Kresse Stine H, Berner Jeanne-Marie, Meza-Zepeda Leonardo A, Gregory Simon G, Kuo Wen-Lin, Gray Joe W, Forus Anne, Myklebost Ola
Department of Tumour Biology, The Norwegian Radium Hospital, Oslo, Norway.
Mol Cancer. 2005 Nov 7;4:39. doi: 10.1186/1476-4598-4-39.
Amplification of the q21-q23 region on chromosome 1 is frequently found in sarcomas and a variety of other solid tumours. Previous analyses of sarcomas have indicated the presence of at least two separate amplicons within this region, one located in 1q21 and one located near the apolipoprotein A-II (APOA2) gene in 1q23. In this study we have mapped and characterized the amplicon in 1q23 in more detail.
We have used fluorescence in situ hybridisation (FISH) and microarray-based comparative genomic hybridisation (array CGH) to map and define the borders of the amplicon in 10 sarcomas. A subregion of approximately 800 kb was identified as the core of the amplicon. The amplification patterns of nine possible candidate target genes located to this subregion were determined by Southern blot analysis. The genes activating transcription factor 6 (ATF6) and dual specificity phosphatase 12 (DUSP12) showed the highest level of amplification, and they were also shown to be over-expressed by quantitative real-time reverse transcription PCR (RT-PCR). In general, the level of expression reflected the level of amplification in the different tumours. DUSP12 was expressed significantly higher than ATF6 in a subset of the tumours. In addition, two genes known to be transcriptionally activated by ATF6, glucose-regulated protein 78 kDa and -94 kDa (GRP78 and GRP94), were shown to be over-expressed in the tumours that showed over-expression of ATF6.
ATF6 and DUSP12 seem to be the most likely candidate target genes for the 1q23 amplification in sarcomas. Both genes have possible roles in promoting cell growth, which makes them interesting candidate targets.
1号染色体q21 - q23区域的扩增在肉瘤和多种其他实体瘤中经常被发现。先前对肉瘤的分析表明,该区域内至少存在两个独立的扩增子,一个位于1q21,另一个位于1q23的载脂蛋白A-II(APOA2)基因附近。在本研究中,我们更详细地绘制并表征了1q23中的扩增子。
我们使用荧光原位杂交(FISH)和基于微阵列的比较基因组杂交(阵列CGH)来绘制并确定10个肉瘤中扩增子的边界。一个约800 kb的子区域被确定为扩增子的核心。通过Southern印迹分析确定了位于该子区域的9个可能的候选靶基因的扩增模式。激活转录因子6(ATF6)和双特异性磷酸酶12(DUSP12)显示出最高水平的扩增,并且通过定量实时逆转录PCR(RT-PCR)也显示它们过表达。总体而言,表达水平反映了不同肿瘤中的扩增水平。在一部分肿瘤中,DUSP12的表达明显高于ATF6。此外,已知由ATF6转录激活的两个基因,78 kDa和 - 94 kDa葡萄糖调节蛋白(GRP78和GRP94),在显示ATF6过表达的肿瘤中也显示出过表达。
ATF6和DUSP12似乎是肉瘤中1q23扩增最可能的候选靶基因。这两个基因在促进细胞生长方面都可能起作用,这使它们成为有趣的候选靶点。