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Identification of novel causative genes in mesothelioma and the elucidation of the carcinogenic mechanism

Research Project

Project/Area Number 23590464
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Experimental pathology
Research InstitutionShimane University

Principal Investigator

KAKAZU Naoki  島根大学, 医学部, 准教授 (20264757)

Project Period (FY) 2011-04-28 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Keywords中皮腫 / 融合転写産物 / 悪性中皮腫 / 融合遺伝子
Outline of Final Research Achievements

Mesothelioma is a poor prognosis tumor due to former exposure to asbestos. We analyzed mesothelioma cells by next generation sequencing to identify novel candidate fusion genes associated with the development of mesothelioma. Firstly, we performed whole transcriptome shotgun sequencing (RNA-Seq) of a mesothelioma cell line and comprehensively detected many fusion transcripts. Secondly, we performed RT-PCR in the cell line and the other five to confirm the presence of these detected fusion transcripts, and narrowed down the candidate fusion genes. These results suggest that two fusion genes (DUS4L-BCAP29, PDPN-PRDM2) are the potential candidates implicated in the pathogenesis of mesothelioma in this study.

Report

(5 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (3 results)

All 2015 2014 2013

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

  • [Journal Article] Identification of the 12q15 Amplicon within the Homogeneously Staining Regions in the Embryonal Rhabdomyosarcoma Cell Line RMS-YM2014

    • Author(s)
      Kakazu N, Yamane H, Miyachi M, Shiwaku K, Hosoi H
    • Journal Title

      Cytogenet Genome Res

      Volume: 142 Issue: 3 Pages: 167-173

    • DOI

      10.1159/000357930

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells2013

    • Author(s)
      Yoshida H, Miyachi M, Hosoi H, et al
    • Journal Title

      Oncogene

      Volume: 11(印刷中) Issue: 49 Pages: 5601-8

    • DOI

      10.1038/onc.2013.491

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] 次世代シークエンサーによる悪性中皮腫における融合転写産物の網羅的同定2015

    • Author(s)
      嘉数直樹、山根史嗣
    • Organizer
      日本衛生学会学術総会
    • Place of Presentation
      ホテルアバローム紀の国(和歌山市)
    • Year and Date
      2015-03-26 – 2015-03-28
    • Related Report
      2014 Annual Research Report

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Published: 2011-08-05   Modified: 2019-07-29  

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