基于DNA载体的RNA干扰稳定抑制肝癌细胞BEL-7402中hLRH-1基因表达谱的芯片分析

WANG Shui-Liang , LAN Feng-Hua , ZHUANG Yue-Peng , LI Hui-Zhong , HUANG Liang-Hu , ZHENG De-Zhu , ZENG Jian , DONG Li-Hong , ZHU Zhong-Yong , FU Ji-Liang
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引用次数: 4

摘要

为了建立永久抑制hLRH-1的细胞系,本研究构建了一个稳定的靶向hLRH-1的RNAi载体(psiineohlrh -1),并将其导入肝癌细胞BEL-7402。通过半定量RT-PCR分析,发现携带pineohlrh -1的BEL-7402细胞中hLRH-1的表达被显著抑制高达60%。此外,通过芯片分析,我们评估了稳定敲低hLRH-1的BEL-7402细胞中基因表达改变的程度。直接比较18000多个基因的表达谱发现,在hLRH-1敲低细胞中,有405个表达基因的表达水平与对照组有显著差异,这表明hLRH-1具有更广泛的生物学功能。有趣的是,在这些差异表达的基因中,有一些是与癌症相关的基因,如Gadd45β和PTEN,它们的表达得到了进一步的验证。尽管这些基因与hLRH-1之间的确切关系有待深入研究,但本研究的发现为hLRH-1参与肿瘤发生的机制提供了新的见解。
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Microarray Analysis of Gene-Expression Profile in Hepatocellular Carcinoma Cell, BEL-7402, with Stable Suppression of hLRH-1 via a DNA Vector-based RNA Interference

To establish a cell line with a permanent suppression of hLRH-1 in this study, a stable RNAi vector (pSineohLRH-1) targeting hLRH-1 was constructed and introduced into hepatocellular carcinoma cell, BEL-7402. By semiquantitative RT-PCR analysis, the expression of hLRH-1 in BEL-7402 cells carrying pSineohLRH-1 was shown to be significantly suppressed by up to ∼60%. In addition, microarray analysis was carried out to assess the extent of altered gene expression in BEL-7402 cells with stable knockdown of hLRH-1. Direct comparison of gene-expression profiles of more than 18 000 genes showed that 405 of the expressed genes in hLRH-1-knockdown cells differed dramatically in expression levels from those in controls, which suggested the even extensive biological functions of hLRH-1. Interestingly, among those differentially expressed genes, some are cancer-associated such as Gadd45β and PTEN, and their expressions were further validated. Although the identification of the exact relationship between these genes and hLRH-1 awaits intensive investigation, the findings of this study provide new insights into the mechanism by which hLRH-1 is involved in tumorigenesis.

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