Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker

被引:38
作者
Fontecha, Nerea [1 ]
Basaras, Miren [1 ]
Hernaez, Silvia [2 ]
Andia, Daniel [3 ]
Cisterna, Ramon [1 ,2 ]
机构
[1] Univ Basque Country, UPV EHU, Fac Med & Odontol, Dept Microbiol Immunol & Parasitol, Leioa 48940, Spain
[2] Basurto Univ Hosp, Clin Microbiol & Infect Control Dept, Bilbao 48013, Spain
[3] Basurto Univ Hosp, Dept Obstet & Gynaecol, Bilbao 48013, Spain
关键词
High-risk HPV genotypes; E6/E7 mRNA detection; Oncogenes; Biomarker; Prognosis marker; HPV GENOTYPE DISTRIBUTION; INTRAEPITHELIAL NEOPLASIA; CANCER; WOMEN; CYTOLOGY; DNA; INFECTION; SEVERITY; TRENDS; ASSAY;
D O I
10.1186/s12885-016-2885-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The aims of this study were to detect HPV E6/E7 mRNA expression in women with high-risk genotypes (HPV-16, -18, -31, -33 and -45) analysing its relationship with tissue pathology and 2) 2-year follow-up of E6/E7 mRNA tested group. Methods: Our samples were genotyped and classified by pathologists according to Bethesda system. After RNA extraction, E6/E7 oncogene mRNA detection was performed by NucliSens((R)) EasyQ((R)) HPV v1 Test (bioMerieux). Results: The results of the present study showed that E6/E7 mRNA positivity rate was 68.29 % in women tested once and 69.56 % in women tested twice. According to tissue pathology, all samples with high-grade lesions were positive for mRNA. Among women with low-grade lesions varied over the years from 89.28 to 84 % in women tested once and from 77.77 to 70 % in tested twice. Among women without lesion, positivity rate maintained in women tested once (from 50 to 41.38 %) and decreased in tested twice, from 63.63 to 44.44 %. Regarding lesion evolution, mRNA positivity was higher in women with lesion progression (53.13 %) and in women with positive results in two tested samples (83.33 %). Conclusion: HPV E6/E7 mRNA detection may be an effective screening test and biomarker for cervical cancer in women infected with these five genotypes. Nonetheless, further studies are needed to standardize as routine triage test.
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