Expression of transcription factor Sp1 in hepatocellular carcinoma

ObjectiveTo determine whether the transcription factor Sp1 is differentially expressed in human hepatocellular carcinoma (HCC) and to investigate the potential pro-apoptotic effect of transforming growth factor beta 1 (TGFβ1) through Sp1 by using the HCC cell line HepG2. MethodsThe Sp1 expression pa...

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Main Author: FENG Jie
Format: Article
Language:zho
Published: Editorial Department of Journal of Clinical Hepatology 2013-01-01
Series:Linchuang Gandanbing Zazhi
Subjects:
Online Access:http://www.lcgdbzz.org/qk_content.asp?id=5224&ClassID=1214134654
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spelling doaj-2600163745ec4c2db7c538d6380e18982020-11-24T23:46:48ZzhoEditorial Department of Journal of Clinical HepatologyLinchuang Gandanbing Zazhi1001-52561001-52562013-01-012916567Expression of transcription factor Sp1 in hepatocellular carcinomaFENG Jie0The Fifth People′s Hospital of Shanghai, Fudan University, Shanghai 200240, ChinaObjectiveTo determine whether the transcription factor Sp1 is differentially expressed in human hepatocellular carcinoma (HCC) and to investigate the potential pro-apoptotic effect of transforming growth factor beta 1 (TGFβ1) through Sp1 by using the HCC cell line HepG2. MethodsThe Sp1 expression patterns were detected by immunohistochemistry in tumors from 51 cases of HCC and 10 specimens of normal liver tissues. HepG2 cells in culture were stimulated by TGFβ1 and the change in Sp1 mRNA expression was detected by RT-PCR while the change in cell apoptosis rate was detected by flow cytometry. Statistical significance of changes were assessed by one-way ANOVA. ResultsThe positive rate of Sp1 expression was significantly higher in HCC tissue than in normal liver tissues (P<001). The level of Sp1 mRNA was significantly lower in HepG2 cells stimulated with TGFβ1 than in the control cells (P<0.01), and the effect was TGFβ1 dose-dependent. The apoptosis rate of HepG2 cells increased in correspondence with increases in TGFβ1 concentration. ConclusionOverexpression of Sp1 may functionally contribute to HCC occurrence and development. TGFβ1 can induce apoptosis of HepG2 HCC cells in vitro, and this apoptotic effect may involve Sp1.http://www.lcgdbzz.org/qk_content.asp?id=5224&ClassID=1214134654transforming growth factor beta 1; Sp1 transcription factor; carcinoma
collection DOAJ
language zho
format Article
sources DOAJ
author FENG Jie
spellingShingle FENG Jie
Expression of transcription factor Sp1 in hepatocellular carcinoma
Linchuang Gandanbing Zazhi
transforming growth factor beta 1; Sp1 transcription factor; carcinoma
author_facet FENG Jie
author_sort FENG Jie
title Expression of transcription factor Sp1 in hepatocellular carcinoma
title_short Expression of transcription factor Sp1 in hepatocellular carcinoma
title_full Expression of transcription factor Sp1 in hepatocellular carcinoma
title_fullStr Expression of transcription factor Sp1 in hepatocellular carcinoma
title_full_unstemmed Expression of transcription factor Sp1 in hepatocellular carcinoma
title_sort expression of transcription factor sp1 in hepatocellular carcinoma
publisher Editorial Department of Journal of Clinical Hepatology
series Linchuang Gandanbing Zazhi
issn 1001-5256
1001-5256
publishDate 2013-01-01
description ObjectiveTo determine whether the transcription factor Sp1 is differentially expressed in human hepatocellular carcinoma (HCC) and to investigate the potential pro-apoptotic effect of transforming growth factor beta 1 (TGFβ1) through Sp1 by using the HCC cell line HepG2. MethodsThe Sp1 expression patterns were detected by immunohistochemistry in tumors from 51 cases of HCC and 10 specimens of normal liver tissues. HepG2 cells in culture were stimulated by TGFβ1 and the change in Sp1 mRNA expression was detected by RT-PCR while the change in cell apoptosis rate was detected by flow cytometry. Statistical significance of changes were assessed by one-way ANOVA. ResultsThe positive rate of Sp1 expression was significantly higher in HCC tissue than in normal liver tissues (P<001). The level of Sp1 mRNA was significantly lower in HepG2 cells stimulated with TGFβ1 than in the control cells (P<0.01), and the effect was TGFβ1 dose-dependent. The apoptosis rate of HepG2 cells increased in correspondence with increases in TGFβ1 concentration. ConclusionOverexpression of Sp1 may functionally contribute to HCC occurrence and development. TGFβ1 can induce apoptosis of HepG2 HCC cells in vitro, and this apoptotic effect may involve Sp1.
topic transforming growth factor beta 1; Sp1 transcription factor; carcinoma
url http://www.lcgdbzz.org/qk_content.asp?id=5224&ClassID=1214134654
work_keys_str_mv AT fengjie expressionoftranscriptionfactorsp1inhepatocellularcarcinoma
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