布鲁顿的酪氨酸激酶抑制剂:癌症、自身免疫性疾病、GVHD和COVID-19的多功能治疗方法。

IF 3.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Swati Paliwal, Uma Agarwal, Rajiv Kumar Tonk
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引用次数: 0

摘要

最近的趋势表明,各种具有重要医学意义的化合物的发展,这些化合物特异性地靶向b细胞受体(BCR)通路的各个片段,这些片段在布鲁顿酪氨酸激酶(BTK)受体中起主要作用,该受体属于激酶家族。这些激酶通常位于细胞膜附近,因此它们参与BCR信号的上游加工。各种分子已被潜在地靶向这些激酶受体的信号通路,以达到药理作用。鉴于BTK在免疫中的核心作用,BTK抑制是治疗多种疾病的一种有希望的治疗方法。BTK抑制剂通过调节b细胞受体信号以及炎症途径和免疫细胞相互作用起作用,与传统疗法相比,提供了更先进的治疗选择。除了BTK抑制剂外,为了更准确地预测患者何时何地需要联合治疗或仅使用一种药物,对这些受体阻断的药理学机制的广泛了解也是必要的。努力促进转化发现、药物再利用概念和精准医疗产品的进一步发展。这项全面的文献研究集中在2025年6月之前发表的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bruton's Tyrosine Kinase Inhibitors: A Versatile Therapeutic Approach for Cancer, Autoimmune Disorders, GVHD, and COVID-19.

Recent trends have shown the development of various medicinally important compounds that specifically target B-cell receptor (BCR) pathways at various segments that have a major role in Bruton's tyrosine kinase (BTK) receptor, which belongs to the family of kinases. These kinases are usually situated close to the cell membrane due to which they participate in upstream processing of BCR signalling. Various molecules have been potentialized to target these signalling pathways of these kinase receptors in order to achieve a pharmacological effect. Given the central role of BTK in immunity, BTK inhibition represents a promising therapeutic approach for the treatment of multiple diseases. BTK inhibitors work by regulating B-cell receptor signalling along with inflammatory pathways and immune cell interactions, offering more advanced treatment options compared to traditional therapies. In addition to BTK inhibitors, an extensive knowledge of the pharmacological mechanisms underlying the blockage of these receptors is necessary in order to more accurately forecast when and where a patient could need combination therapy or just one medication. Efforts have been made to facilitate translational discoveries, drug re-purposing concepts, and further development of precision medicine products. This thorough literature study has focused on studies published until June 2025.

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来源期刊
CiteScore
7.80
自引率
0.00%
发文量
231
审稿时长
6 months
期刊介绍: The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines. Mini-Reviews in Medicinal Chemistry covers all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies. Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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