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Let-7 miRNA-binding site polymorphism in the KRAS 3′UTR; colorectal cancer screening population prevalence and influence on clinical outcome in patients with metastatic colorectal cancer treated with 5-fluorouracil and oxaliplatin +/− cetuximab

机译:KRAS 3UTR中Let-7的miRNA结合位点多态性; 5-氟尿嘧啶和奥沙利铂+/-西妥昔单抗治疗转移性结直肠癌患者的结直肠癌筛查人群患病率及其对临床结局的影响

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摘要

BackgroundRecent studies have reported associations between a variant allele in a let-7 microRNA complementary site (LCS6) within the 3untranslated region (3UTR) of KRAS (rs61764370) and clinical outcome in metastatic colorectal cancer (mCRC) patients receiving cetuximab. The variant allele has also been associated with increased cancer risk. We aimed to reveal the incidence of the variant allele in a colorectal cancer screening population and to investigate the clinical relevance of the variant allele in mCRC patients treated with 1st line Nordic FLOX (bolus 5-fluorouracil/folinic acid and oxaliplatin) +/− cetuximab.
机译:背景最近的研究报道了KRAS的3 '非翻译区(3 ' UTR)内let-7 microRNA互补位点(LCS6)中的变异等位基因之间的关联(rs61764370)西妥昔单抗转移性大肠癌(mCRC)患者的临床和临床结局。变异等位基因也与增加的癌症风险有关。我们旨在揭示在结肠直肠癌筛查人群中变异等位基因的发生率,并研究变异等位基因在接受1 系Nordic FLOX(5-氟尿嘧啶/叶酸单剂量)治疗的mCRC患者中的临床相关性。酸和奥沙利铂)+/-西妥昔单抗。

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