Chromosomal imbalances in sporadic neuroendocrine tumours of the thymus.

Abstract:

:Neuroendocrine (carcinoid) tumours of the thymus are rare neoplasms characterized by a highly malignant clinical behavior. Some of these tumors are associated with MEN1. In this study we evaluated 10 cases of sporadic thymic neuroendocrine tumours using immunohistochemistry and comparative genomic hybridization (CGH). All tumours showed a diffuse expression of neuron specific enolase (NSE) and synaptophysin. Chromosomal imbalances were detected in 8/10 cases, the most frequent gains were seen on chromosome Xp (3/10 cases), 7p, 7q, 11q, 12q, and 20q (2/10 each), losses were most frequently detected at 6q (5/10 each), 6p (3/10 each), 4q (3/10 each), 3p, 10q, 11q and 13 q (2/10 each). These CGH data show a degree of overlap with chromosomal imbalances commonly observed in advanced thymomas.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Rieker RJ,Aulmann S,Penzel R,Schnabel PA,Blaeker H,Esposito I,Morresi-Hauf A,Otto HF,Hecker E,Dienemann H,Schirmacher P,Mechtersheimer G

doi

10.1016/j.canlet.2004.10.027

keywords:

subject

Has Abstract

pub_date

2005-06-01 00:00:00

pages

169-74

issue

1

eissn

0304-3835

issn

1872-7980

pii

S0304-3835(04)00810-9

journal_volume

223

pub_type

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