Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1991 Jul;82(7):807-14.
doi: 10.1111/j.1349-7006.1991.tb02706.x.

Induction of glutathione S-transferase P-form in primary cultured rat hepatocytes by epidermal growth factor and insulin

Affiliations
Comparative Study

Induction of glutathione S-transferase P-form in primary cultured rat hepatocytes by epidermal growth factor and insulin

I Hatayama et al. Jpn J Cancer Res. 1991 Jul.

Abstract

The effects of epidermal growth factor (EGF) (10 ng/ml) and insulin (100 nM) on the expression of glutathione S-transferases (GSTs), especially the GST-P form (GST 7-7), were examined in primary cultured rat hepatocytes in serum-free medium. On culture with EGF and insulin, the GST activities towards 1-chloro-2,4-dinitrobenzene and 1,2-dichloro-4-nitrobenzene were transiently decreased on day 2 to 10% of those of freshly isolated hepatocytes and then increased to 60 to 100% of those of freshly isolated cells on day 4. Western blot analysis of GSTs revealed that GST-P, which is not present in freshly isolated hepatocytes, was markedly induced and that GST subunits 3 and 4 of the Mu class also increased after addition of EGF and/or insulin, while the subunits 1 and 2 of the Alpha class disappeared. Northern blot analysis showed that on addition of EGF and insulin the level of GST-P mRNA was also elevated and expressions of the nuclear oncogenes c-jun and c-fos were enhanced. These results suggest that the enhanced expression of GST-P induced by EGF or insulin in primary cultured rat hepatocytes might be regulated by JUN and FOS proteins.

PubMed Disclaimer

Similar articles

Cited by

References

    1. ) Mannervik , B. and Danielson , U. H.Glutathione transferases– structure and catalytic activity , CRC Crit, Rev. Biochem. Mol. Biol. , 23 , 283 – 337 ( 1988. ). - PubMed
    1. ) Sato , K.Glutathione S‐transferases and hepatocar‐cinogenesis . Jpn. J. Cancer Res. , 79 , 556 – 572 ( 1988. ). - PMC - PubMed
    1. ) Sato , K.Glutathione transferases as markers of pre‐neoplasia and neoplasia . Adv. Cancer Res. , 52 , 205 – 255 ( 1989. ). - PubMed
    1. ) Sato , K. , Kitahara , A. , Satoh , K. , Ishikawa , T. , Tatematsu , M. and Ito , N.The placental form of glu‐tathione S‐transferase as a new marker protein for pre‐neoplasia in rat chemical hepatocarcinogenesis . Gann , 75 , 199 – 202 ( 1984. ). - PubMed
    1. ) Satoh , K. , Kitahara , A. , Soma , Y. , Inaba , Y. , Hatayama , I. and Sato , K.Purification, induction, and distribution of placental glutathione transferase: a new marker enzyme for preneoplastic cells in the rat chemical hepato carcinogenesis . Proc. Natl. Acad. Sci. USA . 82 , 3964 – 3968 ( 1985. ). - PMC - PubMed

Publication types

MeSH terms

LinkOut - more resources