Department of Surgery of Shanghai Ruijin Hospital and Shanghai Institute of Digestive Surgery, Shanghai, PR China.
Oncogene. 2010 Jul 8;29(27):3908-20. doi: 10.1038/onc.2010.143. Epub 2010 May 3.
The IRX1 tumor suppressor gene is located on 5p15.33, a cancer susceptibility locus. Loss of heterozygosity of 5p15.33 in gastric cancer was identified in our previous work. In this study, we analyzed the molecular features and function of IRX1. We found that IRX1 expression was lost or reduced in gastric cancer. However, no mutations were identified in IRX1-encoding regions. IRX1 transcription was suppressed by hypermethylation, and the expression of IRX1 mRNA was partially restored in gastric cancer cells after 5-Aza-dC treatment. Restoring IRX1 expression in SGC-7901 and NCI-N87 gastric cancer cells inhibited growth, invasion and tumorigenesis in vitro and in vivo. We identified a number of target genes by global microarray analysis after IRX1 transfection combined with real-time PCR and chromatin immunoprecipitation assay. BDKRB2, an angiogenesis-related gene, HIST2H2BE and FGF7, cell proliferation and invasion-related genes, were identified as direct IRX1 target genes. The hypermethylation of IRX1 was not only detected in primary gastric cancer tissues but also in the peripheral blood of gastric cancer patients, suggesting IRX1 could potentially serve as a biomarker for gastric cancer.
IRX1 肿瘤抑制基因位于 5p15.33,这是一个癌症易感性位点。在我们之前的工作中已经鉴定出胃癌中 5p15.33 的杂合性丢失。在这项研究中,我们分析了 IRX1 的分子特征和功能。我们发现 IRX1 在胃癌中的表达缺失或减少。然而,在 IRX1 编码区域没有发现突变。IRX1 转录受到超甲基化的抑制,并且在胃癌细胞中用 5-Aza-dC 处理后,IRX1 mRNA 的表达得到部分恢复。在 SGC-7901 和 NCI-N87 胃癌细胞中恢复 IRX1 的表达,在体外和体内抑制了生长、侵袭和肿瘤发生。我们通过 IRX1 转染结合实时 PCR 和染色质免疫沉淀分析,通过全基因组微阵列分析鉴定了一些靶基因。BDKRB2,一个与血管生成相关的基因,HIST2H2BE 和 FGF7,与细胞增殖和侵袭相关的基因,被鉴定为直接的 IRX1 靶基因。IRX1 的高甲基化不仅在原发性胃癌组织中检测到,而且在胃癌患者的外周血中也检测到,这表明 IRX1 可能是胃癌的潜在生物标志物。