Evidence map›Paper›PMID 38746473›Full record

ArticleResearch square2024

Opportunities for targeted therapies: trametinib as a therapeutic approach to canine oral squamous cell carcinomas.

Santiago Peralta, William Katt, Cheryl Balkman, Scott Butler, Patrick Carney, Amy Todd-Donato, Matthew Drozd, Gerald Duhamel, Nadine Fiani, Jordan Ford and 12 more

Abstract readPreprint
In one paragraph

Article in Research square, 2024. 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

22 authors.

Santiago PeraltaCornell University.ORCID 0000-0002-4167-6272
William KattCornell University.ORCID 0000-0001-5104-7667
Cheryl BalkmanCornell University College of Veterinary Medicine.
Scott ButlerCornell University.
Patrick CarneyCornell University.
Amy Todd-DonatoCornell University.
Matthew DrozdCornell University.
Gerald DuhamelCornell University.
Nadine FianiCornell University.
Jordan FordPrism Veterinary Dentistry.
Jennifer GrenierRNA Sequencing Core and Center for Reproductive Genomics. Cornell University, Ithaca, NY.
Jessica HaywardCornell University.
Kristiina HeikinheimoUniversity of Turku.
Kelly HumeCornell University.
Elizabeth MooreCornell University.ORCID 0000-0003-2502-6429
Rishi PuriCornell University.
Skylar SylvesterCornell University.
Sydney WarshawPrism Veterinary Dentistry.
Suzin WebbCornell University.
Andrew WhiteCornell University.ORCID 0000-0002-5436-5377
Alexandra WrightCornell University.
Richard CerioneCornell University.ORCID 0000-0003-4512-5897

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
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 GM082910
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 significant morbidity and can negatively impact functionality and quality of life. OSCCs have significant 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, significantly blocks the growth of several COSCC cell lines established from current patient tumor samples. We further show clinical evidence that the drug is able to cause significant tumor regression in some patients with spontaneously occurring COSCC. Given the limited treatment options available and the high rate of owner rejection of these offered options, these findings provide new hope that more acceptable treatment options may soon enter the veterinary clinic.

Identifiers

PMID38746473
PMCPMC11092801

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.