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The therapeutic research using Autophagy in Tuberous sclerosis complex

Research Project

Project/Area Number 24791074
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pediatrics
Research InstitutionOita University

Principal Investigator

MIYAHARA HIROAKI  大分大学, 医学部, 講師 (00457615)

Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,380,000 (Direct Cost: ¥2,600,000、Indirect Cost: ¥780,000)
Fiscal Year 2014: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2013: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords結節性硬化症 / オートファジー / ウェスタンブロット / 細胞培養 / mTOR
Outline of Final Research Achievements

In this research, I have tried to elucidate the relationship between mTOR signaling pathway and autophagy in Tuberous sclerosis complex (TSC) and establish new therapeutic strategy using induction of autophagy. In western blotting, control fubroblast induced autophagy with starvation, but TSC fbroblast did not at all. p62, which is decrease with induction of autophagy, showed reduction tendency in both fibroblasts.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (1 results)

All 2013

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

  • [Journal Article] Suppressed Expression of Autophagosomal Protein LC3 in Cortical Tubers of2013

    • Author(s)
      Miyahara H, Natsumeda M, Shiga A, Aoki H, Toyoshima Y, Zheng Y, Takeuchi R,
    • Journal Title

      Brain Pathol.

      Volume: 23 Issue: 3 Pages: 254-262

    • DOI

      10.1111/j.1750-3639.2012.00634.x

    • Related Report
      2012 Research-status Report
    • Peer Reviewed

URL: 

Published: 2013-05-31   Modified: 2019-07-29  

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