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About:
TGF-β and WNT signaling pathways in cardiac fibrosis: non-coding RNAs come into focus
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
TGF-β and WNT signaling pathways in cardiac fibrosis: non-coding RNAs come into focus
Creator
Ghasemi, Younes
Hamblin, Michael
Dabiri, Hamed
Derakhshan, Maryam
Mahjoubin-Tehran, Maryam
Mirzaei, Hamed
Movahedpour, Ahmad
Nikoozadeh, Azin
Savardashtaki, Amir
Shabaninejad, Zahra
Vakili, Sina
Yousefi, Fatemeh
source
PMC
abstract
Cardiac fibrosis describes the inappropriate proliferation of cardiac fibroblasts (CFs), leading to accumulation of extracellular matrix (ECM) proteins in the cardiac muscle, which is found in many pathophysiological heart conditions. A range of molecular components and cellular pathways, have been implicated in its pathogenesis. In this review, we focus on the TGF-β and WNT signaling pathways, and their mutual interaction, which have emerged as important factors involved in cardiac pathophysiology. The molecular and cellular processes involved in the initiation and progression of cardiac fibrosis are summarized. We focus on TGF-β and WNT signaling in cardiac fibrosis, ECM production, and myofibroblast transformation. Non-coding RNAs (ncRNAs) are one of the main players in the regulation of multiple pathways and cellular processes. MicroRNAs, long non-coding RNAs, and circular long non-coding RNAs can all interact with the TGF-β/WNT signaling axis to affect cardiac fibrosis. A better understanding of these processes may lead to new approaches for diagnosis and treatment of many cardiac conditions.
has issue date
2020-06-09
(
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bibo:doi
10.1186/s12964-020-00555-4
has license
cc-by
sha1sum (hex)
87d6d2779247358e8c59ffe3446525d257223a3f
schema:url
https://doi.org/10.1186/s12964-020-00555-4
resource representing a document's title
TGF-β and WNT signaling pathways in cardiac fibrosis: non-coding RNAs come into focus
has PubMed Central identifier
PMC7281690
schema:publication
Cell Commun Signal
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covid:87d6d2779247358e8c59ffe3446525d257223a3f#body_text
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of
named entity 'cardiac'
named entity 'long'
named entity 'TGF-β'
named entity 'fibrosis'
named entity 'extracellular matrix'
named entity 'production'
named entity 'signaling pathways'
named entity 'TGF-β'
named entity 'AXIS'
named entity 'PROGRESSION'
named entity 'SIGNALING PATHWAYS'
named entity 'INITIATION'
named entity 'ECM'
named entity 'NEW'
named entity 'INTERACTION'
named entity 'MAIN'
named entity 'FOCUS'
named entity 'SIGNALING'
named entity 'PROTEINS'
named entity 'CELLULAR PROCESSES'
named entity 'molecular'
named entity 'proteins'
named entity 'WNT signaling'
named entity 'non-coding RNAs'
named entity 'ECM'
named entity 'fibroblasts'
named entity 'range'
named entity 'proliferation'
named entity 'pathophysiological'
named entity 'fibrosis'
named entity 'cardiac fibrosis'
named entity 'cardiac conditions'
named entity 'WNT signaling'
named entity 'cardiac fibrosis'
named entity 'WNT signaling'
named entity 'fibroblasts'
named entity 'ECM'
named entity 'CFs'
named entity 'cellular processes'
named entity 'cardiac muscle'
named entity 'cellular processes'
named entity 'TGF-β'
named entity 'lncRNAs'
named entity 'over-expression'
named entity 'TGFβ1'
named entity 'fibrotic'
named entity 'ECM'
named entity 'Smad3'
named entity 'gene expression'
named entity 'cardiac fibrosis'
named entity 'hypertrophy'
named entity 'Wnt signaling'
named entity 'highly conserved'
named entity 'TGF-β'
named entity 'Wnt/β-catenin pathway'
named entity 'Smad-3'
named entity 'expression levels'
named entity 'TGF-β signaling'
named entity 'pharmacological'
named entity 'infarct'
named entity 'signaling pathways'
named entity 'survival rate'
named entity 'signaling pathway'
named entity 'hepatoma'
named entity 'co-receptor'
named entity 'βcatenin'
named entity 'cardiac fibrosis'
named entity 'ligands'
named entity 'Smad4'
named entity 'ncRNAs'
named entity 'miRNAs'
named entity 'receptor'
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