Wang Fenglin, Dai Min, Chen Hongjie, Li Yue, Zhang Jiongshan, Zou Zengcheng, Yang Hongzhi
Department of Traditional Chinese Medicine, The Third Affiliated Hospital of Sun Yet-sen University, Guangzhou, Guangdong 510000, P.R. China.
Oncol Lett. 2018 Jul;16(1):815-820. doi: 10.3892/ol.2018.8710. Epub 2018 May 16.
This study aimed to investigate the expression of microRNA (miRNA) 299 and miRNA-7706 in patients with hepatocellular carcinoma (HCC), and to explore their effects on proliferation of SK-HEP-1 HCC cells. Expression of miRNA-299 and miRNA-7706 in tumor tissue (HCC group) and adjacent healthy tissue (>30 mm away from the tumor tissue) of 179 patients with HCC was determined by real-time polymerase chain reaction (qRT-PCR). miR-299 mimics and miR-7706 mimics were transfected into SK-HEP-1 HCC cells by RNA transfection. The proliferation and invasion of SK-HEP-1 cells were detected by CCK-8 kit and Transwell kit, respectively. Compared with adjacent tissues, expression levels of miRNA-299 and miRNA-7706 in HCC group were significantly downregulated. Analyses on the correlation between the expression of miRNA-299 and miRNA-7706 and clinical factors showed that expression levels of miRNA-299 and miRNA-7706 were significantly correlated with pathological stages and lymph node metastasis. ROC curve analysis showed that the areas under the curve were 0.837 and 0.845 for miRNA-299 and miRNA-7706 in the prediction of HCC, respectively. Survival analysis showed that the 5-year overall survival rate of patients with high expression levels of miRNA-299 and miRNA-7706 was significantly different from that of patients with low expression levels (P=0.016). Compared with cells transfected with scramble mimics, proliferation and invasion abilities of SK-HEP-1 cells transfected with miR-299 mimics and miRNA-7706 were significantly weakened. Results suggested that downregulation of miRNA-299 and miRNA-7706 can inhibit the proliferation of HCC cells and can be used as a new target for the treatment of HCC.
本研究旨在调查肝细胞癌(HCC)患者中微小RNA(miRNA)-299和miRNA-7706的表达情况,并探讨它们对SK-HEP-1肝癌细胞增殖的影响。通过实时聚合酶链反应(qRT-PCR)测定179例HCC患者肿瘤组织(HCC组)和邻近健康组织(距肿瘤组织>30 mm)中miRNA-299和miRNA-7706的表达。通过RNA转染将miR-299模拟物和miR-7706模拟物转染到SK-HEP-1肝癌细胞中。分别使用CCK-8试剂盒和Transwell试剂盒检测SK-HEP-1细胞的增殖和侵袭能力。与邻近组织相比,HCC组中miRNA-299和miRNA-7706的表达水平显著下调。对miRNA-299和miRNA-7706表达与临床因素之间的相关性分析表明,miRNA-299和miRNA-7706的表达水平与病理分期和淋巴结转移显著相关。ROC曲线分析表明,miRNA-299和miRNA-7706在预测HCC中的曲线下面积分别为0.837和0.845。生存分析表明,miRNA-299和miRNA-7706高表达水平患者的5年总生存率与低表达水平患者的5年总生存率有显著差异(P=0.016)。与转染了乱序模拟物的细胞相比,转染了miR-299模拟物和miRNA-7706的SK-HEP-1细胞的增殖和侵袭能力显著减弱。结果表明,miRNA-299和miRNA-7706的下调可抑制肝癌细胞的增殖,并可作为肝癌治疗的新靶点。