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 |
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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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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.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.26058</identifier><identifier>PMID: 30279971</identifier><language>eng</language><publisher>United States: Impact Journals LLC</publisher><subject>Review</subject><ispartof>Oncotarget, 2018-09, Vol.9 (70), p.33416-33439</ispartof><rights>Copyright: © 2018 Singer et al. 2018</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3808-c56f2fdc8c245ca2168292f225d2d97f3f1efbf0c885a4c6eee3d921065794e33</citedby><cites>FETCH-LOGICAL-c3808-c56f2fdc8c245ca2168292f225d2d97f3f1efbf0c885a4c6eee3d921065794e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161786/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161786/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30279971$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singer, Jack W</creatorcontrib><creatorcontrib>Fleischman, Angela</creatorcontrib><creatorcontrib>Al-Fayoumi, Suliman</creatorcontrib><creatorcontrib>Mascarenhas, John O</creatorcontrib><creatorcontrib>Yu, Qiang</creatorcontrib><creatorcontrib>Agarwal, Anupriya</creatorcontrib><title>Inhibition of interleukin-1 receptor-associated kinase 1 (IRAK1) as a therapeutic strategy</title><title>Oncotarget</title><addtitle>Oncotarget</addtitle><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. 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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.</abstract><cop>United States</cop><pub>Impact Journals LLC</pub><pmid>30279971</pmid><doi>10.18632/oncotarget.26058</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record> |
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title | Inhibition of interleukin-1 receptor-associated kinase 1 (IRAK1) as a therapeutic strategy |
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