Abstract
To determine whether Akt activation was sufficient for the transformation of normal prostate epithelial cells, murine prostate restricted Akt kinase activity was generated in transgenic mice (MPAKT mice). Akt expression led to p70S6K activation, prostatic intraepithelial neoplasia (PIN), and bladder obstruction. mRNA expression profiles from MPAKT ventral prostate revealed similarities to human cancer and an angiogenic signature that included three angiogenin family members, one of which was found elevated in the plasma of men with prostate cancer. Thus, the MPAKT model may be useful in studying the role of Akt in prostate epithelial cell transformation and in the discovery of molecular markers relevant to human disease.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Enzyme Activation
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Genotype
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Humans
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Immunoblotting
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Immunohistochemistry
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In Situ Hybridization
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Male
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Mice
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Mice, Transgenic
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Neovascularization, Pathologic
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Oligonucleotide Array Sequence Analysis
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Platelet Endothelial Cell Adhesion Molecule-1 / biosynthesis
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Prostate / enzymology
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Prostate / metabolism
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Prostate / pathology
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Prostatic Intraepithelial Neoplasia / enzymology*
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Prostatic Intraepithelial Neoplasia / etiology*
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Protein Serine-Threonine Kinases*
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Proto-Oncogene Proteins / metabolism*
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Proto-Oncogene Proteins c-akt
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RNA / metabolism
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RNA, Messenger / metabolism
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Ribosomal Protein S6 Kinases, 70-kDa / metabolism
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Transgenes
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Urinary Bladder / pathology
Substances
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Platelet Endothelial Cell Adhesion Molecule-1
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Proto-Oncogene Proteins
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RNA, Messenger
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RNA
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AKT1 protein, human
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Protein Serine-Threonine Kinases
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Proto-Oncogene Proteins c-akt
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Ribosomal Protein S6 Kinases, 70-kDa