APC alterations are frequently involved in the pathogenesis of acinar cell carcinoma of the pancreas, mainly through gene loss and promoter hypermethylation.

Détails

ID Serval
serval:BIB_A2B562B19A10
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
APC alterations are frequently involved in the pathogenesis of acinar cell carcinoma of the pancreas, mainly through gene loss and promoter hypermethylation.
Périodique
Virchows Archiv : An International Journal of Pathology
Auteur⸱e⸱s
Furlan D., Sahnane N., Bernasconi B., Frattini M., Tibiletti M.G., Molinari F., Marando A., Zhang L., Vanoli A., Casnedi S., Adsay V., Notohara K., Albarello L., Asioli S., Sessa F., Capella C., La Rosa S.
ISSN
1432-2307 (Electronic)
ISSN-L
0945-6317
Statut éditorial
Publié
Date de publication
2014
Peer-reviewed
Oui
Volume
464
Numéro
5
Pages
553-564
Langue
anglais
Notes
Publication types: Journal ArticlePublication Status: ppublish
Résumé
Genetic and epigenetic alterations involved in the pathogenesis of pancreatic acinar cell carcinomas (ACCs) are poorly characterized, including the frequency and role of gene-specific hypermethylation, chromosome aberrations, and copy number alterations (CNAs). A subset of ACCs is known to show alterations in the APC/β-catenin pathway which includes mutations of APC gene. However, it is not known whether, in addition to mutation, loss of APC gene function can occur through alternative genetic and epigenetic mechanisms such as gene loss or promoter methylation. We investigated the global methylation profile of 34 tumor suppressor genes, CNAs of 52 chromosomal regions, and APC gene alterations (mutation, methylation, and loss) together with APC mRNA level in 45 ACCs and related peritumoral pancreatic tissues using methylation-specific multiplex ligation probe amplification (MS-MLPA), fluorescence in situ hybridization (FISH), mutation analysis, and reverse transcription-droplet digital PCR. ACCs did not show an extensive global gene hypermethylation profile. RASSF1 and APC were the only two genes frequently methylated. APC mutations were found in only 7 % of cases, while APC loss and methylation were more frequently observed (48 and 56 % of ACCs, respectively). APC mRNA low levels were found in 58 % of cases and correlated with CNAs. In conclusion, ACCs do not show extensive global gene hypermethylation. APC alterations are frequently involved in the pathogenesis of ACCs mainly through gene loss and promoter hypermethylation, along with reduction of APC mRNA levels.
Mots-clé
Carcinoma, Acinar Cell/genetics, DNA Methylation, DNA Mutational Analysis, Gene Dosage, Genes, APC, Genes, Tumor Suppressor, Humans, In Situ Hybridization, Fluorescence, Multiplex Polymerase Chain Reaction, Pancreatic Neoplasms/genetics, Promoter Regions, Genetic, Reverse Transcriptase Polymerase Chain Reaction
Pubmed
Web of science
Création de la notice
06/09/2016 13:49
Dernière modification de la notice
16/03/2023 12:14
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