Signal transduction mechanism in response to aflatoxin B1 exposure: protein kinase C activity.

Abstract:

:A single dose of the carcinogen aflatoxin B1 (7 mg/kg body weight) to male Wistar rats significantly enhanced the hepatic activity of protein kinase C in the particulate and nuclear fractions. The particulate fraction showed stimulation at 4 and 7 h, while the nuclear activity was increased at 17 h following administration of aflatoxin B1. The enzyme activity in cytosol revealed a significant decline corresponding to stimulation in particulate fraction. The carcinogen-activated protein kinase C stimulated autophosphorylation, and was found to accelerate in vitro phosphorylation of two model DNA synthesizing enzymes--the Klenow fragment of replicative DNA polymerase of E. Coli and a DNA primase-polymerase complex of yeast mitochondrial origin. Prior phosphorylation of these enzymes led to significant enhancement of their activities. The results imply that activation of protein kinase C and consequently the activation of DNA synthesizing enzymes may play an important role in the initiation of carcinogenesis.

journal_name

Chem Biol Interact

authors

Mistry KJ,Krishna M,Pasupathy K,Murthy V,Bhattacharya RK

doi

10.1016/0009-2797(96)03698-8

subject

Has Abstract

pub_date

1996-03-25 00:00:00

pages

177-85

issue

2

eissn

0009-2797

issn

1872-7786

pii

0009-2797(96)03698-8

journal_volume

100

pub_type

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