The 12q13-22 amplicon from four liposacroma specimens evaluated by com
parative genomic hybridization was studied analyzing 55 microsatellite
markers by PCR. All four specimens were informative in at least 34 lo
ci; an amplification or allelic imbalance was identified with four to
17 markers. The amplicons were discontinuous; there were non-amplified
marker loci between the amplified marker loci. These findings indicat
e the presence of separate amplicons in the 12q13-22 region. Evidence
of the concomitant gain of one allele and loss of the other allele was
found with several markers in one tumor and with one marker in two tu
mor specimens. Southern blotting showed amplification of CDK4 and MDM2
in all four specimens. (C) 1997 Wiley-Liss, Inc.