Abstract
The major cause of death from prostate cancer is due to metastases that are resistant to therapy. The prognosis and choice of therapy for most patients with prostate cancer are based on the clinical stage, serum prostate-specific antigen (PSA), and histological grade (Gleason score) of the tumor. Since metastases often develop in patients with clinically localized disease which is treated with radical prostatectomy, there is an urgent need to identify new molecular markers of prostate cancer metastasis. To produce metastasis, prostate cancer cells must complete a series of sequential and selective steps which are regulated by discrete and independent genes. We developed a rapid technique for detecting the activity of genes involved in the formation of metastasis: vascularization, invasion, adhesion, and proliferation. Human prostate cancer cells growing in culture or in the prostate of nude mice as well as formalin-fixed paraffin-embedded archival specimens of primary human prostate cancers from patients were examined by a colorimetric in situ hybridization (ISH) technique detecting mRNA of E-cadherin (cell cohesion), collagenase type IV: collagenase type IV and MMP-9 (invasion), and vascular endothelial growth factor/vascular permeability factor (VEGF/VPF) (angiogenesis). Intra- and intertumoral heterogeneity in gene expression was prominent. The relative expression of the MMP-9 and E-cadherin genes that regulate detachment and invasion of cancer cells respectively and the expression of angiogenic factor VEGF/VPF reliably predicted the metastatic potential of individual human prostate cancers.
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Fidler, I.J., Kuniyasu, H., Greene, G.F., Troncoso, P., Pettaway, C.A. (2000). Molecular Diagnosis to Predict the Metastatic Potential of Human Prostate Cancer. In: Khayat, D., Hortobagyi, G.N. (eds) Progress in Anti-Cancer Chemotherapy. Progress in Anti-Cancer Chemotherapy, vol 4. Springer, Paris. https://doi.org/10.1007/978-2-8178-0920-5_10
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DOI: https://doi.org/10.1007/978-2-8178-0920-5_10
Publisher Name: Springer, Paris
Print ISBN: 978-2-287-59692-6
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