Grade Marian, Hörmann Patrick, Becker Sandra, Hummon Amanda B, Wangsa Danny, Varma Sudhir, Simon Richard, Liersch Torsten, Becker Heinz, Difilippantonio Michael J, Ghadimi B Michael, Ried Thomas
Department of General Surgery, University Medical Center, Robert-Koch-Strasse 40, 37075 Göttingen, Germany.
Cancer Res. 2007 Jan 1;67(1):41-56. doi: 10.1158/0008-5472.CAN-06-1514.
To characterize patterns of global transcriptional deregulation in primary colon carcinomas, we did gene expression profiling of 73 tumors [Unio Internationale Contra Cancrum stage II (n = 33) and stage III (n = 40)] using oligonucleotide microarrays. For 30 of the tumors, expression profiles were compared with those from matched normal mucosa samples. We identified a set of 1,950 genes with highly significant deregulation between tumors and mucosa samples (P < 1e-7). A significant proportion of these genes mapped to chromosome 20 (P = 0.01). Seventeen genes had a >5-fold average expression difference between normal colon mucosa and carcinomas, including up-regulation of MYC and of HMGA1, a putative oncogene. Furthermore, we identified 68 genes that were significantly differentially expressed between lymph node-negative and lymph node-positive tumors (P < 0.001), the functional annotation of which revealed a preponderance of genes that play a role in cellular immune response and surveillance. The microarray-derived gene expression levels of 20 deregulated genes were validated using quantitative real-time reverse transcription-PCR in >40 tumor and normal mucosa samples with good concordance between the techniques. Finally, we established a relationship between specific genomic imbalances, which were mapped for 32 of the analyzed colon tumors by comparative genomic hybridization, and alterations of global transcriptional activity. Previously, we had conducted a similar analysis of primary rectal carcinomas. The systematic comparison of colon and rectal carcinomas revealed a significant overlap of genomic imbalances and transcriptional deregulation, including activation of the Wnt/beta-catenin signaling cascade, suggesting similar pathogenic pathways.
为了描述原发性结肠癌中全球转录失调的模式,我们使用寡核苷酸微阵列对73例肿瘤(国际抗癌联盟II期,n = 33;III期,n = 40)进行了基因表达谱分析。对于其中30例肿瘤,将其表达谱与匹配的正常黏膜样本的表达谱进行了比较。我们鉴定出一组1950个基因,这些基因在肿瘤和黏膜样本之间存在高度显著的失调(P < 1e-7)。这些基因中有很大一部分定位于20号染色体(P = 0.01)。17个基因在正常结肠黏膜和癌组织之间的平均表达差异>5倍,包括MYC和假定的癌基因HMGA1的上调。此外,我们鉴定出68个在淋巴结阴性和淋巴结阳性肿瘤之间显著差异表达的基因(P < 0.001),其功能注释显示在细胞免疫反应和监测中起作用的基因占优势。在40多个肿瘤和正常黏膜样本中,使用定量实时逆转录PCR对20个失调基因的微阵列衍生基因表达水平进行了验证,两种技术之间具有良好的一致性。最后,我们建立了特定基因组失衡(通过比较基因组杂交对32例分析的结肠肿瘤进行定位)与全球转录活性改变之间的关系。此前,我们对原发性直肠癌进行了类似的分析。结肠癌和直肠癌的系统比较显示基因组失衡和转录失调存在显著重叠,包括Wnt/β-连环蛋白信号级联的激活,提示致病途径相似。