Department of Oncology, St Olavs Hospital, Trondheim University Hospital, Olav Kyrresgt 17, Trondheim 7006, Norway.
Br J Cancer. 2013 Apr 30;108(8):1712-9. doi: 10.1038/bjc.2013.121. Epub 2013 Apr 4.
microRNAs (miRNAs) exist in blood in an apparently stable form. We have explored whether serum miRNAs can be used as non-invasive early biomarkers of colon cancer.
Serum samples from 30 patients with colon cancer stage IV and 10 healthy controls were examined for the expression of 375 cancer-relevant miRNAs. Based on the miRNA profile in this study, 34 selected miRNAs were measured in serum from 40 patients with stage I-II colon cancer and from 10 additional controls.
Twenty miRNAs were differentially expressed in serum from stage IV patients compared with controls (P<0.01). Unsupervised clustering revealed four subgroups; one corresponding mostly to the control group and the three others to the patient groups. Of the 34 miRNAs measured in the follow-up study of stage I-II patients, 21 showed concordant expression between stage IV and stage I-II patient. Based on the profiles of these 21 miRNAs, a supervised linear regression analysis (Partial Least Squares Regression) was performed. Using this model we correctly assigned stage I-II colon cancer patients based on miRNA profiles of stage IV patients.
Serum miRNA expression profiling may be utilised in early detection of colon cancer.
microRNAs(miRNAs)以明显稳定的形式存在于血液中。我们探索了血清 miRNAs 是否可作为结肠癌的非侵入性早期生物标志物。
检测了 30 例 IV 期结肠癌患者和 10 例健康对照者的血清样本,以检测 375 种与癌症相关的 miRNAs 的表达情况。根据本研究中的 miRNA 图谱,在 40 例 I-II 期结肠癌患者和另外 10 例对照者的血清中测量了 34 种选定的 miRNAs。
与对照组相比,IV 期患者血清中有 20 种 miRNAs 表达差异显著(P<0.01)。无监督聚类显示有四个亚群;一个主要对应对照组,另外三个对应患者组。在 I-II 期患者的随访研究中测量的 34 种 miRNAs 中,有 21 种在 IV 期和 I-II 期患者之间的表达一致。基于这 21 种 miRNAs 的图谱,进行了监督线性回归分析(偏最小二乘回归)。使用该模型,我们根据 IV 期患者的 miRNA 图谱正确分配了 I-II 期结肠癌患者。
血清 miRNA 表达谱分析可用于结肠癌的早期检测。