6533b831fe1ef96bd1299837

RESEARCH PRODUCT

Expression of gelatinases (MMP-2, MMP-9) and cyclooxygenases (COX-1, COX-2) in some benign salivary gland tumors.

Aldo GerbinoA MauroLuana LipariSalvatore GallinaMaria BuscemiSilvia TortoriciStefano Tetè

subject

Settore BIO/17 - IstologiaGelatinasesPathologymedicine.medical_specialtyImmunologyAdenoma PleomorphicBiologyMatrix metalloproteinaselaw.inventionPleomorphic adenomalawSettore MED/28 - Malattie OdontostomatologichemedicineHumansImmunology and AllergyProspective StudiesPathologicalPolymerase chain reactionPharmacologySalivary glandReverse Transcriptase Polymerase Chain Reactionbenign salivary gland tumorsgelatinasescyclooxygenasesAdenolymphomaSalivary Gland Neoplasmsmedicine.diseaseImmunohistochemistryReverse transcriptasemedicine.anatomical_structureSettore MED/31 - OtorinolaringoiatriaMatrix Metalloproteinase 9Cyclooxygenase 2Cyclooxygenase 1Matrix Metalloproteinase 2Immunohistochemistry

description

Salivary gland tumors, most of which are rare benign tumors, represent a histologically heterogenous group with the greatest diversity of morphological and cellular features. The aim of this study is to analyse the expression and possible interactions between gelatinases (MMP-2, MMP-9) and cyclooxygenases (COX-1, COX-2) in some benign salivary gland tumors. We investigated the expression of gelatinases and cyclooxigenases in control salivary gland, Pleomorphic adenoma and Warthin's tumor through immunohistochemistry and Reverse Transcription – Polymerase Chain Reaction (PCR). We identified the expression of both classes of enzyme in normal samples and in the two types of pathological samples without any quantitative differences. From the present data no significant differences emerge in the expression of these enzymes among the different pathologies examined. Nevertheless, due to the small number of samples included in this study, general statements regarding correlation between the degree of severity of the tumoral pathology and the quantitative expression of these potential tumoral markers can not be made.

http://hdl.handle.net/10447/63363