Evidence map›Paper›PMID 41749937›Full record

ArticleCancers2026

In Vitro Model Characterizing Carcinogenic Progression of HPV-Positive Oropharyngeal Cancer.

Jesus Avila Tejeda, Sreejata Chatterjee, Craig Meyers

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jesus Avila TejedaDepartment of Cell and Biological Systems, The Pennsylvania State University College of Medicine, 500 University Drive, Hershey, PA 17033, USA.ORCID 0000-0002-3463-7312
Sreejata ChatterjeeDepartment of Cell and Biological Systems, The Pennsylvania State University College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
Craig MeyersDepartment of Cell and Biological Systems, The Pennsylvania State University College of Medicine, 500 University Drive, Hershey, PA 17033, USA.ORCID 0000-0001-8773-3976

Funding

Understanding the Role of HAART in the Progression of HPV-Associated Oral CancerR01DE032212 · NIDCR · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Craig M Meyers · 2022 to 2026
$2.7M
Effect of HPV16 and ART on the Epigenome Leading to AIDS-Associated Oral CancerR01DE024964 · NIDCR · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MEYERS, CRAIG M · 2014 to 2018
$2.4M
NIDCR NIH HHS R01DE024964NIDCR NIH HHS R01 DE032212NIDCR NIH HHS R01DE032212
6 · The paper itself

Abstract

BACKGROUND/

objectiveHuman papillomavirus (HPV) represents the most widespread sexually transmitted infection globally, with high-risk strains such as HPV16 driving a rising incidence of oropharyngeal squamous cell carcinoma (OPSCC), particularly in developed countries like the United States and United Kingdom. In the U.S., HPV16-associated OPSCC has surpassed cervical cancer as the most common HPV-related malignancy. Despite the availability of preventive vaccines, uptake remains suboptimal among adolescents and shifting sexual behaviors have contributed to increased disease burden. Early detection remains a major clinical challenge due to the absence of defined precursor lesions and the extended latency between viral exposure and disease onset. Most patients present with advanced-stage disease and no prior clinical history of pre-malignancy, limiting access to early-stage samples and hindering biomarker discovery.

methodsTo address these limitations, we developed an in vitro HPV16 oral cancer model, using the three-dimensional organotypic raft culture system that simulates the progression of HPV16-transfected oral epithelium from precancerous states to malignant phenotypes.

resultsUsing HPV16-transfected human tonsil keratinocytes, we generated stratified and differentiated epithelia that mimic the biochemical and structural changes observed in vivo. This system enables detailed monitoring of epithelial differentiation, biochemical shifts, viral genome status, and key oncogenic and metabolic markers associated with HPV16-driven OPSCC. By aligning expression profiles with clinical datasets, we validated the model through the measurement of virologic markers linked to infection and progression, as well as tissue markers indicative of carcinogenic transformation.

conclusionsThis model offers a promising tool for refining early detection strategies and evaluating potential clinical biomarkers, ultimately aiming to improve diagnostic precision and therapeutic outcomes in HPV-associated OPSCC.

Indexed as

head and neck cancerhuman papillomavirus type 16 (HPV16)organotypic raft culturesoropharyngeal canceroropharyngeal squamous cell carcinoma (OPSCC)

Identifiers

PMID41749937
PMCPMC12939338

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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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.