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Overcoming negative predictions of microRNA expressions to gemcitabine response with FOLFIRINOX in advanced pancreatic cancer patients

机译:克服MicroRNA表达对晚期胰腺癌患者Folfirinox的吉西他滨反应的负面预测

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摘要

FOLFIRINOX is superior to gemcitabine in patients with pancreatic cancer, but this regimen is associated with toxicity and biomarkers for response are warranted. MicroRNAs can mediate drug resistance and could provide predictive information. Altered expressions of several microRNAs including miR-21-5p, miR-10b-5p and miR-34a-5p have been previously linked to a worse response to gemcitabine. We investigated the influence of expression levels in tumor tissue of those three microRNAs on outcome to FOLFIRINOX. Twenty-nine patients with sufficient formalin-fixed paraffin-embedded tumor tissue were identified. There was no significant association between high and low expression groups for these three microRNA. We conclude that polychemotherapy combination can overcome intrinsic negative prognostic factors.
机译:Folfirinox优于胰腺癌患者的吉西他滨,但这种方案与毒性有关,保证响应的生物标志物。 MicroRNA可以介导耐药性并提供预测信息。包括miR-21-5p,miR-10b-5p和miR-34a-5p在内的几个微小Rna的改变表达先前已与吉西他滨的更糟糕的反应相关联。我们调查了在结果对叶氟基毒素的那些三个微大稻草的肿瘤组织中表达水平的影响。鉴定了29例足够的足够福尔马林固定的石蜡包埋肿瘤组织。这三个microRNA的高表达组之间没有显着关联。我们得出结论,聚铬疗法组合可以克服内在的阴性预后因素。

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