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Effect of PAK1 gene silencing on proliferation and apoptosis in hepatocellular carcinoma cell lines MHCC97-H and HepG2 and cells in xenograft tumor

机译:PAK1基因沉默对肝细胞癌细胞系MHCC97-H和HepG2中肝细胞增殖和细胞凋亡的影响及异种移植肿瘤的细胞

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摘要

This study intends to explore the effect of the PAK1 gene silencing on apoptosis and proliferation of hepatocellular carcinoma (HCC) MHCC97-H and HepG2 cells and cells in xenograft tumor. MHCC97-H and HepG2 cells and mice with xenograft tumor in vivo were randomly divided into control, empty vector and PAK1 shRNA groups. Morphology and the expression of green fluorescent protein of MHCC97-H and HepG2 cells and cells in xenograft tumor were observed. MTT assay and flow cytometry were used to detect proliferation, cell cycle and apoptosis of MHCC97-H and HepG2 cells and cells in xenograft tumor. The expressions of PAK1, PCNA, Ki67, Cyclin E, CDK2, p21, p53, Bax and Bcl-2 were measured using the quantitative reverse transcription polymerase chain reaction and western blotting. Compared with the control and empty vector groups, number of adherent cells of MHCC97-H and HepG2 cells and cells in xenograft tumor was reduced, and green fluorescent cells became round and reduced in the PAK1 shRNA group. Cell proliferation, the cells at S phase, the mRNA and protein expressions of PAK1, PCNA, Ki67, Cyclin E, CDK2 and Bcl-2 of MHCC97-H and HepG2 cells and cells in xenograft tumor were decreased, while the cells at G1 phase, apoptosis rate, the mRNA and protein expressions of p21, p53 and Bax of MHCC97-H and HepG2 cells and cells in xenograft tumor were increased in the PAK1 shRNA group. PAK1 gene silencing decreases proliferation of MHCC97-H cells, HepG2 cells and cells in xenograft tumor through the p53/p21 pathway.
机译:本研究旨在探讨PAK1基因沉默对肝细胞癌(HCC)MHCC97-H和HepG2细胞和异种移植瘤细胞的凋亡和增殖的影响。将MHCC97-H和HEPG2细胞和小鼠在体内随机分为对照,空载体和PAK1 shRNA组。观察了MHCC97-H和HEPG2细胞的绿色荧光蛋白的形态和表达和异种移植肿瘤中的细胞。 MTT测定和流式细胞仪用于检测MHCC97-H和HepG2细胞的增殖,细胞周期和卵泡2细胞和异种移植瘤细胞的凋亡。使用定量逆转录聚合酶链反应和Western印迹测量PAK1,PCNA,Ki67,Cyclin E,CDK2,P21,P53,Bax和Bcl-2的表达。与对照和空载体组相比,减少了MHCC97-H和HEPG2细胞的粘附细胞数量,降低了异种移植瘤中的细胞,绿色荧光细胞变圆并降低了PAK1 shRNA组。细胞增殖,S相的细胞,PAK1,PCNA,Ki67,Cyclin E,CDK2和Bcl-2的MHCC97-H和HepG2细胞和异种移植瘤中的细胞的细胞均降低,而G1相的细胞在PAK1 shRNA组中增加了凋亡率,p21,p53和肝移植肿瘤中的细胞和肝移植瘤中的细胞的细胞凋亡率,mRNA和蛋白表达。 PAK1基因沉默通过P53 / P21途径降低了异种移植肿瘤中MHCC97-H细胞,HEPG2细胞和细胞的增殖。

著录项

  • 来源
    《Gene therapy》 |2018年第4期|共13页
  • 作者单位

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

    Hebei Med Univ Dept Hepatobiliary Surg Hosp 4 Shijiazhuang 050011 Hebei Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
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