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2023 Fiscal Year Research-status Report

Nanomedicine-based Chemo-Immunotherapy for the Treatment of Pediatric Brain Cancer

Research Project

Project/Area Number 22K12833
Research InstitutionKawasaki Institute of Industrial Promotion Innovation Center of NanoMedicine

Principal Investigator

劉 学瑩  公益財団法人川崎市産業振興財団(ナノ医療イノベーションセンター), ナノ医療イノベーションセンター, 主任研究員 (30777470)

Co-Investigator(Kenkyū-buntansha) 喜納 宏昭  公益財団法人川崎市産業振興財団(ナノ医療イノベーションセンター), ナノ医療イノベーションセンター, 主幹研究員 (70283067)
Quader Sabina  公益財団法人川崎市産業振興財団(ナノ医療イノベーションセンター), ナノ医療イノベーションセンター, 副主幹研究員 (90749699)
Project Period (FY) 2022-04-01 – 2025-03-31
KeywordsNanomedicine / ICIs / medulloblastoma
Outline of Annual Research Achievements

We have successfully developed and confirmed the effectiveness of a syngeneic mouse model for medulloblastoma, a type of brain tumor in our laboratory.
In our research, we have conducted extensive screenings of multiple anticancer drug-loaded nanomedicines against this model, leading to significant findings.
Furthermore, we have also conducted screenings of several immune checkpoint inhibitors (PD1, PDL1, CTLA-4, CD47, CD24, CD276) against the MB syngeneic model, resulting in important and promising research outcomes.

Current Status of Research Progress
Current Status of Research Progress

2: Research has progressed on the whole more than it was originally planned.

Reason

A substantial amount of research-related data has been collected.

Strategy for Future Research Activity

Confirmation of synergistic or combination effect of anticancer drug-loaded nanomedicine and immune checkpoint inhibitors. Additionally, intellectual patent filing and dissemination of results through conference presentation and journal article publication.

Causes of Carryover

Due to other important commitments, it was not possible to attend the planned international conferences, which have been rescheduled for this fiscal year.

  • Research Products

    (1 results)

All 2023

All Journal Article (1 results)

  • [Journal Article] Identifying molecular tags selectively retained on the surface of brain endothelial cells to generate artificial targets for therapy delivery.2023

    • Author(s)
      48.G. M. Porro, I. Lorandi, X. Liu, K. Kataoka, G. Battaglia, D. G.-Carter,
    • Journal Title

      Fluids Barriers CNS

      Volume: 20 Pages: 88

    • DOI

      10.1186/s12987-023-00493-6

URL: 

Published: 2024-12-25  

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