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      Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway

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          Abstract

          Idiopathic pulmonary fibrosis is a progressive lung disease with high mortality and limited therapy that is characterized by epithelial cell damage and fibroblast activation. Ellagic acid is a natural polyphenol compound widely found in fruits and nuts that has multiple pharmacological activities. In this study, we explored the potential effects and mechanisms of Ellagic acid on pulmonary fibrosis in vivo and in vitro. In vivo studies showed that Ellagic acid significantly alleviated bleomycin (BLM)-induced pulmonary fibrosis in mice. In vitro experiments indicated that Ellagic acid could suppress Wnt signaling and attenuate Wnt3a-induced myofibroblast activation and the phosphorylation of Erk2 and Akt. Further studies showed that Ellagic acid could induce autophagy formation in myofibroblasts mainly by suppressing mTOR signaling and promoting apoptosis of myofibroblasts. In vivo experiments revealed that Ellagic acid significantly inhibited myofibroblast activation and promoted autophagy formation. Taken together, our results show that Ellagic acid effectively attenuates BLM-induced pulmonary fibrosis in mice by suppressing myofibroblast activation and promoting autophagy and apoptosis of myofibroblasts by inhibiting the Wnt signaling pathway.

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          Most cited references62

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          Wnt/β-catenin signaling and disease.

          The WNT signal transduction cascade controls myriad biological phenomena throughout development and adult life of all animals. In parallel, aberrant Wnt signaling underlies a wide range of pathologies in humans. In this Review, we provide an update of the core Wnt/β-catenin signaling pathway, discuss how its various components contribute to disease, and pose outstanding questions to be addressed in the future. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Autophagy is a lysosomal degradation pathway that is essential for survival, differentiation, development, and homeostasis. Autophagy principally serves an adaptive role to protect organisms against diverse pathologies, including infections, cancer, neurodegeneration, aging, and heart disease. However, in certain experimental disease settings, the self-cannibalistic or, paradoxically, even the prosurvival functions of autophagy may be deleterious. This Review summarizes recent advances in understanding the physiological functions of autophagy and its possible roles in the causation and prevention of human diseases.
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                12 April 2021
                2021
                : 12
                : 639574
                Affiliations
                [ 1 ]State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin, China
                [ 2 ]Tianjin Key Laboratory of Molecular Drug Research, Tianjin International Joint Academy of Biomedicine, Tianjin, China
                [ 3 ]Department of Thoracic Surgery, Tianjin First Central Hospital, Tianjin, China
                Author notes

                Edited by: Johnatas Dutra Silva, Queen’s University Belfast, United Kingdom

                Reviewed by: Elga Bandeira, Karolinska Institutet (KI), Sweden

                Antonio Molino, University of Naples Federico II, Italy

                Luisa Helena Andrade Da Silva, Northwestern University, United States

                This article was submitted to Respiratory Pharmacology, a section of the journal Frontiers in Pharmacology

                [†]

                These authors have contributed equally to this work and share first authorship

                Article
                639574
                10.3389/fphar.2021.639574
                8072668
                33912053
                bd6737d9-abe5-4a65-a1de-db1a1aa90382
                Copyright © 2021 Li, Huang, Liu, Ruan, Ma, Liang, Cui, Wang, Wu, Li, Wei, Li, Gao, Yang, Li, Yang, Zhou and Yang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 09 December 2020
                : 23 February 2021
                Categories
                Pharmacology
                Original Research

                Pharmacology & Pharmaceutical medicine
                pulmonary fibrosis,ellagic acid,myofibroblasts,autophagy,apoptosis,wnt

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