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The role of circular RNA ITCH in the development of aortic stenosis

Research Project

Project/Area Number 18K15838
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 53020:Cardiology-related
Research InstitutionYamagata University

Principal Investigator

Yoichiro Otaki  山形大学, 医学部, 助教 (80732693)

Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2020: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
KeywordsITCH E3 ligase / cardiac hypertrophy / aortic stenosis / HECT-type E3 ligase ITCH / Dvl / LVH / Aortic sclerosis / HECT type E3 ligase ITCH / Circular ITCH / 大動脈弁狭窄症 / 心肥大 / ITCHとDVLの相互作用 / 左室肥大
Outline of Final Research Achievements

Left ventricular hypertrophy and aortic valve calcification are associated with the development of aortic stenosis. We examined the role of circular ITCH and ITCH on the development of aortic stenosis. Unexpectedly, expression level of miR214, a target of circular ITCH, was not changed after left ventricular hypertrophy induced by transverse aortic constriction. Thus, we focused on the ubiquitin E3 ligase ITCH, but not circular ITCH, and found that ITCH attenuates left ventricular hypertrophy through Wnt/β catenin signaling pathway. Furthermore, mRNA expression level of ITCH in aortic valve was lower in patients with AS than in those without it. These findings suggest a pivotal role of ITCH in the development of aortic stenosis and identify ITCH as a potential treatment target for preventing aortic stenosis.

Academic Significance and Societal Importance of the Research Achievements

ユビキチン転移酵素ITCHが大動脈弁狭窄症発症(左室肥大や大動脈弁硬化)に関連することを示した。左室肥大に関しては、心筋特異的ITCH過剰発現マウスを用いて、ITCHがWnt/βカテニン経路を介して、野生型マウスに比較して心肥大を抑制し、心機能を改善することを示した。大動脈弁硬化に関しては、人大動脈弁サンプルを用いて、大動脈狭窄症の発症に、ITCHの機能低下が関与することを示した。また、ITCHがRunx2の発現を抑制するデータを得た。本研究により得られた新たな知見から、ITCHが左室肥大と大動脈弁硬化に対する新たな治療標的となりうる可能性が示唆された。

Report

(4 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (1 results)

All 2020

All Journal Article (1 results) (of which Peer Reviewed: 1 results)

  • [Journal Article] HECT(Homologous to the E6-AP Carboxyl Terminus)-Type Ubiquitin E3 Ligase ITCH Attenuates Cardiac Hypertrophy by Suppressing the Wnt/β-Catenin Signaling Pathway2020

    • Author(s)
      Jun Goto, Yoichiro Otaki et al.
    • Journal Title

      Hypertension

      Volume: 76 Issue: 6 Pages: 1868-1878

    • DOI

      10.1161/hypertensionaha.120.15487

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed

URL: 

Published: 2018-04-23   Modified: 2022-01-27  

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