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基于新一代测序的HPV基因分型检测方法在福尔马林固定、石蜡包埋的口咽癌和宫颈癌标本中得到验证。

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

作者信息

Ambulos Nicholas P, Schumaker Lisa M, Mathias Trevor J, White Ruth, Troyer Jennifer, Wells David, Cullen Kevin J

机构信息

1 University of Maryland Marlene and Stewart Greenebaum Cancer Center, Baltimore, Maryland 21201, USA; and 2 Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland 21702, USA.

出版信息

J Biomol Tech. 2016 Jul;27(2):46-52. doi: 10.7171/jbt.16-2702-004. Epub 2016 Mar 7.

Abstract

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.

摘要

现有的用于头颈癌的临床人乳头瘤病毒(HPV)诊断方法灵敏度有限,和/或无法确定HPV基因型。常见的HPV基因分型检测成本高且 labor intensive。我们试图开发一种基于新一代测序(NGS)的HPV基因分型检测方法,其灵敏度足以用于福尔马林固定石蜡包埋(FFPE)样本。我们使用带条形码的HPV PCR广谱通用引物5(+)/6(+)(BSGP)5(+)/6(+)开发了一种离子激流NGS HPV基因分型检测方法。为了验证基因分型的特异性以及在存档临床FFPE肿瘤样本中的应用,我们在2个测序中心比较了NGS HPV基因分型与罗氏线性阵列检测法在42份口咽癌和宫颈癌标本中的分型结果,这些标本代表10种HPV基因型以及HPV阴性病例。为了证明能检测多种HPV基因型,我们对一组266例宫颈癌进行了基因分型。将FFPE癌标本的NGS基因分型与线性阵列基因分型进行比较,结果显示在测序位点1的34/37个样本(92%)和测序位点2的39/42个样本(93%)中结果一致。两个位点之间的一致性为92%。该检测方法设计用于10 ng基因组DNA,使用低至1.25 ng FFPE来源的基因组DNA就能检测到HPV。在266例宫颈癌标本中,NGS检测方法鉴定出20种不同的HPV基因型,包括所有13种致癌基因型。这种新型的NGS检测方法提供了一种灵敏、特异的高通量方法,以低样本成本检测和鉴定来自FFPE的一系列临床标本中的HPV。

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