Relationship of microsatellite instability to mismatch repair deficiency in malignant tumors of dogs

  • Sakuya Inanaga
    Laboratory of Molecular Diagnostics and Therapeutics, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,
  • Masaya Igase
    Laboratory of Molecular Diagnostics and Therapeutics, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,
  • Yusuke Sakai
    National Institute of Infectious Diseases Department of Pathology, , Tokyo,
  • Kenji Hagimori
    Kyoto Animal Medical Center , Kyoto,
  • Hiroshi Sunahara
    Laboratory of Veterinary Surgery, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,
  • Hiro Horikirizono
    Laboratory of Veterinary Radiology, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,
  • Kazuhito Itamoto
    Laboratory of Companion Animal Medicine, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,
  • Kenji Baba
    Laboratory of Veterinary Internal Medicine, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,
  • Yoshiharu Ohsato
    Kahotechno Co., Ltd. , Fukuoka,
  • Takuya Mizuno
    Laboratory of Molecular Diagnostics and Therapeutics, Joint Faculty of Veterinary Medicine, Yamaguchi University , Yamaguchi,

書誌事項

公開日
2022-09-01
資源種別
journal article
権利情報
  • https://creativecommons.org/licenses/by-nc-nd/4.0/
  • http://creativecommons.org/licenses/by-nc-nd/4.0/
DOI
  • 10.1111/jvim.16454
公開者
Oxford University Press (OUP)

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説明

<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>Microsatellite instability (MSI) is a type of genomic instability caused by mismatch repair deficiency (dMMR) in tumors. Studies on dMMR/MSI are limited, and the relationship between dMMR and MSI is unknown in tumors of dogs.</jats:p> </jats:sec> <jats:sec> <jats:title>Objectives</jats:title> <jats:p>We aimed to identify the frequency of dMMR/MSI by tumor type and evaluate the relationship between dMMR and MSI in tumors of dogs.</jats:p> </jats:sec> <jats:sec> <jats:title>Animals</jats:title> <jats:p>In total, 101 dogs with 11 types of malignant tumors were included.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>We extracted DNA from fresh normal and tumor tissues. Twelve microsatellite loci from both normal and tumor DNA were amplified by PCR and detected by capillary electrophoresis. Each microsatellite (MS) was defined as MSI if a difference in product size between the tumor and normal DNA was detected. The dMMR was evaluated by immunohistochemistry with formalin-fixed paraffin-embedded tumor tissues. Next, we confirmed whether dMMR induces MSI by serial passaging of MMR gene knockout cell lines for 3 months.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Microsatellite instability was detected frequently in oral malignant melanoma. The number of MSI-positive markers was higher in cases with dMMR than in those with proficient MMR (P &lt; .0001). Statistical analysis indicated that the occurrence of MSI in FH2305 might have relevance to dMMR. Furthermore, MSI occurred in dMMR cell lines 3 months after passaging.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions and Clinical Importance</jats:title> <jats:p>Microsatellite instability and dMMR more frequently were found in oral malignant melanoma than in other tumors, and dMMR has relevance to MSI in both clinical cases and cell lines.</jats:p> </jats:sec>

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