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Identification of peptides which can be applied to cancer vaccine therapy for patients with prostate cancer

Research Project

Project/Area Number 15K10612
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Urology
Research InstitutionKindai University

Principal Investigator

MINAMI Takafumi  近畿大学, 医学部, 講師 (70340809)

Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywordsペプチドワクチン / 前立腺癌
Outline of Final Research Achievements

3~5 prostate cancer-associated antigens (PTH-rP,EGFR,EZH2) -derived peptides that were prepared based on the binding motif to the HLA-A3 supertype alleles (HLA-A11, -A31, and -A33) were functionally screened for their potential to induce peptide-specific cytotoxic T lymphocytes (CTLs) from peripheral blood mononuclear cells (PBMCs) of 12 HLA-A3 supertype allele+ prostate cancer patients. As a result, EZH2733-741 peptide was found to efficiently induce peptide-specific CTLs. To test cytotoxicity of CTLs by a standard 6-h 51Cr-release assay, CD8+ T cells were purified from EZH2733-741 peptide-stimulated PBMCs. The EZH2733-741 peptide-stimulated and purified CD8+ T cells from PBMCs of HLA-A3 supertype allele+ prostate cancer patients showed higher cytotoxicity against HLA-A3 supertype allele-expressing LNCaP prostate cancer cells than against parental LNCaP cells.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (1 results)

All 2015

All Journal Article (1 results) (of which Peer Reviewed: 1 results)

  • [Journal Article] New polycomb group protein enhancer of zeste homolog (EZH) 2-derived peptide with the potential to induce cancer-reactive cytotoxic T lymphocytes in prostate cancer patients with HLA-A3 supertype alleles.2015

    • Author(s)
      Minami T, Minami T, Shimizu N, Yamamoto Y, De Velasco MA, Nozawa M, Yoshimura K, Harashima N, Harada M, Uemura H.
    • Journal Title

      Int Immunopharmacol.

      Volume: 26(1) Pages: 133-138

    • Related Report
      2015 Research-status Report
    • Peer Reviewed

URL: 

Published: 2015-04-16   Modified: 2020-01-20  

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