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Peer-reviewed veterinary case report

Using blood test to monitor oral melanoma in dogs

By Tagawa, Michihito & Aoki, Minori·Published in Frontiers in veterinary science·2023·Obihiro University of Agriculture and Veterinary Medicine, Japan·View original on PubMed

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Original publication title: Clinical utility of liquid biopsy in canine oral malignant melanoma using cell-free DNA.

Species:
dog

Plain-English summary

A group of dogs with oral malignant melanoma (a type of mouth cancer) had their blood tested for cell-free DNA (cfDNA) to see if it could help track the disease's progress. While the overall cfDNA levels were similar to healthy dogs, the DNA integrity index (DII) was lower in the dogs with cancer, and it decreased further as the disease worsened. This suggests that measuring cfDNA and DII could be useful for monitoring how the cancer is developing in dogs. More research is needed, but this could be a promising tool for veterinarians in managing oral malignant melanoma.

People also search for: dog oral cancer treatment · monitoring dog melanoma · canine cancer blood test

Abstract

INTRODUCTION: Cell-free DNA (cfDNA), an extracellular free DNA released into the bloodstream by cells, is a potentially useful noninvasive marker to detect human malignancies and monitor response to treatment. In the present study, we evaluated the utility of circulating cfDNA in canine patients with oral malignant melanoma (OMM) in assessing therapeutic response and clinical outcomes. METHODS: Plasma samples were collected from 12 dogs with OMM and 9 healthy controls. cfDNA concentration was quantified by real-time PCR resulting in short (99bp) and long (218bp) fragments of long interspersed nuclear element-1 (LINE-1), and the DNA integrity index (DII) was then calculated (218/99). A follow-up study was conducted on 6 dogs with OMM, and the plasma cfDNA and DII were quantified throughout disease progression. RESULTS: Although cfDNA levels obtained from dogs with OMM were not significantly different compared to those obtained from healthy controls, the DII was significantly lower in dogs with OMM than in healthy controls. The DII tended to decrease as the disease stage progressed. Moreover, changes in cfDNA concentration and DII along the clinical course were observed when major changes, such as metastasis or apparent tumor progression, were observed. DISCUSSION: The results of our study suggest that measurements of serum cfDNA and DII using LINE-1 might be valuable new biomarkers for monitoring OMM progression in dogs. This preliminary study demonstrated the potential clinical utility of monitoring plasma cfDNA in canine patients with OMM.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/37408834/