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Analysis of the innate immune response to nucleic acids in tumor cells.

Research Project

Project/Area Number 23650586
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Carcinogenesis
Research InstitutionHokkaido University

Principal Investigator

HAYAKAWA Sumio  北海道大学, 遺伝子病制御研究所, 助教 (00368292)

Co-Investigator(Kenkyū-buntansha) KAMEYAMA Takeshi  北海道大学, 遺伝子病制御研究所, 研究員 (40569505)
ADACHI Yoshihiro Christopher  北海道大学, 遺伝子病制御研究所, 研究員 (10616204)
Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords自然免疫 / 腫瘍 / 抗腫瘍 / インターフェロン
Research Abstract

Pattern recognition receptors (PRRs)-mediated activation of the innate immune response is triggered by recognition of pathogen-associated molecular patterns (PAMPs), such as a various bacterial cell wall components, peptidoglycan and lipoprotein, as well as bacterial and viral nucleic acids. In this study, we demonstrate that nucleic acids are recognized by PRRs in some tumor types, and promoted the activation of IRF and NF-kB pathway. However, some types of tumor cells are not activated. Furthermore, we are able to find the relationship between the tissue specificity of innate immune response and apoptosis induction. In in vivo experiment, nucleic acids inhibit growth of transplantation tumor in nude mice. Thus, these finding indicate that nucleic acids may contribute to the progress of material for therapeutic cancer. We consider clarifying the detail mechanism of nucleic acids recognition on innate immune response from the molecular, biochemical and cell biology viewpoints.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (1 results)

All 2011

All Presentation (1 results)

  • [Presentation] ZAPS is a potent stimulator of RIG-I-mediated signaling for antiviral response.2011

    • Author(s)
      Hayakawa S., Shiratori S., Yamato H., Kameyama T., Ohba Y., Miyazaki T., Imamura M & Takaoka A.
    • Organizer
      The 79th Meeting of the Japanese Society for Interferon and Cytokine Research / The 19th International Symposium of Macrophage Molecular and Cellular Biology
    • Place of Presentation
      ANA Gate Tower Hotel Osaka, Japan
    • Related Report
      2011 Research-status Report

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Published: 2011-08-05   Modified: 2019-07-29  

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