Stanley Schwartz

University at Buffalo, The State University of New York, Buffalo, New York, United States

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Publications (2)3.84 Total impact

  • [Show abstract] [Hide abstract]
    ABSTRACT: Prostate-specific antigen (PSA) is a well-known biomarker for diagnosis and management of prostate cancer. PSA has been shown to have anti-angiogenic activity. We used the emerging proteomic research technology to identify proteins in prostate cancer cells whose expression is regulated by enzymatically active PSA. Differentially expressed proteins in PC-3M cells treated with PSA were analyzed by 2D-DIGE analysis and identified by HPLC-MS/MS and SEQUEST data mining. Biological network analysis was carried out using MetaCore integrated software designed for functional analysis of experimental data. Gene expression data for several regulated proteins were confirmed by real-time, quantitative PCR. A total of 41 proteins were significantly (P < 0.05) changed in abundance in PC-3M cells in response to PSA treatment. Proteins from 26 gel-spots were identified. Many of the down-regulated proteins including N8 gene product long isoform, laminin receptor, vimentin, DJ-1 and Hsp60 are known to be involved in tumor progression. The relevance of the level of PSA in prostate tissue microenvironment and its relation to tumor progression has not been elucidated. PSA has been shown to down-regulate several proteins that are known to have involvement in tumor progression. This suggests that normal physiological levels of PSA in prostate tissue microenvironment may be promoting non-angiogenic environment and its down-regulation may promote tumor growth.
    The Prostate 10/2008; 68(14):1531-45. · 3.84 Impact Factor
  • Clinical Immunology - CLIN IMMUNOL. 01/2006; 119.

Publication Stats

7 Citations
3.84 Total Impact Points

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Institutions

  • 2008
    • University at Buffalo, The State University of New York
      • Division of Allergy, Immunology and Rheumatology
      Buffalo, New York, United States