数字聚合酶链反应
多路复用
甲基化
DNA甲基化
癌症
生物
胰腺癌
前列腺癌
结直肠癌
癌症研究
计算生物学
生物信息学
DNA
聚合酶链反应
基因
遗传学
基因表达
作者
Isabelle Neefs,Nele De Meulenaere,Thomas Vanpoucke,Janah Vandenhoeck,Dieter Peeters,Marc Peeters,Guy Van Camp,Ken Op de Beeck
标识
DOI:10.1002/1878-0261.13708
摘要
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.
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