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Prostate stem cell antigen is overexpressed in human transitional cell carcinoma.
N Amara1, G S Palapattu, M Schrage
1Department of Urology, Jonsson Cancer Center, University of California-Los Angeles School of Medicine, Los Angeles, California 90095, USA.
Cancer Research
|June 19, 2001
Summary
Prostate stem cell antigen (PSCA) is overexpressed in most bladder cancers, especially early stages. This finding highlights PSCA as a promising target for transitional cell carcinoma diagnosis and immunotherapy.
Area of Science:
- Urothelial Carcinomas
- Cancer Immunotherapy
- Molecular Oncology
Background:
- Prostate stem cell antigen (PSCA) is expressed in prostate cancer and normal bladder.
- PSCA's role in transitional cell carcinoma (TCC) is not fully understood.
- Assessing PSCA expression is crucial for its potential as an immunotherapeutic target in bladder cancer.
Purpose of the Study:
- To compare PSCA expression in normal and malignant urothelial tissues.
- To evaluate PSCA as a potential immunotherapeutic target for transitional cell carcinoma (TCC).
Main Methods:
- Immunohistochemical analysis of PSCA protein expression in 32 normal bladders and 110 TCC specimens (dysplasia, CIS, STCC, ITCC, metastases).
- Semi-quantitative scoring of PSCA staining intensity and frequency.
- Examination of PSCA mRNA expression using Northern blot.
- Confocal microscopy to determine PSCA localization.
Main Results:
- PSCA expression was weak in normal bladder epithelium, primarily in superficial cells.
- Significantly higher and more uniform PSCA staining in carcinoma in situ (CIS) and superficial TCC (STCC) compared to normal bladder (P < 0.001).
- PSCA detected in 65% of muscle-invasive TCC (ITCC) and 57% of metastatic cancers, with higher expression correlating with increased tumor grade (P < 0.001).
Conclusions:
- PSCA is overexpressed in a majority of human TCCs, particularly CIS and superficial tumors.
- PSCA is localized to the cell surface in TCC.
- PSCA represents a promising target for bladder cancer diagnosis and therapy.