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The role of TGF-β/SMAD4 signaling in cancer

Transforming growth factor β (TGF-β) signaling pathway plays important roles in many biological processes, including cell growth, differentiation, apoptosis, migration, as well as cancer initiation and progression. SMAD4, which serves as the central mediator of TGF-β signaling, is specifically inact...

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Detalles Bibliográficos
Autores principales: Zhao, Ming, Mishra, Lopa, Deng, Chu-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821033/
https://www.ncbi.nlm.nih.gov/pubmed/29483830
http://dx.doi.org/10.7150/ijbs.23230
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author Zhao, Ming
Mishra, Lopa
Deng, Chu-Xia
author_facet Zhao, Ming
Mishra, Lopa
Deng, Chu-Xia
author_sort Zhao, Ming
collection PubMed
description Transforming growth factor β (TGF-β) signaling pathway plays important roles in many biological processes, including cell growth, differentiation, apoptosis, migration, as well as cancer initiation and progression. SMAD4, which serves as the central mediator of TGF-β signaling, is specifically inactivated in over half of pancreatic duct adenocarcinoma, and varying degrees in many other types of cancers. In the past two decades, multiple studies have revealed that SMAD4 loss on its own does not initiate tumor formation, but can promote tumor progression initiated by other genes, such as KRAS activation in pancreatic duct adenocarcinoma and APC inactivation in colorectal cancer. In other cases, such as skin cancer, loss of SMAD4 plays an important initiating role by disrupting DNA damage response and repair mechanisms and enhance genomic instability, suggesting its distinct roles in different types of tumors. This review lists SMAD4 mutations in various types of cancer and summarizes recent advances on SMAD4 with focuses on the function, signaling pathway, and the possibility of SMAD4 as a prognostic indicator.
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spelling pubmed-58210332018-02-26 The role of TGF-β/SMAD4 signaling in cancer Zhao, Ming Mishra, Lopa Deng, Chu-Xia Int J Biol Sci Review Transforming growth factor β (TGF-β) signaling pathway plays important roles in many biological processes, including cell growth, differentiation, apoptosis, migration, as well as cancer initiation and progression. SMAD4, which serves as the central mediator of TGF-β signaling, is specifically inactivated in over half of pancreatic duct adenocarcinoma, and varying degrees in many other types of cancers. In the past two decades, multiple studies have revealed that SMAD4 loss on its own does not initiate tumor formation, but can promote tumor progression initiated by other genes, such as KRAS activation in pancreatic duct adenocarcinoma and APC inactivation in colorectal cancer. In other cases, such as skin cancer, loss of SMAD4 plays an important initiating role by disrupting DNA damage response and repair mechanisms and enhance genomic instability, suggesting its distinct roles in different types of tumors. This review lists SMAD4 mutations in various types of cancer and summarizes recent advances on SMAD4 with focuses on the function, signaling pathway, and the possibility of SMAD4 as a prognostic indicator. Ivyspring International Publisher 2018-01-12 /pmc/articles/PMC5821033/ /pubmed/29483830 http://dx.doi.org/10.7150/ijbs.23230 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Zhao, Ming
Mishra, Lopa
Deng, Chu-Xia
The role of TGF-β/SMAD4 signaling in cancer
title The role of TGF-β/SMAD4 signaling in cancer
title_full The role of TGF-β/SMAD4 signaling in cancer
title_fullStr The role of TGF-β/SMAD4 signaling in cancer
title_full_unstemmed The role of TGF-β/SMAD4 signaling in cancer
title_short The role of TGF-β/SMAD4 signaling in cancer
title_sort role of tgf-β/smad4 signaling in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821033/
https://www.ncbi.nlm.nih.gov/pubmed/29483830
http://dx.doi.org/10.7150/ijbs.23230
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