a Musculoskeletal Pathology Group, Institute IDIS , Santiago University Clinical Hospital , Santiago de Compostela , Spain.
b Research laboratory 9 (NEIRID LAB), Institute of Medical Research, SERGAS , Santiago University Clinical Hospital , Santiago de Compostela , Spain.
Expert Opin Ther Targets. 2019 Jul;23(7):607-618. doi: 10.1080/14728222.2019.1617274. Epub 2019 May 15.
: The rising prevalence of musculoskeletal pathologies in developed countries has caused a dramatic impact on social welfare. Amidst these musculoskeletal pathologies is Rheumatoid arthritis (RA), a chronic systemic autoimmune disease that mostly affects the synovium. RA metabolic-associated alterations, including distorted adipokine production, enhance RA inflammatory environment. Among the altered adipokines, visfatin is particularly involved in RA inflammation and catabolism and stands out as an essential enzyme linked to critical cell features. : We discuss the potential mechanism supporting the contribution of visfatin to RA and the association between RA and obesity. We discuss the repurposing of cancer-tested drugs to inhibit visfatin in the context of RA. Additionally, we address the possibility of combining these drugs with current RA therapy. Finally, we explore the future of visfatin as an RA biomarker or therapeutic target. : Inhibition of visfatin has become an interesting therapeutic approach for RA pathology. Such a feat has already been attained in oncology using small molecule inhibitors, which suggest that a similar course of action would be worth pursuing in the RA context. Visfatin will become an important biomarker and therapeutic target for RA.
: 发达国家肌肉骨骼疾病的患病率不断上升,对社会福利造成了巨大影响。在这些肌肉骨骼疾病中,类风湿关节炎(RA)是一种主要影响滑膜的慢性系统性自身免疫性疾病。RA 的代谢相关改变,包括脂联素产生的扭曲,增强了 RA 的炎症环境。在改变的脂联素中,内脂素特别参与 RA 炎症和分解代谢,并成为与关键细胞特征相关的必需酶。 : 我们讨论了支持内脂素对 RA 贡献的潜在机制以及 RA 和肥胖之间的关联。我们讨论了在 RA 背景下使用经过癌症测试的药物抑制内脂素的重新利用。此外,我们还探讨了将这些药物与当前的 RA 治疗相结合的可能性。最后,我们探讨了内脂素作为 RA 生物标志物或治疗靶点的未来。 : 内脂素抑制已成为 RA 病理学的一种有趣的治疗方法。在肿瘤学中已经使用小分子抑制剂实现了这一目标,这表明在 RA 背景下采取类似的行动是值得的。内脂素将成为 RA 的重要生物标志物和治疗靶点。