Association of serum and fecal microRNA profiles in cats with gastrointestinal cancer and chronic inflammatory enteropathy

Author:

Brogaard Louise1ORCID,Lyngby Janne G.2ORCID,Kristensen Annemarie T.2ORCID,Fredholm Merete1ORCID,Bjørnvad Charlotte R.2ORCID,Salavati Schmitz Silke3ORCID,Skancke Ellen4,Morris Joanna S.5,Dupont Nana2ORCID,Argyle David3,Sánchez Armand67,Spohr Anette8,Graarup‐Hansen Kasper9ORCID,Nielsen Lise N.2ORCID,Cirera Susanna1ORCID

Affiliation:

1. Department of Veterinary and Animal Sciences University of Copenhagen Frederiksberg Denmark

2. Department of Veterinary Clinical Sciences University of Copenhagen Frederiksberg Denmark

3. Hospital for Small Animals, Royal (Dick) School of Veterinary Studies, The Roslin Institute, College of Medicine and Veterinary Medicine, University of Edinburgh Midlothian UK

4. Department of Companion Animal Clinical Sciences Norwegian University of the Life Sciences Oslo Norway

5. College of Medical, Veterinary, and Life Sciences, School of Veterinary Medicine, University of Glasgow Glasgow UK

6. Department of Animal Medicine and Surgery, School of Veterinary Sciences Universitat Autònoma de Barcelona, Cerdanyola del Vallès Barcelona Spain

7. Centre for Research in Agricultural Genomics, The Spanish National Research Council (CSIC) Institute of Agrifood Research and Technology (IRTA), Autonomous University of Barcelona (UAB), and University of Barcelona (UB) Barcelona Spain

8. Evidensia Faxe Animal Hospital Faxe Denmark

9. Evidensia Karlslunde Animal Hospital Greve Denmark

Abstract

AbstractBackgroundDifferentiation of gastrointestinal cancer (GIC) from chronic inflammatory enteropathies (CIE) in cats can be challenging and often requires extensive diagnostic testing. MicroRNAs (miRNAs) have promise as non‐invasive biomarkers in serum and feces for diagnosis of GIC.Hypothesis/ObjectivesCats with GIC will have serum and fecal miRNA profiles that differ significantly from healthy cats and cats with CIE. Identify serum and fecal miRNAs with diagnostic potential for differentiation between cats with GIC and CIE as compared to healthy cats.AnimalsTen healthy cats, 9 cats with CIE, and 10 cats with GIC; all client‐owned.MethodsCats were recruited for an international multicenter observational prospective case‐control study. Serum and feces were screened using small RNA sequencing for miRNAs that differed in abundance between cats with GIC and CIE, and healthy cats. Diagnostic biomarker potential of relevant miRNAs from small RNA sequencing and the literature was confirmed using reverse transcription quantitative real‐time PCR (RT‐qPCR).ResultsSerum miR‐223‐3p was found to distinguish between cats with GIC and CIE with an area under the curve (AUC) of 0.9 (95% confidence interval [CI], 0.760‐1.0), sensitivity of 90% (95% CI, 59.6‐99.5%), and specificity of 77.8% (95% CI, 45.3‐96.1%). Serum miR‐223‐3p likewise showed promise in differentiating a subgroup of cats with small cell lymphoma (SCL) from those with CIE. No fecal miRNAs could distinguish between cats with GIC and CIE.Conclusion and Clinical ImportanceSerum miR‐223‐3p potentially may serve as a noninvasive diagnostic biomarker of GIC in cats, in addition to providing a much needed tool for the differentiation of CIE and SCL.

Funder

Teknologi og Produktion, Det Frie Forskningsråd

Publisher

Wiley

Subject

General Veterinary

Reference65 articles.

1. Feline chronic enteropathy

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3. Differentiating feline inflammatory bowel disease from alimentary lymphoma in duodenal endoscopic biopsies

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