| المساهمون: |
Marini, Francesca, Giusti, Francesca, Fossi, Caterina, Cioppi, Federica, Cianferotti, Luisella, Masi, Laura, Boaretto, Francesca, Zovato, Stefania, Cetani, Filomena, Colao, Annamaria, Davì, Maria Vittoria, Faggiano, Antongiulio, Fanciulli, Giuseppe, Ferolla, Piero, Ferone, Diego, Loli, Paola, Mantero, Franco, Marcocci, Claudio, Opocher, Giuseppe, Beck-Peccoz, Paolo, Persani, Luca, Scillitani, Alfredo, Guizzardi, Fabiana, Spada, Anna, Tomassetti, Paola, Tonelli, Francesco, Brandi, Maria Luisa |
| الوصف: |
Multiple endocrine neoplasia type 1 (MEN1) is caused by germline inactivating mutations of the MEN1 gene. Currently, no direct genotype–phenotype correlation is identified. We aim to analyze MEN1 mutation site and features, and possible correlations between the mutation type and/or the affected menin functional domain and clinical presentation in patients from the Italian multicenter MEN1 database, one of the largest worldwide MEN1 mutation series published to date. The study included the analysis of MEN1 mutation profile in 410 MEN1 patients [370 familial cases from 123 different pedigrees (48 still asymptomatic at the time of this study) and 40 single cases]. We identified 99 different mutations: 41 frameshift [small intra-exon deletions (28) or insertions (13)], 13 nonsense, 26 missense and 11 splicing site mutations, 4 in-frame small deletions, and 4 intragenic large deletions spanning more than one exon. One family had two different inactivating MEN1 mutations on the same allele. Gastro-entero-pancreatic tumors resulted more frequent in patients with a nonsense mutation, and thoracic neuroendocrine tumors in individuals bearing a splicing-site mutation. Our data regarding mutation type frequency and distribution are in accordance with previously published data: MEN1 mutations are scattered through the entire coding region, and truncating mutations are the most common in MEN1 syndrome. A specific direct correlation between MEN1 genotype and clinical phenotype was not found in all our families, and wide intra-familial clinical variability and variable disease penetrance were both confirmed, suggesting a role for modifying, still undetermined, factors, explaining the variable MEN1 tumorigenesis. |
