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Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity
The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF...
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Published in: | Frontiers in cell and developmental biology 2016-02, Vol.4, p.11-11 |
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description | The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF α-subunits also respond to various growth factors, hormones, or cytokines under normoxia indicating involvement of different kinase pathways in their regulation. Because these proteins participate in angiogenesis, glycolysis, programmed cell death, cancer, and ischemia, HIFα regulating kinases are attractive therapeutic targets. Although numerous kinases were reported to regulate HIFα indirectly, direct phosphorylation of HIFα affects HIFα stability, nuclear localization, and transactivity. Herein, we review the role of phosphorylation-dependent HIFα regulation with emphasis on protein stability, subcellular localization, and transactivation. |
doi_str_mv | 10.3389/fcell.2016.00011 |
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Herein, we review the role of phosphorylation-dependent HIFα regulation with emphasis on protein stability, subcellular localization, and transactivation.</description><subject>HIF-1α</subject><subject>hypoxia</subject><subject>kinase</subject><subject>MAPK pathway</subject><subject>Oncology</subject><subject>Phosphorylation</subject><subject>PI3K/PKB pathway</subject><issn>2296-634X</issn><issn>2296-634X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkc9rFDEYhoMottTePckcK3TW_JjJJB4EKa47sKBgBW_hSybpZpmdjMlscf3rzc7W0p4Skud98pEXobcELxgT8oMztu8XFBO-wBgT8gKdUyp5yVn16-WT_Rm6TGl7RGjd1IK9RmeUy4qSRp6j7eowhj8eynbo9sbr3hZLMFOIqbhatcv0voChK75vQho3IR56mHwYPhbtbsxUEYbixwTa9346XBfrYKD3f2fkes7dRhhSBv19Bt6gVw76ZC8f1gv0c_nl9mZVrr99bW8-r0tTUzGVUrquAyowNdoSrB2rGl4LUnNHgXMumeBau6qz1BgtBWHUOUM7pl1Xa8HZBWpP3i7AVo3R7yAeVACv5oMQ7xTEyZveKgaQPc5UttIVNQJEzY0koFn-LF6J7Pp0co17vbOdscMUoX8mfX4z-I26C_cqz8ywaLLg6kEQw--9TZPa-XQsDgYb9kmRpslYw2qZUXxCTQwpResenyFYHRtXc-Pq2LiaG8-Rd0_Hewz875f9Ayxrqg0</recordid><startdate>20160223</startdate><enddate>20160223</enddate><creator>Kietzmann, Thomas</creator><creator>Mennerich, Daniela</creator><creator>Dimova, Elitsa Y</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160223</creationdate><title>Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity</title><author>Kietzmann, Thomas ; Mennerich, Daniela ; Dimova, Elitsa Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>HIF-1α</topic><topic>hypoxia</topic><topic>kinase</topic><topic>MAPK pathway</topic><topic>Oncology</topic><topic>Phosphorylation</topic><topic>PI3K/PKB pathway</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kietzmann, Thomas</creatorcontrib><creatorcontrib>Mennerich, Daniela</creatorcontrib><creatorcontrib>Dimova, Elitsa Y</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in cell and developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kietzmann, Thomas</au><au>Mennerich, Daniela</au><au>Dimova, Elitsa Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity</atitle><jtitle>Frontiers in cell and developmental biology</jtitle><addtitle>Front Cell Dev Biol</addtitle><date>2016-02-23</date><risdate>2016</risdate><volume>4</volume><spage>11</spage><epage>11</epage><pages>11-11</pages><issn>2296-634X</issn><eissn>2296-634X</eissn><abstract>The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF α-subunits also respond to various growth factors, hormones, or cytokines under normoxia indicating involvement of different kinase pathways in their regulation. Because these proteins participate in angiogenesis, glycolysis, programmed cell death, cancer, and ischemia, HIFα regulating kinases are attractive therapeutic targets. Although numerous kinases were reported to regulate HIFα indirectly, direct phosphorylation of HIFα affects HIFα stability, nuclear localization, and transactivity. 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subjects | HIF-1α hypoxia kinase MAPK pathway Oncology Phosphorylation PI3K/PKB pathway |
title | Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity |
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