Literature DB >> 8537397

CCAAT/enhancer-binding proteins alpha and beta interact with the silencer element in the promoter of glutathione S-transferase P gene during hepatocarcinogenesis.

S Osada1, K Takano, T Nishihara, T Suzuki, M Muramatsu, M Imagawa.   

Abstract

We have previously identified a silencer in the glutathione S-transferase P (GST-P) gene which is strongly and specifically expressed during chemical hepatocarcinogenesis. At least three trans-acting factors bind to multiple cis-elements in the silencer. One of them, Silencer Factor-B (SF-B), is identical with CCAAT/enhancer-binding protein beta (C/EBP beta) and binds to GST-P Silencer 1 (GPS1). Many C/EBP beta binding sites are recognized by each of the C/EBP isoforms. Western blot analyses of C/EBP isoforms during chemical hepatocarcinogenesis revealed a decrease of C/EBP alpha expression. However, there was no change in C/EBP beta level. In the nuclear extracts from normal liver, C/EBP alpha was the dominant form that bound to GPS1, whereas both C/EBP alpha and C/EBP beta bound to GPS1 in the nuclear extracts from carcinogenic liver. Furthermore, transfection assays showed that C/EBP alpha not only repressed the GST-P promoter activity but also attenuated the transcriptional stimulation by C/EBP beta. These observations strongly suggest that the ratio of C/EBP alpha to C/EBP beta is one of the important factors for the GST-P silencer activity, and the decrease of this ratio during hepatocarcinogenesis reduces the silencer activity and, consequently, increases the GST-P expression.

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Year:  1995        PMID: 8537397     DOI: 10.1074/jbc.270.52.31288

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  6 in total

1.  Expression, DNA-binding specificity and transcriptional regulation of nuclear factor 1 family proteins from rat.

Authors:  S Osada; T Matsubara; S Daimon; Y Terazu; M Xu; T Nishihara; M Imagawa
Journal:  Biochem J       Date:  1999-08-15       Impact factor: 3.857

2.  Intestinal maturation in mice lacking CCAAT/enhancer-binding protein alpha (C/EPBalpha).

Authors:  T J Oesterreicher; L L Leeper; M J Finegold; G J Darlington; S J Henning
Journal:  Biochem J       Date:  1998-03-15       Impact factor: 3.857

3.  Chronic administration of 2-acetylaminofluorene alters the cellular iron metabolism in rat liver.

Authors:  Svitlana I Shpyleva; Levan Muskhelishvili; Volodymyr P Tryndyak; Igor Koturbash; Erik J Tokar; Michael P Waalkes; Frederick A Beland; Igor P Pogribny
Journal:  Toxicol Sci       Date:  2011-07-23       Impact factor: 4.849

4.  Histone acetyltransferase MOZ acts as a co-activator of Nrf2-MafK and induces tumour marker gene expression during hepatocarcinogenesis.

Authors:  Kumiko Ohta; Megumi Ohigashi; Ayako Naganawa; Hiromi Ikeda; Masaharu Sakai; Jun-ichi Nishikawa; Masayoshi Imagawa; Shigehiro Osada; Tsutomu Nishihara
Journal:  Biochem J       Date:  2007-03-15       Impact factor: 3.857

5.  Regulation of the rat glutathione S-transferase A2 gene by glucocorticoids: crosstalk through C/EBPs.

Authors:  K Cameron Falkner; Russell A Prough
Journal:  Drug Metab Rev       Date:  2007       Impact factor: 4.518

Review 6.  Mechanisms of a tumor marker, glutathione transferase P, expression during hepatocarcinogenesis of the rat.

Authors:  Masami Muramatsu; Masaharu Sakai
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2006-02-12       Impact factor: 3.493

  6 in total

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