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Epidermal growth factor receptor expression and gene amplification in colorectal carcinoma: an immunohistochemical and chromogenic in situ hybridization study

机译:大肠癌中表皮生长因子受体的表达和基因扩增:免疫组织化学和生色原位杂交研究

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Recent data suggest that detection of epidermal growth factor receptor protein by immunohistochemistry (IHC) does not predict response to the antiepidermal growth factor receptor drug, cetuximab, in patients with colorectal carcinoma. In searching for foundation for further investigation to optimize patient selection for cetuximab therapy, this study sought to exploit the tissue microarray and chromogenic in situ hybridization techniques to evaluate the status of epidermal growth factor receptor gene amplification in colorectal cancer and its relationship with protein expression by IHC. The study included 158 primary or metastatic colorectal adenocarcinomas. Immunohistochemical results were scored as 0–3+ based on the intensity of membrane staining. The in situ hybridization signals were counted in 30 nuclei per tissue core. Overall, the rate of tissue loss was 7%, yielding 147 analyzable cases: 123 primary, 24 metastatic. Positive immunohistochemical staining of any intensity was detected in 85% (105/123) of primary and 79% (19/24) of metastatic tumors, whereas gene amplification (>5 gene copiesucleus) was only seen in 12% (15/123) of primary and 8% (2/24) of metastatic tumors. Only 2/15 primary and 1/2 metastatic tumors that showed gene amplification were amplified at a high level (>10 gene copiesucleus). Although a positive correlation was detected between the intensity of protein expression and the likelihood of gene amplification in both the primary (P=0.01) and the metastatic (P=0.05) tumors, IHC had a low specificity (17% in primary, 23% in metastatic) in predicting gene amplification. Conversely, all tumors that did not express the protein by IHC lacked gene amplification. Thus, this study shows that only a small fraction of epidermal growth factor receptor- positive colorectal carcinomas detected by IHC are associated with gene amplification. Additional studies are needed to determine whether epidermal growth factor receptor gene amplification bears any informative value in predicting response to cetuximab-based therapy.
机译:最新数据表明,通过免疫组织化学(IHC)检测表皮生长因子受体蛋白不能预测结直肠癌患者对抗表皮生长因子受体药物西妥昔单抗的反应。在寻找进一步研究以优化西妥昔单抗治疗患者选择的基础时,本研究寻求利用组织芯片和发色原位杂交技术评估大肠癌中表皮生长因子受体基因扩增的状态及其与蛋白表达的关系。 IHC。这项研究包括158例原发性或转移性结直肠腺癌。免疫组织化学结果根据膜染色强度计为0–3 +。原位杂交信号在每个组织核心的30个核中计数。总体而言,组织损失率为7%,可分析147例:原发性123例,转移性24例。在原发性转移性肿瘤的85%(105/123)和转移性肿瘤的79%(19/24)中检测到任何强度的阳性免疫组织化学染色,而基因扩增(> 5个基因拷贝/核)仅在12%中可见(15/123)原发性肿瘤和8%(2/24)转移性肿瘤。仅显示基因扩增的2/15原发性和1/2转移性肿瘤被高水平扩增(> 10个基因拷贝/核)。尽管在原发性(P = 0.01)和转移性(P = 0.05)肿瘤中蛋白表达强度和基因扩增的可能性之间均检测到正相关,但IHC的特异性很低(在原发性肿瘤中为17%,23) %(转移)中预测基因扩增。相反,所有不通过IHC表达该蛋白的肿瘤都缺乏基因扩增。因此,这项研究表明,通过IHC检测到的只有一小部分表皮生长因子受体阳性的结直肠癌与基因扩增有关。需要更多的研究来确定表皮生长因子受体基因扩增在预测基于西妥昔单抗的治疗反应中是否具有任何信息价值。

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