Inhibition of interleukin-1 receptor-associated kinase 1 (IRAK1) as a therapeutic strategy

Interleukin-1 receptor-associated kinases (IRAK1, IRAK2, IRAK3 [IRAK-M], and IRAK4) are serine-threonine kinases involved in toll-like receptor and interleukin-1 signaling pathways, through which they regulate innate immunity and inflammation. Evidence exists that IRAKs play key roles in the pathoph...

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Veröffentlicht in:Oncotarget 2018-09, Vol.9 (70), p.33416-33439
Hauptverfasser: Singer, Jack W, Fleischman, Angela, Al-Fayoumi, Suliman, Mascarenhas, John O, Yu, Qiang, Agarwal, Anupriya
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container_end_page 33439
container_issue 70
container_start_page 33416
container_title Oncotarget
container_volume 9
creator Singer, Jack W
Fleischman, Angela
Al-Fayoumi, Suliman
Mascarenhas, John O
Yu, Qiang
Agarwal, Anupriya
description Interleukin-1 receptor-associated kinases (IRAK1, IRAK2, IRAK3 [IRAK-M], and IRAK4) are serine-threonine kinases involved in toll-like receptor and interleukin-1 signaling pathways, through which they regulate innate immunity and inflammation. Evidence exists that IRAKs play key roles in the pathophysiologies of cancers, and metabolic and inflammatory diseases, and that IRAK inhibition has potential therapeutic benefits. Molecules capable of selectively interfering with IRAK function and expression have been reported, paving the way for the clinical evaluation of IRAK inhibition. Herein, we focus on IRAK1, review its structure and physiological roles, and summarize emerging data for IRAK1 inhibitors in preclinical and clinical studies.
doi_str_mv 10.18632/oncotarget.26058
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title Inhibition of interleukin-1 receptor-associated kinase 1 (IRAK1) as a therapeutic strategy
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