Mo Wenhui, Dai Ying, Chen Jianqing, Liang Liwei, Xu Shuqi, Xu Xuanfu
Department of Gastroenterology, Shidong Hospital of Shanghai, Shanghai 200433, People's Republic of China.
Cancer Manag Res. 2020 Sep 2;12:7949-7960. doi: 10.2147/CMAR.S253496. eCollection 2020.
The purpose of this study was to evaluate the effects and mechanisms of the long noncoding RNA (lncRNA) MT1JP on hepatocellular carcinoma (HCC) in vitro.
Thirty pairs of tumor and adjacent normal tissues were collected from HCC patients. Tissue pathology and MT1JP expression were evaluated by hematoxylin and eosin staining and in situ hybridization (ISH), respectively. The correlation between MT1JP and HCC prognosis was investigated. MTT assays, cloning, flow cytometry, transwell assays, and wound-healing assays were used to evaluate the effects of MT1JP on HCC cell lines. RT-qPCR and Western blot were used to measure the relative mRNA and protein expression levels.
The expression of MT1JP was downregulated in HCC tumor tissues compared with that in adjacent normal tissues, while the percent survival was significantly greater in the high MT1JP expression group than in the low MT1JP expression group (=0.0238). In vitro, overexpression of MT1JP suppressed the proliferation, invasion, and migration, reduced colony cell number, increased cell apoptosis, and induced G1-phase cell cycle arrest in Bel-7402 and Huh-7 cells. Meanwhile, the mRNA and protein expression levels of RUNX3 and P21 were significantly upregulated, whereas those of MMP2 and MMP9 were significantly downregulated, in Bel-7402 and Huh-7 cells overexpressing MT1JP (all <0.001).
LncRNA MT1JP may function as a tumor suppressor in HCC. Overexpression of MT1JP suppressed HCC cell biological activities through the regulation of RUNX3.
本研究旨在评估长链非编码RNA(lncRNA)MT1JP在体外对肝细胞癌(HCC)的影响及机制。
收集30对HCC患者的肿瘤组织及癌旁正常组织。分别采用苏木精-伊红染色和原位杂交(ISH)评估组织病理学及MT1JP表达。研究MT1JP与HCC预后的相关性。采用MTT法、克隆实验、流式细胞术、Transwell实验和伤口愈合实验评估MT1JP对HCC细胞系的影响。采用RT-qPCR和蛋白质免疫印迹法检测相对mRNA和蛋白质表达水平。
与癌旁正常组织相比,MT1JP在HCC肿瘤组织中的表达下调,而MT1JP高表达组的生存率显著高于低表达组(=0.0238)。在体外,MT1JP过表达抑制了Bel-7402和Huh-7细胞的增殖、侵袭和迁移,减少了集落细胞数量,增加了细胞凋亡,并诱导G1期细胞周期阻滞。同时,在过表达MT1JP的Bel-7402和Huh-7细胞中,RUNX3和P21的mRNA和蛋白质表达水平显著上调,而MMP2和MMP9的表达水平显著下调(均<0.001)。
LncRNA MT1JP可能在HCC中发挥肿瘤抑制作用。MT1JP过表达通过调节RUNX3抑制HCC细胞的生物学活性。