Evidence map›Paper›PMID 42008480›Full record

ArticleJournal of visualized experiments : JoVE2026

Translationally-Relevant Tumor Resection Model for Murine Preclinical Models of Oral Squamous Cell Carcinoma.

Gemalene M Sunga, Alejandra Cobos Perez, Andrea H Molina, Nourhan Hussein, Neeraja Dharmaraj, Andrew Sikora, Simon Young

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Gemalene M SungaKatz Department of Oral and Maxillofacial Surgery, The University of Texas Health Science Center at Houston, School of Dentistry; Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center; Gemalene.Sunga@uth.tmc.edu.
Alejandra Cobos PerezKatz Department of Oral and Maxillofacial Surgery, The University of Texas Health Science Center at Houston, School of Dentistry; Department of Bioengineering, Rice University.
Andrea H MolinaKatz Department of Oral and Maxillofacial Surgery, The University of Texas Health Science Center at Houston, School of Dentistry.
Nourhan HusseinKatz Department of Oral and Maxillofacial Surgery, The University of Texas Health Science Center at Houston, School of Dentistry.
Neeraja DharmarajKatz Department of Oral and Maxillofacial Surgery, The University of Texas Health Science Center at Houston, School of Dentistry.
Andrew SikoraDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center.
Simon YoungKatz Department of Oral and Maxillofacial Surgery, The University of Texas Health Science Center at Houston, School of Dentistry.

Funding

SynerGel: A Novel Tumor Microenvironment-Modulating Hydrogel for Local ImmunotherapyR01DE030140 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI YOUNG, SIMON · 2021 to 2025
$3.0M
Engineered bacterial in situ vaccines against oral cancer.R21DE034543 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TABOR, JEFFREY JAY, VEISEH, OMID · 2024 to 2024
$434k
NIDCR NIH HHS R01 DE030140NIDCR NIH HHS R21 DE034543
6 · The paper itself

Abstract

Currently, the first-line treatment for the most common form of head and neck squamous cell carcinoma (HNSCC), oral cavity squamous cell carcinoma (OSCC), is surgical resection, followed by risk-adapted treatments, such as chemoradiotherapy. However, with the current standard of care and even the emergence of new treatments, such as checkpoint blockade, the overall survival for advanced, recurrent disease remains high, and the prevalence of head and neck cancer is projected to continue to increase in the coming years. Thus, deeper investigation into current standard-of-care modalities, in addition to novel therapeutics, is necessary to translate potential and promising treatment options to patients with HNSCC. Preclinical models are utilized to evaluate the safety and efficacy of potential treatment interventions. Unfortunately, current preclinical models fail to fully embody the surgical procedure many patients receive, as they primarily involve non-surgical treatment modalities, like radiation, chemotherapy, or immunotherapy. Furthermore, existing surgical models are limited by additional reagents needed to support the establishment of tumors in orthotopic sites and the requirement of microsurgery for tumor removal. This warrants the generation of improved and simplified preclinical models to investigate therapeutics and gain insight into locoregional tumor recurrence and treatment resistance. This article describes a novel syngeneic clinically relevant orthotopic murine subtotal resection model that recapitulates the standard of care in OSCC. This model simplifies existing models and results in measurable recurrence following surgical resection of buccal mucosal tumors. Use of this model may lead to valuable insights into tumor recurrence and treatment resistance in patients with OSCC. The establishment of this preclinical model paves the way for further work to investigate how OSCC responds to post-resection adjuvant therapies, capturing the tumor state at the clinically relevant window at which patients generally begin such subsequent treatments.

Indexed as

Carcinoma, Squamous CellDisease Models, AnimalMouth NeoplasmsAnimalsFemaleHumansMice

Identifiers

PMID42008480
PMCPMC13316768

What OpenQuestion holds

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Registered trials

None linked

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.