• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Elucidation of the resistance mechanism to the molecular targeting drug in renal cancer using the genome editing technology

Research Project

Project/Area Number 17K16799
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Urology
Research InstitutionKagoshima University

Principal Investigator

YONEMORI Masaya  鹿児島大学, 附属病院, 医員 (00758013)

Research Collaborator Nakagawa Masayuki  
Enokida Hideki  
Yoshino Hirofumi  
Gutkind JS  
Nohata Nijiro  
Sugita Satoshi  
Sakaguchi Satoshi  
Project Period (FY) 2017-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2018: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2017: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords腎癌 / CRISPR/Cas9 / PHGDH / 低酸素誘導因子 / PHGDG / 腎細胞癌 / HIF / microRNA
Outline of Final Research Achievements

We established a sunitinib-resistant RCC cell line, followed by the establishment of HIF2α knockout cell line (HIF2α-KO-SU-R-786-o) by CRISPR/Cas9. By using omics analyses using the cell, we found that serine biosynthesis was significantly activated in HIF2α-KO-SU-R-786-o, and that PHGDH, a key enzyme for serine synthesis, was accelerated in HIF2α-KO-SU-R-786-o. PHGDH inhibitor reduced cell growth in vivo and in vitro by inducing apoptosis in HIF2α-KO-SU-R-786-o more than in parent cells. Public database showed that patients with PHGDH gene amplification had poor overall survival (P = 0.0003) compared to patients without amplification. In conclusion, PHGDH can be a therapeutic target for patients showing activated serine biosynthesis after HIF2α deficiency. Furthermore, PHGDH inhibitor should be considered as a first treatment in patients with PHGDH amplification.

Academic Significance and Societal Importance of the Research Achievements

転移性腎癌の多くは分子標的治療薬に治療抵抗性を獲得し、再発・転移に至るが、低酸素誘導因子(HIF) の恒常的な活性化は腎癌の進展のみでなく、腎癌治療に一時治療として使用されているmTOR阻害剤や血管新生阻害剤の耐性獲得にも重要な役割を果たすとされている。本研究では、CRISPR/Cas9によるゲノム編集技術を用いて当科で作成したスニチニブ(マルチキナーゼ阻害剤)耐性HIFノックアウト腎癌細胞株を使用して、腎癌の増殖・浸潤・転移および薬剤耐性に関わる癌シグナル経路を解明することが出来た。本研究の成果により、転移性腎癌に対する新たな治療戦略の可能性が提案された。

Report

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

    (10 results)

All 2019 2018 2017

All Journal Article (7 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 6 results,  Open Access: 4 results,  Acknowledgement Compliant: 1 results) Presentation (3 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] Tumor suppressive microRNA223 targets WDR62 directly in bladder cancer.2019

    • Author(s)
      Sugita S, Yoshino H, Yonemori M, Miyamoto K, Matsushita R, Sakaguchi T, Itesako T, Tatarano S, Nakagawa M, Enokida H.
    • Journal Title

      Int J Oncol.

      Volume: 54 Pages: 2222-2236

    • DOI

      10.3892/ijo.2019.4762

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Potential tumor-suppressive role of microRNA-99-3p in sunitinib-resistant renal cell carcinoma cells through the regulation of RRM22019

    • Author(s)
      Osako Y, Yoshino H, Sakaguchi T, Sugita S, Yonemori M, Nakagawa M, Enokida H.
    • Journal Title

      International Journal of Oncology

      Volume: 54 Pages: 1759-1770

    • DOI

      10.3892/ijo.2019.4736

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] HRAS as a potential therapeutic target of salirasib RAS inhibitor in bladder cancer.2019

    • Author(s)
      Sugita S, Enokida H, Yoshino H, Miyamoto K, Yonemori M, Sakaguchi T, Osako Y, Nakagawa M.
    • Journal Title

      Int J Oncol.

      Volume: 53 Pages: 725-736

    • DOI

      10.3892/ijo.2018.4435

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Bromodomain protein BRD4 inhibitor JQ1 regulates potential prognostic molecules in advanced renal cell carcinoma.2018

    • Author(s)
      Sakaguchi T, Yoshino H, Sugita S, Miyamoto K, Yonemori M, Osako Y, Meguro-Horike M, Horike SI, Nakagawa M, Enokida H.
    • Journal Title

      Oncotarget

      Volume: 9 Issue: 33 Pages: 23003-23017

    • DOI

      10.18632/oncotarget.25190

    • Related Report
      2018 Annual Research Report
    • Open Access
  • [Journal Article] Downregulation of microRNA-1274a induces cell apoptosis through regulation of2018

    • Author(s)
      Yoshino H, Yonezawa T, Yonemori M, Miyamoto K, Sakaguchi T, Sugita S, Osako Y, Tatarano S, Nakagawa M, Enokida H.
    • Journal Title

      Oncol Rep

      Volume: 39 Pages: 173-181

    • DOI

      10.3892/or.2017.6098

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Journal Article] microRNA-210-3p depletion by CRISPR/Cas9 promoted tumorigenesis through revival of TWIST1 in renal cell carcinoma.2017

    • Author(s)
      Yoshino H, Yonemori M, Miyamoto K, Tatarano S, Kofuji S, Nohata N, Nakagawa M, Enokida H.
    • Journal Title

      Oncotarget

      Volume: 8 Issue: 13 Pages: 20881-20894

    • DOI

      10.18632/oncotarget.14930

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] PHGDH as a Key Enzyme for Serine Biosynthesis in HIF2α-Targeting Therapy for Renal Cell Carcinoma.2017

    • Author(s)
      Yoshino H, Nohata N, Miyamoto K, Yonemori M, Sakaguchi T, Sugita S, Itesako T, Kofuji S, Nakagawa M, Dahiya R, Enokida H.
    • Journal Title

      Cancer Res

      Volume: 77 Pages: 6321-6329

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Presentation] ゲノム編集技術(CRISPR/Cas9)を使用した腎癌における分子標的治療薬への耐性化機序の解明と革新的治療法の開発2018

    • Author(s)
      米森雅也,吉野裕史,宮元一隆,坂口 大,杉田 智,榎田英樹,中川昌之.
    • Organizer
      第106回日本泌尿器科学会総会
    • Related Report
      2018 Annual Research Report
  • [Presentation] 代謝リプログラミングを標的とした腎癌治療薬抵抗性獲得機序の解明と克服2018

    • Author(s)
      吉野裕史、宮元一隆、米森雅也、杉田 智、坂口 大、榎田英樹、中川昌之
    • Organizer
      日本泌尿器科学会総会
    • Related Report
      2017 Research-status Report
  • [Presentation] Elucidation of the resistance mechanism to the molecular target drugs in renal cell carcinoma using the genome editing technology2017

    • Author(s)
      Hideki Enokida, Hirofumi Yoshino, Kazutaka Miyamoto, Masaya Yonemori, Masayuki Nakagawa
    • Organizer
      米国泌尿器科学会
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research

URL: 

Published: 2017-04-28   Modified: 2020-03-30  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi