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Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β

The transforming growth factor (TGF)-βs are potent growth inhibitors of normal epithelial cells. In established tumor cell systems, however, the preponderant experimental evidence suggests that TGF-βs can foster tumor-host interactions that indirectly support the viability and/or progression of canc...

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Detalles Bibliográficos
Autores principales: Dumont, Nancy, Arteaga, Carlos L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139434/
https://www.ncbi.nlm.nih.gov/pubmed/11250702
http://dx.doi.org/10.1186/bcr44
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author Dumont, Nancy
Arteaga, Carlos L
author_facet Dumont, Nancy
Arteaga, Carlos L
author_sort Dumont, Nancy
collection PubMed
description The transforming growth factor (TGF)-βs are potent growth inhibitors of normal epithelial cells. In established tumor cell systems, however, the preponderant experimental evidence suggests that TGF-βs can foster tumor-host interactions that indirectly support the viability and/or progression of cancer cells. The timing of this 'TGF-β switch' during the progressive transformation of epithelial cells is not clear. More recent evidence also suggests that autocrine TGF-β signaling is operative in some tumor cells, and can also contribute to tumor invasiveness and metastases independent of an effect on nontumor cells. The dissociation of antiproliferative and matrix associated effects of autocrine TGF-β signaling at a transcriptional level provides for a mechanism(s) by which cancer cells can selectively use this signaling pathway for tumor progression. Data in support of the cellular and molecular mechanisms by which TGF-β signaling can accelerate the natural history of tumors will be reviewed in this section.
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spelling pubmed-1394342003-02-27 Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β Dumont, Nancy Arteaga, Carlos L Breast Cancer Res Review The transforming growth factor (TGF)-βs are potent growth inhibitors of normal epithelial cells. In established tumor cell systems, however, the preponderant experimental evidence suggests that TGF-βs can foster tumor-host interactions that indirectly support the viability and/or progression of cancer cells. The timing of this 'TGF-β switch' during the progressive transformation of epithelial cells is not clear. More recent evidence also suggests that autocrine TGF-β signaling is operative in some tumor cells, and can also contribute to tumor invasiveness and metastases independent of an effect on nontumor cells. The dissociation of antiproliferative and matrix associated effects of autocrine TGF-β signaling at a transcriptional level provides for a mechanism(s) by which cancer cells can selectively use this signaling pathway for tumor progression. Data in support of the cellular and molecular mechanisms by which TGF-β signaling can accelerate the natural history of tumors will be reviewed in this section. BioMed Central 2000 2000-02-21 /pmc/articles/PMC139434/ /pubmed/11250702 http://dx.doi.org/10.1186/bcr44 Text en Copyright © 2000 Current Science Ltd
spellingShingle Review
Dumont, Nancy
Arteaga, Carlos L
Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β
title Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β
title_full Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β
title_fullStr Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β
title_full_unstemmed Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β
title_short Transforming growth factor-β and breast cancer: Tumor promoting effects of transforming growth factor-β
title_sort transforming growth factor-β and breast cancer: tumor promoting effects of transforming growth factor-β
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139434/
https://www.ncbi.nlm.nih.gov/pubmed/11250702
http://dx.doi.org/10.1186/bcr44
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