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Epigenetic aberrations associated with evolution of hepatoblastoma

Research Project

Project/Area Number 16K15740
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Pediatric surgery
Research InstitutionHokkaido University

Principal Investigator

Sunahara Masao  北海道大学, 医学研究院, 客員研究員 (80750314)

Co-Investigator(Kenkyū-buntansha) 本多 昌平  北海道大学, 大学病院, 助教 (90588089)
宮城 久之  旭川医科大学, 医学部, 助教 (50596442)
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2018: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords肝芽腫 / DNAメチル化 / miRNA / メチル化 / 小児 / エピゲノム / 小児がん / エピジェネティクス / 小児悪性腫瘍
Outline of Final Research Achievements

Epigenetic dysregulation is one of the potential mechanisms associated with pathogenesis of hepatoblastoma(HB). In this study, we aimed to identify mRNA and miRNA profiles in lung metastatic tumors, primary tumors (fetal and embryonal subtypes) and nontumorous surrounding livers, which were obtained from formalin-fixed, paraffin-embedded specimens to establish molecular markers for the diagnostic and prognostic use in clinical setting. By examining miRNA and small nucleolar RNAs expressions through GeneChip® miRNA4.0 Array assay, we found that HB shows distinct miRNA profiles related to tumor types, which could lead to new approaches to treatment and prognosis in progressive HB patients. Learning more about the effects of those epigenetic dysregulations could overcome barriers to innovating better therapeutic strategies to improve clinical outcomes of progressive HB

Academic Significance and Societal Importance of the Research Achievements

肝芽腫の進展におけるepigenetic異常を、DNAメチル化異常およびmiRNA異常を照らし合わせることによって解明した。本研究によって得られる新規分子マーカーが臨床応用されることによって、手術治療では改善できない予後不良な進行肝芽腫症例の治療成績向上につながることが期待され、肝芽腫患児への恩恵は多大なものと考える。今後得られた成果を実臨床に活かせらる様に更なる症例での検討を続けていく所存です。

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (6 results)

All 2018 2017

All Presentation (6 results)

  • [Presentation] Molecular study in JPLT studies2018

    • Author(s)
      Honda S, Hiyama E, Fujiyoshi S, Minato M, Hishiki T, Watanabe K, Ida K, Hoshino K, Iehara T, Aoki Y, Kazama T, Kihira K, Takama Y, Taguchi T, Fujimura J, Matsumoto K, Mori M, Yano M, Yokoi A, Tanaka Y, Fuji H, Miyazaki O, Yoshimura K, Takimoto T, Taketomi A
    • Organizer
      国際小児肝癌会議2018(SIOPEL Meeting 2018)
    • Related Report
      2018 Annual Research Report
  • [Presentation] Identification of aberrant hypermethylation of Cisplatin-resistant associated genes in hepatoblastoma.2017

    • Author(s)
      藤好 直、本多昌平、湊雅嗣、鈴木拓、檜山英三、武冨紹信
    • Organizer
      第76回日本癌学会定期学術集会
    • Related Report
      2017 Research-status Report
  • [Presentation] Investigation of aberrant hypermethylation of DNA in association with cisplatin-resistance in hepatoblastoma.2017

    • Author(s)
      Fujiyoshi S, Honda S, Minato M, Suzuki H, Hiyama E, Taketomi A.
    • Organizer
      第28回消化器癌発生学会
    • Related Report
      2017 Research-status Report
  • [Presentation] 希少がんにおける個別化医療を目指した分子マーカーの確立:肝芽腫エピゲノム異常解析2017

    • Author(s)
      本多昌平、湊 雅嗣、宮城久之、藤好 直、檜山英三、新開真人、北河徳彦、新開真人、田中水緒、田中祐吉、武冨紹信
    • Organizer
      第117回日本外科学会定期学術集会
    • Related Report
      2017 Research-status Report
  • [Presentation] 網羅的DNAメチル化解析を用いた肝芽腫遠隔転移予測マーカーの探求2017

    • Author(s)
      湊 雅嗣、本多昌平、宮城久之、檜山英三、新開真人、北河徳彦、新開真人、田中水緒、田中祐吉、武冨紹信
    • Organizer
      第117回日本外科学会定期学術集会
    • Related Report
      2017 Research-status Report
  • [Presentation] 肝芽腫の分岐進化に関わるmicroRNA発現異常2017

    • Author(s)
      本多昌平、湊 雅嗣、宮城久之、藤好 直、檜山英三、新開真人、北河徳彦、新開真人、田中水緒、田中祐吉、武冨紹信
    • Organizer
      第54回日本小児外科学会学術集会
    • Related Report
      2017 Research-status Report

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Published: 2016-04-21   Modified: 2020-03-30  

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