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Analysis of antiviral activity of 25-hydroxycholesterol

Research Project

Project/Area Number 26860050
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Biological pharmacy
Research InstitutionNational Institute of Health Sciences

Principal Investigator

Shibata Norihito  国立医薬品食品衛生研究所, 遺伝子医薬部, 主任研究官 (30391973)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords酸化コレステロール
Outline of Final Research Achievements

Although it is well known that many viruses can cause severe diseases, existing drugs against viruses are not sufficient and development of novel anti-virus drugs is required. Previously, I found that 25-hydroxycholesterol (25OHC) can inhibit virus replication without affecting on the viability of host cells. In this study, I investigated the molecular mechanism how 25OHC is recognized by the host cells, and how 25OHC induces the expression of specific stress-related genes. These results suggest that 25OHC may be a promising target for development of a novel anti-virus drug.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (11 results)

All 2017 2016 2015 2014

All Journal Article (4 results) (of which Int'l Joint Research: 3 results,  Peer Reviewed: 4 results,  Open Access: 1 results,  Acknowledgement Compliant: 3 results) Presentation (7 results)

  • [Journal Article] Development of BCR-ABL degradation inducers via the conjugation of an imatinib derivative and a cIAP1 ligand.2016

    • Author(s)
      Demizu, Y., Shibata, N., Hattori, T., Ohoka, N., Motoi, H., Misawa, T., Shoda, T., Naito, M. & Kurihara, M.
    • Journal Title

      Bioorg Med Chem Lett

      Volume: 26 Issue: 20 Pages: 4865-4869

    • DOI

      10.1016/j.bmcl.2016.09.041

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Induction of proteasomal degradation of ERα and subsequent cell death in breast cancer cells2016

    • Author(s)
      K. Okuhira, Y. Demizu, T. Hattori, N. Ohoka, N. Shibata, T. Nishimaki-Mogami, H. Okuda, M. Kurihara, M. Naito*
    • Journal Title

      Methods Mol. Biol.

      Volume: 1366 Pages: 549-560

    • DOI

      10.1007/978-1-4939-3127-9_42

    • ISBN
      9781493931262, 9781493931279
    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Protein Knockdown Technology: Application of Ubiquitin Ligase to Cancer Therapy.2016

    • Author(s)
      Ohoka N, Shibata N, Hattori T, Naito M.
    • Journal Title

      Current Cancer Drug Targets

      Volume: 16 Issue: 2 Pages: 136-146

    • DOI

      10.2174/1568009616666151112122502

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Degradation of Stop Codon Read-through Mutant Proteins via the Ubiquitin-Proteasome System Causes Hereditary Disorders.2015

    • Author(s)
      Shibata N, Ohoka N, Sugaki Y, Onodera C, Inoue M, Sakuraba Y, Takakura D, Hashii N, Kawasaki N, Gondo Y, Naito M
    • Journal Title

      J. Biol. Chem.

      Volume: 290 Issue: 47 Pages: 28428-28437

    • DOI

      10.1074/jbc.m115.670901

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] プロテインノックダウン法を利用したアンドロゲン受容体タンパク質分解誘導剤の開発2017

    • Author(s)
      柴田識人、永井克典、森田陽子、宇治川治、大岡伸通、服部隆行、今枝泰宏、奈良洋、長展生、内藤幹彦
    • Organizer
      日本薬学会第137年会
    • Place of Presentation
      仙台
    • Year and Date
      2017-03-24
    • Related Report
      2016 Annual Research Report
  • [Presentation] 発がん因子BCR-ABLを分解する低分子化合物の開発2016

    • Author(s)
      柴田識人、大岡伸通、服部隆行、内藤幹彦
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Related Report
      2016 Annual Research Report
  • [Presentation] BCR-ABLの蛋白質分解誘導剤開発を指向したBCR-ABL結合化合物の探索2016

    • Author(s)
      柴田 識人、大岡 伸通、服部 隆行、橋井 則貴、斎藤 臣雄、近藤 恭光、石井 明子、長田 裕之、内藤 幹彦
    • Organizer
      日本薬学会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2016-03-26
    • Related Report
      2015 Research-status Report
  • [Presentation] 終止コドンリードスルー変異による蛋白質のユビキチン-プロテアソーム依存的な分解はある種の遺伝性疾患の原因となりえる2015

    • Author(s)
      柴田 識人、大岡 伸通、権藤 洋一 、内藤 幹彦
    • Organizer
      日本癌学会学術総会
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Year and Date
      2015-10-08
    • Related Report
      2015 Research-status Report
  • [Presentation] 終止コドンのリードスルー変異によるユビキチン-プロテアソーム系を介した蛋白質の不安定化2015

    • Author(s)
      柴田 識人、大岡 伸通、櫻庭 喜行、権藤 洋一 、内藤 幹彦
    • Organizer
      日本薬学会
    • Place of Presentation
      デザイン・クリエイティブセンター神戸(兵庫県)
    • Year and Date
      2015-03-25 – 2015-03-28
    • Related Report
      2014 Research-status Report
  • [Presentation] 終止コドンのリードスルー変異によるユビキチン-プロテアソーム系を介した蛋白質の不安定化2014

    • Author(s)
      柴田 識人、大岡 伸通、櫻庭 喜行、権藤 洋一 、内藤 幹彦
    • Organizer
      Symposium for young ubiquitin researchers in Japan“New Era in the Ubiquitin Research”
    • Place of Presentation
      国際高等研究所(京都府)
    • Year and Date
      2014-11-10 – 2014-11-12
    • Related Report
      2014 Research-status Report
  • [Presentation] 終止コドンのリードスルー変異によるユビキチン-プロテアソーム系を介した蛋白質の不安定化2014

    • Author(s)
      柴田 識人、大岡 伸通、権藤 洋一 、内藤 幹彦
    • Organizer
      日本癌学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2014-09-25 – 2014-09-27
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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