Comparison of HPV detection rate in formalin‐fixed paraffin‐embedded tissues of head and neck carcinoma using two DNA extraction kits and three amplification methods

• Published in: European journal of oral sciences Vol. 128; no. 6; pp. 501 - 507
• Main Authors: Božić, Ljiljana, Jovanović, Tanja, Šmitran, Aleksandra, Janković, Marko, Knežević, Aleksandra
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01-12-2020
• Subjects: Alphapapillomavirus - genetics; Amplification; Cancer; Carcinoma; Dentistry; Deoxyribonucleic acid; DNA; DNA fragmentation; Formaldehyde; formalin‐fixed paraffin‐embedded; Head & neck cancer; human papilloma virus; Human papillomavirus; Humans; nested PCR; Papillomaviridae - genetics; Papillomavirus Infections - diagnosis; Paraffin; Paraffin Embedding; Paraffins; Polymerase chain reaction; Silica; Silicon dioxide; Spectrophotometry; Squamous cell carcinoma; Statistical methods; Tissue Fixation; Tissues; Viruses; human papilloma virus; nested PCR; formalin-fixed paraffin-embedded; DNA fragmentation
• ISSN: 0909-8836; 1600-0722
• DOI: 10.1111/eos.12746

The potential problems of DNA extraction from formalin‐fixed paraffin‐embedded (FFPE) tissue samples and amplification efficiency of Human papilloma virus (HPV) may occur in the molecular studies of head and neck squamous carcinoma (HNSCC). The aim of this study was to compare HPV detection rate in FFPE tissues of oral, oropharyngeal, hypopharyngeal, and laryngeal cancers using two silica‐based extraction kits and three amplification methods. A total of 50 FFPE specimens from HNSCC tissues were analyzed. The quality and quantity of the extracted DNA were tested by spectrophotometry. HPV DNA was detected using a single polymerase chain reaction (PCR), a nested PCR, and a Real‐time PCR kit. Statistically significantly higher DNA quality and quantity was observed using the QIAamp DNA FFPE Tissue Kit than when using the QIAamp DNA Mini Kit. There was not HPV amplification in any of the 50 FFPE samples using the single PCR and Real‐time PCR kits, whereas HPV DNA was detected in 22% of samples using nested PCR. Comparing results of the three different methods showed that HPV DNA was detected only with nested PCR. The results presented imply that nested PCR is the most appropriate method for the detection of HPV DNA in FFPE samples, along with adequate DNA extraction methods.