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MYC Up-regulation Is a Useful Biomarker for Preoperative Neoadjuvant Chemotherapy Combined With Anti-EGFR in Liver Metastasis from Colorectal Cancer

机译:Myc上调是一种有用的生物标志物用于术前Neoadjuvant化疗与肝脏转移中的抗EGFR联合联合癌症

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Background/Aim: At present, there are no biomarkers to predict the effects of molecular targeted drugs in patients with CRC with liver metastasis. Thus, we performed this study to explore potential biomarkers for these patients. Materials and Methods: We obtained cancer tissue specimens from liver metastasis-bearing CRC patients who received the following preoperative neoadjuvant chemotherapies with molecular targeted drugs: i) no therapy (n=3), ii) 5-FU+oxaliplatin+anti-EGFR (n=3), iii) and 5-FU+oxaliplatin+anti-VEGF (n=3). Results: We investigated the RNA expression of 84 genes related to cancer drug resistance using an RT-PCR array. The MYC gene was the only gene that was significantly up-regulated in CRC tissue specimens from anti-EGFR group in comparison to the anti-VEGF group. Conclusion: MYC up-regulation in the primary CRC tissues may be a potentially useful biomarker for selecting anti-EGFR combination therapy in neoadjuvant chemotherapy for CRC with liver metastasis.
机译:背景/目的:目前,没有生物标志物预测CRC与肝转移患者分子靶向药物的影响。因此,我们进行了这项研究以探索这些患者的潜在生物标志物。材料和方法:我们从肝转移的CRC患者获得癌症组织标本,他们接受了与分子靶向药物的以下术前Neoadjuvant化学疗法:i)没有治疗(n = 3),ii)5-FU + Oxaliplatin +抗EGFR( n = 3),iii)和5-fu + Oxaliplatin +抗VEGF(n = 3)。结果:使用RT-PCR阵列研究了84个基因的RNA表达。使用RT-PCR阵列。与抗VEGF组相比,MYC基因是抗EGFR组的CRC组织标本中显着上调的唯一基因。结论:初级CRC组织中的Myc上调可能是潜在的生物标志物,用于选择肝转移的新辅助化疗中的抗EGFR组合治疗。

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