Histopathological evidence suggests that papillary serous carcinoma of
the peritoneum (PSCP) may be multifocal in origin. Utilizing a PCR ba
sed method to detect tandem repeat polymorphisms in formalin fixed tis
sue, loss of heterozygosity at eight loci on chromosomes 1, 3, 4, and
17 was studied in sir cases of PSCP. Loss of heterozygosity was assess
ed at between 5 and 11 tumor sites/patient. Allelic losses at 4 loci (
1q32-qter, 3p14.3-21.1, 17q12, 17q21.3-23) were noted. Three cases dem
onstrated a different pattern of allelic loss at various anatomic site
s within the same patient. In an additional case, a mutation of the p5
3 gene, detected by quantitative PCR followed by single-strand conform
ation polymorphism analysis, was detected in only 2 of 5 tumor sites.
The pattern of allelic loss and;he mutational pattern of the p53 gene
varied at tumor sites within the same patient in 4 of 6 cases of PSCP.
These findings are consistent with histopathological evidence that PS
CP is multifocal in origin.