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MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis

Systemic sclerosis (SSc) is a multisystem fibrotic and autoimmune disease. Both genetic and epigenetic elements mediate SSc pathophysiology. This review summarizes the role of one epigenetic element, known as microRNAs (miRNAs), involved in different signaling pathways of SSc pathogenesis. The expre...

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Detalles Bibliográficos
Autores principales: Li, Yisha, Huang, Jing, Guo, Muyao, Zuo, Xiaoxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610971/
https://www.ncbi.nlm.nih.gov/pubmed/26365208
http://dx.doi.org/10.1016/j.gpb.2015.07.001
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author Li, Yisha
Huang, Jing
Guo, Muyao
Zuo, Xiaoxia
author_facet Li, Yisha
Huang, Jing
Guo, Muyao
Zuo, Xiaoxia
author_sort Li, Yisha
collection PubMed
description Systemic sclerosis (SSc) is a multisystem fibrotic and autoimmune disease. Both genetic and epigenetic elements mediate SSc pathophysiology. This review summarizes the role of one epigenetic element, known as microRNAs (miRNAs), involved in different signaling pathways of SSc pathogenesis. The expression of key components in transforming growth factor-β (TGF-β) signaling pathway has been found to be regulated by miRNAs both upstream and downstream of TGF-β. We are specifically interested in the pathway components upstream of TGF-β, while miRNAs in other signaling pathways have not been extensively studied. The emerging role of miRNAs in vasculopathy of SSc suggests a promising new direction for future investigation. Elucidation of the regulatory role of miRNAs in the expression of signaling factors may facilitate the discovery of novel biomarkers in SSc and improve the understanding and treatment of this disease.
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spelling pubmed-46109712015-11-20 MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis Li, Yisha Huang, Jing Guo, Muyao Zuo, Xiaoxia Genomics Proteomics Bioinformatics Review Systemic sclerosis (SSc) is a multisystem fibrotic and autoimmune disease. Both genetic and epigenetic elements mediate SSc pathophysiology. This review summarizes the role of one epigenetic element, known as microRNAs (miRNAs), involved in different signaling pathways of SSc pathogenesis. The expression of key components in transforming growth factor-β (TGF-β) signaling pathway has been found to be regulated by miRNAs both upstream and downstream of TGF-β. We are specifically interested in the pathway components upstream of TGF-β, while miRNAs in other signaling pathways have not been extensively studied. The emerging role of miRNAs in vasculopathy of SSc suggests a promising new direction for future investigation. Elucidation of the regulatory role of miRNAs in the expression of signaling factors may facilitate the discovery of novel biomarkers in SSc and improve the understanding and treatment of this disease. Elsevier 2015-08 2015-09-11 /pmc/articles/PMC4610971/ /pubmed/26365208 http://dx.doi.org/10.1016/j.gpb.2015.07.001 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Li, Yisha
Huang, Jing
Guo, Muyao
Zuo, Xiaoxia
MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis
title MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis
title_full MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis
title_fullStr MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis
title_full_unstemmed MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis
title_short MicroRNAs Regulating Signaling Pathways: Potential Biomarkers in Systemic Sclerosis
title_sort micrornas regulating signaling pathways: potential biomarkers in systemic sclerosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610971/
https://www.ncbi.nlm.nih.gov/pubmed/26365208
http://dx.doi.org/10.1016/j.gpb.2015.07.001
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