(2020) TGF-beta and WNT signaling pathways in cardiac fibrosis: non-coding RNAs come into focus. Cell Communication and Signaling.
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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-beta 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-beta 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-beta/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.
Item Type: | Article |
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Keywords: | Cardiac fibrosis TGF-beta WNT signaling Non-coding RNAs PROMOTES MYOCARDIAL FIBROSIS FRIZZLED-RELATED PROTEIN-2 WNT/BETA-CATENIN PATHWAY EXTRACELLULAR-MATRIX TRANSFORMING GROWTH-FACTOR-BETA-1 DOWN-REGULATION HEART-FAILURE MYOFIBROBLAST DIFFERENTIATION DILATED CARDIOMYOPATHY DIASTOLIC DYSFUNCTION |
Subjects: | QZ Pathology > QZ 140-180 Pathologic Processes Cardiovascular System > WG 200-460 Heart. Heart Diseases |
Divisions: | Faculty of Medicine > Departments of Clinical Sciences > Department of Pathology |
Journal or Publication Title: | Cell Communication and Signaling |
Journal Index: | ISI |
Volume: | 18 |
Number: | 1 |
Identification Number: | https://doi.org/10.1186/s12964-020-00555-4 |
Depositing User: | Zahra Otroj |
URI: | http://eprints.mui.ac.ir/id/eprint/13885 |
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