OCGR array: an oral cancer genomic regional array for comparative genomic hybridization analysis

被引:32
作者
Garnis, C
Campbell, J
Zhang, LW
Rosin, MP
Lam, WL
机构
[1] British Columbia Canc Res Ctr, Vancouver, BC V5Z 1L3, Canada
[2] Univ British Columbia, Dept Pathol, Vancouver, BC V6T 2B5, Canada
[3] Univ British Columbia, Dept Lab Med, Vancouver, BC V6T 2B5, Canada
关键词
oral; head and neck; progression; array CGH; profiling; copy number; microamplification; high resolution; cancer;
D O I
10.1016/j.oraloncology.2003.10.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic alterations have been recognized as important events in the carcinogenesis of oral squamous cell carcinoma (OSCC) and have been used as predictors of progression risk. In this study, we have designed an oral cancer-specific human bacterial. artificial chromosome (BAC) array, called the oral cancer genomic regional array (OCGR), to detect and fine map copy number alterations in OSCC. This array contains a total of similar to45 Mbp coverage of nine chromosomal regions reported to be involved in the progression of oral cancer. We demonstrate the detection of copy number alterations in 14 microdissected clinical specimens in each of the nine regions. These include both copy number increases and decreases. Although the number of regions selected for this first generation array is small, we observed multiple segmental changes. In some cases, we observed single BAC clone alterations at 7p11 and 11q13 which contain EGFR and cyclin D1 respectively highlighting the need for high resolution detection techniques. Array comparative genomic hybridization (CGH) complements traditional methods for detecting genetic alterations in OSCC (such as microsatellite and CGH analysis) by improving the detection of segmental copy number alterations to single BAC clone resolution. This work represents the first attempt at the construction of an oral cancer-specific CGH array. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:511 / 519
页数:9
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