Yin Wenjun, Nie Yuehua, Chen Lingying, Wang Quipping, Liu Shuangquan, He Xiusheng, Wang Wenjun
Department of Clinical Laboratory, The First Affiliated Hospital of Nanhua University, Hengyang, Hunan 421001, P.R. China.
Department of Radiation Oncology, The First Affiliated Hospital of Nanhua University, Hengyang, Hunan 421001, P.R. China.
Oncol Lett. 2018 Mar;15(3):2781-2788. doi: 10.3892/ol.2017.7690. Epub 2017 Dec 27.
Deregulation of microRNA (miR)-193b has been revealed to be associated with the proliferation of liver cells. However, the interaction between miR-193b and their targets inducing liver cancer remains largely unknown. The aim of the present study was to investigate the hypothesis that miR-193b affects the proliferation of liver cancer cells. In the present study, the overall survival of patients with liver cancer and low fold change of miR-193b was higher compared with that of patients with liver cancer patients and high fold change of miR-193b. The expression level of myeloid cell leukemia-1 (Mcl-1) in patients with liver cancer was lower compared with in the control group. The results of the present study demonstrated that downregulation of miR-193b suppressed the proliferation and induced apoptosis of liver cancer cells, and inhibited the Mcl-1 protein expression level in liver cancer cells. Upregulation of miR-193b increased cell proliferation and decreased apoptosis of liver cancer cells and promoted the expression level of Mcl-1 protein. The results of the present study demonstrated that the expression of miR-193b as a novel tumor suppressor serves an important role in the proliferation of liver cancer cells by mediating Mcl-1 expression.
微小RNA(miR)-193b的失调已被揭示与肝细胞增殖有关。然而,miR-193b与其诱导肝癌的靶标之间的相互作用在很大程度上仍不清楚。本研究的目的是探讨miR-193b影响肝癌细胞增殖这一假说。在本研究中,与miR-193b高倍数变化的肝癌患者相比,miR-193b低倍数变化的肝癌患者的总生存率更高。肝癌患者中髓样细胞白血病-1(Mcl-1)的表达水平低于对照组。本研究结果表明,miR-193b的下调抑制了肝癌细胞的增殖并诱导其凋亡,并抑制了肝癌细胞中Mcl-1蛋白的表达水平。miR-193b的上调增加了肝癌细胞的增殖并减少了其凋亡,并促进了Mcl-1蛋白的表达水平。本研究结果表明,作为一种新型肿瘤抑制因子,miR-193b的表达通过介导Mcl-1的表达在肝癌细胞增殖中起重要作用。