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2013 Fiscal Year Final Research Report

Roles of Polycomb-group in links between metabolism and cancer

Research Project

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Project/Area Number 25670152
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field General medical chemistry
Research InstitutionInstitute of Physical and Chemical Research

Principal Investigator

ISONO Kyoichi  独立行政法人理化学研究所, 統合生命医科学研究センター, 上級研究員 (90323435)

Project Period (FY) 2013-04-01 – 2014-03-31
Keywordsエネルギー代謝 / ポリコーム群 / 遺伝子制御 / がん
Research Abstract

Massive proliferation of cancer cells needs energy produced mainly by activating glycolysis. On the other hand, it is thought that elevated activities of Polycomb-group (PcG) proteins are one of causes for tumorigenesis. Understanding them will be helpful for cancer therapies. We have already identified mine metabolic kinases, which might affect PcG functions. This evidence has made us speculate interdependence between energy metabolism and PcG functions in cancer cells. In this study, we addressed this hypothesis by using gene knockdown experiments and co-immunoprecipitation assay, revealing that three of them could have something to do with PcG proteins or their functions. These results are supporting our hypothesis. We therefore believe that this project is worth being investigated continuously, contributing to applied medical science.

  • Research Products

    (8 results)

All 2014 2013 Other

All Journal Article (5 results) (of which Peer Reviewed: 4 results) Presentation (2 results) Remarks (1 results)

  • [Journal Article] Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia2014

    • Author(s)
      Matsunawa M, Yamamoto R, Sanada M, Sato-Otsubo A, Shiozawa Y, Otsu M, Isono K, Hoseki H., Nakauchi H, Ogawa S
    • Journal Title

      Leukemia

    • DOI

      10.1038/leu.2014.73

    • Peer Reviewed
  • [Journal Article] HRING1 activates Meis2 by mediating interaction of its promoter with a tissue-specific enhacer2014

    • Author(s)
      Kondo T, Isono K, Kondo K, Endo TA, Itohara S, Vidal M, Koseki
    • Journal Title

      Dev Cell

      Volume: 28 Pages: 94-101

    • Peer Reviewed
  • [Journal Article] SAM domain polymerization links subnuclear clustering of PRC1 to gene silencing2013

    • Author(s)
      Isono K, Endo AT, Ku M, Yamada D, Suzuki R, Sharif J, Ishikura T, Toyoda T, Bernstein BE, Koseki H
    • Journal Title

      Dev Cell

      Volume: 26 Pages: 565-577

    • Peer Reviewed
  • [Journal Article] WIP1, a Homeostatic Regulator of the DNA Damage Response, Is Targeted by HIPK2 for Phosphorylation and Degradation2013

    • Author(s)
      Choi DW, Na W, Kabir MH, Yi E, Kwon S, Yeom J, Ahn JW, Choi HH, Lee Y, Seo KW, Shin MK, Park SH, Yoo HY, Isono K, Koseki H, Kim ST, Lee C, Kwon YK, Choi CY
    • Journal Title

      Mol Cell

      Volume: 51 Pages: 374-385

    • Peer Reviewed
  • [Journal Article] ポリコーム群による遺伝子抑制とエピジェネティック治療への貢献2013

    • Author(s)
      磯野協一
    • Journal Title

      遺伝子医学MOOKエピジェネティクスと病気

      Volume: 25 Pages: 37-42

  • [Presentation] ポリコーム群Phc2リン酸化による遺伝子サイレンシング2013

    • Author(s)
      磯野協一
    • Organizer
      日本分子生物学会
    • Place of Presentation
      神戸ポートピアホテル
    • Year and Date
      2013-12-05
  • [Presentation] 遺伝子サイレンシングにおけるポリコーム群Phc2リン酸化の役割2013

    • Author(s)
      磯野協一
    • Organizer
      エピジェネティクス研究会
    • Place of Presentation
      奈良県新公会堂
    • Year and Date
      2013-05-30
  • [Remarks] プレスリリース 「細胞の運命を左右する新しい分子メカニズムの一端を解明」(2013年10月)

    • URL

      http://www.riken.jp/pr/press/2013/20131001_1/digest/

URL: 

Published: 2015-06-25  

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