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Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma.
Transforming growth factor beta1 (TGF-beta1) is a potent modulator of cell proliferation in vitro, and recent studies have demonstrated its overexpression in several different tumours; nevertheless, the molecular mechanisms of TGF-beta1 action on cell growth and differentiation have not been fully e...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150151/ https://www.ncbi.nlm.nih.gov/pubmed/9579831 |
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author | Perlino, E. Loverro, G. Maiorano, E. Giannini, T. Cazzolla, A. Napoli, A. Fiore, M. G. Ricco, R. Marra, E. Selvaggi, L. |
author_facet | Perlino, E. Loverro, G. Maiorano, E. Giannini, T. Cazzolla, A. Napoli, A. Fiore, M. G. Ricco, R. Marra, E. Selvaggi, L. |
author_sort | Perlino, E. |
collection | PubMed |
description | Transforming growth factor beta1 (TGF-beta1) is a potent modulator of cell proliferation in vitro, and recent studies have demonstrated its overexpression in several different tumours; nevertheless, the molecular mechanisms of TGF-beta1 action on cell growth and differentiation have not been fully elucidated. To clarify the role of TGF-beta and its receptor in human endometrial proliferation and differentiation, TGF-beta1 expression at both the mRNA and protein levels has been evaluated by using Northern blotting and immunohistochemistry, in both normal (atrophic, proliferative and secretory) and neoplastic (adenocarcinoma) endometrial samples. This study demonstrates that TGF-beta1 mRNA expression is dramatically reduced in endometrial carcinomas with respect to non-neoplastic tissues, whereas the immunohistochemical expression of TGF-beta1 is enhanced in the epithelial component of endometrial carcinomas compared with non-neoplastic tissues. These data suggest that TGF-beta1 acts as a paracrine regulator of endometrial cell proliferation and that it may contribute to the carcinogenic mechanisms of endometrial carcinoma. IMAGES: |
format | Text |
id | pubmed-2150151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-21501512009-09-10 Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. Perlino, E. Loverro, G. Maiorano, E. Giannini, T. Cazzolla, A. Napoli, A. Fiore, M. G. Ricco, R. Marra, E. Selvaggi, L. Br J Cancer Research Article Transforming growth factor beta1 (TGF-beta1) is a potent modulator of cell proliferation in vitro, and recent studies have demonstrated its overexpression in several different tumours; nevertheless, the molecular mechanisms of TGF-beta1 action on cell growth and differentiation have not been fully elucidated. To clarify the role of TGF-beta and its receptor in human endometrial proliferation and differentiation, TGF-beta1 expression at both the mRNA and protein levels has been evaluated by using Northern blotting and immunohistochemistry, in both normal (atrophic, proliferative and secretory) and neoplastic (adenocarcinoma) endometrial samples. This study demonstrates that TGF-beta1 mRNA expression is dramatically reduced in endometrial carcinomas with respect to non-neoplastic tissues, whereas the immunohistochemical expression of TGF-beta1 is enhanced in the epithelial component of endometrial carcinomas compared with non-neoplastic tissues. These data suggest that TGF-beta1 acts as a paracrine regulator of endometrial cell proliferation and that it may contribute to the carcinogenic mechanisms of endometrial carcinoma. IMAGES: Nature Publishing Group 1998-04 /pmc/articles/PMC2150151/ /pubmed/9579831 Text en 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 | Research Article Perlino, E. Loverro, G. Maiorano, E. Giannini, T. Cazzolla, A. Napoli, A. Fiore, M. G. Ricco, R. Marra, E. Selvaggi, L. Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. |
title | Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. |
title_full | Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. |
title_fullStr | Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. |
title_full_unstemmed | Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. |
title_short | Down-regulated expression of transforming growth factor beta 1 mRNA in endometrial carcinoma. |
title_sort | down-regulated expression of transforming growth factor beta 1 mrna in endometrial carcinoma. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150151/ https://www.ncbi.nlm.nih.gov/pubmed/9579831 |
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