Persson Fredrik, Olofsson Anita, Sjögren Helene, Chebbo Nihal, Nilsson Bengt, Stenman Göran, Aman Pierre
Lundberg Laboratory for Cancer Research, Department of Pathology, The Sahlgrenska Academy at Göteborg University, Göteborg, Sweden.
Cancer Lett. 2008 Feb 18;260(1-2):37-47. doi: 10.1016/j.canlet.2007.10.032. Epub 2007 Dec 21.
The cytogenetic hallmark of well-differentiated liposarcoma (WDLS) is a giant marker chromosomes containing amplified genes from chromosome 12q13-q15. Here, we have employed SKY and high-resolution 244K oligonucleotide array CGH to characterize rearrangements and amplifications in a new WDLS cell line (GOT3) with a giant marker chromosome derived from chromosomes 12, 1, and X. The most prominent amplifications included 144 genes in 12q11-q21.2, 201 genes in 1q23.3-q44, and six genes in 13q32.1-q32.2. In the 12q amplicons, MDM2 showed the highest level of amplification followed by LYZ, HMGA2 (5'-part), TSPAN8, CNOT2, YEATS4, CDK4, GNS, HELB, and TSFM. Expression analysis of genes from the three major amplicons revealed that several highly amplified potential target genes, including HMGA2, MDM2, YEATS4, CDK4, PKP1, IPO9, and SOX21, were strongly overexpressed. Studies of cell cycle controlling proteins that interact with CDK4 and MDM2 revealed an abnormally strong expression of cyclins D1 and E. The selective high-level amplification of the 5'-part of HMGA2, including the DNA-binding domains, suggests that this gene is a major target of amplifications in WDLS. Our results also identify several novel candidate genes of potential pathogenetic and therapeutic importance for WDLS.
高分化脂肪肉瘤(WDLS)的细胞遗传学特征是一条巨大的标记染色体,其包含来自12q13-q15染色体的扩增基因。在此,我们运用光谱核型分析(SKY)和高分辨率244K寡核苷酸阵列比较基因组杂交技术(CGH),对一个新的WDLS细胞系(GOT3)中的重排和扩增进行特征分析,该细胞系带有一条源自12号、1号和X染色体的巨大标记染色体。最显著的扩增包括12q11-q21.2区域的144个基因、1q23.3-q44区域的201个基因以及13q32.1-q32.2区域的6个基因。在12q扩增子中,MDM2的扩增水平最高,其次是LYZ、HMGA2(5'端部分)、TSPAN8、CNOT2、YEATS4、CDK4、GNS、HELB和TSFM。对来自三个主要扩增子的基因进行表达分析发现,包括HMGA2、MDM2、YEATS4、CDK4、PKP1、IPO9和SOX21在内的几个高度扩增的潜在靶基因均强烈过表达。对与CDK4和MDM2相互作用的细胞周期调控蛋白的研究显示,细胞周期蛋白D1和E异常强烈表达。HMGA2 5'端部分(包括DNA结合结构域)的选择性高水平扩增表明,该基因是WDLS扩增的主要靶点。我们的结果还鉴定出了几个对WDLS具有潜在致病和治疗重要性的新候选基因。