Numerical chromosomal anomalies in latent adenocarcinomas of the prostate

• Published in: The Prostate 1999-02, Vol.38 (2), p.92-99
• Main Authors: Erbersdobler, Andreas, Bardenhagen, Petra, Henke, Rolf-Peter
• Format: Article
• Language: English
• Subjects: Adenocarcinoma - genetics; Aged; Aged, 80 and over; autopsy; Biological and medical sciences; Chromosome Aberrations; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 7; Humans; hybridization; In Situ Hybridization; Male; Medical sciences; Middle Aged; Nephrology. Urinary tract diseases; ploidy; prostatic neoplasms; Prostatic Neoplasms - genetics; Tumors of the urinary system; Urinary tract. Prostate gland; X Chromosome; Y Chromosome
• ISSN: 0270-4137; 1097-0045
• DOI: 10.1002/(SICI)1097-0045(19990201)38:2<92::AID-PROS2>3.0.CO;2-6

BACKGROUND Even the high incidence of clinically diagnosed prostate cancer is exceeded by the frequency of tumors detected at autopsy. However, there is some debate concerning the malignant potential of these so‐called “latent prostate cancers.” In this study, prostate cancers detected at autopsy were investigated for the presence of numerical aberrations of chromosomes 7, 10, 17, X, and Y. METHODS Prostates from 57 autopsies, performed on male patients aged 45 years or older, were histologically investigated for the presence of cancer. Interphase cytogenetics, an in situ hybridization method with chromosome‐specific probes, was performed on paraffin sections. RESULTS Of the 57 specimens investigated, 23 contained foci of prostate cancer. Three prostates contained more than one tumor focus. Interphase cytogenetics could be performed successfully in 19 specimens. Of the 22 tumor foci investigated, 14 were disomic and 8 were nondisomic for the five chromosomes tested. Ploidy correlated significantly with the presence of a Gleason score of 7 or higher (P = 0.0109), but not with a tumor volume larger than 0.5 cm3, or with patient age over 75 years. CONCLUSIONS Some latent prostate cancers display a nondisomic chromosomal status and a low histologic differentiation in spite of a small tumor volume, suggesting a more aggressive potential in a subset of these tumors. Prostate 38:92–99, 1999. © 1999 Wiley‐Liss, Inc.