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Investigation of the Mechanism of Angiogenin-Mediated Cancer Cell Proliferation and Tumor Angiogenesis, and Its Application for Cancer Treatment

Research Project

Project/Area Number 18592220
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Surgical dentistry
Research InstitutionOkayama University

Principal Investigator

KISHIMOTO Koji  Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Assistant Professor (40243480)

Co-Investigator(Kenkyū-buntansha) SASAKI Akira  Okayama University, Graduate School of Medicine, Dentisty and Pharmaceutical Science, Professor (00170663)
Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,850,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥450,000)
Fiscal Year 2007: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2006: ¥1,900,000 (Direct Cost: ¥1,900,000)
Keywordsangiogenin / oral cancer / angiogenesis / proliferation / invasion / ribosome / ribosomal RNA / hvpoxia / 低酸素(hypoxia) / 浸潤・転移
Research Abstract

In this study, we made an antitumor model of oral cancer by RNAi technology targeting angiogenin, and aimed to elucidate the mechanism of angiogenin-mediated cancer cell proliferation and tumor angiogenesis in order to apply it for cancer treatment.
Secreted levels of angiogenin and VEGF in various oral cancer cell lines were measured by ELISA. As a result, HSC-2 cell that secreted high levels of angiogenin and VEGF, and SCCKN cell that secreted low level of angiogenin and high level of VEGF were selected, and transfected with angiogenin RNAi construct. Down-regulation of angiogenin expression by RNAi decreased proliferation in both of the cells in vitro, and resulted in a decrease in 45S ribosomal RNA transcription, ribosome biogenesis and phosphorylation of Akt (Ser473) in HSC-2 cell. Besides, knocking down angiogenin expression in HSC-2 cell strongly decreased tumor volume in athymic mice although it secreted high level of VEGF.
These results suggested that angiogenin plays a key role in not only tumor angiogenesis but also cell proliferation in oral cancer. Moreover, angiogenin may be necessary for tumor angiogenesis by VEGF.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (4 results)

All 2008 2007

All Presentation (4 results)

  • [Presentation] 血管新生因子angiogeninを標的とした悪性黒色腫の制御に関する基礎的研究2008

    • Author(s)
      岸本晃治
    • Organizer
      第26回日本口腔腫瘍学会総会・学術大会
    • Place of Presentation
      別府
    • Year and Date
      2008-01-25
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Annual Research Report 2007 Final Research Report Summary
  • [Presentation] The study for molecular targeting therapy of angiogenic factor, angiogenin in malignant melanoma2008

    • Author(s)
      Koji, Kishimoto
    • Organizer
      26rd Annual Meeting of Japan Society for Oral Tumors
    • Place of Presentation
      Beppu
    • Year and Date
      2008-01-25
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] The expression and role of angiogenin in malignant melanoma2007

    • Author(s)
      岸本 晃治
    • Organizer
      66th Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      横浜
    • Year and Date
      2007-10-03
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Annual Research Report 2007 Final Research Report Summary
  • [Presentation] The expression and role of angiogenin in malignant melanoma2007

    • Author(s)
      Koji, Kishimoto
    • Organizer
      66th Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      Yokohama
    • Year and Date
      2007-10-03
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary

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Published: 2006-04-01   Modified: 2016-04-21  

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