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让我们聚焦于掌腱膜挛缩症中的纤维化:细胞通讯网络因子2作为一个新靶点。

Let's Focus on the Fibrosis in Dupuytren Disease: Cell Communication Network Factor 2 as a Novel Target.

作者信息

Lambi Alex G, Morrell Nathan T, Popoff Steven N, Benhaim Prosper, Barbe Mary F

机构信息

Department of Orthopedics and Rehabilitation, University of New Mexico School of Medicine, Albuquerque, NM.

Department of Surgery Division of Plastic Surgery, University of New Mexico School of Medicine, Albuquerque, NM.

出版信息

J Hand Surg Glob Online. 2023 Aug 1;5(5):682-688. doi: 10.1016/j.jhsg.2023.06.017. eCollection 2023 Sep.

Abstract

Dupuytren disease is a progressive, benign fibroproliferative disorder of the hands that can lead to debilitating hand contractures. Once symptomatic, treatment involves either surgical intervention, specifically fasciectomy or percutaneous needle aponeurotomy, or enzymatic degradation with clostridial collagenase. Currently, collagenase is the only pharmacotherapy that has been approved for the treatment of Dupuytren contracture. There is a need for a pharmacotherapeutic that can be administered to limit disease progression and prevent recurrence after treatment. Targeting the underlying fibrotic pathophysiology is critical. We propose a novel target to be considered in Dupuytren disease-cell communication network factor 2/connective tissue growth factor-an established mediator of musculoskeletal tissue fibrosis.

摘要

掌腱膜挛缩症是一种手部进行性良性纤维增生性疾病,可导致手部挛缩,使人衰弱。一旦出现症状,治疗方法包括手术干预,特别是筋膜切除术或经皮针状腱膜切开术,或使用梭菌胶原酶进行酶降解。目前,胶原酶是唯一被批准用于治疗掌腱膜挛缩症的药物疗法。需要一种可以给药以限制疾病进展并防止治疗后复发的药物疗法。针对潜在的纤维化病理生理学至关重要。我们提出了一个在掌腱膜挛缩症中需要考虑的新靶点——细胞通讯网络因子2/结缔组织生长因子,这是一种已确定的肌肉骨骼组织纤维化介质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e97/10543811/5747c15dcc80/gr1.jpg

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