Genetic expression profiling of parotid neoplasms by cDNA microarrays
- PMID: 16450770
- PMCID: PMC2639868
Genetic expression profiling of parotid neoplasms by cDNA microarrays
Abstract
Differentially expressed genes in various benign and malignant salivary gland tumours were identified by use of cDNA microarrays containing 19,000 human expressed sequence tags. Samples were derived from 5 patients with pleomorphic adenoma, 4 with Warthin's tumour, one with clear cell carcinoma, and 2 with mucoepidermoid carcinoma. Tumours were classified by using a subset of 486 genes. Benign Warthin's tumour and pleomorphic adenoma showed very distinctive gene expression patterns. A total of 133 genes differentiated the single malignant clear cell carcinoma from non-tumour salivary glands (p < 0.01), whereas only 16 genes separated it from the highly related benign pleomorphic adenoma (p < 0.01). A total of 57 cDNAs were associated with mucoepidermoid carcinoma (p < 0.01). The results show gene expression alterations common to all tumours and unique to each benign and malignant tumour. The numerous Expressed Sequence Tags of unknown function we identified could also become useful as tumour markers and represent a set of novel tumour-associated genes.
Sono stati identificati con l’uso di cDNA microarrays contenenti 19.000 sequenze geniche, differenti geni espressi in tumori benigni e maligni delle ghiandole salivari. I campioni sono stati ricavati da 5 pazienti affetti da adenoma pleomorfo, 4 da tumori di Warthin, 1 con carcinoma a cellule chiare e 2 con carcinoma muco-epidermoidale. Questi tumori sono stati classificati usando un subset di 486 geni. Il tumore di Warthin e l’adenoma pleomorfo hanno mostrato un pattern di espressione genica estremamente tipico. Il campione di carcinoma a cellule chiare ha dimostrato 133 geni differenti rispetto al tessuto salivare normale (p < 0.01), solo 16 geni lo differenziano dall’adenoma pleomorfo (p < 0.01), mentre 57 geni erano associati al carcinoma muco epidermoidale (p < 0.01). Questi risultati dimostrano che esistono alterazioni dell’espressione genica comuni a tutti i tumori e altre esclusive per i tumori benigni e/o maligni. Sono stati anche identificati numerosi Espressed Sequence Tags, la cui funzionalità è ancora sconosciuta e che potrebbero essere usati come marker tumorali e rappresentare un nuovo gruppo di geni tumore associati.
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