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The hypermethylation of <jats:italic><jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>16<\/jats:italic>, <jats:italic><jats:styled-content style=\"fixed-case\">TSLC<\/jats:styled-content>\u20101<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101<\/jats:italic> genes was analyzed in squamous cell carcinomas (<jats:styled-content style=\"fixed-case\">SCC<\/jats:styled-content>), cervical intraepithelial lesions (<jats:styled-content style=\"fixed-case\">CIN<\/jats:styled-content>) and adenocarcinomas (<jats:styled-content style=\"fixed-case\">ADC<\/jats:styled-content>) of the uterine cervix (total 181 lesions). Additionally human papillomavirus (<jats:styled-content style=\"fixed-case\">HPV<\/jats:styled-content>) type, <jats:italic><jats:styled-content style=\"fixed-case\">EPB41L3<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">RASSF1<\/jats:styled-content><\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">RASSF2<\/jats:styled-content><\/jats:italic> hypermethylation were tested in <jats:styled-content style=\"fixed-case\">ADC<\/jats:styled-content> and the results were compared with those obtained previously by our group in <jats:styled-content style=\"fixed-case\">SCC<\/jats:styled-content>. <jats:italic><jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>16<\/jats:italic>, <jats:italic><jats:styled-content style=\"fixed-case\">TSLC<\/jats:styled-content>\u20101<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101<\/jats:italic> hypermethylation was more frequent in <jats:styled-content style=\"fixed-case\">SCCs<\/jats:styled-content> than in <jats:styled-content style=\"fixed-case\">CINs<\/jats:styled-content>. These percentages and the corresponding ones for <jats:italic><jats:styled-content style=\"fixed-case\">EPB41L3<\/jats:styled-content><\/jats:italic>, <jats:italic><jats:styled-content style=\"fixed-case\">RASSF1<\/jats:styled-content><\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">RASSF2<\/jats:styled-content><\/jats:italic> genes were also higher in <jats:styled-content style=\"fixed-case\">SCCs<\/jats:styled-content> than in <jats:styled-content style=\"fixed-case\">ADCs<\/jats:styled-content>, except for <jats:italic><jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>16<\/jats:italic>. The presence of <jats:styled-content style=\"fixed-case\">HPV<\/jats:styled-content> in <jats:styled-content style=\"fixed-case\">ADCs<\/jats:styled-content> was lower than reported previously in <jats:styled-content style=\"fixed-case\">SCC<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">CIN<\/jats:styled-content>. Patients with <jats:italic><jats:styled-content style=\"fixed-case\">RASSF1A<\/jats:styled-content><\/jats:italic> hypermethylation showed significantly longer disease\u2010free survival (<jats:italic>P<\/jats:italic> = 0.015) and overall survival periods (<jats:italic>P<\/jats:italic> = 0.009) in <jats:styled-content style=\"fixed-case\">ADC<\/jats:styled-content> patients. To our knowledge, this is the first description of the <jats:italic><jats:styled-content style=\"fixed-case\">EPB41L3<\/jats:styled-content><\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">RASSF2<\/jats:styled-content><\/jats:italic> hypermethylation in <jats:styled-content style=\"fixed-case\">ADCs<\/jats:styled-content>. These results suggest that the involvement of <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> hypermethylation in cervical cancer varies depending on the histological type, which might contribute to explaining the different prognosis of patients with these types of tumors.<\/jats:p>","DOI":"10.1111\/pin.12332","type":"journal-article","created":{"date-parts":[[2015,7,27]],"date-time":"2015-07-27T09:39:53Z","timestamp":1437989993000},"page":"476-485","source":"Crossref","is-referenced-by-count":12,"title":["Differential role of gene hypermethylation in adenocarcinomas, squamous cell carcinomas and cervical intraepithelial lesions of the uterine cervix"],"prefix":"10.1111","volume":"65","author":[{"given":"Idoia","family":"Blanco\u2010Luquin","sequence":"first","affiliation":[{"name":"Cancer Epigenetics Group Navarrabiomed\u2010Fundaci\u00f3n Miguel Servet Instituto de Investigaciones Sanitarias de Navarra\u2010IdiSNA  Pamplona Spain"},{"name":"Cancer 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