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Comprehensive Analysis of Microsatellite Instability in Canine Cancers: Implications for Comparative Oncology and Personalized Veterinary Medicine. | LitMetric

AI Article Synopsis

  • Microsatellite instability (MSI) is an important characteristic in cancer, but its role in dog cancers has not been thoroughly studied, prompting this analysis of 10 types of canine tumors using data from 692 samples.
  • The study found that 64% of tumors had MSI, with B-cell lymphomas showing the highest levels of MSI, differing from findings in human cancers.
  • A new "MSI-burden" score was created, indicating a significant correlation with overall mutation levels, and the results suggest MSI could be a valuable biomarker for prognosis and targeted therapies in canine cancer.

Article Abstract

Microsatellite instability (MSI) is a crucial feature in cancer biology, yet its prevalence and significance in canine cancers remain largely unexplored. This study conducted a comprehensive analysis of MSI across 10 distinct canine cancer histotypes using whole-exome sequencing data from 692 tumor-normal sample pairs. MSI was detected in 64% of tumors, with prevalence varying significantly among cancer types. B-cell lymphomas exhibited the highest MSI burden, contrasting with human studies. A novel "MSI-burden" score was developed, correlating significantly with tumor mutational burden. MSI-high (MSI-H) tumors showed elevated somatic mutation counts compared to MSI-low and microsatellite stable tumors. The study identified 3632 recurrent MSI-affected genomic regions across cancer types. Notably, seven of the ten cancer types exhibited MSI-H tumors, with prevalence ranging from 1.5% in melanomas to 37% in B-cell lymphomas. These findings highlight the potential importance of MSI in canine cancer biology and suggest opportunities for targeted therapies, particularly immunotherapies. The high prevalence of MSI in canine cancers, especially in B-cell lymphomas, warrants further investigation into its mechanistic role and potential as a biomarker for prognosis and treatment response.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11394029PMC
http://dx.doi.org/10.3390/ani14172484DOI Listing

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