Fluorescence in situ hybridization evaluation of c-erbB-2 gene amplification and chromosomal anomalies in bladder cancer

Citation
J. Ohta et al., Fluorescence in situ hybridization evaluation of c-erbB-2 gene amplification and chromosomal anomalies in bladder cancer, CLIN CANC R, 7(8), 2001, pp. 2463-2467
Citations number
25
Categorie Soggetti
Oncology
Journal title
CLINICAL CANCER RESEARCH
ISSN journal
10780432 → ACNP
Volume
7
Issue
8
Year of publication
2001
Pages
2463 - 2467
Database
ISI
SICI code
1078-0432(200108)7:8<2463:FISHEO>2.0.ZU;2-8
Abstract
Oncogene amplification and chromosomal anomalies are found in many solid tu mors and are often associated with aggressiveness of cancer. We evaluated t he frequency and the role of c-erbB-2 gene amplification, relative increase in c-erbB-2 gene copy number, and gain of chromosome 17 in bladder cancer. A total of 29 bladder cancer specimens were examined using fluorescence in situ hybridization (FISH). Dual labeling hybridization with a directly lab eled centromere probe for chromosome 17 together with a probe for the c-erb B-2 locus was performed. c-erbB-2 gene amplification was found in 3.4% (1 o f 29) of specimens. Relative increase in c-erbB-2 gene copy number was foun d in 41.4% (12 of 29) of specimens and was significantly associated with tu mor grade (P = 0.044 by Fisher's exact test). Gain of chromosome 17 was ide ntified in 65.5% (19 of 29) of specimens and was significantly associated w ith tumor grade (P = 0.002 by Fisher's exact test) and tumor stage (P = 0.0 03 by Fisher's exact test). Our results suggest that cerbB-2 gene amplifica tion, relative increase in c-erbB-2 gene copy number, and gain of chromosom e 17 may play important roles in the development and progression of bladder cancers. Moreover, the use of c-erbB-2 amplification, relative increase in c-erbB-2 gene copy number, and gain of chromosome 17 using FISH, together with tumor grade and stage, may provide a more useful clinical indicator in bladder cancer.