Register for email alerts and news feeds:
This journal | BMJ Group
rss
Gut 1994;35:266-269; doi:10.1136/gut.35.2.266
Copyright © 1994 BMJ Publishing Group Ltd & British Society of Gastroenterology.

Expression of glutathione S-transferases in normal and malignant pancreas: an immunohistochemical study.

J D Collier, M K Bennett, A Hall, A R Cattan, R Lendrum, M F Bassendine

Department of Medicine, Freeman Hospital.

The glutathione S-transferases (GSTs) are a family of detoxification and metabolising enzymes, which have been linked with the susceptibility of tissues to environmental carcinogens and resistance of tumours to chemotherapy. Environmental carcinogens have been implicated in the pathogenesis of pancreatic carcinoma, which is also a tumour characterised by marked chemotherapeutic drug resistance. In this study 26 pancreatic adenocarcinoma and 12 normal pancreatic samples were examined immunohistochemically for expression of pi (acidic), alpha (basic), and mu (neutral) GST. Fourteen (54%) of the tumours expressed pi GST alone, two (8%) expressed both pi and alpha GST, and two (8%) showed immunoreactivity with alpha GST alone. In the normal pancreas the intralobular ducts and centroacinar cells expressed pi GST alone whereas the large ducts expressed both pi and alpha GST. The acinar cells showed immunoreactivity only with anti-alpha GST. Mu GST was not expressed by normal or malignant pancreas. Expression of pi GST by pancreatic carcinoma may be a marker of the malignant phenotype and be induced during neoplastic transformation. Alternatively it could possibly reflect cell of origin, suggesting that the tumour arises from the centroacinar cells or intralobular ducts, or both rather than the large ducts.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Duell, E. J., Holly, E. A., Bracci, P. M., Liu, M., Wiencke, J. K., Kelsey, K. T. (2002). A Population-Based, Case-Control Study of Polymorphisms in Carcinogen-Metabolizing Genes, Smoking, and Pancreatic Adenocarcinoma Risk. JNCI J Natl Cancer Inst 94: 297-306 [Abstract] [Full Text]  
  • Ulrich, A. B., Standop, J., Schmied, B. M., Schneider, M. B., Lawson, T. A., Pour, P. M. (2002). Species Differences in the Distribution of Drug-Metabolizing Enzymes in the Pancreas. Toxicol Pathol 30: 247-253 [Abstract]  
  • Coles, B. F., Anderson, K. E., Doerge, D. R., Churchwell, M. I., Lang, N. P., Kadlubar, F. F. (2000). Quantitative Analysis of Interindividual Variation of Glutathione S-Transferase Expression in Human Pancreas and the Ambiguity of Correlating Genotype with Phenotype. Cancer Res. 60: 573-579 [Abstract] [Full Text]  

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Cardiology Jobs

Gastroenterology Jobs