Progress in the development of kinase inhibitors for treating asthma and COPD.

Q1 Pharmacology, Toxicology and Pharmaceutics
Advances in pharmacology Pub Date : 2023-01-01 Epub Date: 2023-05-03 DOI:10.1016/bs.apha.2023.04.004
Nathaniel McClean, Jeffery D Hasday, Paul Shapiro
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引用次数: 0

Abstract

Current therapies to mitigate inflammatory responses involved in airway remodeling and associated pathological features of asthma and chronic obstructive pulmonary disease (COPD) are limited and largely ineffective. Inflammation and the release of cytokines and growth factors activate kinase signaling pathways that mediate changes in airway mesenchymal cells such as airway smooth muscle cells and lung fibroblasts. Proliferative and secretory changes in mesenchymal cells exacerbate the inflammatory response and promote airway remodeling, which is often characterized by increased airway smooth muscle mass, airway hyperreactivity, increased mucus secretion, and lung fibrosis. Thus, inhibition of relevant kinases has been viewed as a potential therapeutic approach to mitigate the debilitating and, thus far, irreversible airway remodeling that occurs in asthma and COPD. Despite FDA approval of several kinase inhibitors for the treatment of proliferative disorders, such as cancer and inflammation associated with rheumatoid arthritis and ulcerative colitis, none of these drugs have been approved to treat asthma or COPD. This review will provide a brief overview of the role kinases play in the pathology of asthma and COPD and an update on the status of kinase inhibitors currently in clinical trials for the treatment of obstructive pulmonary disease. In addition, potential issues associated with the current kinase inhibitors, which have limited their success as therapeutic agents in treating asthma or COPD, and alternative approaches to target kinase functions will be discussed.

激酶抑制剂治疗哮喘和慢性阻塞性肺病的研究进展。
目前缓解哮喘和慢性阻塞性肺病(COPD)气道重塑和相关病理特征所涉及的炎症反应的疗法是有限的,并且在很大程度上是无效的。炎症和细胞因子和生长因子的释放激活激酶信号通路,介导气道间充质细胞(如气道平滑肌细胞和肺成纤维细胞)的变化。间充质细胞的增殖和分泌变化加剧了炎症反应并促进气道重塑,其特征通常是气道平滑肌质量增加、气道高反应性、粘液分泌增加和肺纤维化。因此,抑制相关激酶已被视为一种潜在的治疗方法,可以缓解哮喘和COPD中发生的使人衰弱且迄今为止不可逆的气道重塑。尽管FDA批准了几种激酶抑制剂用于治疗增生性疾病,如癌症和类风湿性关节炎和溃疡性结肠炎相关的炎症,但这些药物均未被批准用于治疗哮喘或COPD。这篇综述将简要概述激酶在哮喘和COPD病理学中的作用,并介绍目前在治疗阻塞性肺病的临床试验中激酶抑制剂的最新情况。此外,还将讨论与当前激酶抑制剂相关的潜在问题,这些问题限制了它们作为治疗哮喘或COPD的治疗剂的成功,以及靶向激酶功能的替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
自引率
0.00%
发文量
45
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