Comparative genomic hybridization array analysis and real time PCR reveals genomic alterations in squamous cell carcinomas of the lung

被引:49
作者
Choi, Yong-Woo
Choi, Jin Soo
Zheng, Long Tai
Lim, Yun Jeong
Yoon, Hyoung Kyu
Kim, Yeul Hong
Wang, Young-Pil
Lim, Young [1 ]
机构
[1] Catholic Univ Seoul, St Marys Hosp, Dept Occupat & Environm Med, Seoul, South Korea
[2] Catholic Univ Seoul, St Marys Hosp, Dept Anesthesiol, Seoul, South Korea
[3] Catholic Univ Seoul, Catholic Neurosci Ctr, Seoul, South Korea
[4] Kyung Hee Univ, Coll Med, Dept Pharmacol, Seoul, South Korea
[5] Catholic Univ Seoul, Coll Med, Dept Med, Div Pulm & Crit Care, Seoul, South Korea
[6] Catholic Univ Seoul, Dept Thorac Surg, Seoul, South Korea
[7] Korea Univ, Med Ctr, Dept Internal Med, Anam Hosp, Seoul 136701, South Korea
[8] Dongguk Univ, Coll Med, Dongguk Univ Int Hosp, Dept Internal Med, Goyang, South Korea
关键词
lung cancer; squamous cell carcinoma; array CGH; real time PCR; chromosomal aberration; gene amplification;
D O I
10.1016/j.lungcan.2006.09.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genomic alterations have been identified in lung cancer tissues and reported in numerous studies. To analyze genomic aberrations in lung cancer patients, we used array comparative genomic hybridization (array CGH) in 14 squamous cell lung carcinoma (SqC) tissues. Copy number gain and loss in chromosomal regions were detected, and the corresponding genes were confirmed by real time PCR. Several frequently altered loci, including gain of 3q (36% of samples), were found. The most frequently identified losses were found at 14q32.33 (21% of samples). The relative degree of chromosomal change was analyzed using log(2) ratios. High-level DNA amptifications (> 0.8 log(2) ratio) were detected at 20 regions in 1p, 2q, 3q, 4q, 6q, 7p, 8q, 9p, 10q, 12q, 14q and 19p. We found that the fold change levels were highest at EVI1 (3q26.2), LPP (3q27-28) and FHF-1 (3q28) gene loci. Our results show that array CGH is a useful tool. for identification of gene alteration in lung cancer, and that the above-mentioned genes might represent potential candidate genes for pathogenesis and diagnosis of lung cancer. (c) 2006 Elsevier Iretand Ltd. All rights reserved.
引用
收藏
页码:43 / 51
页数:9
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