Evidence map›Paper›PMID 42510834›Full record

ReviewGenes2026

Development of Autologous Dendritic Cell Vaccine Therapeutics for Canine Mammary Cancer.

Richard Curtis Bird

Abstract readReview
In one paragraph

Review in Genes, 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

1 author.

Richard Curtis BirdDepartment of Pathobiology, College of Veterinary Medicine, Scott-Ritchey Research Center, Auburn University Research Initiative in Cancer (AURIC), Auburn University, Auburn, AL 36849, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Canine mammary tumors have been investigated to determine the causes of malignancy and to promote the development of more effective therapies. The current standard of care, surgical resection where possible, often still results in recurrence of disease. Thus, there is an unmet need for better, more effective therapies that can suppress recurrence in canine patients. Because canine and human mammary cancers, particularly carcinomas and adenocarcinomas, share many similarities in genetic defects, etiology, natural history, and environment, canine mammary cancer cell lines have also been used as effective models of human disease. The genetics and immune response to canine mammary/breast cancers have been investigated to better understand this disease complex and to promote the development of more effective therapies designed to treat individual canine patients. As cancer is a heterogeneous disease, the potential to determine and possibly predict the mechanisms promoting neoplasia would allow the advancement of targeted therapeutic targets/strategies to combat cancer directly. These investigations have led to the development and evaluation of immunotherapies designed to elicit immune recognition of cancer and its suppression, thus improving survival. Hybrid dendritic-cell fusion vaccines and other autologous cancer vaccine formulations have proven effective in suppressing recurrence and extending survival in canine mammary cancer patients following surgical resection. Although current vaccines are somewhat impractical for direct application in veterinary clinics, reported success points the way toward the development of more practical vaccines designed to promote the treatment of canine mammary cancer. They also suggest a possible mechanism whereby removing a tumor from its microenvironment can promote antigenicity by removing local extracellular vesicle-mediated immunosuppression. This review provides a novel perspective on the potential of canine genetics to inform and promote more successful immunotherapies and their value as models of human disease.

Indexed as

Cancer VaccinesDendritic CellsDog DiseasesMammary Neoplasms, AnimalAnimalsDogsFemaleHumansImmunotherapyCancer Vaccinescancer gene defectscaninecell vaccinedendritic cellmammary cancer

Identifiers

PMID42510834
PMCPMC13410244

What OpenQuestion holds

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LicenceCC BY
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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.