R. Casalone et al., CHROMOSOME CHANGES IN BENIGN PROSTATIC HYPERPLASIA AND THEIR SIGNIFICANCE IN THE ORIGIN OF PROSTATIC-CARCINOMA, Cancer genetics and cytogenetics, 68(2), 1993, pp. 126-130
Cytogenetic studies of benign prostatic hyperplasia (BHP) are scarce.
We analyzed primary cell cultures obtained from biopsies of prostatic
tissues from 10 patients (mean age: 60.7 years) with histologic diagno
sis of BHP to compare the eventual chromosome changes with those repor
ted in prostatic adenocarcinoma. Clonal chromosome abnormalities were
noted in five of the 10 cases, with loss of Y chromosome in all. In on
e case, a clonal t(1;20) was observed with a -Y clone. Different numer
ical and structural sporadic abnormalities were evident in eight. Chro
mosome 1 was the chromosome most frequently involved in sporadic rearr
angements. We concluded that -Y is a frequent nonrandom chromosome abn
ormality in BHP in this sample of patients. Immunohistochemical studie
s showed that loss of Y occurs in fibroblasts and not in epithelial ce
lls; therefore, this anomaly is not related to cancer development.