Evidence map›Paper›PMID 40626980›Full record

ArticleRadiology and oncology2025

Human papillomavirus (HPV) genotyping and prognostic value of HPV E4 protein and transcription factors NANOG and SOX11 in atypical p16 patchy squamous epithelium of cervix.

Maja Kebe Radulovic, Anja Ostrbenk, Mario Poljak, Margareta Strojan-Flezar

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Article in Radiology and oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Maja Kebe RadulovicInstitute of Pathology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Anja OstrbenkInstitute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Mario PoljakInstitute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Margareta Strojan-FlezarInstitute of Pathology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunohistochemical staining for p16 is used to differentiate precancerous cervical lesions in tissue samples, but the interpretation of patchy p16 expression remains challenging. We performed human papillomavirus (HPV) genotyping and evaluated immunohistochemical expression of HPV E4 protein - a marker for transient infections, stem cell transcription factor NANOG, and transcription factor SOX11 to detect possible high-grade squamous lesions in atypical p16 patchy squamous epithelium. MATERIALS AND

methodsWe analyzed 24 cervical tissue samples with atypical squamous epithelium and patchy p16 expression along with the following controls: 11 cases of atypical squamous epithelium with null p16 expression, 9 condylomas, 12 cases of cervical intraepithelial neoplasia (CIN) grade 1, 11 cases of CIN2, and 9 cases of CIN3. In addition, HPV genotyping of tissue and related cervical smears from up to two years prior to biopsy was performed. Immunohistochemical staining for Ki67, HPV E4, NANOG, and SOX11 was performed and compared with follow-up data.

resultsHigh-risk HPV infection was detected in 6/24 cases with patchy p16 expression and HPV E4 was expressed in 1/24 cases with patchy p16, weak NANOG expression was found in 11/24 cases with patchy p16 expression while no SOX11 expression was observed. During 10 months of follow-up, additional CIN1 and two CIN3 were identified, and another CIN1 and CIN3 after 5 and 6 years, accordingly.

conclusionsOur study showed that atypical squamous epithelium with patchy p16 expression poses a risk for highgrade precancerous lesions, harbouring high-risk HPV infection. Novel markers may hold diagnostic value in other specific contexts.

Indexed as

Nanog Homeobox ProteinOncogene Proteins, ViralPapillomaviridaePapillomavirus InfectionsSOXC Transcription FactorsUterine Cervical DysplasiaUterine Cervical NeoplasmsAdultBiomarkers, TumorCervix UteriCyclin-Dependent Kinase Inhibitor p16FemaleGenotypeHuman Papillomavirus VirusesHumansImmunohistochemistryBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16Nanog Homeobox ProteinNANOG protein, humanOncogene Proteins, ViralSOX11 protein, humanSOXC Transcription Factorscervical intraepithelial neoplasiagenotypehuman papillomavirusNANOGp16SOX11

Identifiers

PMID40626980
PMCPMC12441885

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