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Next-Generation Sequencing-Based HPV Genotyping Assay Validated in Formalin-Fixed Paraffin-Embedded Oropharyngeal and Cervical Cancer Specimens

机译:在福尔马林固定石蜡包埋的口咽和宫颈癌标本中验证了基于下一代测序的HPV基因分型方法

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摘要

Available clinical human papilloma virus (HPV) diagnostics for head and neck cancer have limited sensitivity and/or fail to define the HPV genotype. Common HPV genotyping assays are costly and labor intensive. We sought to develop a next-generation sequencing (NGS)-based HPV genotyping assay that was sensitive enough to work on formalin-fixed paraffin-embedded (FFPE) samples. We developed an ion torrent NGS HPV genotyping assay using barcoded HPV PCR broad-spectrum general primers 5+/6+ (BSGP)5+/6+. To validate genotype specificity and use in archived clinical FFPE tumor samples, we compared NGS HPV genotyping at 2 sequencing centers with typing by Roche Linear Array assay in 42 oropharyngeal and cervical cancer specimens representing 10 HPV genotypes, as well as HPV-negative cases. To demonstrate the detection of a broad range of HPV genotypes, we genotyped a cohort of 266 cervical cancers. A comparison of NGS genotyping of FFPE cancer specimens with genotyping by Linear Array showed concordant results in 34/37 samples (92%) at sequencing site 1 and 39/42 samples (93%) at sequencing site 2. Concordance between sites was 92%. Designed for use with 10 ng genomic DNA, the assay detected HPV using as little as 1.25 ng FFPE-derived genomic DNA. In 266 cervical cancer specimens, the NGS assay identified 20 different HPV genotypes, including all 13 carcinogenic genotypes. This novel NGS assay provides a sensitive and specific high-throughput method to detect and genotype HPV in a range of clinical specimens derived from FFPE with low per-sample cost.
机译:现有的用于头颈癌的临床人乳头瘤病毒(HPV)诊断方法敏感性有限和/或无法确定HPV基因型。常见的HPV基因分型测定既昂贵又费力。我们寻求开发一种基于下一代测序(NGS)的HPV基因分型测定法,该测定法足够灵敏,可用于福尔马林固定石蜡包埋(FFPE)样品。我们使用条形码HPV PCR广谱通用引物5 + / 6 + (BSGP)5 + /开发了一种离子洪峰NGS HPV基因型分析方法6 + 。为了验证基因型特异性并在已存档的FFPE临床肿瘤样本中使用,我们比较了2个测序中心的NGS HPV基因分型和Roche线性阵列分析的分型,对42例代表10种HPV基因型的口咽和宫颈癌标本以及HPV阴性病例进行了比较。为了证明检测到广泛的HPV基因型,我们对266例子宫颈癌进行了基因分型。 FFPE癌症标本的NGS基因分型与线性阵列基因分型的比较显示,测序位点1的34/37样品(92%)和测序位点2的39/42样品(93%)的结果一致。 。该分析法设计用于10 ng基因组DNA,可使用低至1.25 ng FFPE衍生的基因组DNA检测HPV。在266例宫颈癌标本中,NGS分析鉴定出20种不同的HPV基因型,包括所有13种致癌基因型。这种新颖的NGS分析方法提供了一种灵敏且特异的高通量方法,可以检测和鉴定FFPE衍生的一系列临床标本中的HPV并对其进行基因分型,且每次采样成本低。

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