Expression profile of circulating serum microRNAs in dogs with lymphoma

Aki Fujiwara-Igarashi1, Hirotaka Igarashi2, Noriyuki Mizutani2

  • 1Department of Veterinary Internal Medicine, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan; Division of Therapeutic Science I, Department of Clinical Veterinary Medicine, Nippon Veterinary and Life Science University, 1-7-1 Kyonan-cho, Musashino-shi, Tokyo 183-0023, Japan.

Insights

Serum microRNAs (miRNAs) show altered expression in dogs with lymphoma, with four key miRNAs decreasing and one increasing. These findings suggest potential non-invasive biomarkers for canine lymphoma diagnosis and understanding its pathogenesis.

Area of Science:

  • Veterinary Medicine
  • Molecular Biology
  • Oncology

Background:

  • Serum microRNAs (miRNAs) are stable molecules involved in cell communication and can be altered in various cancers.
  • Altered circulating miRNAs show potential as non-invasive biomarkers for human and animal diseases.
  • Canine lymphoma is a common cancer, and identifying reliable biomarkers is crucial for diagnosis and treatment.

Purpose of the Study:

  • To investigate the expression profile of circulating miRNAs in the serum of dogs diagnosed with lymphoma.
  • To identify specific miRNAs that are differentially expressed in canine lymphoma patients compared to healthy controls.
  • To explore the potential of these miRNAs as diagnostic biomarkers for canine lymphoma.

Main Methods:

  • Serum samples were collected from 61 dogs with lymphoma and 40 control dogs.
  • Real-time reverse transcription-polymerase chain reaction (RT-PCR) was employed for quantitative miRNA measurement.
  • A comprehensive expression analysis was performed to select candidate miRNAs, followed by validation.

Main Results:

  • Out of 277 analyzed miRNAs, five candidates (let-7b, miR-223, miR-25, miR-92a, and miR-423a) were identified.
  • The expression of let-7b, miR-223, miR-25, and miR-92a was significantly decreased in dogs with lymphoma.
  • miR-423a levels were significantly increased in the lymphoma group compared to controls.

Conclusions:

  • Specific circulating miRNA profiles, including decreased let-7b, miR-223, miR-25, miR-92a and increased miR-423a, are associated with canine lymphoma.
  • These miRNAs hold promise as potential non-invasive biomarkers for canine lymphoma.
  • Further research into the functional roles of these serum miRNAs could elucidate the pathogenesis of canine lymphoma.