Evidence map›Paper›PMID 41928992›Full record

ArticlebioRxiv : the preprint server for biology2026

Transcriptomic atlas of premalignant oral squamous cell carcinoma in an aging mouse model reveals an enhanced immune response and dysregulation of head and neck tissue stem cells.

Heidi Kletzien, Nguyen-Ahn Nguyen, Siddhartha G Jena, Jason D Buenrostro, Amy J Wagers

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

5 authors.

Heidi KletzienDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0002-8643-1834
Nguyen-Ahn NguyenDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
Siddhartha G JenaDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0002-9750-0225
Jason D BuenrostroDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
Amy J WagersDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.

Funding

TUFTS--FIELDINGP30AG031679 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI Thomas Glenn Travison · 2008 to 2026
$23.9M
Regulation and Function of Growth Differentiation Factor 11 During Development and AgingR01AG048917 · NIA · HARVARD UNIVERSITY · PI WAGERS, AMY JO · 2016 to 2020
$2.8M
Rapid functional genetics to study stem cell-niche interactions in the skinR01AR080110 · NIAMS · HARVARD UNIVERSITY · PI Ya-Chieh Hsu · 2022 to 2026
$2.5M
Aging and Rejuvenation of Skin Stem CellsR01AR083416 · NIAMS · HARVARD UNIVERSITY · PI Ya-Chieh Hsu · 2024 to 2026
$1.6M
Regulation and function of Growth Differentiation Factor 11 during development and agingR56AG048917 · NIA · HARVARD UNIVERSITY · PI WAGERS, AMY JO · 2015 to 2015
$338k
Mechanisms of stem cell aging that contribute to clonal outgrowth in head and neck tissuesF32AG071208 · NIA · HARVARD UNIVERSITY · PI KLETZIEN, HEIDI · 2021 to 2023
$205k
NIAMS NIH HHS R01 AR080110NIAMS NIH HHS R01 AR083416NIA NIH HHS F32 AG071208NIA NIH HHS P30 AG031679NIA NIH HHS R01 AG048917NIA NIH HHS R56 AG048917
6 · The paper itself

Abstract

Oral squamous cell carcinomas (OSCC) account for ~90% of all oral malignancies and have devastating effects on overall health and quality of life. However, little is known about the early initiating events that drive the development of oral leukoplakia-like premalignant lesions (OPLs) and disease progression. Here, we create a mouse model of tobacco-related premalignant OSCC that takes into consideration its primary risk factors, including advancing age and male sex. This model notably recapitulates the age variant patterns of OSCC risk observed in humans, with a higher prevalence of oral premalignant lesions in older mice. In addition, by building a transcriptomic atlas with this system, we reveal genetic signatures associated with oncogenic progression in the tongue and buccal epithelium, and their resident somatic tissue stem cells. We also identify several novel transcriptomic signatures of premalignancy in OSCC, including enhanced immune response and expansion and dysregulation of head and neck tissue stem cells. These findings offer a new framework for investigating physiologically-relevant risk factors and drivers of OSCC and illuminate novel biological pathways underlying its pathology.

Identifiers

PMID41928992
PMCPMC13041973

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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 OpenQuestion graph.