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Partners in crime: the TGFβ and MAPK pathways in cancer progression

The TGFβ and Ras-MAPK pathways play critical roles in cell development and cell cycle regulation, as well as in tumor formation and metastasis. In the absence of cellular transformation, these pathways operate in opposition to one another, where TGFβ maintains an undifferentiated cell state and supp...

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Detalles Bibliográficos
Autores principales: Chapnick, Douglas A, Warner, Lisa, Bernet, Jennifer, Rao, Timsi, Liu, Xuedong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275500/
https://www.ncbi.nlm.nih.gov/pubmed/22204556
http://dx.doi.org/10.1186/2045-3701-1-42
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author Chapnick, Douglas A
Warner, Lisa
Bernet, Jennifer
Rao, Timsi
Liu, Xuedong
author_facet Chapnick, Douglas A
Warner, Lisa
Bernet, Jennifer
Rao, Timsi
Liu, Xuedong
author_sort Chapnick, Douglas A
collection PubMed
description The TGFβ and Ras-MAPK pathways play critical roles in cell development and cell cycle regulation, as well as in tumor formation and metastasis. In the absence of cellular transformation, these pathways operate in opposition to one another, where TGFβ maintains an undifferentiated cell state and suppresses proliferation, while Ras-MAPK pathways promote proliferation, survival and differentiation. However, in colorectal and pancreatic cancers, the opposing pathways' mechanisms are simultaneously activated in order to promote cancer progression and metastasis. Here, we highlight the roles of the TGFβ and Ras-MAPK pathways in normal and malignant states, and provide an explanation for how the concomitant activation of these pathways drives tumor biology. Finally, we survey potential therapeutic targets in these pathways.
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spelling pubmed-32755002012-02-09 Partners in crime: the TGFβ and MAPK pathways in cancer progression Chapnick, Douglas A Warner, Lisa Bernet, Jennifer Rao, Timsi Liu, Xuedong Cell Biosci Review The TGFβ and Ras-MAPK pathways play critical roles in cell development and cell cycle regulation, as well as in tumor formation and metastasis. In the absence of cellular transformation, these pathways operate in opposition to one another, where TGFβ maintains an undifferentiated cell state and suppresses proliferation, while Ras-MAPK pathways promote proliferation, survival and differentiation. However, in colorectal and pancreatic cancers, the opposing pathways' mechanisms are simultaneously activated in order to promote cancer progression and metastasis. Here, we highlight the roles of the TGFβ and Ras-MAPK pathways in normal and malignant states, and provide an explanation for how the concomitant activation of these pathways drives tumor biology. Finally, we survey potential therapeutic targets in these pathways. BioMed Central 2011-12-28 /pmc/articles/PMC3275500/ /pubmed/22204556 http://dx.doi.org/10.1186/2045-3701-1-42 Text en Copyright ©2011 Chapnick et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Chapnick, Douglas A
Warner, Lisa
Bernet, Jennifer
Rao, Timsi
Liu, Xuedong
Partners in crime: the TGFβ and MAPK pathways in cancer progression
title Partners in crime: the TGFβ and MAPK pathways in cancer progression
title_full Partners in crime: the TGFβ and MAPK pathways in cancer progression
title_fullStr Partners in crime: the TGFβ and MAPK pathways in cancer progression
title_full_unstemmed Partners in crime: the TGFβ and MAPK pathways in cancer progression
title_short Partners in crime: the TGFβ and MAPK pathways in cancer progression
title_sort partners in crime: the tgfβ and mapk pathways in cancer progression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275500/
https://www.ncbi.nlm.nih.gov/pubmed/22204556
http://dx.doi.org/10.1186/2045-3701-1-42
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