Rosetta Genomics Ltd., Rehovot, Israel.
Mod Pathol. 2010 Jun;23(6):814-23. doi: 10.1038/modpathol.2010.57. Epub 2010 Mar 26.
Identification of the tissue of origin of a tumor is vital to its management. Previous studies showed tissue-specific expression patterns of microRNA and suggested that microRNA profiling would be useful in addressing this diagnostic challenge. MicroRNAs are well preserved in formalin-fixed, paraffin-embedded (FFPE) samples, further supporting this approach. To develop a standardized assay for identification of the tissue origin of FFPE tumor samples, we used microarray data from 504 tumor samples to select a shortlist of 104 microRNA biomarker candidates. These 104 microRNAs were profiled by proprietary quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) on 356 FFPE tumor samples. A total of 48 microRNAs were chosen from this list of candidates and used to train a classifier. We developed a clinical test for the identification of the tumor tissue of origin based on a standardized protocol and defined the classification criteria. The test measures expression levels of 48 microRNAs by qRT-PCR, and predicts the tissue of origin among 25 possible classes, corresponding to 17 distinct tissues and organs. The biologically motivated classifier combines the predictions generated by a binary decision tree and K-nearest neighbors (KNN). The classifier was validated on an independent, blinded set of 204 FFPE tumor samples, including nearly 100 metastatic tumor samples. The test predictions correctly identified the reference diagnosis in 85% of the cases. In 66% of the cases the two algorithm predictions (tree and KNN) agreed on a single-tissue origin, which was identical to the reference diagnosis in 90% of cases. Thus, a qRT-PCR test based on the expression profile of 48 tissue-specific microRNAs allows accurate identification of the tumor tissue of origin.
鉴定肿瘤的组织来源对于其治疗至关重要。先前的研究表明,miRNA 具有组织特异性表达模式,并提示 miRNA 谱分析将有助于解决这一诊断难题。miRNA 在福尔马林固定、石蜡包埋(FFPE)样本中保存完好,进一步支持了这种方法。为了开发一种用于鉴定 FFPE 肿瘤样本组织来源的标准化检测方法,我们使用了来自 504 个肿瘤样本的微阵列数据,从中选择了 104 个 miRNA 生物标志物候选物。对 356 个 FFPE 肿瘤样本进行了这 104 个 miRNA 的专有定量逆转录聚合酶链反应(qRT-PCR)分析。从候选名单中总共选择了 48 个 miRNA 并用于训练分类器。我们基于标准化方案开发了一种用于鉴定肿瘤组织来源的临床检测方法,并定义了分类标准。该检测通过 qRT-PCR 测量 48 个 miRNA 的表达水平,并预测 25 种可能类别中的组织来源,对应于 17 个不同的组织和器官。基于生物启发的分类器结合了二叉决策树和 K 近邻(KNN)生成的预测。该分类器在一个独立的、盲法的 204 个 FFPE 肿瘤样本集上进行了验证,包括近 100 个转移性肿瘤样本。该检测在 85%的病例中正确识别了参考诊断。在 66%的病例中,两种算法(树和 KNN)的预测一致,单一组织来源与参考诊断相同,在 90%的病例中。因此,基于 48 个组织特异性 miRNA 表达谱的 qRT-PCR 检测可准确鉴定肿瘤的组织来源。