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Development of a new treatment for colorectal cancer using the glucose metabolism characteristics.

Research Project

Project/Area Number 17H03599
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Tumor therapeutics
Research InstitutionSapporo Medical University

Principal Investigator

Kato Junji  札幌医科大学, 医学部, 教授 (20244345)

Co-Investigator(Kenkyū-buntansha) 早坂 尚貴  札幌医科大学, 医学部, 研究員 (00792665)
高田 弘一  札幌医科大学, 医学部, 講師 (90398321)
大須賀 崇裕  札幌医科大学, 医学部, 助教 (40619714)
宮西 浩嗣  札幌医科大学, 医学部, 准教授 (60372819)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥17,680,000 (Direct Cost: ¥13,600,000、Indirect Cost: ¥4,080,000)
Fiscal Year 2019: ¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2018: ¥5,590,000 (Direct Cost: ¥4,300,000、Indirect Cost: ¥1,290,000)
Fiscal Year 2017: ¥8,190,000 (Direct Cost: ¥6,300,000、Indirect Cost: ¥1,890,000)
Keywords大腸癌 / ドラッグデリバリーシステム / ドラッグデリバリー / 糖代謝特性
Outline of Final Research Achievements

Metastatic / recurrent colorectal cancer is a disease with a poor prognosis, and the number of deaths continues to increase, and the development of more effective treatment methods is awaited. The FDG-PET examination, which utilizes the characteristics of increased sugar uptake in colorectal cancer, is useful for diagnosing colorectal cancer. Therefore, anticancer drugs using FDG as a carrier are promising as therapeutic agents for colorectal cancer. Therefore, we aimed to prepare an FDG-binding anticancer drug and examine its effect. A fluorescent reagent directly bound to FDG was prepared and examined, but no difference of anticancer effect from other sugar was observed. Considering that the stability of the reagent was a problem, we prepared a fluorescent reagent in which FDG was bound to liposomes, and found that it was taken up by cancer cells. In the future, we would like to promote the development of new anticancer agents that utilize this mechanism using FDG-binding liposomes.

Academic Significance and Societal Importance of the Research Achievements

大腸がん細胞特異的に送達される薬剤の開発は、より高い有効性と弱い副作用の治療を実現しうる有望な治療戦略である。FDG-PET検査に用いられるFDGはがん細胞に取り込まれるため抗がん剤にFDGを結合することでがん特異的送達性を狙った。リポソームにFDGを結合させ、蛍光試薬を内包化した薬剤を作製したところ、がん細胞への取り込みを認め、今後のFDGを利用した新規抗がん剤の開発の足掛かりとなった。

Report

(4 results)
  • 2020 Final Research Report ( PDF )
  • 2019 Annual Research Report
  • 2018 Annual Research Report
  • 2017 Annual Research Report
  • Research Products

    (6 results)

All 2019 2018 2017

All Journal Article (6 results) (of which Int'l Joint Research: 5 results,  Peer Reviewed: 6 results,  Open Access: 3 results)

  • [Journal Article] The role of iron in hepatic inflammation and hepatocellular carcinoma2019

    • Author(s)
      Miyanishi K, Tanaka S, Sakamoto H, Kato J
    • Journal Title

      Free Radic Biol Med

      Volume: 133 Pages: 200-205

    • DOI

      10.1016/j.freeradbiomed.2018.07.006

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Increased Duodenal Iron Absorption through Upregulation of Ferroportin 1 due to the Decrement in Serum Hepcidin in Patients with Chronic Hepatitis C2018

    • Author(s)
      Sato Masanori、Miyanishi Koji、Tanaka Shingo、Sakurada Akira、Sakamoto Hiroki、Kawano Yutaka、Takada Kohichi、Kobune Masayoshi、Kato Junji
    • Journal Title

      Canadian Journal of Gastroenterology and Hepatology

      Volume: 2018 Pages: 1-9

    • DOI

      10.1155/2018/2154361

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] An intronic single nucleotide polymorphism in the MUTYH gene is associated with increased risk for HCV-induced hepatocellular carcinoma2018

    • Author(s)
      Sakurada Akira、Miyanishi Koji、Tanaka Shingo、Sato Masanori、Sakamoto Hiroki、Kawano Yutaka、Takada Kohichi、Nakabeppu Yusaku、Kobune Masayoshi、Kato Junji
    • Journal Title

      Free Radical Biology and Medicine

      Volume: 129 Pages: 88-96

    • DOI

      10.1016/j.freeradbiomed.2018.09.010

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Small molecule CP-31398 induces reactive oxygen species-dependent apoptosis in human multiple myeloma2017

    • Author(s)
      Arihara Yohei、Takada Kohichi、Kamihara Yusuke、Hayasaka Naotaka、Nakamura Hajime、Murase Kazuyuki、Ikeda Hiroshi、Iyama Satoshi、Sato Tsutomu、Miyanishi Koji、Kobune Masayoshi、Kato Junji
    • Journal Title

      Oncotarget

      Volume: 8 Issue: 39 Pages: 65889-65899

    • DOI

      10.18632/oncotarget.19508

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] A phase II study of modified docetaxel, cisplatin, and S-1 (mDCS) chemotherapy for unresectable advanced gastric cancer2017

    • Author(s)
      Uemura Naoki、Kikuchi Shohei、Sato Yasushi、Ohnuma Hiroyuki、Okamoto Koichi、Miyamoto Hiroshi、Hirakawa Masahiro、Sagawa Tamotsu、Fujikawa Koshi、Takahashi Yasuo、Okuda Toshinori、Minami Shinya、Takahashi Minoru、Okamoto Tetsuro、Takada Kohichi、Miyanisi Koji、Takayama Tetsuji、Kato Junji
    • Journal Title

      Cancer Chemother Pharmacol

      Volume: 80 Issue: 4 Pages: 707-713

    • DOI

      10.1007/s00280-017-3404-8

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Hepatitis C virus reactivation due to antiemetic steroid therapy during treatment of hepatocellular carcinoma2017

    • Author(s)
      Kawano Yutaka、Miyanishi Koji、Takahashi Satoshi、Kubo Tomohiro、Ishikawa Kazuma、Sugita Shintaro、Takada Kohichi、Kobune Masayoshi、Hasegawa Tadashi、Kato Junji
    • Journal Title

      J Infect Chemother

      Volume: 23 Issue: 5 Pages: 323-325

    • DOI

      10.1016/j.jiac.2016.12.008

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Int'l Joint Research

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Published: 2017-04-28   Modified: 2022-01-27  

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