TRAF6 Upregulates Expression of HIF-1a and Promotes Tumor Angiogenesis

نویسندگان

  • Heng Sun
  • Xue-Bing Li
  • Ya Meng
  • Li Fan
  • Min Li
  • Jing Fang
چکیده

TNF receptor (TNFR)–associated factor TRAF6 is a key activator of NF-kB, playing a critical role in the regulation of innate immune responses and their connection to adaptive immune responses. TRAF6 interactions determine receptor-induced cell death versus survival. TRAF6 has been implicated in cancer but its contributions have not been investigated deeply. In this study, we show that TRAF6 upregulates expression of hypoxia-inducible factor (HIF)–1a. TRAF6 affects HIF-1a protein levels but has little effect on mRNA level. TRAF6 increases HIF-1a protein independent of oxygen. We found that TRAF6 binds HIF-1a and mediates its K63-linked polyubiquitination. The E3 ligase activity of TRAF6 was required to increase HIF-1a protein levels. Finally, we showed that TRAF6 promoted tumor angiogenesis and growth. Our results reveal how TRAF6 functions to upregulate HIF-1a expression and promote tumor angiogenesis. Cancer Res; 73(15);

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تاریخ انتشار 2013