Institute of Pathology, University Hospital Basel, Basel, Switzerland.
Department of Biomedicine, University of Basel, Basel, Switzerland.
J Mol Diagn. 2018 Nov;20(6):836-848. doi: 10.1016/j.jmoldx.2018.07.003. Epub 2018 Aug 22.
Commercially available targeted panels miss genomic regions frequently altered in hepatocellular carcinoma (HCC). We sought to design and benchmark a sequencing assay for genomic screening of HCC. We designed an AmpliSeq custom panel targeting all exons of 33 protein-coding and two long noncoding RNA genes frequently mutated in HCC, TERT promoter, and nine genes with frequent copy number alterations. By using this panel, the profiling of DNA from fresh-frozen (n = 10, 1495×) and/or formalin-fixed, paraffin-embedded (FFPE) tumors with low-input DNA (n = 36, 530×) from 39 HCCs identified at least one somatic mutation in 90% of the cases. Median of 2.5 (range, 0 to 74) and 3 (range, 0 to 76) mutations were identified in fresh-frozen and FFPE tumors, respectively. Benchmarked against the mutations identified from Illumina whole-exome sequencing (WES) of the corresponding fresh-frozen tumors (105×), 98% (61 of 62) and 100% (104 of 104) of the mutations from WES were detected in the 10 fresh-frozen tumors and the 36 FFPE tumors, respectively, using the HCC panel. In addition, 18 and 70 somatic mutations in coding and noncoding genes, respectively, not found by WES were identified by using our HCC panel. Copy number alterations between WES and our HCC panel showed an overall concordance of 86%. In conclusion, we established a cost-effective assay for the detection of genomic alterations in HCC.
市售的靶向面板会遗漏肝癌(HCC)中经常发生改变的基因组区域。我们试图设计和基准测试 HCC 基因组筛选的测序检测。我们设计了一种 AmpliSeq 定制面板,靶向 HCC 中经常突变的 33 个蛋白编码和两个长非编码 RNA 基因(TERT 启动子)以及九个经常发生拷贝数改变的基因的所有外显子。通过使用该面板,对来自 39 个 HCC 的新鲜冷冻(n=10,1495×)和/或低输入 DNA 的福尔马林固定、石蜡包埋(FFPE)肿瘤(n=36,530×)的 DNA 进行分析,在 90%的病例中至少鉴定出一个体细胞突变。在新鲜冷冻和 FFPE 肿瘤中分别鉴定出中位数为 2.5(范围,0 至 74)和 3(范围,0 至 76)个突变。与相应新鲜冷冻肿瘤的 Illumina 全外显子组测序(WES)中鉴定出的突变进行基准测试(105×),使用 HCC 面板在 10 个新鲜冷冻肿瘤和 36 个 FFPE 肿瘤中分别检测到 WES 的 98%(61 个中的 62 个)和 100%(104 个中的 104 个)突变。此外,使用我们的 HCC 面板还鉴定出了 WES 未发现的编码和非编码基因中的 18 个和 70 个体细胞突变。WES 和我们的 HCC 面板之间的拷贝数改变总体一致性为 86%。总之,我们建立了一种用于检测 HCC 中基因组改变的具有成本效益的检测方法。