BACKGROUND. Cytogenetic, molecular cytogenetic, and molecular studies of pr
ostate cancer have revealed an enormous amount of data regarding chromosoma
l loci that are aberrant in prostate tumors.
METHODS. These data have been compared and condensed in this review to dete
rmine which chromosomes and chromosome sites have been most frequently repo
rted.
RESULTS. Loss of the Y chromosome, gain of 7, 8, and chi, and interstitial
deletions on 6q, 7q, 8p, 10q, 13q, 16q, 17q, and 18q are the most prevalent
.
CONCLUSIONS. A potential model for genetic control of tumor progression is
presented, as are data regarding the evaluation of a new series of tumors.
(C) 1999 Wiley-Liss, Inc.