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首页> 外文期刊>Cancer Biomarkers >Circulating miR-17-3p, miR-29a, miR-92a and miR-135b in serum: Evidence against their usage as biomarkers in colorectal cancer
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Circulating miR-17-3p, miR-29a, miR-92a and miR-135b in serum: Evidence against their usage as biomarkers in colorectal cancer

机译:血清中循环的miR-17-3p,miR-29a,miR-92a和miR-135b:反对将其用作大肠癌生物标志物的证据

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BACKGROUND: Colorectal cancer (CRC) is one of the leading causes of cancer-related death in the world. Therefore, there isna high demand for cost-effective and non-invasive biomarkers that would enable an early detection of asymptomatic and curablendisease with high sensitivity and specificity.nOBJECTIVE: The main objective of this study was to investigate the potential of circulating miRNAs as biomarkers of CRC.nMETHODS: Total RNA enriched for small RNAs was isolated from 100 sera of patients with CRC and 30 sera of healthyndonors. The expression levels of miR-17-3p, miR-29a, miR-92a and miR-135b were determined using quantitative real-timenPCR. The average expression levels of particular miRNAs were normalized to miR-16 levels and statistically evaluated.nRESULTS: Using Mann-Whitney U test, no significant differences were observed in miR-17-3p (P = 0.18), miR-29a (P =n0.14) and miR-92a (P = 0.60) levels between sera of CRC patients and controls. The levels of miR-135b in serum were too lownto be quantified accurately. Subsequently, we tried to correlate expression levels of analyzed miRNAs to clinical-pathologicalnfeatures of CRC patients. Only levels of mir-29a were correlated with the clinical stage (P = 0.04). Expression levels of thenother miRNAs were correlated neither with the clinical stage, nor with the grade.nCONCLUSIONS: Interestingly, our results are contradictory to previous studies performed on the CRC patients from Chinesenpopulation, providing an evidence against usage of serum miR-17-3p, miR-29a, miR-92a and miR-135b as new biomarkers fornearly detection of CRC.
机译:背景:大肠癌(CRC)是世界上与癌症相关的死亡的主要原因之一。因此,对具有成本效益的,非侵入性的生物标志物的需求很高,能够以高灵敏度和特异性早期检测无症状和可治愈的疾病。目的:本研究的主要目的是研究循环miRNAs作为生物标志物的潜力。 CRC.nMETHODS:从小儿CRC患者的100血清和健康人的30血清中分离出富含小分子RNA的总RNA。使用实时定量PCR检测miR-17-3p,miR-29a,miR-92a和miR-135b的表达水平。将特定miRNA的平均表达水平标准化为miR-16水平并进行统计学评估。n结果:使用Mann-Whitney U检验,在miR-17-3p(P = 0.18),miR-29a(P = CRC患者血清与对照组之间的n0.14)和miR-92a(P = 0.60)水平。血清中的miR-135b水平太低,无法准确定量。随后,我们试图将分析的miRNA的表达水平与CRC患者的临床病理特征相关联。 mir-29a的水平仅与临床阶段相关(P = 0.04)。结论:有趣的是,我们的结果与先前对中国人群的CRC患者进行的研究相矛盾,提供了反对使用血清miR-17-3p的证据, miR-29a,miR-92a和miR-135b是近来检测CRC的新生物标记。

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