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Analysis of molecular pathways in sporadic neuroendocrine tumors of the gastro‐entero‐pancreatic system
Author(s) -
Arnold Christian N.,
Sosnowski Andrea,
SchmittGräff Annette,
Arnold Rudolf,
Blum Hubert E.
Publication year - 2007
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.22569
Subject(s) - loss of heterozygosity , microsatellite instability , epigenetics , biology , neuroendocrine tumors , methylation , dna methylation , phenotype , cancer research , immunohistochemistry , pathogenesis , medicine , pathology , oncology , microsatellite , endocrinology , gene , gene expression , genetics , allele , immunology
Abstract Little is known about the molecular pathogenesis of neuroendocrine tumors (NET) of the gastro‐entero‐pancreatic (GEP) system. We analyzed genetic and epigenetic alterations as well as the CpG island methylator phenotype (CIMP). The study comprised 118 well‐differentiated fore‐ and mid‐gut GEP‐NET from 71 patients. In addition to loss of heterozygosity (LOH), microsatellite instability (MSI) and the methylation status of various tumor associated genes were examined. The expression profile of p16, APC and MENIN was investigated by immunohistochemistry. None of the tumors was highly microsatellite unstable, LOH was found in 22.2%. Significant differences in promoter hypermethylation were identified in the RUNX3 and the O 6 ‐ MGMT genes. We found a significant loss of p16 expression in insulinomas ( p = 0.05) and functional NET ( p = 0.01), respectively. APC was expressed less in gastrinomas ( p = 0.01) and functional GEP‐NET ( p = 0.05) vs. nonfunctional tumors. MENIN expression was reduced in pancreatic vs . extrapancreatic NET ( p = 0.008) and in insulinomas vs. nonfunctional GEP‐NET ( p = 0.019) and NET associated with the carcinoid syndrome ( p = 0.029). Further CIMP and a Ki‐67 index >10% showed a close correlation. Outcome analysis of 19 patients showed a better survival for CIMP‐negative patients. The analyses identified significant genetic and epigenetic alterations in well‐differentiated fore‐ and mid‐gut NET. CIMP, similar to Ki‐67, might turn out to be of prognostic relevance. © 2007 Wiley‐Liss, Inc.