Identification of a Five-MiRNA Expression Assay to Aid Colorectal Cancer Diagnosis

IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY
M. Davey, G. Feeney, H. Annuk, Maxwell Paganga, E. Holian, A. Lowery, M. Kerin, N. Miller
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引用次数: 1

Abstract

Introduction: One-third of colorectal cancer (CRC) patients present with advanced disease, and establishing control remains a challenge. Identifying novel biomarkers to facilitate earlier diagnosis is imperative in enhancing oncological outcomes. We aimed to create miRNA oncogenic signature to aid CRC diagnosis. Methods: Tumour and tumour-associated normal (TAN) were extracted from 74 patients during surgery for CRC. RNA was isolated and target miRNAs were quantified using real-time reverse transcriptase polymerase chain reaction. Regression analyses were performed in order to identify miRNA targets capable of differentiating CRC from TAN and compared with two endogenous controls (miR-16 and miR-345) in each sample. Areas under the curve (AUCs) in Receiver Operating Characteristic (ROC) analyses were determined. Results: MiR-21 (β-coefficient:3.661, SE:1.720, p = 0.033), miR-31 (β-coefficient:2.783, SE:0.918, p = 0.002), and miR-150 (β-coefficient:−4.404, SE:0.526, p = 0.004) expression profiles differentiated CRC from TAN. In multivariable analyses, increased miR-31 (β-coefficient:2.431, SE:0.715, p < 0.001) and reduced miR-150 (β-coefficient:−4.620, SE:1.319, p < 0.001) independently differentiated CRC from TAN. The highest AUC generated for miR-21, miR-31, and miR-150 in an oncogenic expression assay was 83.0% (95%CI: 61.7–100.0, p < 0.001). In the circulation of 34 independent CRC patients and 5 controls, the mean expression of miR-21 (p = 0.001), miR-31 (p = 0.001), and miR-150 (p < 0.001) differentiated CRC from controls; however, the median expression of miR-21 (p = 0.476), miR-31 (p = 0.933), and miR-150 (p = 0.148) failed to differentiate these groups. Conclusion: This study identified a five-miRNA signature capable of distinguishing CRC from normal tissues with a high diagnostic test accuracy. Further experimentation with this signature is required to elucidate its diagnostic relevance in the circulation of CRC patients.
五-三核糖核酸表达检测法辅助大肠癌癌症诊断的鉴定
简介:1/3的癌症(CRC)患者患有晚期疾病,建立控制仍然是一个挑战。识别新的生物标志物以促进早期诊断对于提高肿瘤学结果至关重要。我们的目的是创建miRNA致癌特征,以帮助CRC诊断。方法:从74例CRC患者中提取肿瘤和肿瘤相关正常(TAN)。分离RNA,并使用实时逆转录聚合酶链反应对靶miRNA进行定量。进行回归分析以鉴定能够区分CRC和TAN的miRNA靶标,并与每个样品中的两种内源性对照(miR-16和miR-345)进行比较。测定受试者操作特征(ROC)分析中的曲线下面积(AUCs)。结果:MiR-21(β-系数:3.661,SE:1.720,p=0.033)、MiR-31(β-系数值:2.783,SE:0.918,p=0.002)和MiR-150(β系数:−4.404,SE:0.526,p=0.004)的表达谱将CRC与TAN区分开来。在多变量分析中,miR-31增加(β-系数:2.431,SE:0.715,p<0.001)和miR-150减少(β系数:−4.620,SE:1.319,p<001)独立区分CRC和TAN。在致癌表达测定中,miR-21、miR-31和miR-150产生的最高AUC为83.0%(95%CI:61.7–100.0,p<0.001)。在34名独立CRC患者和5名对照组的循环中,miR21(p=0.001)、miR-31(p=001)和miR-150(p<001)的平均表达将CRC与对照组区分开来;然而,miR-21(p=0.476)、miR-31(p=0.933)和miR-150(p=0.148)的中值表达未能区分这些组。结论:本研究鉴定了一种能够以高诊断准确性区分CRC和正常组织的五种miRNA特征。需要对该特征进行进一步的实验,以阐明其在CRC患者循环中的诊断相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.50
自引率
0.00%
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审稿时长
10 weeks
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