The origin of intraductal carcinoma of the prostate (IDC-P) in presence of prostate adenocarcinoma (PCa) is a matter of debate. This study evaluates trophoblast cell-surface antigen 2 (Trop-2) expression in prostatic high-grade intraepithelial neoplasia (HGPIN), IDC-P and PCa to explain the possible mechanism for IDC-P arising. Trop-2 was localized in the luminal epithelium of normal prostate gland, HGPIN and IDC-P. The quantitative analysis of immunohistochemistry showed no difference of Trop-2 expression between HGPIN and IDC-P, while statistically significant differences were observed comparing the two pathologies with normal tissues. Contrarily, Trop-2 was expressed in 2.5% of the basal cells in normal prostate gland and in 1% of HGPIN while Trop-2 was expressed in 8% of cells in IDC-P samples. We suggest that Trop-2 present in the basal cells may acquire neoplastic changes. The neoplastic cells could grow into the glandular lumen as HGPIN and/or spread into the duct as IDC-P or spread into the stroma as PCa. In conclusion, our data in part support the theory of intraductal carcinoma origin through retrograde glandular colonization.

Trophoblast cell-surface antigen 2 evaluation in intraepithelial neoplasia and intraductal carcinoma of the prostate: An immunopathological study

Tossetta, Giovanni;
2026-01-01

Abstract

The origin of intraductal carcinoma of the prostate (IDC-P) in presence of prostate adenocarcinoma (PCa) is a matter of debate. This study evaluates trophoblast cell-surface antigen 2 (Trop-2) expression in prostatic high-grade intraepithelial neoplasia (HGPIN), IDC-P and PCa to explain the possible mechanism for IDC-P arising. Trop-2 was localized in the luminal epithelium of normal prostate gland, HGPIN and IDC-P. The quantitative analysis of immunohistochemistry showed no difference of Trop-2 expression between HGPIN and IDC-P, while statistically significant differences were observed comparing the two pathologies with normal tissues. Contrarily, Trop-2 was expressed in 2.5% of the basal cells in normal prostate gland and in 1% of HGPIN while Trop-2 was expressed in 8% of cells in IDC-P samples. We suggest that Trop-2 present in the basal cells may acquire neoplastic changes. The neoplastic cells could grow into the glandular lumen as HGPIN and/or spread into the duct as IDC-P or spread into the stroma as PCa. In conclusion, our data in part support the theory of intraductal carcinoma origin through retrograde glandular colonization.
2026
Intraductal carcinoma of the prostate
Prostate cancer
Prostatic intraepithelial neoplasia
Trop-2
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12078/37666
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