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This Article Full Text Full Text (PDF) All Versions of this Article: ERC-08-0241v1 16/2/505    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Google Scholar Articles by van Nederveen, F. H Articles by de Krijger, R. R PubMed PubMed Citation Articles by van Nederveen, F. H Articles by de Krijger, R. R

Department of Pathology, Josephine Nefkens Institute, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands
¹ Department of Cancer Genetics, British Columbia Cancer Research Centre, Vancouver, Canada
² Departments of Pathology and Internal Medicine, University Medical Center St Radboud Nijmegen, Nijmegen, The Netherlands

(Correspondence should be addressed to F H van Nederveen who is now at Department of Pathology, Erasmus MC, Josephine Nefkens Institute, Room Be210a, PO Box 2040, 3000 CA Rotterdam, The Netherlands; Email: f.vannederveen{at}erasmusmc.nl)

^* (A A V is now deceased)

Pheochromocytomas (PCC) are catecholamine-producing tumors arising from the adrenal medulla that occur either sporadically or in the context of hereditary cancer syndromes, such as multiple endocrine neoplasia type 2 (MEN2), von Hippel-Lindau disease (VHL), neurofibromatosis type 1, and the PCC-paraganglioma syndrome. Conventional comparative genomic hybridization studies have shown loss of 1p and 3q in the majority of sporadic and MEN2-related PCC, and 3p and 11p loss in VHL-related PCC. The development of a submegabase tiling resolution array enabled us to perform a genome-wide high-resolution analysis of 36 sporadic benign PCC. The results show that there are two distinct patterns of abnormalities in these sporadic PCC, one consisting of loss of 1p with or without concomitant 3q loss in 20/36 cases (56%), the other characterized by loss of 3p with or without concomitant 11p loss in 11/36 (31%). In addition, we found loss of chromosome 22q at high frequency (35%), as well as the novel finding of high frequency chromosome 21q loss (21%). We conclude that there appear to be two subgroups of benign sporadic PCC, one of which has a pattern of chromosomal abnormalities that is comparable with PCC from patients with MEN2 and the other that is comparable with the PCC that arise in patients with VHL disease. In addition, genes on 21q and 22q might play a more important role in PCC pathogenesis than had been assumed thus far.

This article has been cited by other articles:

				J. Gaal, F. H. van Nederveen, Z. Erlic, E. Korpershoek, R. Oldenburg, C. C. Boedeker, U. Kontny, H. P. Neumann, W. N. M. Dinjens, and R. R. de Krijger Parasympathetic Paragangliomas Are Part of the Von Hippel-Lindau Syndrome J. Clin. Endocrinol. Metab., November 1, 2009; 94(11): 4367 - 4371. [Abstract] [Full Text] [PDF]