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
{"title":"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","authors":"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","doi":"10.1016/S0379-4172(06)60122-4","DOIUrl":null,"url":null,"abstract":"<div><p>To establish a cell line with a permanent suppression of hLRH-1 in this study, a stable RNAi vector (pSineo<em>hLRH-1</em>) targeting <em>hLRH-1</em> was constructed and introduced into hepatocellular carcinoma cell, BEL-7402. By semiquantitative RT-PCR analysis, the expression of <em>hLRH-1</em> in BEL-7402 cells carrying pSineo<em>hLRH-1</em> 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.</p></div>","PeriodicalId":100017,"journal":{"name":"Acta Genetica Sinica","volume":"33 10","pages":"Pages 881-891"},"PeriodicalIF":0.0000,"publicationDate":"2006-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60122-4","citationCount":"4","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1016/S0379-4172(06)60122-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>To establish a cell line with a permanent suppression of hLRH-1 in this study, a stable RNAi vector (pSineo<em>hLRH-1</em>) targeting <em>hLRH-1</em> was constructed and introduced into hepatocellular carcinoma cell, BEL-7402. By semiquantitative RT-PCR analysis, the expression of <em>hLRH-1</em> in BEL-7402 cells carrying pSineo<em>hLRH-1</em> 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.</p></div>\",\"PeriodicalId\":100017,\"journal\":{\"name\":\"Acta Genetica Sinica\",\"volume\":\"33 10\",\"pages\":\"Pages 881-891\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60122-4\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Genetica Sinica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0379417206601224\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Genetica Sinica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0379417206601224","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.