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The role of exosome derived melanoma cells in tumor immunity

Research Project

Project/Area Number 26660294
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Applied molecular and cellular biology
Research InstitutionYamaguchi University

Principal Investigator

Noguchi Shunsuke  山口大学, 共同獣医学部, 准教授 (10701295)

Co-Investigator(Renkei-kenkyūsha) AKAO Yukihiro  岐阜大学, 大学院連合創薬医療情報研究科, 教授 (00222505)
Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywordsエクソソーム / Exosome / microRNA-205 / CD9 / メラノーマ / exosome / TGF-β
Outline of Final Research Achievements

This study revealed that TGF-β, which promotes the differentiation of T cells to regulatory T cells, was included in the exosomes derived from melanoma cells. This finding indicates that melanoma cells inhibit anti-tumor immunity via exosome secretion.
Visualization of exosomes is important to elucidate the role of exosomes in cell to cell comunication. Therefore, we constructed the expression vector of CD/GFP fusion protein using pEGFP-N1 vector. This vector makes us trace exosomes in vitro and in vivo.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report

URL: 

Published: 2014-04-04   Modified: 2017-05-10  

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