Strazisar Mojca, Rott Tomaz, Glavac Damjan
Department of Molecular Genetics, Faculty of Medicine, University of Ljubljana, Korytkova 2, 1000 Ljubljana, Slovenia.
Lung Cancer. 2009 Mar;63(3):354-9. doi: 10.1016/j.lungcan.2008.06.005. Epub 2008 Jul 24.
Contrary to the recent hypothesis that S100A2 is a tumour suppressor, no somatic mutations have yet been identified. We therefore screened 90 non-small cell lung carcinoma (NSCLC) samples, initially for mutations in S100A2 and then also for mutations in P53 and K-RAS genes. Alterations were detected in 46.7% of squamous lung cancer (SCC) samples, but we detected only one novel tumour specific mutation, Q23X in squamous carcinoma. We detected four polymorphisms, two of them published for the first time (144+109 C/G and 297+75A/G) and two already published: S62N, in the coding region and related to squamous cell carcinoma (SCC), and 297+17T/C. Analysis of S100A2 expression revealed that expression in adenocarcinomas and squamous cell carcinomas is significantly different, but not related to any of the found alterations. In one tumour with S62N polymorphism, P53 and K-RAS genes were also mutated, while two tumours with the Q23X mutation have a P53 but no K-RAS mutation. To the best of our knowledge, this is the first report describing alterations in the S100A2 gene proving a relation between changes in predominantly squamous lung cancer.
与最近关于S100A2是一种肿瘤抑制因子的假说相反,目前尚未发现体细胞突变。因此,我们对90份非小细胞肺癌(NSCLC)样本进行了筛查,首先检测S100A2基因的突变,然后检测P53和K-RAS基因的突变。在46.7%的肺鳞状细胞癌(SCC)样本中检测到了改变,但我们仅在鳞状细胞癌中检测到一种新的肿瘤特异性突变,即Q23X。我们检测到4种多态性,其中2种是首次发表(144+109 C/G和297+75A/G),另外2种已发表:编码区与鳞状细胞癌(SCC)相关的S62N,以及297+17T/C。对S100A2表达的分析显示,腺癌和鳞状细胞癌中的表达存在显著差异,但与任何已发现的改变均无关联。在1例具有S62N多态性的肿瘤中,P53和K-RAS基因也发生了突变,而2例具有Q23X突变的肿瘤有P53突变但无K-RAS突变。据我们所知,这是第一份描述S100A2基因改变并证明其与主要为肺鳞状细胞癌变化之间存在关联的报告。