The journey of p38 MAP kinase inhibitors: From bench to bedside in treating inflammatory diseases

被引:1
|
作者
Yang, Fuwei [1 ]
Zhao, Li-Jie [3 ]
Xu, Qinli [2 ]
Zhao, Jianhui [2 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Dept Neurosurg, Changchun, Peoples R China
[2] Jilin Univ, China Japan Union Hosp, Dept Orthoped, Changchun, Peoples R China
[3] Univ Michigan, Rogel Canc Ctr, Dept Internal Med, Ann Arbor, MI 48109 USA
关键词
p38 MAP inhibitors; Clinical trials; Inflammation; MAPK; ACTIVATED PROTEIN-KINASE; PYRIMIDINYLIMIDAZOLE INHIBITORS; DISCOVERY; DESIGN; POTENT; DRUG; PROLIFERATION; BIRB796; STRESS; SD0006;
D O I
10.1016/j.ejmech.2024.116950
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The p38 mitogen-activated protein kinase (MAPK) pathway is pivotal in regulating inflammatory responses and has emerged as a key target for the development of small-molecule inhibitors aimed at treating inflammatory diseases. In arthritis, especially rheumatoid arthritis (RA), the p38 MAPK pathway contributes to chronic inflammation and joint destruction by promoting the production of pro-inflammatory cytokines. Preclinical studies have shown that small-molecule inhibitors targeting the p38 MAPK pathway hold significant promise, exhibiting the potential to reduce inflammation and preserve joint integrity. Targeting this pathway presents a novel therapeutic approach to mitigating inflammation. This review traces the evolution of p38 MAP kinase inhibitors from initial laboratory studies to clinical candidates, underscoring their potential to significantly alter the treatment approach for inflammatory diseases.
引用
收藏
页数:17
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