatopancreatobiliary Surgery, The Affiliated Hospital of Qingdao University, No. 16, Jiangsu Road, Qingdao, 266003, China.
Department of ICU, The Affiliated Hospital of Qingdao University, Qingdao, China.
Dig Dis Sci. 2017 Mar;62(3):715-722. doi: 10.1007/s10620-016-4429-2. Epub 2017 Jan 3.
Aberrant expression of microRNAs contributes to tumor growth and progression.
This study was designed to explore the prognostic and biological significance of miR-330 in hepatocellular carcinoma (HCC).
The expression of miR-330 and its associations with tumor parameters and overall survival were analyzed in HCC patients. The biological functions of miR-330 in HCC cell growth, invasion, and tumorigenesis were investigated. Bioinformatic analysis and luciferase reporter assays were performed to search for potential targets of miR-330.
The miR-330 level was significantly higher in HCCs than in adjacent normal tissues (P = 0.0085). High expression of miR-330 was significantly associated with more aggressive phenotypes and shorter overall survival in HCC. Loss- and gain-of-function studies indicated the favorable effect of miR-330 on tumor cell growth, invasion, and tumorigenesis. Inhibitor of growth 4 (ING4) was identified to be a direct target of miR-330. Overexpression of miR-330 reduced the expression of ING4 in HCC cells. Importantly, restoration of ING4 almost completely reversed the promotion of HCC cell proliferation and invasion by miR-330.
Altogether, this study demonstrates that upregulation of miR-330 is associated with poor prognosis and contributes to more aggressive phenotypes of HCC. The oncogenic role of miR-330 in HCC is linked to downregulation of ING4.
微小RNA的异常表达促进肿瘤生长和进展。
本研究旨在探讨miR-330在肝细胞癌(HCC)中的预后及生物学意义。
分析HCC患者中miR-330的表达及其与肿瘤参数和总生存期的关系。研究miR-330在HCC细胞生长、侵袭和肿瘤发生中的生物学功能。进行生物信息学分析和荧光素酶报告基因检测以寻找miR-330的潜在靶点。
HCC中miR-330水平显著高于癌旁正常组织(P = 0.0085)。miR-330的高表达与HCC更具侵袭性的表型及更短的总生存期显著相关。功能缺失和功能获得研究表明miR-330对肿瘤细胞生长、侵袭和肿瘤发生具有促进作用。生长抑制因子4(ING4)被确定为miR-330的直接靶点。miR-330的过表达降低了HCC细胞中ING4的表达。重要的是,ING4的恢复几乎完全逆转了miR-330对HCC细胞增殖和侵袭的促进作用。
总之,本研究表明miR-330的上调与预后不良相关,并促进HCC更具侵袭性的表型。miR-330在HCC中的致癌作用与ING4的下调有关。