Dataset Information
Rational genomic optimization of DNA detection for human papillomavirus type 16 in head and neck squamous cell carcinoma.
Ontology highlight
ABSTRACT: Background
We aimed to use genomic data for optimizing polymerase chain reaction (PCR) primer/probe sets for detection of human papillomavirus (HPV)-16 in body fluids of patients with HPV-related head and neck squamous cell carcinoma (HPV-HNSCC).Methods
We used genomic HPV-HNSCC sequencing data from a single institutional and a TCGA cohort. Optimized primer/probe sets were designed and tested for analytical performance in CaSki HPV-16 genome and confirmed in salivary rinse samples from patients with HPV-HNSCC.Results
The highest read density was observed between E5 and L2 regions. The E1 region contained a region that was universally present. Among candidate PCR primer/probe sets created, six reliably detected 30 HPV-16 copy number. In a CLIA certified laboratory setting, the combination of two novel primer/probe with E7 sets improved performance in salivary rinse samples with a sensitivity of 96% and specificity of 100%.Conclusions
PCR-based detection of HPV-16 DNA in HPV-HNSCC can be improved using rational genomic design.
SUBMITTER: Saito Y
PROVIDER: S-EPMC7699136 | biostudies-literature | 2020 Apr
REPOSITORIES: biostudies-literature
Publications
Rational genomic optimization of DNA detection for human papillomavirus type 16 in head and neck squamous cell carcinoma.
Head & neck 20191218 4
<h4>Background</h4>We aimed to use genomic data for optimizing polymerase chain reaction (PCR) primer/probe sets for detection of human papillomavirus (HPV)-16 in body fluids of patients with HPV-related head and neck squamous cell carcinoma (HPV-HNSCC).<h4>Methods</h4>We used genomic HPV-HNSCC sequencing data from a single institutional and a TCGA cohort. Optimized primer/probe sets were designed and tested for analytical performance in CaSki HPV-16 genome and confirmed in salivary rinse sample ...[more]
