ETV4 promotes metastasis in response to activation of PI3-kinase and Ras signaling in a mouse model of advanced prostate cancer Journal Article


Authors: Aytes, A.; Mitrofanova, A.; Kinkade, C. W.; Lefebvre, C.; Lei, M.; Phelan, V.; LeKaye, H. C.; Koutcher, J. A.; Cardiff, R. D.; Califano, A.; Shen, M. M.; Abate-Shen, C.
Article Title: ETV4 promotes metastasis in response to activation of PI3-kinase and Ras signaling in a mouse model of advanced prostate cancer
Abstract: Combinatorial activation of PI3-kinase and RAS signaling occurs frequently in advanced prostate cancer and is associated with adverse patient outcome. We now report that the oncogenic Ets variant 4 (Etv4) promotes prostate cancer metastasis in response to coactivation of PI3-kinase and Ras signaling pathways in a genetically engineered mouse model of highly penetrant, metastatic prostate cancer. Using an inducible Cre driver to simultaneously inactivate Pten while activating oncogenic Kras and a fluorescent reporter allele in the prostate epithelium, we performed lineage tracing in vivo to define the temporal and spatial occurrence of prostate tumors, disseminated tumor cells, and metastases. These analyses revealed that though disseminated tumors cells arise early following the initial occurrence of prostate tumors, there is a significant temporal lag in metastasis, which is temporally coincident with the up-regulation of Etv4 expression in primary tumors. Functional studies showed that knockdown of Etv4 in a metastatic cell line derived from the mouse model abrogates the metastatic phenotype but does not affect tumor growth. Notably, expression and activation of ETV4, but not other oncogenic ETS genes, is correlated with activation of both PI3-kinase and Ras signaling in human prostate tumors and metastases. Our findings indicate that ETV4 promotes metastasis in prostate tumors that have activation of PI3-kinase and Ras signaling, and therefore, ETV4 represents a potential target of therapeutic intervention for metastatic prostate cancer.
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 110
Issue: 37
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2013-09-10
Start Page: E3506
End Page: E3515
Language: English
DOI: 10.1073/pnas.1303558110
PROVIDER: scopus
PMCID: PMC3773788
PUBMED: 23918374
DOI/URL:
Notes: --- - Cited By (since 1996):1 - "Export Date: 1 October 2013" - "CODEN: PNASA" - "Source: Scopus"
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  1. Hongbiao Carl Lekaye
    32 Lekaye
  2. Jason A Koutcher
    278 Koutcher