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Development of new therapy using EBV episomal vector in model mouse of EBV infectious diseases

Research Project

Project/Area Number 15K06819
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Laboratory animal science
Research InstitutionNational Center for Child Health and Development

Principal Investigator

Matsuda Go  国立研究開発法人国立成育医療研究センター, 高度先進医療研究室, 研究員 (60392130)

Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywordsトランスレーショナルリサーチ / ウイルス / 感染症 / 癌 / ゲノム
Outline of Final Research Achievements

Epstein-Barr virus (EBV) is associated with various neoplastic diseases. The development of new therapy is desired because there is not a specific cure for EBV. The aim of this study is to develop the therapy which induce apoptosis to specific infected cells with EBV episomal vector and Herpesvirus TK-GCV therapy in model mouse of EBV disease.
In this research, at the culture cell level we showed that the inhibitory effect of EBV was enough but the effect was not observed in the mice because decreasing the expression level of TK. However, the new therapy may be developed by increasing the expression level of TK.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (7 results)

All 2017 2016

All Presentation (7 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] EBV関連悪性腫瘍に対する新規治療法の開発2017

    • Author(s)
      松田 剛、川野 布由子、今留 謙一
    • Organizer
      第65回日本ウイルス学会
    • Related Report
      2017 Annual Research Report
  • [Presentation] EBV関連悪性腫瘍に対する新規治療法の開発2017

    • Author(s)
      松田 剛、川野 布由子、今留 謙一
    • Organizer
      第40回日本分子生物学会
    • Related Report
      2017 Annual Research Report
  • [Presentation] Structure-function relationship of Epstein-Barr Virus EBNA3C NLS and transport receptor2017

    • Author(s)
      Go Matsuda, Takashi Nagata, Masato Katahira and Ken-ichi Imadome
    • Organizer
      The 8th International Symposium of Advanced Energy Science
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] EBウイルス核遺伝子EBNA3Cの新たな核局在化シグナル(NLS)の発見と複数のNLSの戦略的使用2016

    • Author(s)
      松田 剛、今留 謙一
    • Organizer
      第39回日本分子生物学会
    • Place of Presentation
      パシフィコ横浜(神奈川県横浜市)
    • Year and Date
      2016-11-30
    • Related Report
      2016 Research-status Report
  • [Presentation] Identification and functional analysis of Epstein-Barr virus EBNA3C Nuclear localization signal 4 (NLS4)2016

    • Author(s)
      Go Matsuda and Ken-Ichi Imadome
    • Organizer
      第64回日本ウイルス学会
    • Place of Presentation
      札幌コンベンションセンター(北海道札幌市)
    • Year and Date
      2016-10-23
    • Related Report
      2016 Research-status Report
  • [Presentation] Identification and functional analysis of Epstein-Barr virus EBNA3C Nuclear localization signal 4 (NLS4)2016

    • Author(s)
      松田 剛、今留 謙一
    • Organizer
      第13回EBウイルス研究会
    • Place of Presentation
      東京医科歯科大学(東京都文京区)
    • Year and Date
      2016-07-09
    • Related Report
      2016 Research-status Report
  • [Presentation] EBウイルス EBNA3Cの新たな核局在化シグナル2016

    • Author(s)
      松田 剛、今留 謙一
    • Organizer
      第30回ヘルペスウイルス研究会
    • Place of Presentation
      セミナーハウス クロス・ウェーブ府中(東京都府中市)
    • Year and Date
      2016-06-16
    • Related Report
      2016 Research-status Report

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Published: 2015-04-16   Modified: 2019-03-29  

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