Evidence map›Paper›PMID 42511543›Full record

ArticleInternational journal of molecular sciences2026

A Comparative Species Framework to Identify Candidate Salivary miRNAs Associated with Breast Cancer Risk.

James L Miller, Mariza DaCosta, Kimaya M Bakhle, Lisa Lai, Dawn E Post, Rebecca M Harman, Gerlinde R Van de Walle

Abstract readComparative Study
In one paragraph

Article in International journal of molecular sciences, 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

7 authors.

James L MillerBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-6559-1310
Mariza DaCostaBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.ORCID 0009-0000-2451-9964
Kimaya M BakhleBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-7122-0989
Lisa LaiDepartment of Surgery, SUNY Upstate Medical University, Syracuse, NY 13210, USA.ORCID 0000-0002-8520-8286
Dawn E PostBiorepository Core and Department of Urology, Syracuse, NY 13210, USA.
Rebecca M HarmanBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-8715-2562
Gerlinde R Van de WalleBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-2064-8029

Funding

Cornell University Combined DVM-PhD Medical Scientist Training Program (MSTP)T32GM150453 · NIGMS · CORNELL UNIVERSITY · PI Renata Ivanek Miojevic · 2023 to 2026
$941k
The mammary cell secretome as a novel biologic for triple-negative breast cancerR21CA285521 · NCI · CORNELL UNIVERSITY · PI HARMAN, REBECCA M · 2024 to 2025
$404k
Albert C. Bostwick Foundation not applicableCarol M. Baldwin Breast Cancer Research Fund Not applicableNCI NIH HHS 1R21CA285521-01NCI NIH HHS R21 CA285521NIGMS NIH HHS T32 GM150453
6 · The paper itself

Abstract

Accurate assessment of early indicators of breast cancer (BC) is critical to improve detection strategies and patient prognosis. Our research group takes a comparative species approach to study early BC detection by capitalizing on data from species with inherently low or high incidence of mammary cancer to supplement rare human samples. Circulating microRNAs (c-miRNAs) are a promising class of molecules that have the potential to serve as biomarkers for BC risk and disease detection. The expression of these non-coding RNAs controls numerous cellular processes and their dysregulation is associated with various pathological conditions, including cancer. To explore whether c-miRNA expression profiles can identify individuals with early-stage BC, we conducted a multi-species pilot study. We analyzed biofluid samples (i.e., saliva, serum, and plasma) from patients with early-stage BC and patients with no prior history of cancer and mammosphere-derived epithelial cells (MDECs) from dogs (canines) and horses (equines), species with a relatively high and low incidence of mammary cancer, respectively. We identified 16 candidate c-miRNAs that were upregulated in saliva from patients in the early-stage BC group when compared to the control patient group. Notably, 6 of these c-miRNAs (i.e., miR-361, miR-148b, miR-205, miR-186, miR-223, and miR-197) were also found to be secreted at higher levels by canine MDECs when compared to equine MDECs. Although individual and combinatorial assessment of these six c-miRNAs in a larger human cohort did not confirm their potential association with early breast cancer detection, the data in this study do introduce a novel comparative framework in which species-to-species variation in cancer susceptibility may inform the identification of candidate biomarkers for human disease.

Indexed as

Biomarkers, TumorBreast NeoplasmsMicroRNAsSalivaAnimalsDogsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHorsesHumansMiddle AgedSpecies SpecificityBiomarkers, TumorMicroRNAsbiomarkersbreast cancermammary epithelial cellsmicroRNAsspecies-to-species variation

Identifiers

PMID42511543
PMCPMC13410475

What Socratic 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 Socratic graph.