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血小板衍生生长因子/血小板衍生生长因子受体:硬皮病纤维化的一个可能的分子靶点。

PDGF/PDGFR: A Possible Molecular Target in Scleroderma Fibrosis.

机构信息

Department of Clinical and Molecular Sciences, Università Politecnica delle Marche, 60126 Ancona, Italy.

Department of Internal Medicine, Clinica Medica, Ospedali Riuniti "Umberto I-G.M. Lancisi-G. Salesi", 60126 Ancona, Italy.

出版信息

Int J Mol Sci. 2022 Mar 31;23(7):3904. doi: 10.3390/ijms23073904.

Abstract

Systemic sclerosis (SSc) is a clinically heterogeneous disorder of the connective tissue characterized by vascular alterations, immune/inflammatory manifestations, and organ fibrosis. SSc pathogenesis is complex and still poorly understood. Therefore, effective therapies are lacking and remain nonspecific and limited to disease symptoms. In the last few years, many molecular and cellular mediators of SSc fibrosis have been described, providing new potential options for targeted therapies. In this review: (i) we focused on the PDGF/PDGFR pathway as key signaling molecules in the development of tissue fibrosis; (ii) we highlighted the possible role of stimulatory anti-PDGFRα autoantibodies in the pathogenesis of SSc; (iii) we reported the most promising PDGF/PDGFR targeting therapies.

摘要

系统性硬化症(SSc)是一种结缔组织的临床异质性疾病,其特征为血管改变、免疫/炎症表现和器官纤维化。SSc 的发病机制复杂,目前仍知之甚少。因此,有效的治疗方法缺乏,而且仍然是非特异性的,仅限于疾病症状。在过去的几年中,已经描述了许多 SSc 纤维化的分子和细胞介质,为靶向治疗提供了新的潜在选择。在这篇综述中:(i)我们重点关注 PDGF/PDGFR 途径作为组织纤维化发展中的关键信号分子;(ii)我们强调了刺激抗 PDGFRα 自身抗体在 SSc 发病机制中的可能作用;(iii)我们报告了最有前途的 PDGF/PDGFR 靶向治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e7/8999630/e070d57460a8/ijms-23-03904-g001.jpg

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