Expression of lncRNA MSC-AS1 in hepatocellular carcinoma cell lines and its effect on proliferation, apoptosis, and migration.

Xiaoni Kou, Jiang Zhu, Xinke Xie, Mingxia Hao, Yingren Zhao
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引用次数: 4

Abstract

Background/aims: This study aimed to explore the expression of long non-coding RNA MSC-AS1 in hepatocellular carcinoma (HCC) cells and its effect on the proliferation, migration, and apoptosis of HCC cells.

Materials and methods: The expression of MSC-AS1 in HCC cell lines BEL7402, SMMC7721, Huh7, HepG2, MHCC97-H, and normal hepatocyte line L02 was detected by reverse transcriptase polymerase chain reaction. The HCC cells were divided into blank, negative control (NC)-small interfering RNA (siRNA) (transfected with negative siRNA), and MSC-AS1 siRNA (transfected with MSC-AS1 siRNA) groups. Cell counting kit-8 and colony formation assays were used to determine the proliferation, and cell apoptosis, migration, and invasion were detected by flow cytometry, wound healing, and transwell assays, respectively. Western blot was used to detect the expression of related proteins.

Results: The expression of MSC-AS1 in HCC cell lines was significantly higher than that in L02. In the MSC-AS1 siRNA group, the proliferation and colony formation of HCC cells were inhibited, whereas the apoptosis rate was significantly higher than that in the blank and NC-siRNA groups. The rate of wound healing and the number of invasion cells in the MSC-AS1 siRNA group were significantly lower than that in the blank and NC-siRNA groups.

Conclusion: MSC-AS1 was upregulated in HCC cells, and the downregulation of MSC-AS1 could inhibit cell proliferation, migration, and invasion and promote apoptosis of HCC cells.

lncRNA MSC-AS1在肝癌细胞系中的表达及其对增殖、凋亡和迁移的影响
背景/目的:本研究旨在探讨长链非编码RNA MSC-AS1在肝细胞癌(HCC)细胞中的表达及其对肝癌细胞增殖、迁移和凋亡的影响。材料与方法:采用逆转录聚合酶链反应法检测HCC细胞系BEL7402、SMMC7721、Huh7、HepG2、MHCC97-H和正常肝细胞系L02中MSC-AS1的表达。将HCC细胞分为空白、阴性对照(NC)-小干扰RNA (siRNA)组(转染阴性siRNA)和MSC-AS1 siRNA组(转染MSC-AS1 siRNA)。细胞计数试剂盒-8和集落形成法检测细胞增殖,流式细胞术检测细胞凋亡,伤口愈合和transwell检测细胞迁移和侵袭。Western blot检测相关蛋白的表达。结果:MSC-AS1在HCC细胞系中的表达明显高于L02。在MSC-AS1 siRNA组中,HCC细胞的增殖和集落形成受到抑制,而凋亡率明显高于空白组和NC-siRNA组。与空白组和NC-siRNA组相比,MSC-AS1 siRNA组创面愈合率和侵袭细胞数量显著降低。结论:HCC细胞中MSC-AS1表达上调,下调MSC-AS1可抑制细胞增殖、迁移、侵袭,促进HCC细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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