Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics

Citation
M. Granzow et al., Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics, CANC GENET, 130(1), 2001, pp. 79-83
Citations number
26
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CANCER GENETICS AND CYTOGENETICS
ISSN journal
01654608 → ACNP
Volume
130
Issue
1
Year of publication
2001
Pages
79 - 83
Database
ISI
SICI code
0165-4608(20011001)130:1<79:I1AAEG>2.0.ZU;2-P
Abstract
Data concerning cytogenetic features of childhood ependymoma are rare. In t his article, a gain of 1q was identified as the sole alteration in a primar y childhood infratentorial ependymoma by comparative genomic hybridization (CGH). A recurrence of this brain tumor was studied using multiplex-fluores cence in situ hybridization (M-FISH) in addition to CGH and G-banding analy sis. In accordance with the primary tumor, a gain of Iq corresponding to an isochromosome Iq was observed indicating an early event in the tumor devel opment. Furthermore, M-FISH classified several other rearranged chromosomes including 6q and 17p that have previously been found to be involved in the development and progression of childhood ependymoma. (C) 2001 Elsevier Sci ence Inc. All rights reserved.