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Development of a new type of microRNA inhibitor

Research Project

Project/Area Number 26670054
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Drug development chemistry
Research InstitutionTokyo Medical and Dental University

Principal Investigator

YOKOTA Takanori  東京医科歯科大学, 医歯(薬)学総合研究科, 教授 (90231688)

Project Period (FY) 2014-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2014: ¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
KeywordsmicroRNA / microRNA阻害薬 / exon skipping
Outline of Final Research Achievements

Here we developed a new class of therapeutics oligonucleotide, hetero-chimera-duplex oligonucleotide (HCDO). HCDO has DNA/RNA double strand and antisense oligonucleotide integrated into the RNA strand. We assessed in vivo efficacy of HCDO integrated with microRNA122 inhibitor which had a variety of length of DNA/RNA double strand. We revealed that the length of double strand ranging from 7 to 17mer did not affect efficacy of HCDO. Next, we evaluated in vitro efficacy of HCDO integrated with oligonucleotides regulating splicing. We revealed that HCDO had more efficient ability to regulate splicing than the original single strand oligonucleotide.

Report

(2 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • Research Products

    (1 results)

All 2014

All Presentation (1 results)

  • [Presentation] 新規二本鎖ヘテロキメラ構造によるマイクロRNA抑制薬の増強効果.2014

    • Author(s)
      吉岡耕太郎, 筋野裕美子, 田中規恵, 朴文英, 仁科智子, 桑原宏哉, 仁科一隆, 横田隆徳.
    • Organizer
      第6回日本RNAi研究会
    • Place of Presentation
      広島
    • Year and Date
      2014-08-28
    • Related Report
      2014 Annual Research Report

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Published: 2014-04-04   Modified: 2016-06-03  

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