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Possible molecular mechanisms of normal cells and invasive breast cancer cells after radiation treatment

Research Project

Project/Area Number 25861050
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Radiation science
Research InstitutionHokkaido University

Principal Investigator

NAM JINMIN  北海道大学, 国際連携研究教育局, 助教 (60414132)

Research Collaborator ONODERA YASUHITO  北海道大学, 大学院医学研究科, 講師 (90435561)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2015: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2014: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords放射線 / 乳癌 / 3次元培養 / 3次元培養
Outline of Final Research Achievements

In this study, we investigated molecular mechanisms to improve the radiation therapy by targeting specific molecules which are involved in not only preservation of the functions in normal cell structure but also suppressing tumor growth, recurrence and metastasis. To find candidate genes, we performed microarray analysis in a mammary epithelial cell line which has basal polarity, or invasive breast cancer cell lines in three-dimensional laminin rich extracellular matrix (3D lrECM). We found that β1-integrin and its downstream molecules are involved in the disruption of basal polarity structure and invasive transition on non-malignant mammary epithelial cells in 3D lrECM. In addition, we also found that up-regulated integrin expression on the cell surface may have important roles in the invasive activity after radiation treatment in breast cancer cells.

Report

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

    (9 results)

All 2016 2015 2014 2013 Other

All Int'l Joint Research (1 results) Journal Article (3 results) (of which Peer Reviewed: 3 results) Presentation (5 results) (of which Int'l Joint Research: 1 results,  Invited: 1 results)

  • [Int'l Joint Research] UCSF(米国)

    • Related Report
      2015 Annual Research Report
  • [Journal Article] Increased sugar uptake promotes oncogenesis via EPAC/RAP1 and O-GlcNAc pathways.2014

    • Author(s)
      Onodera Y, Nam JM, Bissell MJ
    • Journal Title

      The Journal of Clinical Investigation

      Volume: 124 Issue: 1 Pages: 367-384

    • DOI

      10.1172/jci63146

    • NAID

      120005372327

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] β1-integrin via NF-κB signaling is essential for acquisition of invasiveness in a model of radiation treated in situ breast cancer.2013

    • Author(s)
      Nam JM, Ahmed KM, Costes S, Zhang H, Onodera Y, Olshen AB, Hatanaka KC, Kinoshita R, Ishikawa M, Sabe H, Shirato H, Park CC
    • Journal Title

      Breast Cancer Res

      Volume: 15

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Co-overexpression of GEP100 and AMAP1 proteins correlates with rapid local recurrence after breast conservative therapy.2013

    • Author(s)
      Kinoshita R, Nam JM, Ito YM, Hatanaka KC, Hashimoto A, Handa H, Otsuka Y, Hashimoto S, Onodera Y, Hosoda M, Onodera S, Shimizu S, Tanaka S, Shirato H, Tanino M, Sabe H.
    • Journal Title

      PLoS One.

      Volume: 8 Issue: 10 Pages: e76791-e76791

    • DOI

      10.1371/journal.pone.0076791

    • NAID

      120005348196

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] Targeting integrin signaling to improve the efficacy of radiation treatment on breast cancer cells2016

    • Author(s)
      Jin-Min Nam
    • Organizer
      The 3rd GI-CoRE Medical Science and Engineering Symposium
    • Place of Presentation
      北海道大学(北海道)
    • Year and Date
      2016-03-03
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] 放射線照射後の乳腺上皮細胞の3次元構造維持に関わる分子機序の解析2015

    • Author(s)
      南ジンミン、小野寺康仁、佐邊壽孝、白土博樹
    • Organizer
      第74回日本癌学会学術総会
    • Place of Presentation
      名古屋国際会議場(名古屋)
    • Year and Date
      2015-10-08
    • Related Report
      2015 Annual Research Report
  • [Presentation] 乳癌における放射線照射後の浸潤能獲得過程に関わる分子機序の解析2014

    • Author(s)
      南ジンミン、小野寺康仁、佐邊壽孝、白土博樹
    • Organizer
      第73回日本癌学会学術総会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2014-09-25 – 2014-09-27
    • Related Report
      2014 Research-status Report
  • [Presentation] 放射線照射後の乳癌再発に関わるシグナルの解析2013

    • Author(s)
      南ジンミン、小野寺康仁、石川正純、佐邊壽孝、白土博樹
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Related Report
      2013 Research-status Report
  • [Presentation] Possible mechanisms of non-invasive to invasive phenotypic conversion of breast cancer cells upon radiation2013

    • Author(s)
      Nam JM, Onodera Y, Sabe H, Shirato H
    • Organizer
      The 11th International Symposium for Future Drug Discovery and Medical Care
    • Place of Presentation
      北海道大学(北海道)
    • Related Report
      2013 Research-status Report

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

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