Mouse Gene Set: QI_HYPOXIA_TARGETS_OF_HIF1A_AND_FOXA2

For the Human gene set with the same name, see QI_HYPOXIA_TARGETS_OF_HIF1A_AND_FOXA2

Standard name QI_HYPOXIA_TARGETS_OF_HIF1A_AND_FOXA2
Systematic name MM885
Brief description Genes up-regulated by hypoxia in TRAMP-C cells (prostatic cancer) expressing HIF1A and FOXA2 [GeneID=3091] [GeneID=3170] off plasmid vectors.
Full description or abstract Neuroendocrine (NE) phenotype, seen in >30% of prostate adenocarcinomas (PCa), and NE prostate tumors are implicated in aggressive prostate cancer. Formation of NE prostate tumors in the TRAMP mouse model was suppressed in mice lacking the ubiquitin ligase Siah2, which regulates HIF-1alpha availability. Cooperation between HIF-1alpha and FoxA2, a transcription factor expressed in NE tissue, promotes recruitment of p300 to transactivate select HIF-regulated genes, Hes6, Sox9, and Jmjd1a. These HIF-regulated genes are highly expressed in metastatic PCa and required for hypoxia-mediated NE phenotype, metastasis in PCa, and the formation of NE tumors. Tissue-specific expression of FoxA2 combined with Siah2-dependent HIF-1alpha availability enables a transcriptional program required for NE prostate tumor development and NE phenotype in PCa.
Collection M2: Curated
      CGP: Chemical and Genetic Perturbations
Source publication Pubmed 20609350   Authors: Qi J,Nakayama K,Cardiff RD,Borowsky AD,Kaul K,Williams R,Krajewski S,Mercola D,Carpenter PM,Bowtell D,Ronai ZA
Exact source Table 3S
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Source species Mus musculus
Contributed by Arthur Liberzon (MSigDB Team)
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identifier namespace		 Mouse_RefSeq
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Version history 2022.1.Mm: First Introduced.

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