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TGF-β Pathway in Salivary Gland Fibrosis
Fibrosis is presented in various physiologic and pathologic conditions of the salivary gland. Transforming growth factor beta (TGF-β) pathway has a pivotal role in the pathogenesis of fibrosis in several organs, including the salivary glands. Among the TGF-β superfamily members, TGF-β1 and 2 are pro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730716/ https://www.ncbi.nlm.nih.gov/pubmed/33266300 http://dx.doi.org/10.3390/ijms21239138 |
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author | Zhang, Xianglan Yun, Jun Seop Han, Dawool Yook, Jong In Kim, Hyun Sil Cho, Eunae Sandra |
author_facet | Zhang, Xianglan Yun, Jun Seop Han, Dawool Yook, Jong In Kim, Hyun Sil Cho, Eunae Sandra |
author_sort | Zhang, Xianglan |
collection | PubMed |
description | Fibrosis is presented in various physiologic and pathologic conditions of the salivary gland. Transforming growth factor beta (TGF-β) pathway has a pivotal role in the pathogenesis of fibrosis in several organs, including the salivary glands. Among the TGF-β superfamily members, TGF-β1 and 2 are pro-fibrotic ligands, whereas TGF-β3 and some bone morphogenetic proteins (BMPs) are anti-fibrotic ligands. TGF-β1 is thought to be associated with the pro-fibrotic pathogenesis of sialadenitis, post-radiation salivary gland dysfunction, and Sjögren’s syndrome. Potential therapeutic strategies that target multiple levels in the TGF-β pathway are under preclinical and clinical research for fibrosis. Despite the anti-fibrotic effect of BMPs, their in vivo delivery poses a challenge in terms of adequate clinical efficacy. In this article, we will review the relevance of TGF-β signaling in salivary gland fibrosis and advances of potential therapeutic options in the field. |
format | Online Article Text |
id | pubmed-7730716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77307162020-12-12 TGF-β Pathway in Salivary Gland Fibrosis Zhang, Xianglan Yun, Jun Seop Han, Dawool Yook, Jong In Kim, Hyun Sil Cho, Eunae Sandra Int J Mol Sci Review Fibrosis is presented in various physiologic and pathologic conditions of the salivary gland. Transforming growth factor beta (TGF-β) pathway has a pivotal role in the pathogenesis of fibrosis in several organs, including the salivary glands. Among the TGF-β superfamily members, TGF-β1 and 2 are pro-fibrotic ligands, whereas TGF-β3 and some bone morphogenetic proteins (BMPs) are anti-fibrotic ligands. TGF-β1 is thought to be associated with the pro-fibrotic pathogenesis of sialadenitis, post-radiation salivary gland dysfunction, and Sjögren’s syndrome. Potential therapeutic strategies that target multiple levels in the TGF-β pathway are under preclinical and clinical research for fibrosis. Despite the anti-fibrotic effect of BMPs, their in vivo delivery poses a challenge in terms of adequate clinical efficacy. In this article, we will review the relevance of TGF-β signaling in salivary gland fibrosis and advances of potential therapeutic options in the field. MDPI 2020-11-30 /pmc/articles/PMC7730716/ /pubmed/33266300 http://dx.doi.org/10.3390/ijms21239138 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Zhang, Xianglan Yun, Jun Seop Han, Dawool Yook, Jong In Kim, Hyun Sil Cho, Eunae Sandra TGF-β Pathway in Salivary Gland Fibrosis |
title | TGF-β Pathway in Salivary Gland Fibrosis |
title_full | TGF-β Pathway in Salivary Gland Fibrosis |
title_fullStr | TGF-β Pathway in Salivary Gland Fibrosis |
title_full_unstemmed | TGF-β Pathway in Salivary Gland Fibrosis |
title_short | TGF-β Pathway in Salivary Gland Fibrosis |
title_sort | tgf-β pathway in salivary gland fibrosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730716/ https://www.ncbi.nlm.nih.gov/pubmed/33266300 http://dx.doi.org/10.3390/ijms21239138 |
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