Academic Journal

Xenobiotic metabolising enzyme expression in colonic neoplasia.

التفاصيل البيبلوغرافية
العنوان: Xenobiotic metabolising enzyme expression in colonic neoplasia.
المؤلفون: McKay, J A, Murray, G I, Weaver, R J, Ewen, S W, Melvin, W T, Burke, M D
بيانات النشر: BMJ Publishing Group Ltd
سنة النشر: 1993
المجموعة: HighWire Press (Stanford University)
مصطلحات موضوعية: Research Article
الوصف: The cytochrome P450, epoxide hydrolase, and glutathione S-transferase enzyme families play an important part in the metabolism of many carcinogens and anti-cancer drugs. The expression of two forms of cytochrome P450 (P450 1A and P450 3A), epoxide hydrolase and of the alpha, mu, and pi forms of glutathione S-transferase in normal colon, colonic adenomas, and adenocarcinoma of the colon were studied by immunohistochemistry. This allowed the precise cellular site and distribution of each enzyme to be determined. Expression of all the xenobiotic metabolising enzymes studied was almost wholly confined to the epithelial cells, whether in normal, adenoma or carcinoma samples, except that cytochrome P450 3A was also identified in mast cells and glutathione S-transferase pi was also present in chronic inflammatory cells. Cytochrome P450 was present in only a small proportion of normal colon samples, whereas epoxide hydrolase and glutathione S-transferase mu were identified in about half, and glutathione S-transferase alpha and pi in most normal samples. By contrast all the enzyme forms studied were expressed in virtually all adenomas and in over half the carcinomas. These results suggest that cytochrome P450 1A and cytochrome P450 3A are more specific markers of colonic neoplasia than epoxide hydrolase or glutathione S-transferases alpha, mu, and pi.
نوع الوثيقة: text
وصف الملف: text/html
اللغة: English
Relation: http://gut.bmj.com/cgi/content/short/34/9/1234; http://dx.doi.org/10.1136/gut.34.9.1234
DOI: 10.1136/gut.34.9.1234
الاتاحة: http://gut.bmj.com/cgi/content/short/34/9/1234
https://doi.org/10.1136/gut.34.9.1234
Rights: Copyright (C) 1993, BMJ Publishing Group
رقم الانضمام: edsbas.33E09E98
قاعدة البيانات: BASE