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Construction of tumor blood vessels involved in hepatobalstoma stem cells and role of tumor microenvironment.

Research Project

Project/Area Number 16K11353
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Pediatric surgery
Research InstitutionSaitama Medical University

Principal Investigator

Fujita Keiko  埼玉医科大学, 医学部, 准教授 (80173425)

Project Period (FY) 2016-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2018: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2017: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2016: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords肝芽腫 / 腫瘍血管新生 / がん幹細胞 / がん微小環境 / 細胞膜ナノチューブ / ニッチ / 細胞間結合 / ニッチェ / 培養 / がんの微小環境
Outline of Final Research Achievements

The conventional notion of tumor vasculature is that new tumor blood vessels sprout from preexisting vasculature near the tumor; hence, tumor endothelial cells are derived from normal endothelial cells. However, the results in this report suggest that CD133‐positive hepatoblastoma stem cells (CSCs) differentiate into tumor vascular endothelial cells and might be able to form tumor vessels.
The hepatoblastoma stem cells using flow cytometry were identified. The side population cells were injected into NOD/SCID mice. The digested xenograft tumor fragments were cultured and the tumor sphere assay was performed. The spheres were cultivated using 3D culture methods. Some spheres formed CD133 positive capillary-like structures. The membrane nanotubes, which conduit for direct cell-to-cell communication, have been suggested to play an important role in tumor microenvironments. The structure of membrane nanotubes in hepatoblastoma cells was investigated.

Academic Significance and Societal Importance of the Research Achievements

肝芽腫の発がん機構を解明し新たな治療法の開発を進めていく上で、肝芽腫幹細胞をとりまく微小環境、腫瘍血管の新生機序とがん幹細胞との相互作用の解明、がん幹細胞から血管内皮細胞へ分化するメカニズムの解明が重要である。肝芽腫幹細胞を選択的に死滅させることができれば、再発・転移を抑制できる可能性が高いことから、治療法が確立されていなかった再発・転移した肝芽腫に対する解決にも本研究の結果が期待される。

Report

(5 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (7 results)

All 2020 2019 2018 2017 2016

All Presentation (6 results) Book (1 results)

  • [Presentation] 肝芽腫細胞間を連結する細胞膜ナノチューブの構造と機能2020

    • Author(s)
      藤田恵子,松本幸子,藤田一正,穐田真澄,永島雅文
    • Organizer
      第125回 日本解剖学会総会・全国学術集会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 細胞膜ナノチューブによるヒト肝芽腫細胞間の連絡2019

    • Author(s)
      藤田恵子,松本幸子,藤田一正,穐田真澄,永島雅文
    • Organizer
      第124回 日本解剖学会総会・全国学術集会
    • Related Report
      2018 Research-status Report
  • [Presentation] ヒト肝芽腫における細胞膜ナノチューブの形成2018

    • Author(s)
      藤田恵子,松本幸子,藤田一正,穐田真澄,永島雅文
    • Organizer
      第123回 日本解剖学会総会・全国学術集会
    • Related Report
      2017 Research-status Report
  • [Presentation] ヒト肝芽腫細胞におけるがん微小環境ストレスに対する適応応答2017

    • Author(s)
      藤田恵子,松本幸子,藤田一正,穐田真澄,永島雅文
    • Organizer
      第122回 日本解剖学会総会・全国学術集会
    • Place of Presentation
      長崎大学坂本キャンパス(長崎県長崎市)
    • Year and Date
      2017-03-30
    • Related Report
      2016 Research-status Report
  • [Presentation] ヒト肝芽腫における細胞間ネットワークの形成2017

    • Author(s)
      藤田恵子,松本幸子,村井則子,穐田真澄
    • Organizer
      第49回 日本臨床分子形態学会総会・学術集会
    • Related Report
      2017 Research-status Report
  • [Presentation] 腫瘍血管構築に関与する肝芽腫幹細胞について2016

    • Author(s)
      藤田恵子,松本幸子,小松久美子,村井則子,穐田真澄
    • Organizer
      第48回日本臨床分子形態学会総会・学術集会
    • Place of Presentation
      くまもと県民交流館パレア(熊本県熊本市)
    • Year and Date
      2016-09-24
    • Related Report
      2016 Research-status Report
  • [Book] Physiologic and Pathologic Angiogenesis - Signaling Mechanisms and Targeted Therapy. Chapter12 Tumor Angiogenesis: A Focus on the Role of Cancer Stem Cells.2017

    • Author(s)
      Keiko Fujita, Masumi Akita
    • Publisher
      INTECH
    • Related Report
      2016 Research-status Report

URL: 

Published: 2016-04-21   Modified: 2021-02-19  

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