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The elucidation of macrophage regulating factor in tumor microenvironment of Ewing sarcoma

Research Project

Project/Area Number 16H07056
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Orthopaedic surgery
Research InstitutionKyushu University

Principal Investigator

Iida Keiichiro  九州大学, 大学病院, 助教 (70782621)

Project Period (FY) 2016-08-26 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywordsマクロファージ / Ewing肉腫 / がん微小環境 / 血管新生 / 癌微小環境 / MCP-1
Outline of Final Research Achievements

We established stable MCP-1 overexpressed EWS cell lines and transplanted to nude mice. The xenografts of MCP-1 overexpressed Ewing sarcoma(EWS) cells had more vascular invasion. The Tumor associated macrophages(TAMs) isolated from the xenograft of MCP-1 overexpressed EWS cells were analyzed and the expression of matrix protease was upregulated in the macrophage. When RAW 264.7, mouse macrophage like cell, was cultured by the culture supernatant of MCP-1 overexpressed EWS cells, the expression of matrix protease was increased and the expression was suppressed by the MCP-1 inhibitor. These findings indicate the secretion of MCP-1 from EWS cells promotes the expression of matrix protease from TAM and induce angiogenesis in tumor microenvironment.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Annual Research Report
  • Research Products

    (1 results)

All 2017

All Presentation (1 results)

  • [Presentation] Ewing 肉腫においてMCP-1 はマクロファージを介し血管新生を誘導する2017

    • Author(s)
      八尋健一郎
    • Organizer
      第50回 日本整形外科学会 骨軟部腫瘍学術集会
    • Related Report
      2017 Annual Research Report

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Published: 2016-09-02   Modified: 2019-03-29  

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