TY  - JOUR
IS  - 11
AV  - public
PB  - S. Karger AG
VL  - 35
ID  - heidok17825
EP  - 688
JF  - Onkologie
N2  - Background: Desmoid tumors are neoplastic proliferations of connective tissues. The mutation status of the gene coding for catenin (cadherin-associated protein) beta 1 (CTNNB1) and trisomy 8 on the chromosomal level have been described to have prognostic relevance. Patients and Methods: In order to elucidate new molecular mechanisms underlying these tumors, we carried out a molecular analysis with a genome-wide human high-density single-nucleotide polymorphism (SNP) array, in 9 patients. Results: Single samples showed numerical aberrations on chromosomes (Chrs) 20 and 6 with either trisomy 20 or monosomy 6. No trisomy 8 could be detected. Recurrent heterozygous deletions were found in Chr 5q (including the APC gene locus, n = 3) and Chr 8p23 (n = 4, containing coding regions for the potential tumor suppressor gene CSMD1). This novel deletion in 8p23 showed an association with local recurrence. In addition, structural chromosomal changes (gain of Chrs 8 and 20) were found in a minority of cases. Conclusion: The genomic alteration affecting the candidate gene CSMD1 could be important in the development of desmoid tumors.
UR  - https://archiv.ub.uni-heidelberg.de/volltextserver/17825/
SP  - 684
A1  - Erben, Philipp
A1  - Nowak, Daniel
A1  - Sauer, Christian
A1  - Ströbel, Philipp
A1  - Hofmann, Wolf-Karsten
A1  - Hofheinz, Ralf-Dieter
A1  - Hohenberger, Peter
A1  - Kasper, Bernd
SN  - 0378-584X
TI  - Molecular analysis of desmoid tumors with a high-density single-nucleotide polymorphism array identifies new molecular candidate lesions
Y1  - 2012///
ER  -