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基质金属蛋白酶 13 作为治疗骨关节炎有前景的靶点概述。

Overview of MMP-13 as a Promising Target for the Treatment of Osteoarthritis.

机构信息

Department of Biomedical Engineering, University of North Texas, Denton, TX 76203, USA.

出版信息

Int J Mol Sci. 2021 Feb 9;22(4):1742. doi: 10.3390/ijms22041742.

Abstract

Osteoarthritis (OA) is a common degenerative disease characterized by the destruction of articular cartilage and chronic inflammation of surrounding tissues. Matrix metalloproteinase-13 (MMP-13) is the primary MMP involved in cartilage degradation through its particular ability to cleave type II collagen. Hence, it is an attractive target for the treatment of OA. However, the detailed molecular mechanisms of OA initiation and progression remain elusive, and, currently, there are no interventions available to restore degraded cartilage. This review fully illustrates the involvement of MMP-13 in the initiation and progression of OA through the regulation of MMP-13 activity at the molecular and epigenetic levels, as well as the strategies that have been employed against MMP-13. The aim of this review is to identify MMP-13 as an attractive target for inhibitor development in the treatment of OA.

摘要

骨关节炎(OA)是一种常见的退行性疾病,其特征为关节软骨破坏和周围组织的慢性炎症。基质金属蛋白酶-13(MMP-13)是通过其特定的切割 II 型胶原的能力而主要参与软骨降解的 MMP。因此,它是治疗 OA 的一个有吸引力的靶点。然而,OA 起始和进展的详细分子机制仍不清楚,目前尚无可用于恢复退化软骨的干预措施。本综述通过在分子和表观遗传水平上调节 MMP-13 的活性,全面说明了 MMP-13 参与 OA 的起始和进展,以及针对 MMP-13 所采用的策略。本综述的目的是确定 MMP-13 作为治疗 OA 的抑制剂开发的有吸引力的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cd7/7916132/17b05dd9ffc7/ijms-22-01742-g001.jpg

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