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Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay
Intestinal injury that results from chemotherapy belongs to the major factors of dose-limitation in tumour therapy. The tyrphostins AG1714 and AG1801 reduce cisplatin and 5-FU-induced small intestinal mucosal damage, using a quantitative biochemical assay. The assay is based on the determination of...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361831/ https://www.ncbi.nlm.nih.gov/pubmed/15655545 http://dx.doi.org/10.1038/sj.bjc.6602324 |
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author | Zlotnik, Y Patya, M Vanichkin, A Novogrodsky, A |
author_facet | Zlotnik, Y Patya, M Vanichkin, A Novogrodsky, A |
author_sort | Zlotnik, Y |
collection | PubMed |
description | Intestinal injury that results from chemotherapy belongs to the major factors of dose-limitation in tumour therapy. The tyrphostins AG1714 and AG1801 reduce cisplatin and 5-FU-induced small intestinal mucosal damage, using a quantitative biochemical assay. The assay is based on the determination of the enzymatic activity of gamma-glutamyl transpeptidase, a marker of the brush border epithelium of the small intestine. |
format | Text |
id | pubmed-2361831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23618312009-09-10 Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay Zlotnik, Y Patya, M Vanichkin, A Novogrodsky, A Br J Cancer Translational Therapeutics Intestinal injury that results from chemotherapy belongs to the major factors of dose-limitation in tumour therapy. The tyrphostins AG1714 and AG1801 reduce cisplatin and 5-FU-induced small intestinal mucosal damage, using a quantitative biochemical assay. The assay is based on the determination of the enzymatic activity of gamma-glutamyl transpeptidase, a marker of the brush border epithelium of the small intestine. Nature Publishing Group 2005-01-31 2005-01-18 /pmc/articles/PMC2361831/ /pubmed/15655545 http://dx.doi.org/10.1038/sj.bjc.6602324 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Translational Therapeutics Zlotnik, Y Patya, M Vanichkin, A Novogrodsky, A Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
title | Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
title_full | Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
title_fullStr | Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
title_full_unstemmed | Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
title_short | Tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
title_sort | tyrphostins reduce chemotherapy-induced intestinal injury in mice: assessment by a biochemical assay |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361831/ https://www.ncbi.nlm.nih.gov/pubmed/15655545 http://dx.doi.org/10.1038/sj.bjc.6602324 |
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