Previous cytogenetic investigations have revealed frequent deletions a
nd other unbalanced structural rearrangements of 3p in human malignant
mesothelioma. We have performed a restriction fragment length polymor
phism analysis by using the polymerase chain reaction and primer sets
for seven DNA markers to examine loss of heterozygosity (LOH) from 3p
in 25 malignant mesotheliomas. Among 24 cases informative at one or mo
re 3p loci, 15 (62.5%) exhibited LOH with at least one marker. Deletio
n mapping in these tumors indicates that the common region of chromoso
mal loss resides within band 3p21, in the vicinity of the D3F 15S2 loc
us. These results suggest that allelic loss from 3p21 is a frequent oc
currence in malignant mesothelioma and that one or more putative tumor
suppressor genes at this site contribute to the pathogenesis of this
malignancy. (C) 1994 Wiley-Liss, Inc.