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Progression of prostate cancer bone metastasis by exosomal micro RNA regulated-chemokine

Research Project

Project/Area Number 17K11126
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Urology
Research InstitutionSt. Luke's International University

Principal Investigator

NARIMOTO Kazutaka  聖路加国際大学, 聖路加国際病院, 医幹 (50645207)

Co-Investigator(Kenkyū-buntansha) 溝上 敦  金沢大学, 医学系, 教授 (50248580)
泉 浩二  金沢大学, 附属病院, 講師 (80646787)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2019: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2018: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2017: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywords前立腺癌 / 腫瘍免疫 / 去勢抵抗性前立腺癌 / ケモカイン
Outline of Final Research Achievements

The cell-cell interaction between bone stromal cells and prostate cancer cells produced CCL5 which in turn increased migration abiliy of prostate cancer cells. Immunohistochemistry revealed CCR5, a receptor of CCL5, expressed in prostate cancer tissue stronger than normal prostate tissue. Coffee ingredients, cafestol and kahweol, synergistically inhibited both proliferation and migration ability of prostate cancer cells in a dose dependent manner. Cafestol and kahweol inhibited the expression of androgen receptor and its nuclear translocation, and also inhibited CCR5 expression in prostate cancer cells. In prostate cancer bone metastasis, CCL5-CCR5 signaling may increase the metastatic ability of prostate cencer cells and cafestol and kahweol have a potential ability to inhibit prostate cancer metastasis via inhibition of CCL5-CCR5 signaling.

Academic Significance and Societal Importance of the Research Achievements

骨転移が多い前立腺癌における骨から骨への転移促進機構は未だ未解明であったが、本研究により、骨転移巣でのCCL5-CCR5経路の活性化が、前立腺癌細胞の転移能を亢進させ、さらなる骨転移を誘発する可能性が示唆された。さらに、コーヒーの成分の中で、カーウェオールとカフェストールはCCL5-CCR5経路の抑制を介し、前立腺癌の転移を抑制できる可能性が示唆された。CCL5-CCR5経路が新規治療ターゲットとして明らかにされただけではなく、カーウェオールとカフェストールが前立腺癌治療薬となる潜在性も明らかになった。

Report

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

    (2 results)

All 2019 2018

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

  • [Journal Article] Coffee diterpenes kahweol acetate and cafestol synergistically inhibit the proliferation and migration of prostate cancer cells.2019

    • Author(s)
      Iwamoto H, Izumi K*, Natsagdorj A, Naito R, Makino T, Kadomoto S, Hiratsuka K, Shigehara K, Kadono Y, Narimoto K, Saito Y, Nakagawa-Goto K, Mizokami A.
    • Journal Title

      Prostate

      Volume: 79 Issue: 5 Pages: 468-479

    • DOI

      10.1002/pros.23753

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] C-C motif ligand 5 promotes migration of prostate cancer cells in the prostate cancer bone metastasis microenvironment.2018

    • Author(s)
      Urata S, Izumi K, Hiratsuka K, Maolake A, Natsagdorj A, Shigehara K, Iwamoto H, Kadomoto S, Makino T, Naito R, Kadono Y, Lin WJ, Wufuer G, Narimoto K, Mizokami A
    • Journal Title

      Cancer Science

      Volume: 109 Issue: 3 Pages: 724-731

    • DOI

      10.1111/cas.13494

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research

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

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