The p38α mitogen-activated protein kinase as a central nervous system drug discovery target

被引:34
作者
Borders, Aaron S. [1 ]
de Almeida, Lucia [2 ]
Van Eldik, Linda J. [1 ,2 ]
Watterson, Martin [1 ,3 ]
机构
[1] Northwestern Univ, Ctr Drug Discovery & Chem Biol, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Cell & Mol Biol, Chicago, IL 60611 USA
[3] Northwestern Univ, Dept Mol Pharmacol & Biol Chem, Chicago, IL 60611 USA
关键词
D O I
10.1186/1471-2202-9-S2-S12
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Protein kinases are critical modulators of a variety of cellular signal transduction pathways, and abnormal phosphorylation events can be a cause or contributor to disease progression in a variety of disorders. This has led to the emergence of protein kinases as an important new class of drug targets for small molecule therapeutics. A serine/threonine protein kinase, p38 alpha mitogen-activated protein kinase ( MAPK), is an established therapeutic target for peripheral inflammatory disorders because of its critical role in regulation of proinflammatory cytokine production. There is increasing evidence that p38a MAPK is also an important regulator of proinflammatory cytokine levels in the central nervous system, raising the possibility that the kinase may be a drug discovery target for central nervous system disorders where cytokine overproduction contributes to disease progression. Development of bioavailable, central nervous system-penetrant p38a MAPK inhibitors provides the required foundation for drug discovery campaigns targeting p38a MAPK in neurodegenerative disorders.
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页数:8
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