A study of chromosome 6 allele loss in human colorectal carcinomas.

Matched normal/tumor DNA pairs from patients with sporadic and hereditary (FAP = familial adenomatous polyposis) colorectal carcinoma were examined for tumor-specific allele loss on chromosome 6 using cDNA probes for the avian myeloblastosis viral oncogene homologue (MYB on 6q22-q23), the estrogen receptor (ESR on 6q24-q27), and for the alpha polypeptide of human chorionic gonadotropin (CGA on 6q14-q21). No chromosome 6 allele loss was observed at these gene loci among 22 colorectal carcinomas examined, although such losses were relatively frequent (37.5% of informative individuals) at the D17S28 locus on chromosome 17. These results are consistent with karyological studies and indicate that chromosome 6 allele loss from colorectal carcinomas may occur less frequently than previously reported.

Chromosome 18 allele loss at the D18S6 locus in human colorectal carcinomas.

This is the first report of chromosome 18 allele loss in colorectal carcinomas from FAP patients and concurrent allele losses on chromosomes 5 and 18 in sporadic colorectal cancer. This is based on our investigation of twenty-two colorectal carcinomas from sporadic cases and FAP patients which revealed tumor-specific allele loss of at least 44% at the D18S6 locus on chromosome 18 in informative cases. These results coupled with the tentative assignment of an HNPCC gene to chromosome 18 suggests that a gene on chromosome 18 may be involved in the etiology of some colon cancers. Possible mechanisms involving genetic changes on chromosome 18 in colon cancer are discussed in relation to tumor- or growth-suppressor genes.