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Transforming growth factor-beta: possible roles in carcinogenesis.
TGF-beta is the prototype of a large family of multifunctional regulatory proteins. The principal sources of the peptide, platelets and bone, suggest that it plays a role in healing and remodeling processes. In vitro, TGF-beta is chemotactic for monocytes and fibroblasts and can greatly enhance accu...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1988
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246450/ https://www.ncbi.nlm.nih.gov/pubmed/3044431 |
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author | Roberts, A. B. Thompson, N. L. Heine, U. Flanders, C. Sporn, M. B. |
author_facet | Roberts, A. B. Thompson, N. L. Heine, U. Flanders, C. Sporn, M. B. |
author_sort | Roberts, A. B. |
collection | PubMed |
description | TGF-beta is the prototype of a large family of multifunctional regulatory proteins. The principal sources of the peptide, platelets and bone, suggest that it plays a role in healing and remodeling processes. In vitro, TGF-beta is chemotactic for monocytes and fibroblasts and can greatly enhance accumulation of extracellular matrix components by fibroblasts. Its ability to stimulate the formation of granulation tissue locally and the demonstration of specific time- and tissue-dependent expression in embryogenesis suggest that similar mechanisms are operative in vivo. By analogy to its effects in wound healing and embryogenesis, it is proposed that TGF-beta, secreted by tumour cells, can augment tumour growth indirectly by effects on the stromal elements. These effects include suppression of the immune response, and enhancement of both angiogenesis and formation of connective tissue. Many tumour cells have escaped from direct growth inhibitory effects of TGF-beta by a variety of mechanisms including inability to activate the latent form of the peptide, loss of cellular receptors for TGF-beta, and loss of functional intracellular signal transduction pathways. IMAGES: |
format | Text |
id | pubmed-2246450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22464502009-09-10 Transforming growth factor-beta: possible roles in carcinogenesis. Roberts, A. B. Thompson, N. L. Heine, U. Flanders, C. Sporn, M. B. Br J Cancer Research Article TGF-beta is the prototype of a large family of multifunctional regulatory proteins. The principal sources of the peptide, platelets and bone, suggest that it plays a role in healing and remodeling processes. In vitro, TGF-beta is chemotactic for monocytes and fibroblasts and can greatly enhance accumulation of extracellular matrix components by fibroblasts. Its ability to stimulate the formation of granulation tissue locally and the demonstration of specific time- and tissue-dependent expression in embryogenesis suggest that similar mechanisms are operative in vivo. By analogy to its effects in wound healing and embryogenesis, it is proposed that TGF-beta, secreted by tumour cells, can augment tumour growth indirectly by effects on the stromal elements. These effects include suppression of the immune response, and enhancement of both angiogenesis and formation of connective tissue. Many tumour cells have escaped from direct growth inhibitory effects of TGF-beta by a variety of mechanisms including inability to activate the latent form of the peptide, loss of cellular receptors for TGF-beta, and loss of functional intracellular signal transduction pathways. IMAGES: Nature Publishing Group 1988-06 /pmc/articles/PMC2246450/ /pubmed/3044431 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 Roberts, A. B. Thompson, N. L. Heine, U. Flanders, C. Sporn, M. B. Transforming growth factor-beta: possible roles in carcinogenesis. |
title | Transforming growth factor-beta: possible roles in carcinogenesis. |
title_full | Transforming growth factor-beta: possible roles in carcinogenesis. |
title_fullStr | Transforming growth factor-beta: possible roles in carcinogenesis. |
title_full_unstemmed | Transforming growth factor-beta: possible roles in carcinogenesis. |
title_short | Transforming growth factor-beta: possible roles in carcinogenesis. |
title_sort | transforming growth factor-beta: possible roles in carcinogenesis. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246450/ https://www.ncbi.nlm.nih.gov/pubmed/3044431 |
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