Assessment of the genetic instability of a microsatellite has indicate
d a new mechanism in human carcinogenesis. Examination was made to det
ermine whether microsatellite instability is associated with the onset
of prostate cancer. Twenty-nine DNA samples from 24 primary prostate
cancer, two metastatic lymph-node and three benign prostatic hypertrop
hy patients were used. Differences in unrelated microsatellites for tu
mor and normal DNA were detected in nine of 24 (37.5%) cases. Seven of
11 (63.6%) with poorly differentiated adenocarcinomas and seven of 15
(46.7%) stage D metastatic patients showed somatic instability in a n
umber of microsatellites. Statistically significant differences in wel
l to moderately differentiated tumors and poorly differentiated cancer
(P=0.015, Chi-square test), were detected but not for stages A-C and
D (P=0.2311). Genetic alterations would thus appear to be rare in low
grade and/or early prostate cancers but more common in high grade and/
or advanced prostate cancers.