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TGF-β in pancreatic cancer initiation and progression: two sides of the same coin

Pancreatic cancer is highly lethal malignant tumor with characterised rapid progression, invasiveness and resistance to radiochemotherapy. Transforming growth factor-β (TGF-β) signaling plays a dual role in both pro-tumorigenic and tumor suppressive of pancreatic cancer, depending on tumor stage and...

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Autores principales: Shen, Wei, Tao, Guo-qing, Zhang, Yu, Cai, Bing, Sun, Jian, Tian, Zhi-qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545849/
https://www.ncbi.nlm.nih.gov/pubmed/28794854
http://dx.doi.org/10.1186/s13578-017-0168-0
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author Shen, Wei
Tao, Guo-qing
Zhang, Yu
Cai, Bing
Sun, Jian
Tian, Zhi-qiang
author_facet Shen, Wei
Tao, Guo-qing
Zhang, Yu
Cai, Bing
Sun, Jian
Tian, Zhi-qiang
author_sort Shen, Wei
collection PubMed
description Pancreatic cancer is highly lethal malignant tumor with characterised rapid progression, invasiveness and resistance to radiochemotherapy. Transforming growth factor-β (TGF-β) signaling plays a dual role in both pro-tumorigenic and tumor suppressive of pancreatic cancer, depending on tumor stage and microenvironment. TGF-β signaling components alteration are common in pancreatic cancer, and its leading role in tumor formation and metastases has received increased attention. Many therapies have investigated to target TGF-β signaling in the preclinical and clinical setting. In this review, we highlight the dual roles of TGF-β and touch upon the perspectives on therapeutic target of TGF-β signaling in pancreatic cancer.
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spelling pubmed-55458492017-08-09 TGF-β in pancreatic cancer initiation and progression: two sides of the same coin Shen, Wei Tao, Guo-qing Zhang, Yu Cai, Bing Sun, Jian Tian, Zhi-qiang Cell Biosci Review Pancreatic cancer is highly lethal malignant tumor with characterised rapid progression, invasiveness and resistance to radiochemotherapy. Transforming growth factor-β (TGF-β) signaling plays a dual role in both pro-tumorigenic and tumor suppressive of pancreatic cancer, depending on tumor stage and microenvironment. TGF-β signaling components alteration are common in pancreatic cancer, and its leading role in tumor formation and metastases has received increased attention. Many therapies have investigated to target TGF-β signaling in the preclinical and clinical setting. In this review, we highlight the dual roles of TGF-β and touch upon the perspectives on therapeutic target of TGF-β signaling in pancreatic cancer. BioMed Central 2017-08-07 /pmc/articles/PMC5545849/ /pubmed/28794854 http://dx.doi.org/10.1186/s13578-017-0168-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Shen, Wei
Tao, Guo-qing
Zhang, Yu
Cai, Bing
Sun, Jian
Tian, Zhi-qiang
TGF-β in pancreatic cancer initiation and progression: two sides of the same coin
title TGF-β in pancreatic cancer initiation and progression: two sides of the same coin
title_full TGF-β in pancreatic cancer initiation and progression: two sides of the same coin
title_fullStr TGF-β in pancreatic cancer initiation and progression: two sides of the same coin
title_full_unstemmed TGF-β in pancreatic cancer initiation and progression: two sides of the same coin
title_short TGF-β in pancreatic cancer initiation and progression: two sides of the same coin
title_sort tgf-β in pancreatic cancer initiation and progression: two sides of the same coin
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545849/
https://www.ncbi.nlm.nih.gov/pubmed/28794854
http://dx.doi.org/10.1186/s13578-017-0168-0
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