Institute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Cancer Biomark. 2010;8(1):11-9. doi: 10.3233/DMA-2011-0814.
Thirteen laryngeal squamous cell carcinoma cell lines were recently studied by array comparative genomic hybridization (array-CGH) in order to identify recurrent DNA copy number alterations in the tumor genome. A highly amplified region 22q11.2 was found in two of the thirteen cell lines. Two established oncogenes CRKL and MAPK1 are localized in this region, but only CRKL was amplified in both cell lines. Therefore, to check if amplification of either CRKL or MAPK1 genes may be important in the pathogenesis of laryngeal squamous cell carcinoma, the DNA copy number and mRNA expression were measured in a cohort of 17 LSCC cell lines by quantitative real-time PCR (qPCR). For the CRKL gene gains of the copy number were found in 3/17 cell lines, while overexpression was found in 6/17 cell lines. Gains in the copy number for the MAPK1 gene were found in 1/17 cell lines, but overexpression was not detected in any cell line. A highly significant correlation between DNA copy number and expression for CRKL gene, but not for MAPK1 gene was established using the Pearson test. Thereafter, 46 primary samples of laryngeal cancer were tested by qPCR to check for possible gains in copy number of the CRKL gene. Gains were found in 3/46 cases. These results suggest that CRKL, but not MAPK1 is the target oncogene of the rare but recurrent amplification at 22q11.2 in laryngeal squamous cell carcinoma.
最近,通过阵列比较基因组杂交(array-CGH)研究了 13 种喉鳞状细胞癌细胞系,以鉴定肿瘤基因组中反复出现的 DNA 拷贝数改变。在这 13 种细胞系中的两种中发现了一个高度扩增的区域 22q11.2。两个已建立的癌基因 CRKL 和 MAPK1 位于该区域,但只有 CRKL 在这两个细胞系中被扩增。因此,为了检查 CRKL 或 MAPK1 基因的扩增是否可能在喉鳞状细胞癌的发病机制中很重要,通过定量实时 PCR(qPCR)在 17 种 LSCC 细胞系中测量了 DNA 拷贝数和 mRNA 表达。对于 CRKL 基因,发现 3/17 种细胞系中的拷贝数获得,而在 6/17 种细胞系中发现过表达。在 1/17 种细胞系中发现了 MAPK1 基因的拷贝数获得,但在任何细胞系中均未检测到过表达。使用 Pearson 检验建立了 CRKL 基因的 DNA 拷贝数与表达之间高度显著的相关性,但 MAPK1 基因则没有。此后,通过 qPCR 测试了 46 个喉癌原发性样本,以检查 CRKL 基因的拷贝数是否可能增加。在 3/46 例中发现了增益。这些结果表明,CRKL 是 22q11.2 罕见但反复扩增的喉鳞状细胞癌的靶癌基因,而不是 MAPK1。