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Development of nucleic acids carriers equipped with tumor microenvironment-sensitive peptides for the therapy of metastatic liver cancer(Fostering Joint International Research)

Research Project

Project/Area Number 15KK0357
Research Category

Fund for the Promotion of Joint International Research (Fostering Joint International Research)

Allocation TypeMulti-year Fund
Research Field Physical pharmacy
Research InstitutionKyoto Pharmaceutical University

Principal Investigator

Hama Susumu  京都薬科大学, 薬学部, 講師 (60438041)

Research Collaborator Kopecek Jindrich  University of Utah, Center for Controlled Chemical Delivery, 教授
Hasan Mahadi  
Itagaki Nagisa  
Marukawa Hiroki  
Watanabe Yuya  
Kamei Kazuho  
Maeda Shizuka  
Project Period (FY) 2016 – 2018
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥14,560,000 (Direct Cost: ¥11,200,000、Indirect Cost: ¥3,360,000)
Keywordsドラッグデリバリーシステム / 腫瘍微小環境 / 幹細胞 / DDS / がん幹細胞
Outline of Final Research Achievements

Cancer stem cells, which exist at deep region of tumor, have been implicated in tumor metastasis and chemotherapy resistance. Therefore, it is required to develop a novel therapy that can induce potent cytotoxicity in cancer stem cells. In this study, low-molecular drugs or nucleic acids, which can inhibit the essential signaling pathway for the survival and maintenance of cancer stem cells, were encapsulated into tumor microenvironment-sensitive drug carriers that can achieve the targeting to cancer stem cells as well as effective tumor delivery. These nanoparticles are expected as a nanomedicine for the therapy of cancer stem cells.

Academic Significance and Societal Importance of the Research Achievements

本研究で開発したナノメディシンは、腫瘍透過性が高いだけでなく、腫瘍微小環境下のがん細胞特異的に薬物送達可能なナノ粒子を基盤としているため、既存の送達方法に比べて、がん幹細胞へ効果的に薬物を送達できることが期待される。また、現在精力的にがん幹細胞の特性解析が行われているが、本ナノ粒子は低分子薬物に限らず、核酸を効率的に細胞質へ送達可能であり、がん幹細胞に細胞死を誘導することができる。今後、がん幹細胞に有効な標的分子が見出されることで、それらの機能を阻害可能な薬物を搭載したナノメディシンによる高い治療効果が期待される。

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (7 results)

All 2018 2017 Other

All Int'l Joint Research (1 results) Journal Article (1 results) (of which Open Access: 1 results) Presentation (4 results) (of which Int'l Joint Research: 1 results,  Invited: 1 results) Remarks (1 results)

  • [Int'l Joint Research] ユタ大学(米国)2017

    • Year and Date
      2017-03-03
    • Related Report
      2018 Annual Research Report
  • [Journal Article] Develop liposome-based drug carriers in response to tumour microenvironment2018

    • Author(s)
      Hama S
    • Journal Title

      Impact

      Volume: 12 Issue: 12 Pages: 73-75

    • DOI

      10.21820/23987073.2018.12.73

    • Related Report
      2018 Annual Research Report
    • Open Access
  • [Presentation] Tumor-penetrable nanoparticles for delivering drugs into cells in response to tumor microenvironment.2018

    • Author(s)
      Hama S, Suzuki S, Itakura S, Kogure K
    • Organizer
      BIT's 8th Annual World Congress Of Nano Science and Technology 2018
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] Development of a tumor-penetrable drug carrier in response to tumor microenvironment.2018

    • Author(s)
      Hama S, Itakura S
    • Organizer
      第77回日本癌学会学術総会
    • Related Report
      2018 Annual Research Report
  • [Presentation] 微弱低pH応答性リポソームの腫瘍内透過におけるiRGD修飾の影響2018

    • Author(s)
      板垣 渚、松井 諒、板倉 祥子、濱 進
    • Organizer
      日本薬剤学会 第33年会
    • Related Report
      2018 Annual Research Report
  • [Presentation] 新規血中滞留性素子を搭載した腫瘍低pH応答性リポソームの開発2018

    • Author(s)
      丸川裕己、板倉祥子、斎藤博幸、宗慶太郎、濱 進
    • Organizer
      日本薬学会第138年会
    • Related Report
      2017 Research-status Report
  • [Remarks] 京都薬科大学薬品物理化学分野

    • URL

      http://labo.kyoto-phu.ac.jp/bukka/

    • Related Report
      2018 Annual Research Report 2016 Research-status Report

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Published: 2016-10-04   Modified: 2020-03-30  

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