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血管生成抑制作为炎症性滑膜炎的一种治疗方法。

Angiogenesis inhibition as a therapeutic approach for inflammatory synovitis.

作者信息

Lainer-Carr Dahlia, Brahn Ernest

机构信息

Rheumatology Fellowship Program, UCLA School of Medicine, University of California-Los Angeles, 1000 Veteran Avenue, Los Angeles, CA 90095, USA.

出版信息

Nat Clin Pract Rheumatol. 2007 Aug;3(8):434-42. doi: 10.1038/ncprheum0559.

Abstract

Angiogenesis inhibition, long studied in the treatment of malignancies, has begun to emerge as a potential therapeutic approach in managing inflammatory arthritis, particularly rheumatoid arthritis. The growth of new vessels is required for the development of the rheumatoid pannus, which then leads to extensive synovial inflammation and joint destruction. Vascular endothelial growth factor is the best studied mediator of angiogenesis, and several therapies have been developed that specifically target this molecule. Several other angiogenesis mediators, such as the angiopoietin-TIE system, hypoxia inducible factor and integrin alpha(V)beta(3), as well as naturally occurring inhibitors of angiogenesis, are also being investigated as potential therapeutic targets. Additionally, there are a number of drugs, including paclitaxel, 2-methoxyestradiol and fumagillin analogs, that might have a role in inhibiting angiogenesis and, thus, in treating proliferative synovitis.

摘要

血管生成抑制在恶性肿瘤治疗领域已被研究多年,如今开始成为治疗炎性关节炎(尤其是类风湿性关节炎)的一种潜在治疗方法。类风湿性血管翳的形成需要新血管的生长,进而导致广泛的滑膜炎和关节破坏。血管内皮生长因子是研究最为深入的血管生成介质,目前已开发出多种特异性靶向该分子的疗法。其他几种血管生成介质,如血管生成素 - TIE系统、缺氧诱导因子和整合素α(V)β(3),以及天然存在的血管生成抑制剂,也正在作为潜在的治疗靶点进行研究。此外,还有多种药物,包括紫杉醇、2 - 甲氧基雌二醇和烟曲霉素类似物,可能在抑制血管生成以及治疗增生性滑膜炎方面发挥作用。

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