Chromosomal instability is more frequent in metastasized than in non-metastasized pulmonary carcinoids but is not a reliable predictor of metastatic potential.
10.3858/emm.2009.41.5.039
- Author:
Arne WARTH
1
;
Esther HERPEL
;
Sabine KRYSA
;
Hans HOFFMANN
;
Philipp A SCHNABEL
;
Peter SCHIRMACHER
;
Gunhild MECHTERSHEIMER
;
Hendrik BLAKER
Author Information
1. Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany. arne.warth@med.uni-heidelberg.de
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
biological markers;
carcinoid tumor;
comparative genomic hybridization;
lung neoplasms;
microsatellite instability;
neoplasm metastasis
- MeSH:
Carcinoid Tumor/*genetics/pathology/*secondary;
Chromosomal Instability/*genetics;
Comparative Genomic Hybridization;
Humans;
Lung Neoplasms/*genetics/pathology;
Lymphatic Metastasis;
Prognosis
- From:Experimental & Molecular Medicine
2009;41(5):349-353
- CountryRepublic of Korea
- Language:English
-
Abstract:
Pulmonary carcinoids are infrequent neoplasms of the lung that normally display a less aggressive biological behavior compared to small cell and non-small cell lung cancers. Approximately 15-25% of carcinoids, in particular atypical carcinoids, show lymph node metastasis and have a worse prognosis than their non-metastasized counterparts. To date, there is no morphological or molecular marker that may help to differentiate between carcinoids that metastasize and carcinoids of identical differentiation that show only local tumor growth. In this study, we analyzed 7 metastasized and 10 non-metastasized pulmonary carcinoids for chromosomal and microsatellite instability in order to determine whether microsatellite instability or chromosomal imbalances are associated with metastasis. Due to the rare occurrence of metastasized carcinoids we compared our results of chromosomal instability with the hitherto published comparative genomic hybridization (CGH) profiles of pulmonary carcinoids, for which information about the absence or presence of metastasis was available. While microsatellite instability was not detected we found chromosomal instability as a common event in pulmonary carcinoids with an increase of frequency and extent of chromosomal alterations in atypical and metastasized carcinoids. These findings are in accordance with the collected and herein compiled data of previous studies and indicate increasing numbers of chromosomal imbalances to play a role in the sequential process of tumor development and metastasis.
