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首页|期刊导航|中国癌症防治杂志|慢病毒介导过表达组织蛋白酶S基因对肝癌MHCC97H细胞增殖和迁移的作用

慢病毒介导过表达组织蛋白酶S基因对肝癌MHCC97H细胞增殖和迁移的作用

张智 朱广志 彭涛 赵国良 徐静

中国癌症防治杂志Issue(4):244-249,250,7.
中国癌症防治杂志Issue(4):244-249,250,7.DOI:10.3969/j.issn.1674-5671.2015.04.02

慢病毒介导过表达组织蛋白酶S基因对肝癌MHCC97H细胞增殖和迁移的作用

Effects of lentivirus-mediated overexpression of Cat S gene on proliferation and migration of hepatocellular carcinoma cell MHCC97H

张智 1朱广志 1彭涛 1赵国良 1徐静1

作者信息

  • 1. 530021 南宁 广西医科大学第一附属医院肝胆外科
  • 折叠

摘要

Abstract

Objective To construct a lentivirus expression vector to drive stable Cat S overexpression in the hepatocellular carcinoma (HCC)cell line MHCC97H,and to investigate the effects of overexpression on cell proliferation and migration. Methods The Cat S gene was inserted into the lentiviral expression vector pLVX-EGFP-3FLAG-Puro using Age I and EcoR I restriction enzymes and transfected into 293T cells to generate recombinant lentivirus. This virus was used to infect MHCC97H cells,and positive cells were selected using puromycin. Real-time quantitative PCR,Western blots,MTT assay,the transwell migration assay and the wound healing migration assay were used to assess the effects of Cat S overexpression on proliferation and migration of MHCC97H cells. Results A lentiviral vector containing the Cat S gene was constructed,and an MHCC97H cell line stably overexpressing Cat S was established. Cat S overexpression was associated with significantly shorter cell doubling time,as well as significantly greater invasion and migration abilities. Conclusions Lentivirus-mediated Cat S overexpression can increase MHCC97H proliferationand migration,opening the door to future studies of molecular mechanisms of liver cancer invasion and metastasis.

关键词

肝肿瘤/组织蛋白酶S/过表达/慢病毒/增殖/迁移

Key words

Liver neoplasm/Cathepsin S/Overexpression/Lentivirus infections/Proliferation/Migration

分类

医药卫生

引用本文复制引用

张智,朱广志,彭涛,赵国良,徐静..慢病毒介导过表达组织蛋白酶S基因对肝癌MHCC97H细胞增殖和迁移的作用[J].中国癌症防治杂志,2015,(4):244-249,250,7.

基金项目

国家自然科学基金资助项目(81360372);广西自然科学基金资助项目(2011GXNSFA018284);广西卫生厅科研基金资助项目 ()

中国癌症防治杂志

1674-5671

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