COMPARATIVE GENOMIC HYBRIDIZATION IN THE DETECTION OF DNA COPY NUMBER ABNORMALITIES IN UVEAL MELANOMA

被引:0
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作者
GORDON, KB
THOMPSON, CT
CHAR, DH
OBRIEN, JM
KROLL, S
GHAZVINI, S
GRAY, JW
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT OPHTHALMOL,OCULAR ONCOL UNIT,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,MOLEC CYTOMETRY LAB,SAN FRANCISCO,CA 94143
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genomic instability appears to play an important role in the development, growth, invasiveness, and eventual metastasis of the neoplastic cell. We have used a powerful new technique, comparative genomic hybridization, to evaluate genetic alterations in 10 fresh frozen uveal melanomas. Comparative genomic hybridization utilizes dual fluorescence in situ hybridization to characterize chromosome deletions and duplications, allowing for simultaneous evaluation of the entire human genome. Several consistent chromosomal abnormalities were detected. This study confirmed previous findings obtained using standard cytogenetic techniques but demonstrated an increased incidence in abnormalities of chromosomes 3 and 8; there was loss of chromosome 3 and duplication of 8q. In addition, we identified, although less frequently, other recurrent abnormal regions including alterations on chromosomes 6p, 7q, 9p, and 13q.
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页码:4764 / 4768
页数:5
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