Prediction of human papillomavirus 16 e6 gene expression and cervical intraepithelial neoplasia progression by methylation status
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19407553
DOI
10.1111/igc.0b013e31819d8a5c
PII: S1048-891X(24)02692-6
Knihovny.cz E-zdroje
- MeSH
- DNA virů analýza MeSH
- dospělí MeSH
- dysplazie děložního hrdla genetika patologie virologie MeSH
- infekce papilomavirem genetika patologie virologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- lidský papilomavirus 16 genetika metabolismus MeSH
- messenger RNA genetika metabolismus MeSH
- metylace DNA * MeSH
- mladiství MeSH
- mladý dospělý MeSH
- nádorová transformace buněk MeSH
- nádory děložního čípku genetika patologie virologie MeSH
- onkogenní proteiny virové genetika MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- prognóza MeSH
- progrese nemoci MeSH
- promotorové oblasti (genetika) genetika MeSH
- represorové proteiny genetika MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA virů MeSH
- E6 protein, Human papillomavirus type 16 MeSH Prohlížeč
- messenger RNA MeSH
- onkogenní proteiny virové MeSH
- represorové proteiny 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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