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血清中循环 miR-17-3p、miR-29a、miR-92a 和 miR-135b:其作为结直肠癌生物标志物的证据不足。

Circulating miR-17-3p, miR-29a, miR-92a and miR-135b in serum: Evidence against their usage as biomarkers in colorectal cancer.

机构信息

Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Brno, Czech Republic.

出版信息

Cancer Biomark. 2012;12(4):199-204. doi: 10.3233/CBM-130308.

Abstract

BACKGROUND

Colorectal cancer (CRC) is one of the leading causes of cancer-related death in the world. Therefore, there is a high demand for cost-effective and non-invasive biomarkers that would enable an early detection of asymptomatic and curable disease with high sensitivity and specificity.

OBJECTIVE

The main objective of this study was to investigate the potential of circulating miRNAs as biomarkers of CRC.

METHODS

Total RNA enriched for small RNAs was isolated from 100~sera of patients with CRC and 30 sera of healthy donors. The expression levels of miR-17-3p, miR-29a, miR-92a and miR-135b were determined using quantitative real-time PCR. The average expression levels of particular miRNAs were normalized to miR-16 levels and statistically evaluated.

RESULTS

Using Mann-Whitney U test, no significant differences were observed in miR-17-3p (P=0.18), miR-29a (P=0.14) and miR-92a (P=0.60) levels between sera of CRC patients and controls. The levels of miR-135b in serum were too low to be quantified accurately. Subsequently, we tried to correlate expression levels of analyzed miRNAs to clinical-pathological features of CRC patients. Only levels of mir-29a were correlated with the clinical stage (P=0.04). Expression levels of the other miRNAs were correlated neither with the clinical stage, nor with the grade.

CONCLUSIONS

Interestingly, our results are contradictory to previous studies performed on the CRC patients from Chinese population, providing an evidence against usage of serum miR-17-3p, miR-29a, miR-92a and miR-135b as new biomarkers for early detection of CRC.

摘要

背景

结直肠癌(CRC)是全球癌症相关死亡的主要原因之一。因此,人们非常需要具有成本效益且非侵入性的生物标志物,以便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 miRNA 作为 CRC 生物标志物的潜力。

方法

从 100 例 CRC 患者和 30 例健康供体的血清中分离富含小 RNA 的总 RNA。使用定量实时 PCR 测定 miR-17-3p、miR-29a、miR-92a 和 miR-135b 的表达水平。特定 miRNA 的平均表达水平与 miR-16 水平归一化,并进行统计学评估。

结果

使用 Mann-Whitney U 检验,CRC 患者和对照组血清中 miR-17-3p(P=0.18)、miR-29a(P=0.14)和 miR-92a(P=0.60)水平无显著差异。miR-135b 血清水平太低,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。只有 miR-29a 的水平与临床分期相关(P=0.04)。其他 miRNA 的表达水平与临床分期或分级均无关。

结论

有趣的是,我们的结果与之前在中国人群 CRC 患者中进行的研究结果相反,这表明血清 miR-17-3p、miR-29a、miR-92a 和 miR-135b 不能作为早期检测 CRC 的新生物标志物。

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