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Establishment of a novel anti-angiogenic treatment targeting Tumor endothelial cell specific non-coding RNA

Research Project

Project/Area Number 18K15831
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 53010:Gastroenterology-related
Research InstitutionKurume University

Principal Investigator

Hideki Iwamoto  久留米大学, 医学部, 助教 (40529541)

Project Period (FY) 2018-04-01 – 2022-03-31
Project Status Completed (Fiscal Year 2021)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2021: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2020: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords癌血管 / マイクロRNA / 肝細胞癌 / 癌血管内皮細胞 / 血管新生
Outline of Final Research Achievements

It is known that tumor endothelial cells (TECs) are functionally and genetically different from normal ECs. In this study, we have clarified morphologic, functional, and genetic differences between TEC and liver sinusoidal endothelial cells (LSEC) to find a specific molecular target that can only inhibit tumor angiogenesis without inhibition of normal vessels. In the study, TEC showed disorganized, leaky, and less perfused vessels, compared with LSECs, which resulted in increased hypoxia within tumors. We have detected the top 5 downregulated TEC-specific miRs. Downregulation of TEC-specific miRs showed significantly increased tube formation. Notably, TEC-specific miRs agonists significantly inhibited tumor growth in HCC orthotopic model mice with only inhibiting tumor vessels. Our detected TEC-specific miRs were strongly correlated with tumor angiogenesis, which can be novel and promising therapeutic targets for HCC.

Academic Significance and Societal Importance of the Research Achievements

本研究の新規性として、一つ目は癌血管に特異的なマイクロRNAの発見が挙げられる。二つ目は、同定されたマイクロRNAを制御する事で癌血管のみを抑制する事ができるという点である。現在、癌血管を標的とした治療は、様々な癌種の標準的な治療であり、その治療における問題点を本研究では解決した。従って、本研究の達成による癌患者への貢献は大きいものと考える。また、遺伝子導入により癌治療を行う事は、今後の癌治療の大きな進歩の一つであり、本研究の達成により新たな可能性が見いだされた。

Report

(5 results)
  • 2021 Annual Research Report   Final Research Report ( PDF )
  • 2020 Research-status Report
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (3 results)

All 2021 2018

All Presentation (3 results) (of which Int'l Joint Research: 2 results)

  • [Presentation] 肝細胞癌における癌血管特異的micro RNAを利用した新規血管新生抑制治療2021

    • Author(s)
      岩本英希
    • Organizer
      第57回肝臓学会総会
    • Related Report
      2021 Annual Research Report
  • [Presentation] Novel anti-angiogenic therapy using tumor endothelial cell-specific micro RNA in hepatocellular carcinoma2021

    • Author(s)
      Hideki Iwamoto
    • Organizer
      JSH Internaltional liver conference 2021
    • Related Report
      2021 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Fatty liver environment confers antiangiogenic drug resistance to hepatocellular carcinoma and metastatic liver cancer of colorectal cancer through activation of lipid dependent metabolic pathway2018

    • Author(s)
      岩本英希
    • Organizer
      アメリカ肝臓学会年次総会
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research

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Published: 2018-04-23   Modified: 2023-01-30  

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