Department of Pathology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium.
Virchows Arch. 2011 Feb;458(2):197-203. doi: 10.1007/s00428-010-1012-7. Epub 2010 Nov 27.
The aim of this study was to investigate murine double minute-2 (MDM2) gene copy number changes in colon carcinoma and to correlate these findings with an immunohistochemical analysis of MDM2 protein expression and histopathologic prognostic indicators of the tumors. The study included 80 cases of sporadic colon carcinomas. MDM2 protein expression was assessed by immunohistochemistry, and MDM2 gene status by fluorescence in situ hybridization. MDM2 gene amplification was detected in 18% of the 80 cases examined. A strong correlation was found between MDM2 gene amplification and the presence, intensity, and staining proportion of cytoplasmic MDM2 protein expression (p = 0.01). No correlation was found between MDM2 gene amplification and the well-established histopathologic prognostic factors. Given the correlation with gene amplification, we clearly demonstrated that cytoplasmic expression of MDM2 protein is true and relevant and that this finding has to be taken into account when immunohistochemistry would be used as a screening for MDM2 gene amplification in the near future. Targeting MDM2 could be a new approach in colon cancer therapy. The amplification status could be a predictive factor of the response to MDM2-targeted therapy.
本研究旨在探讨结肠癌中鼠双微体 2(MDM2)基因拷贝数的变化,并将这些发现与 MDM2 蛋白表达的免疫组织化学分析以及肿瘤的组织病理学预后指标相关联。本研究纳入了 80 例散发性结肠癌病例。通过免疫组织化学评估 MDM2 蛋白表达,通过荧光原位杂交评估 MDM2 基因状态。在 80 例检查的病例中,检测到 18%存在 MDM2 基因扩增。我们发现 MDM2 基因扩增与细胞质 MDM2 蛋白表达的存在、强度和染色比例之间存在强烈相关性(p=0.01)。MDM2 基因扩增与既定的组织病理学预后因素之间没有相关性。鉴于与基因扩增的相关性,我们明确证实细胞质 MDM2 蛋白的表达是真实且相关的,在不久的将来,当免疫组织化学被用作 MDM2 基因扩增的筛选时,这一发现必须被考虑在内。靶向 MDM2 可能成为结肠癌治疗的新方法。扩增状态可能是对 MDM2 靶向治疗反应的预测因素。