Evidence map›Paper›PMID 41401057›Full record

ArticleRadiology and oncology2025

Human papillomavirus-related oropharyngeal squamous cell carcinoma exhibits enhanced radiosensitivity despite limited activation of cytosolic DNA sensing pathways and innate immune responses.

Kristina Levpuscek, Tanja Jesenko, Tilen Komel, Simona Kranjc Brezar, Gregor Sersa, Maja Cemazar, Primoz Strojan

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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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Kristina Levpuscek1Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Tanja Jesenko1Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Tilen Komel1Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Simona Kranjc Brezar1Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Gregor Sersa1Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Maja Cemazar1Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Primoz Strojan2Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPharyngeal squamous cell carcinoma (PSCC) is a significant health concern, with human papillomavirus 16 (HPV16) playing a key role in the etiology of oropharyngeal squamous cell carcinoma (OPSCC). HPV16-related OPSCC exhibits enhanced radiosensitivity compared to HPV16-unrelated PSCC, yet the underlying mechanisms remain poorly understood. As HPV16 oncoproteins E6 and E7 are known to interfere with innate immune signaling, we investigated how modulation of cytosolic DNA sensing pathways and innate immune responses changes after irradiation (IR) and whether this contributes to enhanced radiosensitivity in HPV16-related OPSCC. MATERIALS AND

methodsUsing HPV16-related and -unrelated PSCC models, we examined baseline expression levels of DNA sensors and cytokines and assessed the effects of IR on double-stranded DNA (dsDNA) accumulation, activation of cytosolic DNA sensors, cytokines, and immune cell infiltration both

resultsHPV16-related OPSCC exhibited a distinct baseline expression profile of DNA sensors and cytokines, consistent with suppression of the stimulator of interferon genes (STING) pathway. While IR-induced activation of DNA sensors was dose- and time-dependent across models, HPV16-related OPSCC showed selective activation of cyclic GMP-AMP synthase (cGAS) and STING without significant cytokine upregulation or immune activation. In contrast, HPV16-related and unrelated PSCCs displayed activation of multiple DNA sensors, increased cytokine expression, and enhanced immune cell infiltration following IR.

conclusionsThe key finding was that the involvement of cytosolic DNA sensing pathways and innate immune system do not increase radiosensitivity of HPV16-related OPSCC. In PSCC models, DNA sensor and cytokine expression varied depending on IR dose and fractionation.

Indexed as

Carcinoma, Squamous CellHuman papillomavirus 16Immunity, InnateOropharyngeal NeoplasmsPapillomavirus InfectionsRadiation ToleranceSquamous Cell Carcinoma of Head and NeckAnimalsCell Line, TumorCytokinesCytosolHuman Papillomavirus VirusesHumansMiceOncogene Proteins, ViralSignal TransductionCytokinesOncogene Proteins, Viralcytosolic DNA sensing pathwayshuman papillomavirus type 16innate immune responsepharyngeal squamous cell carcinomaradiation responseIntroduction

Identifiers

PMID41401057
PMCPMC12707452

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.