Center of Molecular Medicine, Institute of Prevention and Occupational Medicine of the German Social Accident Insurance-Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
PLoS One. 2012;7(1):e30221. doi: 10.1371/journal.pone.0030221. Epub 2012 Jan 11.
To date, no biomarkers with reasonable sensitivity and specificity for the early detection of malignant mesothelioma have been described. The use of microRNAs (miRNAs) as minimally-invasive biomarkers has opened new opportunities for the diagnosis of cancer, primarily because they exhibit tumor-specific expression profiles and have been commonly observed in blood of both cancer patients and healthy controls. The aim of this pilot study was to identify miRNAs in the cellular fraction of human peripheral blood as potential novel biomarkers for the detection of malignant mesothelioma.
METHODOLOGY/PRINCIPAL FINDINGS: Using oligonucleotide microarrays for biomarker identification the miRNA levels in the cellular fraction of human peripheral blood of mesothelioma patients and asbestos-exposed controls were analyzed. Using a threefold expression change in combination with a significance level of p<0.05, miR-103 was identified as a potential biomarker for malignant mesothelioma. Quantitative real-time PCR (qRT-PCR) was used for validation of miR-103 in 23 malignant mesothelioma patients, 17 asbestos-exposed controls, and 25 controls from the general population. For discrimination of mesothelioma patients from asbestos-exposed controls a sensitivity of 83% and a specificity of 71% were calculated, and for discrimination of mesothelioma patients from the general population a sensitivity of 78% and a specificity of 76%.
CONCLUSIONS/SIGNIFICANCE: The results of this pilot study show that miR-103 is characterized by a promising sensitivity and specificity and might be a potential minimally-invasive biomarker for the diagnosis of mesothelioma. In addition, our results support the concept of using the cellular fraction of human blood for biomarker discovery. However, for early detection of malignant mesothelioma the feasibility of miR-103 alone or in combination with other biomarkers needs to be analyzed in a prospective study.
迄今为止,尚无具有合理灵敏度和特异性的生物标志物可用于恶性间皮瘤的早期检测。使用 microRNAs(miRNAs)作为微创生物标志物为癌症的诊断开辟了新的机会,主要是因为它们表现出肿瘤特异性的表达谱,并且在癌症患者和健康对照者的血液中都经常观察到。本初步研究的目的是鉴定人外周血细胞部分中的 miRNAs,作为恶性间皮瘤检测的潜在新型生物标志物。
方法/主要发现:使用寡核苷酸微阵列进行生物标志物鉴定,分析了间皮瘤患者和接触石棉的对照组人外周血细胞部分中的 miRNA 水平。使用三倍表达变化结合 p<0.05 的显著性水平,鉴定 miR-103 为恶性间皮瘤的潜在生物标志物。采用定量实时 PCR(qRT-PCR)对 23 名恶性间皮瘤患者、17 名接触石棉的对照组和 25 名普通人群对照进行了 miR-103 的验证。为了区分间皮瘤患者和接触石棉的对照组,计算出敏感性为 83%,特异性为 71%,而区分间皮瘤患者和普通人群,敏感性为 78%,特异性为 76%。
结论/意义:本初步研究结果表明,miR-103 具有有前途的灵敏度和特异性,可能是间皮瘤诊断的潜在微创生物标志物。此外,我们的结果支持使用人血液细胞部分进行生物标志物发现的概念。然而,为了恶性间皮瘤的早期检测,需要在前瞻性研究中分析 miR-103 单独或与其他生物标志物联合的可行性。