Uterine leiomyomas are the most common benign tumor that arise from smooth
muscle cells of the myometrium. Little is known about the etiology and path
ogenesis of this tumor. To investigate the molecular pathogenesis of these
tumors, we have conducted an allelotype of 102 leiomyomas from 12 patients,
using 67 fluorescently-tagged oligonucleotide primers amplifying microsate
llite loci covering all autosomes. No areas of the genome showed frequent l
oss of heterozygosity (LOH); however, the highest rate of LOH (9%) was obse
rved on 7q, consistent with previous cytogenetic observations. Uterine leio
myomas are sometimes multiple. In general, multiplicity of other types of n
eoplasm is associated with genetic predisposition to the disease. Because m
ultiple tumors were available from each of the 12 patients studied we looke
d for evidence of allele-specific LOH, which might indicate the presence of
an underlying predisposition gene. However, no evidence fbr allele-specifi
c LOH was detected, indicating that if cases of multiple uterine leiomyoma
are due to an underlying predisposition gene, it is unlikely to be a recess
ive oncogene. (C) Elsevier Science Inc., 1999. All rights reserved.