Article Summary
邱新毓 杨建栋 张毅 李燕 李成花 张兰慧 刘新平 郑瑾.NDRG2 通过调控CD24 影响肝癌细胞侵袭能力的研究[J].现代生物医学进展英文版,2014,14(9):1637-1640.
NDRG2 通过调控CD24 影响肝癌细胞侵袭能力的研究
NDRG2 Expression Regulates CD24 and Invasion ability of Hepatocellularcarcinoma Cells
  
DOI:
中文关键词: NDRG2  CD24  肝癌细胞  侵袭
英文关键词: NDRG2  CD24  Hepatocellular carcinoma cell  Adhesion
基金项目:国家自然科学基金项目(81072973)
Author NameAffiliation
QIU Xin-yu, YANG Jian-dong, ZHANG Yi, LI Cheng-hua, ZHANG Lan-hui, LIU Xin-ping, ZHENG Jin 第四军医大学2009级口腔医学系2 队
65547部队医院
第四军医大学唐都医院中医科暨中西医结合肿瘤科
第四军医大学生物化学与分子生物学教研室
解放军总医院中医院 
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中文摘要:
      目的:阐明NDRG2(N-Myc downstream-regulated gene 2)在肝癌细胞中对CD24 的调控及其对乳腺癌细胞侵袭能力的影响。 方法:Western blot 检测低转移性的肝癌细胞Huh7、高转移性的肝癌细胞系MHCC97h 及正常人肝细胞系L-02 中NDRG2 和 CD24 的表达;通过腺病毒载体上调MHCC97h 细胞中NDRG2 的水平,或利用siRNA 下调Huh7 细胞中NDRG2 的表达,检测 CD24 的变化以及细胞侵袭能力的改变。结果:MHCC97h 细胞中NDRG2 基因和蛋白的表达水平低于Huh7 细胞,而CD24 的表达 水平高于Huh7 细胞;在MHCC97h 细胞中上调NDRG2 可以抑制CD24 的表达并抑制其侵袭能力,而在Huh7 细胞中下调 NDRG2 的表达可以提高CD24 的水平及细胞的侵袭能力。结论:NDRG2 可能通过影响CD24 参与调控肝癌细胞的侵袭能力。
英文摘要:
      Objective:To explore the regulative role of N-Myc downstream-regulated gene2 (NDRG2) on CD24 expression and the invasion ability of hepatocellular carcinoma cells.Methods:The mRNA and protein expressions of CD24 and NDRG2 in MHCC97H, Huh7 and L-02 cells were analyzed. Changes in cell invasion were detected when NDRG2 was up- or down-regulated by adenovirus or siRNA. The expression pattern of NDRG2 and CD24 in HCC cells and the relationship between NDRG2 and invision features were analyzed.Results:NDRG2 expression was negatively correlated with malignancy in HCC. CD24 protein decreased when the hepatocellular cacinoma cell MHCC97H was infected by Ad-NDRG2. CD24 protein increased when the hepatocellular cacinoma cell Huh7 was transfected by siRNA-NDRG2. The up-regulation of NDRG2 decreased CD24 expression and cell invasion. By contrast, the down-regulation of NDRG2 enhanced CD24 expression and invasion.Conclusion:The results suggest that NDRG2 exerted anti-tumor activity by regulating CD24, which mediates that cell-cell interaction, tumor proliferation and adhesion.
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