Literature DB >> 2546957

Heterogeneous alterations of UDP-glucuronosyltransferases in mouse hepatic foci.

K W Bock1, A B Kobusch, G Fischer.   

Abstract

UDP-glucuronosyltransferase (UDPGT) was studied immunohistochemically in hepatic foci and nodules of N-nitrosomorpholine-treated mice. Serial sections were stained for glucose-6-phosphatase (G6Pase). It was found that a high percentage of G6Pase-negative liver foci and nodules were also UDPGT-negative (34%). In addition, G6Pase-negative foci without altered UDPGT phenotype (30%) and UDPGT-negative foci without altered G6Pase phenotype (8%) were detected. G6Pase-positive foci were also present (24%). Interestingly, most G6Pase-positive foci were UDPGT-positive (16%). Some G6Pase-positive lesions without altered UDPGT phenotype were also found (8%). The major phenotype observed in rat hepatocarcinogenesis models (UDPGT-positive/G6Pase-negative foci) was not detectable in the mouse model. These results demonstrate heterogeneous alterations of UDPGTs in mouse hepatic foci. They furthermore suggest marked differences between the mouse and the rat in the regulation of UDPGTs in similarly induced rat hepatic foci.

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Year:  1989        PMID: 2546957     DOI: 10.1007/BF00391704

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  22 in total

Review 1.  Metabolism of xenobiotics in hepatocyte nodules.

Authors:  L C Eriksson; A Blanck; K W Bock; B Mannervik
Journal:  Toxicol Pathol       Date:  1987       Impact factor: 1.902

2.  Effects of N-nitrosomorpholine and phenobarbital on UDP-glucuronyltransferase in putative preneoplastic foci of rat liver.

Authors:  G Fischer; D Ulrich; K W Bock
Journal:  Carcinogenesis       Date:  1985-04       Impact factor: 4.944

Review 3.  The sequential analysis of cancer development.

Authors:  E Farber; R Cameron
Journal:  Adv Cancer Res       Date:  1980       Impact factor: 6.242

Review 4.  The first relevant cell stage in rat liver carcinogenesis. A quantitative approach.

Authors:  P Emmelot; E Scherer
Journal:  Biochim Biophys Acta       Date:  1980-05-06

5.  Intralobular distribution of UDP-glucuronosyltransferase in livers from untreated, 3-methylcholanthrene- and phenobarbital-treated rats.

Authors:  D Ullrich; G Fischer; N Katz; K W Bock
Journal:  Chem Biol Interact       Date:  1984-02       Impact factor: 5.192

6.  Purification of rat-liver microsomal UDP-glucuronyltransferase. Separation of two enzyme forms inducible by 3-methylcholanthrene or phenobarbital.

Authors:  K W Bock; D Josting; W Lilienblum; H Pfeil
Journal:  Eur J Biochem       Date:  1979-07

7.  The histopathology and biochemistry of phenobarbitone-induced liver nodules in C3H mice.

Authors:  S D Gangolli; B G Lake; J G Evans
Journal:  Arch Toxicol Suppl       Date:  1987

Review 8.  Endogenous substrates for UDP-glucuronosyltransferases.

Authors:  T Tephly; M Green; J Puig; Y Irshaid
Journal:  Xenobiotica       Date:  1988-11       Impact factor: 1.908

9.  Electroimmunochemical quantification of UDP-glucuronosyltransferase in rat liver microsomes.

Authors:  H Pfeil; K W Bock
Journal:  Eur J Biochem       Date:  1983-04-05

10.  Separation of different UDP glucuronosyltransferase activities according to charge heterogeneity by chromatofocusing using mouse liver microsomes. Three major types of aglycones.

Authors:  P I Mackenzie; M M Joffe; P J Munson; I S Owens
Journal:  Biochem Pharmacol       Date:  1985-03-15       Impact factor: 5.858

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