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Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication

Bone morphogenetic proteins (BMPs) comprise a major subgroup of the transforming growth factor (TGF)-β superfamily. They play pivotal roles in embryonic development and tissue homeostasis in adults. Deregulation of BMP and TGF-β signaling contributes to developmental anomalies and multiple diseases....

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Autores principales: Cao, Yanna, Drake, Madeline, Davis, Joy, Yang, Baibing, Ko, Tien C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093075/
https://www.ncbi.nlm.nih.gov/pubmed/32211568
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author Cao, Yanna
Drake, Madeline
Davis, Joy
Yang, Baibing
Ko, Tien C
author_facet Cao, Yanna
Drake, Madeline
Davis, Joy
Yang, Baibing
Ko, Tien C
author_sort Cao, Yanna
collection PubMed
description Bone morphogenetic proteins (BMPs) comprise a major subgroup of the transforming growth factor (TGF)-β superfamily. They play pivotal roles in embryonic development and tissue homeostasis in adults. Deregulation of BMP and TGF-β signaling contributes to developmental anomalies and multiple diseases. In this mini-review, we focus on BMP signaling in inflammatory disorders of the pancreas, acute and chronic pancreatitis, in contrast to TGF-β signaling. We then discuss molecular mechanisms that interact with and connect between the BMP and TGF-β signaling pathways. Lastly, we review potential implications of these molecular mechanisms for therapeutic development. In summary, BMP signaling pathway plays different roles during pancreatitis disease development, and the antagonism between BMP and TGF-β signaling can be manipulated for therapeutic development against pancreatitis.
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spelling pubmed-70930752020-03-24 Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication Cao, Yanna Drake, Madeline Davis, Joy Yang, Baibing Ko, Tien C Adv Res Gastroenterol Hepatol Article Bone morphogenetic proteins (BMPs) comprise a major subgroup of the transforming growth factor (TGF)-β superfamily. They play pivotal roles in embryonic development and tissue homeostasis in adults. Deregulation of BMP and TGF-β signaling contributes to developmental anomalies and multiple diseases. In this mini-review, we focus on BMP signaling in inflammatory disorders of the pancreas, acute and chronic pancreatitis, in contrast to TGF-β signaling. We then discuss molecular mechanisms that interact with and connect between the BMP and TGF-β signaling pathways. Lastly, we review potential implications of these molecular mechanisms for therapeutic development. In summary, BMP signaling pathway plays different roles during pancreatitis disease development, and the antagonism between BMP and TGF-β signaling can be manipulated for therapeutic development against pancreatitis. 2019 2019-09-04 /pmc/articles/PMC7093075/ /pubmed/32211568 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under Creative Commons Attribution 4.0 License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Cao, Yanna
Drake, Madeline
Davis, Joy
Yang, Baibing
Ko, Tien C
Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication
title Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication
title_full Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication
title_fullStr Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication
title_full_unstemmed Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication
title_short Opposing Roles of BMP and TGF-β Signaling Pathways in Pancreatitis: Mechanisms and Therapeutic Implication
title_sort opposing roles of bmp and tgf-β signaling pathways in pancreatitis: mechanisms and therapeutic implication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093075/
https://www.ncbi.nlm.nih.gov/pubmed/32211568
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