The cytogenetic evaluation of prostatic adenocarcinoma has shown no co
nsistent cytogenetic abnormalities. Despite manipulation of culture co
nditions, the majority of low-stage, untreated prostatic adenocarcinom
as show a normal karyotype. We have performed cytogenetic analysis on
eight primary prostate adenocarcinomas, using several control measures
to increase the probability that any normal karyotype was derived fro
m neoplastic cells rather than accompanying normal cells. Tumors were
grown in media that encourages epithelial growth; DNA ploidy studies w
ere performed before and after tissue culture; and immunohistochemical
confirmation of the prostatic and epithelial nature of the cells was
done following culture. Percentage of tumor on tissue sections adjacen
t to those submitted for culture was >75% in all cases. Seven of eight
cases were evaluable, and six cases showed no clonal abnormalities an
d were diploid. One tumor showed a population of tetraploid cells, wit
hout structural abnormalities. Three additional tumors showed evidence
of tetraploidy by DNA analysis. One case showed nonclonal marker chro
mosomes and was aneuploid. This patient was pathologic Stage D. We con
clude that the majority of prostatic adenocarcinomas at their inceptio
n may not show routinely detectable cytogenetic abnormalities. However
, tetraploidy may play a role in the evolution of prostatic adenocarci
noma.