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Investigation of tumor heterogeneity based on analyses of transcriptomic entropy

Research Project

Project/Area Number 25430139
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Tumor diagnostics
Research InstitutionKeio University

Principal Investigator

WAKUI MASATOSHI  慶應義塾大学, 医学部, 講師 (90240465)

Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywordsがんの個性診断 / 腫瘍不均一性 / 遺伝子発現 / エントロピー / 情報理論 / 代謝経路 / トランスクリプトーム / シャノンのエントロピー / 相互情報量 / ヒトがん細胞株 / 癌
Outline of Final Research Achievements

We successfully applied information theory represented by Shannon’s entropy and mutual information to quantification of the tumor heterogeneity reflected in the transcriptome in each of biological pathways. In fact, metabolic pathways exhibiting high or low heterogeneity were detected among a number of human cancer cell lines as well as between different oxygen environments of cell culture. These results provide insights into tumor heterogeneity from the perspective of metabolic biology, suggesting the potential of diagnostic and therapeutic application.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (4 results)

All 2016 2015 2014 2013

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

  • [Journal Article] nnate Response to Human Cancer Cells with or without IL-2 Receptor Common γ-Chain Function in NOD Background Mice Lacking Adaptive Immunity.2015

    • Author(s)
      Nishime C, Kawai K, Yamamoto T, Katano I, Monnai M, Goda N, Mizushima T, Suemizu H, Nakamura M, Murata M, Suematsu M, Wakui M.
    • Journal Title

      J Immunol

      Volume: 195 Issue: 4 Pages: 1883-1890

    • DOI

      10.4049/jimmunol.1402103

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Bevacizumab terminates homeobox B9-induced tumor proliferation by silencing microenvironmental communication2014

    • Author(s)
      Yoshinori Hoshino, Tetsu Hayashida, Akira Hirata, Hidena Takahashi, Naokazu Chiba, Mitsuyo Ohmura, Masatoshi Wakui, Hiromitsu Jinno, Hirotoshi Hasegawa, Shyamala Maheswaran, Makoto Suematsu, Yuko Kitagawa,
    • Journal Title

      Molecular Cancer

      Volume: 13 Issue: 1 Pages: 102-102

    • DOI

      10.1186/1476-4598-13-102

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Lewis Lung Carcinoma Progression Is Facilitated by TIG-3 Fibroblast Cells.2013

    • Author(s)
      Yamauchi Y, Izumi Y, Asakura K, Kawai K, Wakui M, Ohmura M, Suematsu M, Nomori H
    • Journal Title

      Anticancer Res.

      Volume: 33 Pages: 3791-3798

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] Innate Effector Mechanisms for Elimination of Human Cancer Cells in the NOD-Background Mice Lacking Adaptive Immunity.2016

    • Author(s)
      Nishime C, Wakui M, Kawai K, Yamamoto T, Katano I, Monnai M, Goda N, Mizushima T, Suemizu H, Nakamura M, Murata M, Suematsu M
    • Organizer
      5th International Workshop on Humanized Mice (IWHM5)
    • Place of Presentation
      チューリッヒ(スイス)
    • Year and Date
      2016-01-28
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research

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Published: 2014-07-25   Modified: 2019-07-29  

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