Prediction of human papillomavirus 16 e6 gene expression and cervical intraepithelial neoplasia progression by methylation status
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19407553
DOI
10.1111/igc.0b013e31819d8a5c
PII: 00009577-200904000-00004
Knihovny.cz E-resources
- MeSH
- DNA, Viral analysis MeSH
- Adult MeSH
- Uterine Cervical Dysplasia genetics pathology virology MeSH
- Papillomavirus Infections genetics pathology virology MeSH
- Middle Aged MeSH
- Humans MeSH
- Human papillomavirus 16 genetics metabolism MeSH
- RNA, Messenger genetics metabolism MeSH
- DNA Methylation * MeSH
- Adolescent MeSH
- Young Adult MeSH
- Cell Transformation, Neoplastic MeSH
- Uterine Cervical Neoplasms genetics pathology virology MeSH
- Oncogene Proteins, Viral genetics MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Prognosis MeSH
- Disease Progression MeSH
- Promoter Regions, Genetic genetics MeSH
- Repressor Proteins genetics MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA, Viral MeSH
- E6 protein, Human papillomavirus type 16 MeSH Browser
- RNA, Messenger MeSH
- Oncogene Proteins, Viral MeSH
- Repressor Proteins MeSH
INTRODUCTION: Human papillomavirus (HPV) infection represents the most important risk factor for the development of cervical intraepithelial neoplasia (CIN) and cervical cancer. We aimed to analyze the consequences of methylation of the E6 gene promoter in distinct stages of HPV-16-induced cellular transformation to assess its importance for disease progression. METHODS: Human papillomavirus 16 was detected by sensitive polymerase chain reaction (PCR). Determination of E6 gene promoter methylation was analyzed by digestion with specific restriction endonuclease McrBC followed by PCR amplification. Expression of the E6 gene was determined by quantitative real-time PCR. RESULTS: Of 103 cervical smears from asymptomatic women with no cytological and colposcopic abnormalities, 20.4% were HPV-16-positive. Human papillomavirus 16 was present in 44.4% of 18 patients with CIN I, in 62.2% of 143 patients with CIN II/III, and in 74.2% of 31 cervix carcinoma specimens. The incidence of HPV-16 in all lesions compared with asymptomatic women was statistically significant (P < 0.001, Pearson chi test). Methylation was detected in 81% (n = 21) of HPV-16-positive asymptomatic smears compared with 62.5% in CIN I (n = 8), 31.5% (n = 89) in CIN II/III, and 43.4% (n = 23) in carcinomas; a statistical significance between lesions and healthy women was found (P < 0.001, Pearson chi test). Expression of E6 mRNA correlated with methylation status (P = 0.010, Mann-Whitney U test). CONCLUSIONS: We conclude that methylation of the E6 gene promoter in HPV-16 genome is a predictive biomarker for cervical cancer progression by regulating the expression of the E6 oncogene.
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