Sun Chunhui, Yao Xun, Jiang Qingyu, Sun Xiuyong
Department of Hepatobiliary Surgery, The Third People's Hospital of Qingdao, Qingdao, Shandong 266041, P.R. China.
Oncol Lett. 2018 Sep;16(3):3063-3069. doi: 10.3892/ol.2018.8970. Epub 2018 Jun 15.
MicroRNAs (miRNAs) have been proven to have important effects on the proliferation and metastasis of multiple cancers, including hepatocellular carcinoma (HCC). In the present study, our aim was to explore the biological function of miR-106b in HCC cell proliferation and metastasis. qPCR analysis showed that miR-106b was expressed at higher levels, while disabled homolog 2 (DAB2) was expressed at lower levels in HCC tissues and cells. Moreover, the aberrant miR-106b expression in HCC affected the cell proliferative and migratory ability by MTT and Transwell assay. DAB2 was identified as a specific target of miR-106b in HCC by luciferase reporter assay and regression analysis showed a negative correlation between DAB2 and miR-106b expression. In addition, DAB2 may attenuate the miR-106b promotion effect on HCC cell proliferation and migration. In short, miR-106b may promote HCC cell proliferation and migration by targeting DAB2.
微小RNA(miRNA)已被证明对包括肝细胞癌(HCC)在内的多种癌症的增殖和转移具有重要影响。在本研究中,我们的目的是探讨miR-106b在肝癌细胞增殖和转移中的生物学功能。qPCR分析表明,miR-106b在肝癌组织和细胞中表达水平较高,而失活同源物2(DAB2)表达水平较低。此外,通过MTT和Transwell实验,肝癌中异常的miR-106b表达影响了细胞的增殖和迁移能力。通过荧光素酶报告基因实验确定DAB2是肝癌中miR-106b的特异性靶标,回归分析显示DAB2与miR-106b表达呈负相关。此外,DAB2可能减弱miR-106b对肝癌细胞增殖和迁移的促进作用。简而言之,miR-106b可能通过靶向DAB2促进肝癌细胞的增殖和迁移。