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2022 Fiscal Year Final Research Report

Rapid and specific diagnosis for tumor using exosome and cfDNA

Research Project

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Project/Area Number 20K21375
Research Category

Grant-in-Aid for Challenging Research (Exploratory)

Allocation TypeMulti-year Fund
Review Section Medium-sized Section 42:Veterinary medical science, animal science, and related fields
Research InstitutionKagoshima University

Principal Investigator

Miura Naoki  鹿児島大学, 農水産獣医学域獣医学系, 教授 (80508036)

Co-Investigator(Kenkyū-buntansha) 高橋 雅  鹿児島大学, 農水産獣医学域獣医学系, 准教授 (40750419)
古澤 悠  鹿児島大学, 共同獣医学部, 特任助教 (30791793)
畑井 仁  岩手大学, 農学部, 特任教授 (40566535)
川原 幸一  大阪工業大学, 工学部, 教授 (10381170)
Project Period (FY) 2020-07-30 – 2023-03-31
Keywords犬 / エクソソーム / non-coding RNA / cfDNA / 腫瘍
Outline of Final Research Achievements

Tumor-specific exosome analysis revealed differences in surface lectin expression between cell lines, including decreased expression associated with canine mammary tumor metastasis. Exosome-containing RNA analysis identified specific changes in metastatic and primary canine melanoma cell lines. Clinical canine samples were used to determine the sensitivity and specificity of exosome-containing target microRNAs in case-control studies. In addition, we found specificity for the inclusion of non-coding RNAs other than microRNAs and reported the results. In tumor-specific cfDNA analysis, we selected SNPs in canine melanoma tissues by next-generation sequencing and confirmed mutations in four completely novel SNPs. Still, we could not confirm mutations in clinical samples.

Free Research Field

臨床獣医学

Academic Significance and Societal Importance of the Research Achievements

本研究では,獣医臨床領域では初めてとなるエクソソームの腫瘍特異的な表面レクチンの発現の違いを確認できた.この結果は,今後,腫瘍マーカのより選択的な選別の一助となると同時に,エクソソームを利用したDDSの標的ともなる.次にエクソソームに特異的に含有されるnon-coding RNAの網羅的解析から,腫瘍に特異的な発現含有パターンを確認することができ,今後の臨床バイオマーカーとして,より適切な指標が作成可能となる.特に転移病変と原発病変の細胞から分泌されるエクソソームの違いを確認できたことで,腫瘍のより選択的な病態の把握が可能となる.

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Published: 2024-01-30  

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