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使用多重液滴数字PCR分析法同时检测八种癌症类型。

Simultaneous detection of eight cancer types using a multiplex droplet digital PCR assay.

作者信息

Neefs Isabelle, De Meulenaere Nele, Vanpoucke Thomas, Vandenhoeck Janah, Peeters Dieter, Peeters Marc, Van Camp Guy, Op de Beeck Ken

机构信息

Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.

Center for Oncological Research, University of Antwerp and Antwerp University Hospital, Wilrijk, Belgium.

出版信息

Mol Oncol. 2025 Jan;19(1):188-203. doi: 10.1002/1878-0261.13708. Epub 2024 Sep 6.

DOI:10.1002/1878-0261.13708
PMID:39239847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11705734/
Abstract

DNA methylation biomarkers have emerged as promising tools for cancer detection. Common methylation patterns across tumor types allow multi-cancer detection. Droplet digital PCR (ddPCR) has gained considerable attention for methylation detection. However, multi-cancer detection using multiple targets in ddPCR has never been performed before. Therefore, we developed a multiplex ddPCR assay for multi-cancer detection. Based on previous data analyses using The Cancer Genome Atlas (TCGA), we selected differentially methylated targets for eight frequent tumor types (lung, breast, colorectal, prostate, pancreatic, head and neck, liver, and esophageal cancer). Three targets were validated using ddPCR in 103 tumor and 109 normal adjacent fresh frozen samples. Two distinct ddPCR assays were successfully developed. Output data from both assays is combined to obtain a read-out from the three targets together. Our overall ddPCR assay has a cross-validated area under the curve (cvAUC) of 0.948. Performance between distinct cancer types varies, with sensitivities ranging from 53.8% to 100% and specificities ranging from 80% to 100%. Compared to previously published single-target parameters, we show that combining targets can drastically increase sensitivity and specificity, while lowering DNA input. In conclusion, we are the first to report a multi-cancer methylation ddPCR assay, which allows for highly accurate tumor predictions.

摘要

DNA甲基化生物标志物已成为癌症检测的有前景的工具。不同肿瘤类型的常见甲基化模式可实现多癌检测。液滴数字PCR(ddPCR)在甲基化检测方面备受关注。然而,此前从未在ddPCR中使用多个靶点进行多癌检测。因此,我们开发了一种用于多癌检测的多重ddPCR检测方法。基于先前使用癌症基因组图谱(TCGA)进行的数据分析,我们为八种常见肿瘤类型(肺癌、乳腺癌、结直肠癌、前列腺癌、胰腺癌、头颈癌、肝癌和食管癌)选择了差异甲基化靶点。在103个肿瘤和109个正常相邻新鲜冷冻样本中使用ddPCR验证了三个靶点。成功开发了两种不同的ddPCR检测方法。将两种检测方法的输出数据合并,以共同获得三个靶点的读数。我们的整体ddPCR检测方法的交叉验证曲线下面积(cvAUC)为0.948。不同癌症类型之间的性能有所不同,灵敏度范围为53.8%至100%,特异性范围为80%至100%。与先前发表的单靶点参数相比,我们表明组合靶点可大幅提高灵敏度和特异性,同时降低DNA输入量。总之,我们首次报道了一种多癌甲基化ddPCR检测方法,该方法可实现高度准确的肿瘤预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/21180d1505c1/MOL2-19-188-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/63cbc69cdc46/MOL2-19-188-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/4e06ef0efd8a/MOL2-19-188-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/f3ba99ce01aa/MOL2-19-188-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/21180d1505c1/MOL2-19-188-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/63cbc69cdc46/MOL2-19-188-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/4e06ef0efd8a/MOL2-19-188-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/f3ba99ce01aa/MOL2-19-188-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b077/11705734/21180d1505c1/MOL2-19-188-g005.jpg

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