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Study of cell death-inducing effect enhanced by combined use of anatase-type titanium dioxide and a physiologically active substance

Research Project

Project/Area Number 24651054
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Risk sciences of radiation/Chemicals
Research InstitutionTokyo University of Science

Principal Investigator

YOSHIMI Yoji  東京理科大学, 理工学部, 助教 (70609362)

Co-Investigator(Renkei-kenkyūsha) IKEKITA Masahiko  東京理科大学, 理工学部応用生物科学科, 教授 (70138981)
SHINOMIYA Takahisa  東京理科大学, 理工学部応用生物科学科, 教授 (30196414)
Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,380,000 (Direct Cost: ¥2,600,000、Indirect Cost: ¥780,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywords光触媒 / 酸化チタン / 細胞死 / 活性酸素 / 酸化ストレス / 脂質過酸化 / ネクローシス / アポトーシス / ナノパーティクル / 皮膚がん / 紫外線
Research Abstract

The present study analyzes the mechanism of cell damage by photocatalytic effect of titanium dioxide, was done for the purpose of basic research in order to help in the treatment of cancer. Research is composed of three modes, 1) to establish the effective induction and measurement method for the cell cytotoxicity, 2) to classify the type of cell death, and 3) to analyze of the induction mechanism of the cell death. It was possible to establish a system in which they have found a condition that injury effectively the cell, to measure. Further, it was suggested that cell death by the photocatalyst is not apoptosis of various features. Furthermore, the lipid peroxidation of the cell membrane is caused remarkably was confirmed. It is considered that cell death by photocatalyst to cause necrosis by membrane collapses ROS generated by photocatalytic effect has prompted the lipid peroxidation of the cell membrane.

Report

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

    (14 results)

All 2013 2012 Other

All Journal Article (2 results) (of which Peer Reviewed: 2 results) Presentation (11 results) Remarks (1 results)

  • [Journal Article] Novel tamoxifen derivative Ridaifen-B induces Bcl-2 independent autophagy without estrogen receptor involvement2013

    • Author(s)
      M Takeyoshi, S Sakemoto, I Shiina, K Nakata, K Fujimori, Y Wang, E Umeda, C Watanabe, S Uetake, T Yamori, S Dan, Y Yoshimi, T Shinomiya, M Ikekita
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: In press

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] SUTAF, a novel β-methoxyacrylate derivative, promotes neurite outgrowth with extracellular signal-regulated kinase and c-jun N-terminal kinase activation.2012

    • Author(s)
      Nagahara Y, Suzuki E, Sekine Y, Uchiro H, Yoshimi Y, Shinomiya T, Ikekita M
    • Journal Title

      Europian Juornal of Pharmacology

      Volume: 694 Issue: 1-3 Pages: 53-59

    • DOI

      10.1016/j.ejphar.2012.08.018

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Presentation] カバノアナタケから同定された抗癌剤候補化合物DDTCTの作用機構解析2012

    • Author(s)
      北川純子, 吉見 陽児, 望月万里, 森田明典, 菅原二三男, 池北雅彦
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] 腎細胞がんの診断マーカーの探索2012

    • Author(s)
      田中信太郎, 金子直樹, 吉見陽児, 四宮貴久, 池北雅彦
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] 新規抗癌剤候補化合物DDTCT誘導性細胞増殖抑制に関連する遺伝子の解析2012

    • Author(s)
      内田知紗, 望月万里, 吉見陽児, 森田明典, 羽染芳宗, 井田紀子, 船津修, 菅原二三男, 池北雅彦
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] 環状グアニジン構造を有する新規化合物RK-96の制がん剤としての可能性2012

    • Author(s)
      清水理加, 吉見陽児, 横山翔, 岩下治弘, 袴田真矢, 斎藤隆夫, 四宮貴久, 池北雅彦
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] 新規タモキシフェン類縁体リダイフェン-Bによるオートファジー誘導2012

    • Author(s)
      長原礼宗, 酒本聖也, 梅田絵梨, 渡邊千尋, 植竹祥子, 吉見陽児, 四宮貴久, 池北雅彦, 椎名勇
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] リダイフェン-Gは強力なオートファジー誘導剤である2012

    • Author(s)
      山本卓, 吉見陽児, 四宮貴久, 羽鳥麻奈美, 長原礼宗, 梅田絵梨, 渡邊千尋, 植竹祥子, 椎名勇, 池北雅彦
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] 新規細胞死誘導剤リダイフェンGの作用機構の解析並びに標的分子の同定2012

    • Author(s)
      羽鳥麻奈美, 山本卓, 友光裕子, 椎名勇, 梅田絵梨, 戸田年総, 大篭友博, 岩本真知子, 森田明典, 渡邊千尋, 植竹祥子, 矢守隆夫, 吉見陽児, 四宮貴久, 池北雅彦
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] TiO2の光触媒効果が引き起こす細胞死誘導における細胞膜脂質過酸化解析光触媒

    • Author(s)
      伊藤駿、小松原直人、吉見陽児、中田一弥、池北雅彦
    • Organizer
      光機能材料研究会第20回記念シンポジウム
    • Place of Presentation
      東京
    • Related Report
      2013 Final Research Report
  • [Presentation] 光触媒効果による細胞死誘導機構の分子機構解析光触媒

    • Author(s)
      小松原直人、吉見陽児、中田一弥、池北雅彦
    • Organizer
      光機能材料研究会第20回記念シンポジウム
    • Place of Presentation
      東京
    • Related Report
      2013 Final Research Report
  • [Presentation] 光触媒効果による細胞死誘導の分子機構解析

    • Author(s)
      小松原直人、吉見陽児、中田一弥、池北雅彦
    • Organizer
      光触媒、光機能材料研究会 第20回記念シンポジウム
    • Place of Presentation
      東京大学生産技術研究所
    • Related Report
      2013 Annual Research Report
  • [Presentation] TiO2の光触媒効果が引き起こす細胞死誘導における細胞膜脂質過酸化解析

    • Author(s)
      伊藤駿、小松原直人、吉見陽児、中田一弥、池北雅彦
    • Organizer
      光触媒、光機能材料研究会 第20回記念シンポジウム
    • Place of Presentation
      東京大学生産技術研究所
    • Related Report
      2013 Annual Research Report
  • [Remarks]

    • URL

      http://www.rs.tus.ac.jp/nakata/

    • Related Report
      2013 Final Research Report

URL: 

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

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