Correlation Between PSMA and VEGF Expression as Markers for LNCaP Tumor Angiogenesis

Author:

Tsui Paulus1,Rubenstein Marvin123,Guinan Patrick134

Affiliation:

1. Division of Cellular Biology, Hektoen Institute for Medical Research, Chicago, IL 60612, USA

2. Department of Biochemistry, Rush Presbyterian St Lukes Medical Center, Chicago, IL 60612, USA

3. Department of Urology, Rush Presbyterian St Lukes Medical Center, Chicago, IL 60612, USA

4. Department of Urology, University of Illinois at Chicago, Chicago, IL 60612, USA

Abstract

Our aim is the identification and correlation of changes in tumor-associated protein expression which results from therapy. LNCaP tumors, excised from nude mice treated either by orchiectomy or with the chemotherapeutic agent paclitaxel, were evaluated for the expression of proteins and receptors associated with growth, differentiation, and angiogenesis using immunohistologic procedures. Compared to untreated control tumors, both treatments reduced the expression of vascular endothelial growth factor (VEGF), prostate-specific membrane antigen (PSMA), prostate-specific antigen (PSA), androgen receptor (AR), and epidermal growth factor receptor (EGFR). The effect of paclitaxel treatment on AR expression was the most significant(P=.005). Of particular interest was identifying a significant correlation(P<.000801)between PSMA and VEGF expression regardless of treatment modality. These altered expressions suggest that PSMA may also be a marker for angiogenesis and could represent a target for deliverable agents recognizing either prostatic tumors or endothelial development. Cell surface PSMA would then present a unique target for treatment of patients early in their development of prostatic metastases.

Funder

Blum-Kovler Foundation

Publisher

Hindawi Limited

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology,Molecular Medicine,General Medicine,Biotechnology

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