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Effect of bile acid with elevated levels in human serum on cancer cell proliferation and sensitivity to anticancer drugs.

Research Project

Project/Area Number 17K08424
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Medical pharmacy
Research InstitutionKeio University

Principal Investigator

SUZUKI Sayo  慶應義塾大学, 薬学部(芝共立), 教授 (90424134)

Co-Investigator(Kenkyū-buntansha) 中村 智徳  慶應義塾大学, 薬学部(芝共立), 教授 (30251151)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2019: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2018: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywordsがん / 胆汁酸 / 抗がん剤感受性 / 細胞増殖 / 薬剤反応性 / 治療個別化 / 癌
Outline of Final Research Achievements

Recently, many standard-of-care chemotherapy regimens have been established and new approaches to improve the prevention and early detection of cancer have also been developed. However, unfortunately, they leave much to be desired.
In this study, we focused on the cancer treatments of patients with conditions like cholestasis. As a first step of this study, we mainly used several human cancer cells and deoxycholate (DCA) or chenodeoxycholate (CDCA) which are components in bile acids. We showed that DCA and / or CDCA with concentrations corresponding to elevated serum levels in such as cholestasis or biliary obstruction by tumors enhanced cell proliferation and / or decreased sensitivity to anticancer drugs depending on the kinds of cancer cells and conditions of bile acids exposure.

Academic Significance and Societal Importance of the Research Achievements

本研究により、臨床で生じ得る血中胆汁酸濃度の上昇・変動ががん細胞の増殖や抗がん剤の抗腫瘍効果に及ぼす影響やそのメカニズムを明らかにすることができれば、例えば肝障害があり血液中に胆汁酸が滞っている胆汁うっ滞などが生じている場合等で抗がん剤治療を行う必要がある場合に、あらかじめ手術で摘出した腫瘍組織中の関連タンパク質や関連遺伝子を分析することにより個々の患者に合わせた適切な薬物治療の選択が可能となる(治療の個別化)。さらにそれが可能となれば、治療開始段階から効果の期待できる抗がん剤を選択できるため医療経済の観点からも有意義であり、社会的貢献も大きいと考える。

Report

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

    (3 results)

All 2019 2018 Other

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

  • [Journal Article] Renal dysfunction and anemia associated with long-term imatinib treatment in patients with chronic myelogenous leukemia.2019

    • Author(s)
      Sakurai Masatoshi, Karigane Daiki, Kasahara Hidenori, Matsuki Eri, Hashida Risa, Yamane Yusuke, Abe Ryohei, Koda Yuya, Toyama Takaaki, Kikuchi Taku, Kato Jun, Shimizu Takayuki, Yokoyama Yuta, Suzuki Sayo, Nakamura Tomonori, Okamoto Shinichiro, and Mori Takehiko.
    • Journal Title

      Int J Hematol.

      Volume: 109 Issue: 3 Pages: 292-298

    • DOI

      10.1007/s12185-019-02596-z

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Book] Principal Pharmacotherapy 改訂版2018

    • Author(s)
      水谷顕洋,中村智徳,林哲也,武藤章弘,齋藤義正,齋藤英胤,細山田真,末岡浩,小佐野博史,小川郁,佐藤卓美,柴田洋孝,加藤宏一,落合高徳,田邊稔,櫻井正寿,岡本真一郎,鈴木小夜,大井一弥,宮地勇人など
    • Total Pages
      1199
    • Publisher
      ネオメディカル
    • ISBN
      9784904634240
    • Related Report
      2017 Research-status Report
  • [Remarks] 慶應義塾研究者情報データベース

    • URL

      https://k-ris.keio.ac.jp/html/100012960_ja.html

    • Related Report
      2019 Annual Research Report

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

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