Department of Cancer Prevention and Controls, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
PLoS One. 2010 Oct 29;5(10):e13735. doi: 10.1371/journal.pone.0013735.
To date, there are no highly sensitive and specific minimally invasive biomarkers for detection of breast cancer at an early stage. The occurrence of circulating microRNAs (miRNAs) in blood components (including serum and plasma) has been repeatedly observed in cancer patients as well as healthy controls. Because of the significance of miRNA in carcinogenesis, circulating miRNAs in blood may be unique biomarkers for early and minimally invasive diagnosis of human cancers. The objective of this pilot study was to discover a panel of circulating miRNAs as potential novel breast cancer biomarkers.
METHODOLOGY/PRINCIPAL FINDINGS: Using microarray-based expression profiling followed by Real-Time quantitative Polymerase Cycle Reaction (RT-qPCR) validation, we compared the levels of circulating miRNAs in plasma samples from 20 women with early stage breast cancer (10 Caucasian American (CA) and 10 African American (AA)) and 20 matched healthy controls (10 CAs and 10 AAs). Using the significance level of p<0.05 constrained by at least two-fold expression change as selection criteria, we found that 31 miRNAs were differentially expressed in CA study subjects (17 up and 14 down) and 18 miRNAs were differentially expressed in AA study subjects (9 up and 9 down). Interestingly, only 2 differentially expressed miRNAs overlapped between CA and AA study subjects. Using receiver operational curve (ROC) analysis, we show that not only up-regulated but also down-regulated miRNAs can discriminate patients with breast cancer from healthy controls with reasonable sensitivity and specificity. To further explore the potential roles of these circulating miRNAs in breast carcinogenesis, we applied pathway-based bioinformatics exploratory analysis and predicted a number of significantly enriched pathways which are predicted to be regulated by these circulating miRNAs, most of which are involved in critical cell functions, cancer development and progression.
Our observations from this pilot study suggest that the altered levels of circulating miRNAs might have great potential to serve as novel, noninvasive biomarkers for early detection of breast cancer.
迄今为止,还没有高度敏感和特异的微创生物标志物用于早期检测乳腺癌。在癌症患者和健康对照者的血液成分(包括血清和血浆)中,循环 microRNAs(miRNAs)的出现已被反复观察到。由于 miRNA 在致癌作用中的重要性,血液中的循环 miRNAs 可能是人类癌症早期和微创诊断的独特生物标志物。本初步研究的目的是发现一组循环 miRNAs 作为潜在的新型乳腺癌生物标志物。
方法/主要发现:我们使用基于微阵列的表达谱分析,然后使用实时定量聚合酶链反应(RT-qPCR)验证,比较了 20 名早期乳腺癌(10 名白种人(CA)和 10 名非裔美国人(AA))和 20 名匹配健康对照者(10 名 CA 和 10 名 AA)血浆样本中的循环 miRNAs 水平。使用至少两倍表达变化的显著性水平(p<0.05)作为选择标准,我们发现 CA 研究对象中有 31 个 miRNAs 表达差异(17 个上调和 14 个下调),AA 研究对象中有 18 个 miRNAs 表达差异(9 个上调和 9 个下调)。有趣的是,CA 和 AA 研究对象中仅重叠 2 个差异表达的 miRNAs。使用接收者操作特性曲线(ROC)分析,我们表明不仅上调的 miRNAs,而且下调的 miRNAs 都可以以合理的灵敏度和特异性将乳腺癌患者与健康对照者区分开来。为了进一步探索这些循环 miRNAs 在乳腺癌发生中的潜在作用,我们应用基于途径的生物信息学探索性分析,并预测了许多显著富集的途径,这些途径预计受这些循环 miRNAs 的调节,其中大多数与关键的细胞功能、癌症发展和进展有关。
本初步研究的观察结果表明,循环 miRNAs 水平的改变可能具有作为乳腺癌早期检测的新型无创生物标志物的巨大潜力。