Detection of AMACR (P504S), P63 and 34betaE12 cocktail in the early diagnosis of prostate cancer.
- Author:
Tao YU
1
;
Shao-xing ZHU
;
Song ZHENG
;
Shi-ping CHEN
Author Information
- Publication Type:Journal Article
- MeSH: Aged; Carcinoma, Basal Cell; diagnosis; metabolism; Early Diagnosis; Humans; Immunohistochemistry; Keratins; biosynthesis; Male; Membrane Proteins; biosynthesis; Middle Aged; Prostatic Hyperplasia; diagnosis; metabolism; Prostatic Neoplasms; diagnosis; metabolism; Racemases and Epimerases; biosynthesis
- From: National Journal of Andrology 2007;13(3):222-225
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the value of detection of AMACR (P504S), P63 and 34betaE12 cocktail in the early diagnosis of prostate cancer (PCa).
METHODSThe expressions of AMACR, P63 and 34betaE12 were examined in the biopsy specimens of 42 cases of prostate cancer, 12 cases of high-grade prostatic intraepithelial neoplasia (HGPIN) and 30 cases of benign prostatic hyperplasia (BPH) using the Maxvision single-step immunohistochemical method with triple-antibody cocktail (AMACR/P63/34betaE12) staining and double-color chromogens in single paraffin sections .
RESULTSThe expressions of AMACR, P63 and 34betaE12 were significantly different between PCa and BPH (P < 0.01). The staining of PCa was positive for AMACR and negative for P63 and 34betaE12, and the positivity rate of AMACR was 100%. BPH was strongly expressed for P63 and 34betaE12, but negatively for AMACR. The expression of AMACR was significantly different between HGPIN and BPH (P < 0.01), but not between HGPIN and PCa (P > 0.05), and the positivity rate of AMACR in HGPIN was 91.67%. However, the expressions of P63 and 34betaE12 were significantly different between HGPIN and PCa (P < 0.01), but not between HGPIN and BPH (P > 0.05), and the positivity rate of AMACR in HGPIN was 100%. The level of AMACR expression was not correlated with PCa Gleason score (P > 0.05).
CONCLUSIONAMACR is a sensitive and specific marker for PCa. P63 and 34betaE12 cocktail staining can increase the sensitivity and specificity of the basal cell detection. The immunohistochemical analysis with triple-antibody cocktail (AMACR/P63/34betaE12) staining and double-color chromogens can improve diagnostic accuracy and has an important applied value for the early diagnosis of prostate cancer.