The Prostate · 2002 · 73 citations · 18 references
Life SciencesCell BiologyUrologyCell AdhesionSignal TransductionTumor ProgressionCancer Cell SignalingFocal AdhesionsIntegrin SignalingProstate CancerProstate PathologyProstatic PathologyFocal Adhesion Kinase SignalingIntegrin Signaling In CancerMetastasis Of Prostate CancerProstate AdenocarcinomaProstate CarcinogenesisProstate SpecimensProstatic AdenocarcinomaSecretory Epithelium
BACKGROUND: Focal adhesion kinase (FAK) regulates multiple cellular processes including growth, differentiation, adhesion, motility, and apoptosis. In tumor cells, including prostate adenocarcinoma, FAK overexpression has been linked to cancer progression. METHODS: By using immunohistochemistry, FAK expression was investigated in human prostate specimens. RESULTS: FAK was expressed predominantly in the basal layer of normal prostate epithelium but not in secretory epithelium. FAK was expressed at similar levels in all stages of prostate tumorigenesis, including preinvasive carcinoma and metastatic disease. Elevated FAK expression was observed at the earliest stages of transformation and expression continued during cancer progression. CONCLUSION: Given the established role for FAK in the regulation of integrin signaling, we suggest that the sustained elevated levels of FAK expression during prostate tumor cell progression is consistent with a role for FAK in the development and maintenance of prostate carcinoma.
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Disruption of epithelial cell-matrix interactions induces apoptosis
SM Frisch, H. Francis · The Journal of Cell Biology · 1994 · 3.3K citations · Full text
Control of adhesion-dependent cell survival by focal adhesion kinase.
Steven M. Frisch, Kristiina Vuori, Erkki Ruoslahti et al. · The Journal of Cell Biology · 1996 · 1.1K citations · Full text
Molecular classification of human carcinomas by use of gene expression signatures.
Andrew I. Su, John Welsh, Lisa M. Sapinoso et al. · PubMed · 2001 · 692 citations
Overexpression of the focal adhesion kinase (p125FAK) in invasive human tumors.
Lewis V. Owens, Li Xu, Rolf J. Craven et al. · PubMed · 1995 · 616 citations
Medicine, Cell Biology, Oncology +17