Biology of hypoxia-inducible factor-2α in development and disease
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作者:
Patel, S. A.
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Univ Penn, Dept Cell & Dev Biol, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USAUniv Penn, Dept Cell & Dev Biol, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
Patel, S. A.
[1
]
Simon, M. C.
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Univ Penn, Dept Cell & Dev Biol, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
Howard Hughes Med Inst, Dept Cell & Dev Biol, Philadelphia, PA USAUniv Penn, Dept Cell & Dev Biol, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
Simon, M. C.
[1
,2
]
机构:
[1] Univ Penn, Dept Cell & Dev Biol, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Howard Hughes Med Inst, Dept Cell & Dev Biol, Philadelphia, PA USA
The transcriptional response to hypoxia is primarily mediated by two hypoxia-inducible factors -HIF-1 alpha and HIF-2 alpha. While these proteins are highly homologous, increasing evidence suggests they have unique transcriptional targets and differential impact on tumor growth. Furthermore, non-transcriptional effects of the HIF-alpha subunits, including effects on the Notch and c-Myc pathways, contribute to their distinct functions. HIF-2 alpha transcriptional targets include genes involved in erythropoiesis, angiogenesis, metastasis, and proliferation. Therefore, HIF-2 alpha contributes significantly to both normal physiology as well as tumorigenesis. Here, we summarize the function of HIF-2 alpha during development as well as its contribution to pathologic conditions, such as tumors and vascular disease.