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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Manson, M.M.
Right arrow Articles by Neal, G.E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Manson, M.M.
Right arrow Articles by Neal, G.E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1981 Oxford University Press

research-article

An examination of the relative resistances to aflatoxin B1 and susceptibilities to {gamma}-glutamyl p-phenylene diamine mustard of {gamma}-glutamyl transferase negative and positive cell lines

M.M. Manson 1, R.F. Legg 1, J.V. Watson 2, J.A. Green 1 and G.E. Neal 1

1Toxicology Unit, MRC Laboratories Wood-mansterne Road, Carshalton, Surrey
2Clinical Oncology and Radiotherapeutics Unit, MRC Centre, University Medical School Hills Road, Cambridge, UK

Two epithelial cell lines have been derived from rat liver. One, containing only low levels of {gamma}glutamyl transferase (GGT) was obtained from normal liver and the other, containing high levels of the enzyme was isolated from an aflatoxin B1induced hepatoma. The GGT levels present in the two cell lines have been examined by histochemical staining, by a fluorescence assay using disrupted cells, and also by intact fluorescence-labelled cells in a laser flow cytofluori-meter. The cells containing high levels of GGT have been found to be less sensitive to microsomally-activated aflatoxin B1 than are the GGT negative cells, a feature of the in vivo situation. Evidence for activation of the {gamma}-glutamyl derivative of an alkylating mustard analogue of p-phenylene diamine by the GGT positive cells is presented. This finding could be of relevance to the possible chemotherapy of GGT-rich lesions in vivo.


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
A.G. Shepherd, M. M. Manson, H. W.L. Ball, and L. I. McLellan
Regulation of rat glutamate-cysteine ligase ({gamma}-glutamylcysteine synthetase) subunits by chemopreventive agents and in aflatoxin B1-induced preneoplasia
Carcinogenesis, October 1, 2000; 21(10): 1827 - 1834.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
A. Bayly, N. French, C Dive, and R. Roberts
Non-genotoxic hepatocarcinogenesis in vitro: the FaO hepatoma line responds to peroxisome proliferators and retains the ability to undergo apoptosis
J. Cell Sci., January 2, 1993; 104(2): 307 - 315.
[Abstract] [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.