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Establishment of cell lines from rare thoracic malignancies and its genetic alterations

Research Project

Project/Area Number 17K10808
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Respiratory surgery
Research InstitutionNagoya University

Principal Investigator

Fukui Takayuki  名古屋大学, 医学部附属病院呼吸器外科, 講師 (70463198)

Co-Investigator(Kenkyū-buntansha) 羽切 周平  名古屋大学, 医学部附属病院, 病院助教 (40647476)
川口 晃司  名古屋大学, 医学部附属病院, 病院准教授 (10402611)
横井 香平  名古屋大学, 医学系研究科, 教授 (60378007)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2019: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2018: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2017: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords胸腺腫 / 胸腺癌 / 細胞株 / 胸腺上皮性腫瘍 / PD-L1 / PD1 / PD-1 / PDL-1 / 胸部悪性腫瘍 / 中皮腫
Outline of Final Research Achievements

Among the rare thoracic malignancies, we established cell lines from thymoma since 2017, and succeeded in culturing them for more than 10 passages in 2 cases. Furthermore, in thymic epithelial tumors, PD-L1 staining was performed using paraffin blocks of surgical specimens. As a result, it was revealed that PD-L1 positivity (staining 1% or more) was significantly higher in B2 and B3 thymoma, advanced stage thymoma of Masaoka stage 3 or 4. In addition, FDG accumulation (maxSUV value) and PD-L1 expression in FDG-PET scan were significantly correlated. The results could be presented at academic conferences in Japan and overseas. Furthermore, we performed additional PD-Ll staining using 240 cases of resected thymic epithelial tumor, but the evaluation could not be completed due to changes in the evaluator.

Academic Significance and Societal Importance of the Research Achievements

胸部に発生するまれな腫瘍のうち、胸腺腫では研究に利用可能な細胞株が国内外でほとんど存在しないため、未熟ながらも初代培養に成功した意義はあると思われる。また、胸腺上皮性腫瘍と腫瘍内のPD-L1タンパク発現の頻度や臨床病理学的因子との関係を明らかにできたことで、現在は有効な薬物治療が他癌腫に比べて限られている進行胸腺腫や胸腺癌患者に対する各種免疫チェックポイント阻害薬の臨床効果が期待できる。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (3 results)

All 2019 2018 2017

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (2 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] Clinicopathological Features of Thymoma with expression of Programmed Death Ligand 12019

    • Author(s)
      Shuhei Hakiri, Takayuki Fukui, Shunsuke Mori, Koji Kawaguchi, Shota Nakamura, Naoki Ozeki, Taketo Kato, Masaki Goto, Yasushi Yatabe, Kohei Yokoi
    • Journal Title

      Annals of Thoracic Surgery

      Volume: 107 Issue: 2 Pages: 418-424

    • DOI

      10.1016/j.athoracsur.2018.08.037

    • Related Report
      2019 Annual Research Report 2018 Research-status Report
    • Peer Reviewed
  • [Presentation] Clinicopathological Features of Thymoma with the Expression of Programmed Death-Ligand 12018

    • Author(s)
      Shuhei Hakiri, Takayuki Fukui, Shunsuke Mori, Koji Kawaguchi, Shota Nakamura, Naoki Ozeki, Masaki Goto, Yasushi Yatabe, Kohei Yokoi
    • Organizer
      ESMO 2018
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research
  • [Presentation] 胸腺上皮性腫瘍におけるPD-L1発現の意義 PD-L1は予後因子となりうるか?2017

    • Author(s)
      羽切周平 福井高幸 岡阪敏樹 川口晃司 福本紘一 中村彰太 尾関直樹 加藤毅人 横井香平
    • Organizer
      第34回日本呼吸器外科学会総会
    • Related Report
      2017 Research-status Report

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Published: 2017-04-28   Modified: 2021-02-19  

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