Effect of HPV on tumor expression levels of the most commonly used markers in HNSCC
Language English Country United States Media print-electronic
Document type Comparative Study, Journal Article
PubMed
26666815
DOI
10.1007/s13277-015-4569-6
PII: 10.1007/s13277-015-4569-6
Knihovny.cz E-resources
- Keywords
- Head and neck cancer, Human papillomavirus, Kaplan-Meier analysis, Tumor markers,
- MeSH
- DNA, Viral genetics MeSH
- Adult MeSH
- Papillomavirus Infections complications virology MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger genetics MeSH
- Survival Rate MeSH
- Biomarkers, Tumor genetics MeSH
- Head and Neck Neoplasms etiology pathology MeSH
- Follow-Up Studies MeSH
- Papillomaviridae genetics MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Prognosis MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Carcinoma, Squamous Cell etiology pathology MeSH
- Neoplasm Staging MeSH
- Gene Expression Profiling MeSH
- Case-Control Studies MeSH
- Neoplasm Grading MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- DNA, Viral MeSH
- RNA, Messenger MeSH
- Biomarkers, Tumor MeSH
Approximately 90 % of head and neck cancers are squamous cell carcinomas (HNSCC), and the overall 5-year survival rate is not higher than 50 %. There is much evidence that human papillomavirus (HPV) infection may influence the expression of commonly studied HNSCC markers. Our study was focused on the possible HPV-specificity of molecular markers that could be key players in important steps of cancerogenesis (MKI67, EGF, EGFR, BCL-2, BAX, FOS, JUN, TP53, MT1A, MT2A, VEGFA, FLT1, MMP2, MMP9, and POU5F). qRT-PCR analysis of these selected genes was performed on 74 biopsy samples of tumors from patients with histologically verified HNSCC (22 HPV-, 52 HPV+). Kaplan-Meier analysis was done to determine the relevance of these selected markers for HNSCC prognosis. In conclusion, our study confirms the impact of HPV infection on commonly studied HNSCC markers MT2A, MMP9, FLT1, VEGFA, and POU5F that were more highly expressed in HPV-negative HNSCC patients and also shows the relevance of studied markers in HPV-positive and HPV-negative HNSCC patients.
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