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2017 Fiscal Year Annual Research Report

Overcoming physical barriers arising in the drug delivery of nanomedicines to lung metastases

Research Project

Project/Area Number 16F16731
Research InstitutionThe University of Tokyo

Principal Investigator

Cabral Horacio  東京大学, 医学(系)研究科(研究院), その他 (10533911)

Co-Investigator(Kenkyū-buntansha) MARTIN JOHN  東京大学, 工学(系)研究科(研究院), 外国人特別研究員
Project Period (FY) 2016-07-27 – 2018-03-31
KeywordsNanomedicine / Tumor microenvironment / Tumor normalization / Tumor stffness / Lung metastasis
Outline of Annual Research Achievements

Normalizing the tumor microenvironment (TME), i.e. components of solid tumors other than cancer cells, increases oxygen and drug delivery thereby making it a treatment strategy combinable with conventional chemo-, radio-, and immune therapies. Normalizing tumor vessels increases intratumor transport of oxygen and drug delivery systems (DDS) up to 30 nanometers (nm) in diameter, while normalization of cancer-associated fibroblasts (CAFs) and extracellular matrix (ECM) increases delivery of DDS up to at least 120nm. The existence of an agent that does both types of normalization and whether such an agent would affect DDS in a size-dependent manner is unknown. We hypothesize there is a size-window of DDS that benefits from TME normalization and reduces hematological toxicity. Steroids like dexamethasone are given to patients post-chemotherapy to manage side effects, yet the potential of such drugs to normalize the TME is unclear. Here, we propose repurposing dexamethasone to a pre-chemotherapy schedule (Pre-TX DEX) to potentiate existing treatments through TME normalization. We elucidated the size-dependent changes of DDS delivery during Pre-TX DEX treatment. We found that Pre-TX DEX normalized the TEM and reduced the stiffness of the tumors, which promoted the enhanced accumulation of nanomedicines in tumors. Thus, Pre-TX DEX improved the efficacy of polymeric micelles loaded with platinum drugs in breast tumor and their lung metastasis.

Research Progress Status

29年度が最終年度であるため、記入しない。

Strategy for Future Research Activity

29年度が最終年度であるため、記入しない。

  • Research Products

    (4 results)

All 2017

All Journal Article (2 results) Presentation (2 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] Effective treatment of drug resistant recurrent breast tumors harboring cancer stem-like cells by staurosporine/epirubicin co-loaded polymeric micelles2017

    • Author(s)
      Zhang Juanjuan、Kinoh Hiroaki、Hespel Louise、Liu Xueying、Quader Sabina、Martin John、Chida Tsukasa、Cabral Horacio、Kataoka Kazunori
    • Journal Title

      Journal of Controlled Release

      Volume: 264 Pages: 127~135

    • DOI

      10.1016/j.jconrel.2017.08.025

  • [Journal Article] Proteasome Inhibitor Loaded Micelles Enhance Antitumor Activity Through Macrophage Reprogramming by NF-κB Inhibition2017

    • Author(s)
      Wu Hailiang、Tao Anqi、Martin John D.、Quader Sabina、Liu Xueying、Takahashi Kei、Hespel Louise、Miura Yutaka、Hayakawa Yoshihiro、Irimura Tatsuro、Cabral Horacio、Kataoka Kazunori
    • Journal Title

      Journal of Pharmaceutical Sciences

      Volume: 106 Pages: 2438~2446

    • DOI

      10.1016/j.xphs.2017.03.031

  • [Presentation] Proteasome inhibitor loaded micelles enhance antitumor activity through macrophage reprogramming by NF-kB inhibition2017

    • Author(s)
      John Martin, Horacio Cabral, Kazunori Kataoka
    • Organizer
      Cancer Nanotechnology Gordon Research Conference, Mt. Snow, VT,
    • Int'l Joint Research
  • [Presentation] Proteasome inhibitor loaded micelles enhance antitumor activity through macrophage reprogramming2017

    • Author(s)
      John Martin, Horacio Cabral, Kazunori Kataoka
    • Organizer
      11th Annual Symposium on Nanobiotechnology, Kawasaki, Japan
    • Int'l Joint Research

URL: 

Published: 2018-12-17  

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