Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (17)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Bager, Y.
Right arrow Articles by Wärngàrd, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bager, Y.
Right arrow Articles by Wärngàrd, L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1994 Oxford University Press

research-article

Alteration in expression of gap junction proteins in rat liver after treatment with the tumour promoter 3,4,5,3',4'-pentachiorobiphenyl

Yvonne Bager, Kerstin Kenne, Vladimir Krutovskikh 1, Marc Mesnil 1, Otto Traub 2 and Lars Wärngàrd 3

Institute of Environmental Medicine, Karolinska Institutet Box 210, S-171 77 Stockholm, Sweden
1International Agency for Research on Cancer 150 cours Albert-Thomas, 69372 Lyon Cédex 08, France
2Institut für Genetik Abteilung für Molekulargenetik, Universfärt Bonn, 53117 Bonn, Germany

3To whom correspondence should be addressed

Polychiorinated biphenyls (PCBs) are industrial chemicals which are highly persistent and widely distributed in the environment. We have previously shown that 3,4,5,3',4'-pentachiorobiphenyl (PCB 126) is a potent tumour promoter in two separate 20 week initiation–promotion studies. In the present study, rat livers from these two studies were further investigated for connexin expression. The results demonstrated that treatment with PCB 126 caused a decrease in the amount of the two major liver connexins, cx 26 and cx 32, In livers of treated animals. This reduction was also prominent after treatment at low doses, although {gamma}-glutamyl transpeptidase-positive foci had not developed in these livers. The quantity of cx 26 and cx 32 in iminunostained liver sections was determined using a computerized fluorescence image analyzer. Western blot analysis of liver extracts conlinned these results. No changes in the RNA levels in the treated rats were seen, suggesting that the down-regulation of cx 26 and cx 32 is post-transcriptional.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
CarcinogenesisHome page
I. Plante, M. Charbonneau, and D. G. Cyr
Decreased gap junctional intercellular communication in hexachlorobenzene-induced gender-specific hepatic tumor formation in the rat
Carcinogenesis, July 1, 2002; 23(7): 1243 - 1249.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
C. Campagna, M.-A. Sirard, P. Ayotte, and J. L. Bailey
Impaired Maturation, Fertilization, and Embryonic Development of Porcine Oocytes Following Exposure to an Environmentally Relevant Organochlorine Mixture
Biol Reprod, August 1, 2001; 65(2): 554 - 560.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
O. Moennikes, A. Buchmann, A. Romualdi, T. Ott, J. Werringloer, K. Willecke, and M. Schwarz
Lack of Phenobarbital-mediated Promotion of Hepatocarcinogenesis in Connexin32-Null Mice
Cancer Res., September 1, 2000; 60(18): 5087 - 5091.
[Abstract] [Full Text]


Home page
Toxicol SciHome page
J. S. Isenberg, L. M. Kamendulis, J. H. Smith, D. C. Ackley, G. Pugh Jr., A. W. Lington, and J. E. Klaunig
Effects of Di-2-Ethylhexyl Phthalate (DEHP) on Gap-Junctional Intercellular Communication (GJIC), DNA Synthesis, and Peroxisomal Beta Oxidation (PBOX) in Rat, Mouse, and Hamster Liver
Toxicol. Sci., July 1, 2000; 56(1): 73 - 85.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.