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Development of interferon cancer gene therapy by optimizing structure/pharmacokinetics/activity of transgene product

Research Project

Project/Area Number 25713003
Research Category

Grant-in-Aid for Young Scientists (A)

Allocation TypePartial Multi-year Fund
Research Field Physical pharmacy
Research InstitutionKyoto University

Principal Investigator

Takahashi Yuki  京都大学, 薬学研究科(研究院), 助教 (00547870)

Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥24,050,000 (Direct Cost: ¥18,500,000、Indirect Cost: ¥5,550,000)
Fiscal Year 2015: ¥6,240,000 (Direct Cost: ¥4,800,000、Indirect Cost: ¥1,440,000)
Fiscal Year 2014: ¥5,590,000 (Direct Cost: ¥4,300,000、Indirect Cost: ¥1,290,000)
Fiscal Year 2013: ¥12,220,000 (Direct Cost: ¥9,400,000、Indirect Cost: ¥2,820,000)
Keywordsインターフェロン / 遺伝子治療 / DDS / ルシフェラーゼ
Outline of Final Research Achievements

In the present study, we designed IFNγ derivatives fused with a fibrin-binding pentapeptide (CREKA) for the development of effective IFNγ cancer gene therapy. We constructed plasmid DNA (pDNA) expressing an IFNγ-CREKA fusion protein and administered the pDNA into tumor-bearing mice by hydrodynamic injection. The fusion protein was detected to bind to fibrin clots in the tumor tissue. Moreover, tumor growth was suppressed by the administration of the pDNA. In conclusion, it was shown that IFNγ-CREKA fusion protein can be used to improve therapeutic effect of IFNγ cancer gene therapy.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Annual Research Report
  • 2013 Annual Research Report
  • Research Products

    (4 results)

All 2015 2014 2013

All Presentation (4 results)

  • [Presentation] 血栓結合型インターフェロンγ誘導体の遺伝子導入によるインターフェロンγ癌遺伝子治療効果の増強2015

    • Author(s)
      藤本眞衣、安藤満、高橋有己、西川元也、濵名温志、高倉喜信
    • Organizer
      第65回日本薬学会近畿支部総会・大会
    • Place of Presentation
      大阪大谷大学 (大阪府 富田林市)
    • Year and Date
      2015-10-17
    • Related Report
      2015 Annual Research Report
  • [Presentation] 血栓結合型インターフェロンγ誘導体の遺伝子導入によるインターフェロンγ癌遺伝子治療効果の増強2015

    • Author(s)
      濵名温志、安藤 満、藤本眞衣、高橋有己、西川元也、高倉喜信
    • Organizer
      日本薬学会第135年会
    • Place of Presentation
      兵庫医療大学(神戸)
    • Year and Date
      2015-03-26 – 2015-03-28
    • Related Report
      2014 Annual Research Report
  • [Presentation] 腫瘍血栓結合性ペプチド融合インターフェロンの設計と遺伝子導入による腫瘍指向性インターフェロン遺伝子治療法の開発2014

    • Author(s)
      藤本眞衣、安藤 満、高橋有己、濵名温志、西川元也、高倉喜信
    • Organizer
      アンチセンス・遺伝子・デリバリーシンポジウム2014
    • Place of Presentation
      東京医科歯科大学M&Dタワー(東京)
    • Year and Date
      2014-09-08 – 2014-09-09
    • Related Report
      2014 Annual Research Report
  • [Presentation] ヒト肝細胞キメラマウスを用いたインターフェロンγ遺伝子導入による治療抵抗性慢性C型肝炎治療.2013

    • Author(s)
      安藤 満、高橋有己、西川元也、平賀信彦、今村道雄、茶山一彰、高倉喜信
    • Organizer
      第29回日本DDS学会学術集会
    • Place of Presentation
      京都テルサ (京都市南区)
    • Related Report
      2013 Annual Research Report

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Published: 2013-05-21   Modified: 2019-07-29  

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