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Chromosome 7 Multiplication in EGFR-positive Lung Carcinomas Based on Tissue Microarray Analysis

机译:基于组织芯片分析的EGFR阳性肺癌的染色体7增殖。

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摘要

Background/Aim: Epidermal growth factor receptor (EGFR) over-activation is observed in significant proportions of non-small cell lung carcinomas (NSCLC). Our aim was to investigate the role of chromosome 7 multiplication with regard to its influence in EGFR expression, combined or not with gene amplification. Materials and Methods: Using tissue microarray technology, fifty (n=50) primary NSCLCs were cored and re-embedded into the final recipient block. Immunohistochemistry (IHC) and also chromogenic in situ hybridization (CISH) were performed. Results: EGFR expression at any level was detected in 40/50 (80%) cores. Over-expression was observed in 23/40 (57.5%) cases. Gene amplification was identified in 11/50 (22%) cases whereas chromosome 7 polysomy in 8/50 (16%) cases. Pure chromosome 7 multiplication alone led to low or moderate levels of expression. Overall EGFR expression was correlated with gene (p=0.001) and interestingly with chromosome 7 centromere numerical imbalances (p=0.004). Conclusion: EGFR expression is associated not only with amplification, but also with chromosome 7 centromere multiple copies. Chromosome 7 multiplication –due to centromere region amplification or true polysomy– is critical for applying monoclonal antibody targeted therapeutic strategies excluding the pure non-amplified cases.
机译:背景/目的:在很大比例的非小细胞肺癌(NSCLC)中观察到表皮生长因子受体(EGFR)过度活化。我们的目的是研究染色体7倍增在EGFR表达中的影响,以及是否与基因扩增相结合的作用。材料和方法:使用组织微阵列技术,将五十个(n = 50)原发性NSCLC取芯并重新嵌入最终的受体区。进行了免疫组织化学(IHC)和生色原位杂交(CISH)。结果:在40/50(80%)核心中检测到任何水平的EGFR表达。在23/40(57.5%)的病例中观察到过表达。在11/50(22%)的病例中发现了基因扩增,而在8/50(16%)的病例中发现了7号染色体多态性。单纯的第7号染色体增殖导致低或中等水平的表达。总体EGFR表达与基因相关(p = 0.001),有趣的是与7号染色体着丝粒的数字失衡(p = 0.004)。结论:EGFR的表达不仅与扩增有关,而且与7号染色体着丝粒多拷贝有关。由于着丝粒区域扩增或真正的多体性,染色体7的增殖对于应用靶向单克隆抗体的治疗策略(不包括纯非扩增病例)至关重要。

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