{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Hollenhorst PC"],"funding":["NCI NIH HHS","NIGMS NIH HHS"],"pagination":["1044-1052"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3046414"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["1(10)"],"pubmed_abstract":["Chromosomal abnormalities that give rise to elevated expression levels of the ETS genes ETV1, ETV4, ETV5, or ERG are prevalent in prostate cancer, but the function of these transcription factors in carcinogenesis is not clear. Previous work in cell lines implicates ERG, ETV1, and ETV5 as regulators of invasive growth but not transformation. Here we show that the PC3 prostate cancer cell line provides a model system to study the over-expression of ETV4. Migration assays, anchorage independent growth assays, and microarray analysis indicate that high ETV4 expression contributes to both transformation and cellular motility in PC3 cells. ETV4 directly bound the 5' and 3' MYC enhancers and modulated expression of both MYC and other cell proliferation genes, demonstrating a potential role in cel"],"journal":["Genes & cancer"],"pubmed_title":["The ETS gene ETV4 is required for anchorage-independent growth and a cell proliferation gene expression program in PC3 prostate cells."],"pmcid":["PMC3046414"],"funding_grant_id":["P30 CA042014","P30 CA042014-21","R01 GM038663"],"pubmed_authors":["Paul L","Graves BJ","Hollenhorst PC","Ferris MW"],"additional_accession":[]},"is_claimable":false,"name":"The ETS gene ETV4 is required for anchorage-independent growth and a cell proliferation gene expression program in PC3 prostate cells.","description":"Chromosomal abnormalities that give rise to elevated expression levels of the ETS genes ETV1, ETV4, ETV5, or ERG are prevalent in prostate cancer, but the function of these transcription factors in carcinogenesis is not clear. Previous work in cell lines implicates ERG, ETV1, and ETV5 as regulators of invasive growth but not transformation. Here we show that the PC3 prostate cancer cell line provides a model system to study the over-expression of ETV4. Migration assays, anchorage independent growth assays, and microarray analysis indicate that high ETV4 expression contributes to both transformation and cellular motility in PC3 cells. ETV4 directly bound the 5' and 3' MYC enhancers and modulated expression of both MYC and other cell proliferation genes, demonstrating a potential role in cel","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Jan","modification":"2025-04-05T16:04:07.721Z","creation":"2019-06-06T22:41:20Z"},"accession":"S-EPMC3046414","cross_references":{"pubmed":["21373373"],"doi":["10.1177/1947601910395578"]}}