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miR‐125b‐1 and miR‐378a are predictive biomarkers for the efficacy of vaccine treatment against colorectal cancer

机译:miR-125b-1和miR-378a是疫苗治疗结直肠癌疗效的预测性生物标志物

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摘要

Many clinical trials of peptide vaccines have been conducted. However, these vaccines have provided clinical benefits in only a small fraction of patients. The purpose of the present study was to explore microRNAs (miRNAs) as novel predictive biomarkers for the efficacy of vaccine treatment against colorectal cancer. First, we carried out microarray analysis of pretreatment cancer tissues in a phase I study, in which peptide vaccines alone were given. Candidate miRNAs were selected by comparison of the better prognosis group with the poorer prognosis group. Next, we conducted microarray analysis of cancer tissues in a phase II study, in which peptide vaccines combined with chemotherapy were given. Candidate miRNAs were further selected by a similar comparison of prognosis. Subsequently, we carried out reverse‐transcription PCR analysis of phase II cases, separating cancer tissues into cancer cells and stromal tissue using laser capture microdissection. Treatment effect in relation to overall survival (OS) and miRNA expression was analyzed. Three miRNA predictors were negatively associated with OS: miR‐125b‐1 in cancer cells (P = 0.040), and miR‐378a in both cancer cells (P = 0.009) and stromal cells (P < 0.001). Multivariate analysis showed that expression of miR‐378a in stromal cells was the best among the three predictors (HR, 2.730; 95% CI, 1.027–7.585; P = 0.044). In conclusion, miR‐125b‐1 and miR‐378a expression might be considered as novel biomarkers to predict the efficacy of vaccine treatment against colorectal cancer.
机译:肽疫苗已进行了许多临床试验。但是,这些疫苗仅在一小部分患者中提供了临床益处。本研究的目的是探索微小RNA(miRNA)作为新型预测生物标记物,用于疫苗治疗结肠直肠癌的功效。首先,在I期研究中,我们对预处理的癌症组织进行了微阵列分析,其中仅给予了肽疫苗。通过比较预后较好的组和预后较差的组来选择候选miRNA。接下来,我们在一项II期研究中对癌症组织进行了微阵列分析,该研究中给出了结合化学疗法的肽疫苗。通过相似的预后比较进一步选择候选miRNA。随后,我们对II期病例进行了逆转录PCR分析,使用激光捕获显微切割术将癌症组织分为癌细胞和基质组织。分析了与总生存期(OS)和miRNA表达有关的治疗效果。三种miRNA预测因子与OS呈负相关:癌细胞中的miR-125b-1(P = 0.040),癌细胞中的miR-378a(P = 0.009)和基质细胞(P <0.001)。多变量分析显示,在三个预测因子(HR,2.730; 95%CI,1.027-7.585; P = 0.044)中,基质细胞中miR-378a的表达最好。总之,miR-125b-1和miR-378a的表达可能被视为预测疫苗治疗结直肠癌疗效的新生物标记。

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