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。
Objective: To explore the regulative role of N-Myc downstream-regulated gene 2 (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. Remits: 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.
出处
《现代生物医学进展》
CAS
2014年第9期1637-1640,共4页
Progress in Modern Biomedicine
基金
国家自然科学基金项目(81072973)