Evidence map›Paper›PMID 40016294›Full record

ArticleScientific reports2025

The MEK inhibitor trametinib is effective in inhibiting the growth of canine oral squamous cell carcinoma.

William P Katt, Cheryl E Balkman, Scott D Butler, Michael Byron, Patrick C Carney, Amy B Todd-Donato, Matthew E Drozd, Gerald E Duhamel, Jacquelyn M Evans, Nadine Fiani and 14 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

24 authors.

William P Katt *Department of Molecular Medicine, Cornell University, Ithaca, NY, USA. wpk8@cornell.edu.
Cheryl E BalkmanDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Scott D ButlerDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Michael ByronDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Patrick C CarneyDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Amy B Todd-DonatoDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Matthew E DrozdDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Gerald E DuhamelDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Jacquelyn M EvansDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Nadine FianiDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Jordan C FordGenomics Facility, Institute of Biotechnology, Cornell University, Ithaca, NY, USA.
Jennifer K GrenierGenomics Facility, Institute of Biotechnology, Cornell University, Ithaca, NY, USA.
Jessica J HaywardDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Kristiina HeikinheimoDepartment of Oral and Maxillofacial Surgery, Institute of Dentistry, University of Turku and Turku University Hospital, Turku, Finland.
Kelly R HumeDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Elizabeth S MooreDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Rishi PuriDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Skylar R SylvesterDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Sydney L WarshawPrism Veterinary Dentistry, New York, NY, USA.
Suzin M WebbDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Andrew C WhiteDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Alexandra L WrightDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Richard A CerioneDepartment of Molecular Medicine, Cornell University, Ithaca, NY, USA.
Santiago Peralta *Department of Clinical Sciences, Cornell University, Ithaca, NY, USA. sp888@cornell.edu.

Funding

The unique roles of the GTP-binding/protein crosslinking enzyme transglutaminase-2 and signaling partners in aggressive cancersR01CA201402 · NCI · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2016 to 2024
$4.3M
Studies of Global Signal TransductionR35GM152206 · NIGMS · CORNELL UNIVERSITY · PI RICHARD A. CERIONE · 2024 to 2026
$1.7M
Tools for Genetic and Genomic Studies in the DogR24GM082910 · NIGMS · CORNELL UNIVERSITY · PI ACLAND, GREGORY M · 2008 to 2011
$1.5M
NCI NIH HHS R01 CA201402NIGMS NIH HHS R24 GM082910NIGMS NIH HHS R35 GM152206
6 · The paper itself

Abstract

Oral tumors are relatively common in dogs, and canine oral squamous cell carcinoma (COSCC) is the most prevalent oral malignancy of epithelial origin. COSCC is locally aggressive with up to 20% of patients showing regional or distant metastasis at the time of diagnosis. The treatment of choice most typically involves wide surgical excision. Although long-term remission is possible, treatments are associated with considerable morbidity and can negatively impact functionality and quality of life. OSCCs have substantial upregulation of the RAS-RAF-MEK-MAPK signaling axis, and we had previously hypothesized that small-molecule inhibitors that target RAS signaling might effectively inhibit tumor growth and progression. Here, we demonstrate that the MEK inhibitor trametinib, an FDA-approved drug for human cancers, substantially inhibits the growth of six COSCC cell lines established from current patient tumor samples. We further show preliminary clinical evidence that the drug is able to cause ~ 40% and ~ 80% tumor regression in two out of four patients with spontaneously occurring COSCC, a partial response according to commonly used RECIST criteria. Given the limited treatment options available and the number of dogs for which standard of care is not acceptable, these preliminary findings provide new hope that more suitable treatment options may soon enter the veterinary clinic.

Indexed as

Antineoplastic AgentsCarcinoma, Squamous CellDog DiseasesMouth NeoplasmsProtein Kinase InhibitorsPyridonesPyrimidinonesAnimalsCell Line, TumorCell ProliferationDogsFemaleHumansMaleMitogen-Activated Protein Kinase KinasesAntineoplastic AgentsMitogen-Activated Protein Kinase KinasesProtein Kinase InhibitorsPyridonesPyrimidinonestrametinibCanine cancerOral squamous cell carcinomaRAS signalingTrametinib

Identifiers

PMID40016294
PMCPMC11868584

What OpenQuestion holds

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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.