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dc.contributor.authorØvestad, Irene Tveiterås
dc.contributor.authorEngesæter, Birgit Øvstebø
dc.contributor.authorHalle, Mari Kyllesø
dc.contributor.authorAkbari, Saleha
dc.contributor.authorBicskei, Beatrix
dc.contributor.authorLapin, Morten
dc.contributor.authorAustdal, Marie
dc.contributor.authorJanssen, Emiel
dc.contributor.authorKrakstad, Camilla
dc.contributor.authorLillesand, Melinda
dc.contributor.authorNordhus, Marit
dc.contributor.authorMunk, Ane Cecilie Dæhli
dc.contributor.authorGudlaugsson, Einar
dc.date.accessioned2022-02-17T09:03:05Z
dc.date.available2022-02-17T09:03:05Z
dc.date.created2022-02-10T14:09:47Z
dc.date.issued2021
dc.identifier.issn1422-0067
dc.identifier.urihttps://hdl.handle.net/11250/2979565
dc.description.abstractImplementation of high-risk human papilloma virus (HPV) screening and the increasing proportion of HPV vaccinated women in the screening program will reduce the percentage of HPV positive women with oncogenic potential. In search of more specific markers to identify women with high risk of cancer development, we used RNA sequencing to compare the transcriptomic immune-profile of 13 lesions with cervical intraepithelial neoplasia grade 3 (CIN3) or adenocarcinoma in situ (AIS) and 14 normal biopsies from women with detected HPV infections. In CIN3/AIS lesions as compared to normal tissue, 27 differential expressed genes were identified. Transcriptomic analysis revealed significantly higher expression of a number of genes related to proliferation, (CDKN2A, MELK, CDK1, MKI67, CCNB2, BUB1, FOXM1, CDKN3), but significantly lower expression of genes related to a favorable immune response (NCAM1, ARG1, CD160, IL18, CX3CL1). Compared to the RNA sequencing results, good correlation was achieved with relative quantitative PCR analysis for NCAM1 and CDKN2A. Quantification of NCAM1 positive cells with immunohistochemistry showed epithelial reduction of NCAM1 in CIN3/AIS lesions. In conclusion, NCAM1 and CDKN2A are two promising candidates to distinguish whether women are at high risk of developing cervical cancer and in need of frequent follow-up.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleHigh-Grade Cervical Intraepithelial Neoplasia (CIN) Associates with Increased Proliferation and Attenuated Immune Signalingen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 by the authorsen_US
dc.source.articlenumber373en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.3390/ijms23010373
dc.identifier.cristin2000029
dc.source.journalInternational Journal of Molecular Sciencesen_US
dc.identifier.citationInternational Journal of Molecular Sciences. 2021, 23 (1), 373.en_US
dc.source.volume23en_US
dc.source.issue1en_US


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