Henderson L-J, Coe B P, Lee E H L, Girard L, Gazdar A F, Minna J D, Lam S, MacAulay C, Lam W L
British Columbia Cancer Research Centre, 675 West 10th Avenue, Vancouver, BC, V5Z 1L3, Canada.
Br J Cancer. 2005 Apr 25;92(8):1553-60. doi: 10.1038/sj.bjc.6602452.
Genetic alterations occurring on human chromosome arm 1p are common in many types of cancer including lung, breast, neuroblastoma, pheochromocytoma, and colorectal. The identification of tumour suppressors and oncogenes on this arm has been limited by the low resolution of current technologies for fine mapping. In order to identify genetic alterations on 1p in small-cell lung carcinoma, we developed a new resource for fine mapping segmental DNA copy number alterations. We have constructed an array of 642 ordered and fingerprint-verified bacterial artificial chromosome clones spanning the 120 megabase (Mb) 1p arm from 1p11.2 to p36.33. The 1p arm of 15 small-cell lung cancer cell lines was analysed at sub-Mb resolution using this arm-specific array. Among the genetic alterations identified, two regions of recurrent amplification emerged. They were detected in at least 45% of the samples: a 580 kb region at 1p34.2-p34.3 and a 270 kb region at 1p11.2. We further defined the potential importance of these genomic amplifications by analysing the RNA expression of the genes in these regions with Affymetrix oligonucleotide arrays and semiquantitative reverse transcriptase-polymerase chain reaction. Our data revealed overexpression of the genes HEYL, HPCAL4, BMP8, IPT, and RLF, coinciding with genomic amplification.
人类染色体1p臂上发生的基因改变在许多类型的癌症中都很常见,包括肺癌、乳腺癌、神经母细胞瘤、嗜铬细胞瘤和结直肠癌。由于目前精细定位技术的分辨率较低,该染色体臂上肿瘤抑制基因和癌基因的鉴定受到了限制。为了鉴定小细胞肺癌中1p上的基因改变,我们开发了一种用于精细定位节段性DNA拷贝数改变的新资源。我们构建了一个由642个有序且经过指纹验证的细菌人工染色体克隆组成的阵列,覆盖了从1p11.2到p36.33的120兆碱基(Mb)的1p臂。使用这个特定于1p臂的阵列,以亚Mb分辨率分析了15个小细胞肺癌细胞系的1p臂。在鉴定出的基因改变中,出现了两个反复扩增的区域。它们在至少45%的样本中被检测到:一个位于1p34.2 - p34.3的580 kb区域和一个位于1p11.2的270 kb区域。我们通过使用Affymetrix寡核苷酸阵列和半定量逆转录聚合酶链反应分析这些区域中基因的RNA表达,进一步确定了这些基因组扩增的潜在重要性。我们的数据显示,基因HEYL、HPCAL4、BMP8、IPT和RLF的表达上调,与基因组扩增一致。