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Published in: Virchows Archiv 1/2011

Open Access 01-01-2011 | Original Article

Chromosome 3p alterations in pancreatic endocrine neoplasia

Authors: Eliana Amato, Stefano Barbi, Giorgio Malpeli, Samantha Bersani, Giuseppe Pelosi, Paola Capelli, Aldo Scarpa

Published in: Virchows Archiv | Issue 1/2011

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Abstract

Pancreatic endocrine tumors (PET) are rare neoplasms classified as functioning (F-PET) or non-functioning (NF-PET) according to the presence of a clinical syndrome due to hormonal hypersecretion. PETs show variable degrees of clinical aggressiveness and loss of chromosome 3p has been suggested to be associated with an advanced stage of disease. We assessed chromosome 3p copy number in 113 primary PETs and 32 metastases by fluorescence in situ hybridization (FISH) using tissue microarrays. The series included 56 well-differentiated endocrine tumors (WDET), 62 well-differentiated endocrine carcinomas (WDEC), and 6 poorly differentiated endocrine carcinomas (PDEC). Chromosome 3p alterations were found in 23/113 (20%) primary tumors, with losses being predominant over gains (14% vs. 6%). Loss of 3p was found in 5/55 (9%) WDET, 11/52 (21%) WDEC, and never in PDEC. Gains of 3p were detected in 4/55 (7%) WDET, no WDEC, but notably in 3/6 (50%) PDEC (OR 23.6; P = 0.003). Metastases were more frequently monosomic for 3p compared to primary tumors (OR 3.6; P = 0.005). Monosomy was significantly associated with larger tumor size, more advanced tumor stage, and metastasis. No association was found with survival. Chromosome 3p copy number alterations are frequent events in advanced stage PET, with gains prevailing in PDEC while losses are more frequent in WDEC, supporting the view that a specific pattern of alterations are involved in these diverse disease subtypes.
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Metadata
Title
Chromosome 3p alterations in pancreatic endocrine neoplasia
Authors
Eliana Amato
Stefano Barbi
Giorgio Malpeli
Samantha Bersani
Giuseppe Pelosi
Paola Capelli
Aldo Scarpa
Publication date
01-01-2011
Publisher
Springer-Verlag
Published in
Virchows Archiv / Issue 1/2011
Print ISSN: 0945-6317
Electronic ISSN: 1432-2307
DOI
https://doi.org/10.1007/s00428-010-1001-x

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