Phytochemicals targeting JAK/STAT pathway in the treatment of rheumatoid arthritis: Is there a future?

托法替尼 斯达 医学 JAK-STAT信号通路 类风湿性关节炎 贾纳斯激酶 耐受性 药理学 免疫学 不利影响 托珠单抗 细胞因子 内科学 信号转导 受体 车站3 生物 酪氨酸激酶 生物化学
作者
Gurleen Kour,Rupali Choudhary,Sobia Anjum,Asha Bhagat,Bijender Kumar Bajaj,Zabeer Ahmed
出处
期刊:Biochemical Pharmacology [Elsevier BV]
卷期号:197: 114929-114929 被引量:19
标识
DOI:10.1016/j.bcp.2022.114929
摘要

Rheumatoid arthritis (RA) is a chronic autoimmune disorder and the treatment involves the use of traditional and biological disease modifying anti-rheumatic drugs (DMARDs). Recent studies have shown JAK/STAT signaling pathway as potential target for the treatment of RA. Novel JAK/STAT inhibitors viz tofacitinib and baricitinib have been recently approved by FDA for RA treatment and have attained substantial importance. However, the discernible risks of thromboembolism, gastrointestinal (GIT) perforations, hepatotoxicity and serious infections including tuberculosis, herpes zoster associated with their administration cannot be overlooked. Furthermore, these are highly expensive which limits their application for a broader use. These limitations provide the basis of exploring novel JAK/STAT inhibitors of natural origin with increased tolerability, safety and cost-effectiveness. In this review we confer an account of various natural compounds/phytochemicals that have proved to be beneficial in attenuating inflammation in RA via modulation of JAK/STAT signaling pathway. Some of these natural compounds including resveratrol have clearly indicated biochemical and clinically significant therapeutic effects in ameliorating RA both in vivo and in clinical settings. We further discuss the physicochemical challenges of poor solubility and absorption coupled with the use of natural JAK/STAT inhibitors. We thereafter discuss and summarize various drug delivery systems (DDS) to confront the physicochemical limitations of natural JAK/STAT inhibitors with the aim to enhance the therapeutic efficacy. Overall the review unveils the potential of natural JAK/STAT inhibitors as a cost-effective approach in ameliorating RA without incorporating the risks of adverse repercussions, thus setting the stage for clinical exploration of these compounds that may possibly complement the present RA therapy.
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