High-resolution chromosome arm 5p array CGH analysis of small cell lung carcinoma cell lines

被引:35
作者
Coe, BR
Henderson, LJ
Garnis, C
Tsao, MS
Gazdar, AF
Minna, J
Lam, S
MacAulay, C
Lam, WL
机构
[1] British Columbia Canc Res Ctr, Vancouver, BC V5Z 3L1, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 1M9, Canada
[3] Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
[4] Univ Texas, SW Med Ctr, Hamon Ctr Therapeut Oncol Res, Dallas, TX 75230 USA
关键词
D O I
10.1002/gcc.20137
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genomic amplification of regions on chromosome arm 5p has been observed frequently in small cell lung cancer (SCLC), implying the presence of multiple oncogenes on this arm. Although conventional comparative genomic hybridization (CGH) detects gross chromosomal copy number changes, gene discovery requires a higher-resolution approach in order to identify regions of alteration precisely. To identify candidate genes on this chromosome arm, we developed a high-resolution, 10-clone-per-megabase bacterial artificial chromosome CGH array for 5p and examined a panel of 15 SCLC cell lines. Utilization of this CGH array has allowed the fine-mapping of breakpoints to regions as small as 200 kb in a single experiment. In addition to reporting our observations of aberrations at the well-characterized SKP2 and TERT loci, we describe the identification of microdeletions that have escaped detection by conventional screens and the identification TRIO and ANKH as novel putative oncogenes.(C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:308 / 313
页数:6
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