GENOTYPIC ALTERATIONS IN BENIGN AND MALIGNANT SALIVARY-GLAND TUMORS -HISTOGENETIC AND CLINICAL IMPLICATIONS

Loss of heterozygosity (LOH) and microsatellite instability (MI) were examined at 24 microsatellite loci in 46 primary benign and malignant salivary gland tumors. Among the 27 benign tumors, 11 (40.7%), manifes ted microsatellite alterations in at least one locus; of these, five ( 18.5%) showed LOH and four (14.8%) had microsatellite instability at t wo or more loci. Four of 11 pleomorphic adenomas (36.4%) had allele lo ss on the long arm of chromosome 8. Among the 19 malignant neoplasms e xamined, 10 (52.6%) and one (5.2%) had allele losses and MI, respectiv ely, at multiple loci; three tumors showed MI at only one locus. Frequ ent LOH was detected at D8S166 (8q11-12), D17S799, and D17S122 (17p-17 p11-2) loci, with an incidence of 40%, 37.5%, and 43%, respectively. I n general, malignant neoplasms with LOH exhibited aggressive tumor cha racteristics. Statistically significant correlation's were found betwe en LOH and pathologic classification (chi(2), p = 0.05), higher grade (p = 0.02), DNA aneuploidy (p = 0.005), and a proliferative index of > 6% (p = 0.005) of the malignant tumors. Carcinomas with 17p loci alter ations, including two carcinomas expleomorphic adenoma with concurrent 8q LOH, showed more aggressive features. The results suggested that ( a) loci on chromosome sq may harbor a tumor suppressor gene or genes a ssociated with the development or progression of some salivary neoplas ms; (b) alterations on the short arm of chromosome 17 may represent an event related to tumor progression; and (c) tumors with LOH at multip le loci have aggressive biologic characteristics.