Literature DB >> 25305493

Dimethyl fumarate protection against collagen II degradation.

Ye Li, Jie Tang, Yong Hu.   

Abstract

Degradation of collagen type II caused by pro-inflammatory cytokines such as tumor necrosis factor alpha (TNF-α) is one of the major pathological characteristics of osteoarthritis (OA). Dimethyl fumarate (DMF) is a medication approved by the US Food and Drug Administration (FDA) as an oral multiple sclerosis (MS) therapy. In this study, we found that DMF ameliorated collagen type II degradation by inhibiting the expression of MMP-1, MMP-3, and MMP-13 caused by TNF-α. Mechanistically, DMF attenuated MMPs expression by suppressing JAK/STAT3 pathway. These findings imply that DMF treatment might be a potential therapeutic strategy for chondroprotective therapy.

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Year:  2014        PMID: 25305493     DOI: 10.1016/j.bbrc.2014.10.005

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Activation of the cannabinoid receptor 1 by ACEA suppresses senescence in human primary chondrocytes through sirt1 activation.

Authors:  Dawei Zhang; Gang Zhang; Zongyu Li; Bingsheng Li
Journal:  Exp Biol Med (Maywood)       Date:  2018-02-14

Review 2.  Utilization of Dimethyl Fumarate and Related Molecules for Treatment of Multiple Sclerosis, Cancer, and Other Diseases.

Authors:  Zaidoon Al-Jaderi; Azzam A Maghazachi
Journal:  Front Immunol       Date:  2016-07-22       Impact factor: 7.561

Review 3.  Lymphocyte Counts and Multiple Sclerosis Therapeutics: Between Mechanisms of Action and Treatment-Limiting Side Effects.

Authors:  Stefanie Fischer; Undine Proschmann; Katja Akgün; Tjalf Ziemssen
Journal:  Cells       Date:  2021-11-15       Impact factor: 6.600

Review 4.  Nrf2-mediated anti-inflammatory polarization of macrophages as therapeutic targets for osteoarthritis.

Authors:  Lin Wang; Chengqi He
Journal:  Front Immunol       Date:  2022-08-12       Impact factor: 8.786

  4 in total

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