| Literature DB >> 19717424 |
Gerald B W Wertheim1, Thomas W Yang, Tien-chi Pan, Anna Ramne, Zhandong Liu, Heather P Gardner, Katherine D Dugan, Petra Kristel, Bas Kreike, Marc J van de Vijver, Robert D Cardiff, Carol Reynolds, Lewis A Chodosh.
Abstract
We previously identified a SNF1/AMPK-related protein kinase, Hunk, from a mammary tumor arising in an MMTV-neu transgenic mouse. The function of this kinase is unknown. Using targeted deletion in mice, we now demonstrate that Hunk is required for the metastasis of c-myc-induced mammary tumors, but is dispensable for normal development. Reconstitution experiments revealed that Hunk is sufficient to restore the metastatic potential of Hunk-deficient tumor cells, as well as defects in migration and invasion, and does so in a manner that requires its kinase activity. Consistent with a role for this kinase in the progression of human cancers, the human homologue of Hunk is overexpressed in aggressive subsets of carcinomas of the ovary, colon, and breast. In addition, a murine gene expression signature that distinguishes Hunk-wild type from Hunk-deficient mammary tumors predicts clinical outcome in women with breast cancer in a manner consistent with the pro-metastatic function of Hunk in mice. These findings identify a direct role for Hunk kinase activity in metastasis and establish an in vivo function for this kinase.Entities:
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Year: 2009 PMID: 19717424 PMCID: PMC2734880 DOI: 10.1073/pnas.0906993106
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205