Zhang Fengjuan, Yang Chao, Xing Zhiyuan, Liu Pei, Zhang Bo, Ma Xiang, Huang Liuye, Zhuang Likun
Department of Infectious Diseases, The Affiliated Hospital of Qingdao University, Qingdao 266003, People's Republic of China.
Department of General Surgery, The Second Affiliated Hospital of Qingdao University, Qingdao 266003, People's Republic of China.
Onco Targets Ther. 2019 May 21;12:4013-4023. doi: 10.2147/OTT.S209439. eCollection 2019.
MiR-1323 was identified in 2006. Until now, the roles and mechanisms of miR-1323 in the progression of cancers including hepatocellular carcinoma (HCC) remain unknown. The aim of this study was to investigate the expressions, roles and mechanisms of miR-1323 in HCC development. QRT-PCR was used to evaluate the expressions of miR-1323, GAS5 and TP53INP1 in HCC tissues and cell lines. CCK-8 assay, transwell invasion assay and flow cytometry assay were conducted to evaluate the proliferation, invasion and apoptosis of HCC cells. Luciferase assay was used to identify microRNA-target interaction. Firstly, our results showed that miR-1323 promoted proliferation and invasion, and inhibited apoptosis of HCC cells. Secondly, we found that TP53INP1 was a direct target of miR-1323 and could reverse the effects of miR-1323 on proliferation, invasion and apoptosis of HCC cells. Thirdly, our results showed that long non-coding RNA (lncRNA) GAS5 and miR-1323 could interact with each other and affect biological processes of HCC cells. Furthermore, we identified the negative correlations between miR-1323 and TP53INP1, and between miR-1323 and GAS5 in tumor tissues of patients with HCC. Taken together, our study revealed the important roles of GAS5/miR-1323/TP53INP1 axis in HCC progression. This study also provided promising strategies for targeted therapy of patients with HCC.
miR - 1323于2006年被发现。迄今为止,miR - 1323在包括肝细胞癌(HCC)在内的癌症进展中的作用和机制仍不清楚。本研究的目的是探讨miR - 1323在HCC发生发展中的表达、作用及机制。采用定量逆转录聚合酶链反应(QRT - PCR)检测miR - 1323、生长停滞特异性转录本5(GAS5)和TP53诱导蛋白1(TP53INP1)在HCC组织和细胞系中的表达。采用细胞计数试剂盒 - 8(CCK - 8)检测、Transwell侵袭实验和流式细胞术检测评估HCC细胞的增殖、侵袭和凋亡。采用荧光素酶报告基因实验鉴定微小RNA - 靶标相互作用。首先,我们的结果表明miR - 1323促进HCC细胞的增殖和侵袭,并抑制其凋亡。其次,我们发现TP53INP1是miR - 1323的直接靶标,并且可以逆转miR - 1323对HCC细胞增殖、侵袭和凋亡的影响。第三,我们的结果表明长链非编码RNA(lncRNA)GAS5和miR - 1323可以相互作用并影响HCC细胞的生物学过程。此外,我们在HCC患者的肿瘤组织中鉴定出miR - 1323与TP53INP1之间以及miR - 1323与GAS5之间呈负相关。综上所述,我们的研究揭示了GAS5/miR - 1323/TP53INP1轴在HCC进展中的重要作用。本研究还为HCC患者的靶向治疗提供了有前景的策略。