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lncRNA GIHCG通过调节miR-429在原发性肝癌发生发展中的作用
引用本文:陈恩利,楼俊晓,王镇,黄瑛,郝敬铎. lncRNA GIHCG通过调节miR-429在原发性肝癌发生发展中的作用[J]. 中华全科医学, 2019, 17(5): 779-783. DOI: 10.16766/j.cnki.issn.1674-4152.000790
作者姓名:陈恩利  楼俊晓  王镇  黄瑛  郝敬铎
作者单位:1. 宁波市第七医院(镇海区人民医院)院感科, 浙江 宁波 315202;
基金项目:浙江省医药卫生一般研究计划项目(2019KY626)
摘    要:目的 探讨lncRNA GIHCG通过调节miR-429在原发性肝癌发生发展中的作用。 方法 选择宁波市第七医院2017年1—12月60例原发性肝癌手术患者的肝癌组织及相应的癌旁组织。将HepG2细胞根据随机数字法分为空白对照组、阴性对照组和lncRNA GIHCG-siRNA组。采用RT-PCR测定肝癌组织和细胞中lncRNA GIHCG mRNA和miR-429水平,采用WST-1测定细胞增殖,采用Transwell法测定细胞侵袭和迁移能力。 结果 肝癌组织中lncRNA GIHCG mRNA水平高于癌旁组织(P<0.05),miR-429水平低于癌旁组织(P<0.05)。肝癌细胞中lncRNA GIHCG mRNA水平高于正常肝细胞(P<0.05),miR-429水平低于正常肝细胞(P<0.05)。肝癌组织及肝癌细胞中lncRNA GIHCG mRNA和miR-429呈负相关(P<0.05)。第3天和第5天,GIHCG-siRNA组细胞OD值低于空白对照组和阴性对照组(均P<0.05)。与空白对照组和阴性对照组比较,lncRNA GIHCG-siRNA组HepG2细胞中lncRNA GIHCG mRNA水平、细胞侵袭和迁移能力降低(均P<0.05),miR-429水平升高(均P<0.05)。 结论 原发性肝癌组织中lncRNA GIHCG水平升高,lncRNA GIHCG可能通过调节miR-429促进肝癌细胞增殖和侵袭迁移。 

关 键 词:lncRNA GIHCG   miR-429   肝癌   增殖   侵袭   迁移
收稿时间:2018-10-12

Role of lncRNA GIHCG in the development of primary liver cancer by regulating miR-429
Affiliation:Department of Nosocomial Infection Disease, the Seventh Hospital of Ningbo (Zhenhai People's Hospital), Ningbo, Zhejiang 315202, China
Abstract:Objective To investigate the role of lncRNA GIHCG in the development of primary liver cancer by regulating miR-429. Methods The hepatocellular carcinoma and adjacent tissues of 60 cases of liver cancer in our hospital were prepared from January 2017 to December 2017. HepG2 cells were randomly divided into the blank control group, negative control group and lncRNA GIHCG-siRNA group with random number method. The levels of lncRNA GIHCG mRNA and miR-429 in the tissues and cells were determined by RT-PCR. The proliferations of cells were determined by WST-1. The invasion and migration ability of cells were determined by Transwell method. Results In the hepatocarcinoma tissues, the level of lncRNA GIHCG mRNA was higher than that in the adjacent tissues (P<0.05), however, the level of miR-429 was lower than that in the adjacent tissues (P<0.05). The level of lncRNA GIHCG mRNA of the liver cancer cells were higher than that of the normal hepatocytes (P<0.05), however, the level of miR-429 of the liver cancer cells were lower than that of the normal hepatocytes (P<0.05). There were negative correlation between lncRNA GIHCG mRNA and miR-429 in the liver cancer tissues and liver cancer cells (P<0.05). On D3 and D5, the OD value of cells in the GIHCG-siRNA group were lower than those in the blank control group and the negative control group (all P<0.05). When compared with the blank control group and the negative control group, the lncRNA GIHCG mRNA level, cell invasion and migration ability of the lncRNA GIHCG-siRNA group were decreased (all P<0.05), the miR-429 level was increased (all P<0.05). Conclusion The level of lncRNA GIHCG is elevated in primary liver cancer tissues, and lncRNA GIHCG may promote hepatoma cell proliferation and invasion and migration through regulating the expression of miR-429. 
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