Back to Search Start Over

Expression of Contactin 4 is associated with malignant behavior in pheochromocytomas and paragangliomas.

Authors :
UCL - SSS/DDUV/GEHU - Génétique
UCL - SSS/IREC/MIRO - Pôle d'imagerie moléculaire, radiothérapie et oncologie
UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition
UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire
UCL - (SLuc) Service de pathologie cardiovasculaire
UCL - (SLuc) Service d'anatomie pathologique
UCL - (SLuc) Service d'endocrinologie et de nutrition
UCL - (SLuc) Service d'oto-rhino-laryngologie
UCL - (SLuc) Centre du cancer
Evenepoel, Lucie
van Nederveen, Francien H
Oudijk, Lindsey
Papathomas, Thomas G
Restuccia, David F
Belt, Eric J T
de Herder, Wouter W
Feelders, Richard A
Franssen, Gaston J H
Hamoir, Marc
Maiter, Dominique
Perren, Aurel
Timmers, Henri J L M
van Eeden, Susanne
Vroonen, Laurent
Aydin, Selda
Robledo, Mercedes
Vikkula, Miikka
de Krijger, Ronald R
Dinjens, Winand N M
Persu, Alexandre
Korpershoek, Esther
UCL - SSS/DDUV/GEHU - Génétique
UCL - SSS/IREC/MIRO - Pôle d'imagerie moléculaire, radiothérapie et oncologie
UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition
UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire
UCL - (SLuc) Service de pathologie cardiovasculaire
UCL - (SLuc) Service d'anatomie pathologique
UCL - (SLuc) Service d'endocrinologie et de nutrition
UCL - (SLuc) Service d'oto-rhino-laryngologie
UCL - (SLuc) Centre du cancer
Evenepoel, Lucie
van Nederveen, Francien H
Oudijk, Lindsey
Papathomas, Thomas G
Restuccia, David F
Belt, Eric J T
de Herder, Wouter W
Feelders, Richard A
Franssen, Gaston J H
Hamoir, Marc
Maiter, Dominique
Perren, Aurel
Timmers, Henri J L M
van Eeden, Susanne
Vroonen, Laurent
Aydin, Selda
Robledo, Mercedes
Vikkula, Miikka
de Krijger, Ronald R
Dinjens, Winand N M
Persu, Alexandre
Korpershoek, Esther
Source :
Journal of Clinical Endocrinology and Metabolism, Vol. 103, no. 1, p. 46-55 (2018)
Publication Year :
2018

Abstract

Context: Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine, usually benign, tumors. Currently, the only reliable criterion of malignancy is the presence of metastases. Objective: The aim of this study was to identify genes associated with malignancy in PPGLs. Design: Transcriptomic profiling was performed on 40 benign and 11 malignant PPGLs. Genes showing a significantly different expression between benign and malignant PPGLs with a ratio ≥4 were confirmed and tested in an independent series by quantitative real-time polymerase chain reaction (qRT-PCR). Immunohistochemistry was performed for the validated genes on 109 benign and 32 malignant PPGLs. Functional assays were performed with hPheo1 cells. Setting: This study was conducted at the Department of Pathology of the Erasmus MC University Medical Center Rotterdam Human Molecular Genetics laboratory of the de Duve Institute, University of Louvain. Patients: PPGL samples from 179 patients, diagnosed between 1972 and 2015, were included. Main outcome measures: Associations between gene expression and malignancy were tested using supervised clustering approaches. Results: Ten differentially expressed genes were selected based on messenger RNA (mRNA) expression array data. Contactin 4 (CNTN4) was overexpressed in malignant vs benign tumors [4.62-fold; false discovery rate (FDR), 0.001]. Overexpression at the mRNA level was confirmed using qRT-PCR (2.90-fold, P = 0.02; validation set: 4.26-fold, P = 0.005). Consistent findings were obtained in The Cancer Genome Atlas cohort (2.7-fold; FDR, 0.02). CNTN4 protein was more frequently expressed in malignant than in benign PPGLs by immunohistochemistry (58% vs 17%; P = 0.002). Survival after 7 days of culture under starvation conditions was significantly enhanced in hPheo1 cells transfected with CNTN4 complementary DNA. Conclusion: CNTN4 expression is consistently associated with malignant behavior in PPGLs.

Details

Database :
OAIster
Journal :
Journal of Clinical Endocrinology and Metabolism, Vol. 103, no. 1, p. 46-55 (2018)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130457771
Document Type :
Electronic Resource