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Genome-Wide Association Study for Central Nervous System Germ Cell Tumor

Research Project

Project/Area Number 18K15230
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 50010:Tumor biology-related
Research InstitutionNational Center for Child Health and Development

Principal Investigator

Terashima Keita  国立研究開発法人国立成育医療研究センター, 小児がんセンター, 診療部長 (70649681)

Project Period (FY) 2018-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2019: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2018: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords中枢神経胚細胞腫瘍 / GWAS / WGS / SNPアレイ / 胚細胞腫瘍 / 脳腫瘍 / 中枢神経系胚細胞腫瘍
Outline of Final Research Achievements

The purpose of this study is to identify disease susceptibility genes in central nervous system germ cell tumors by genome-wide association analysis. DNA was extracted from 138 peripheral blood samples of patients and survivors who obtained consent to participate in the study at 8 medical institutions nationwide.
The DNA sample was sent to Osaka University, which is a research cooperation institute, and subjected to gene decoding using a single nucleotide polymorphism array customized for Japanese population. Currently, data analysis is being performed to identify the genotypes and genes associated with the development of this disease.
In addition, the sample was sent to the University of Connecticut, and gene analysis using a new technique called whole genome sequencing is in progress.

Academic Significance and Societal Importance of the Research Achievements

感受性遺伝子の解明によって、本腫瘍の、個人の遺伝情報に応じた発がん機構をつきとめることが可能となる。その分子機構を阻害する分子標的薬によって、従来の非特異的治療を代替・補完するオーダーメイド治療の開発が成功すれば、本腫瘍に罹患した子どもや若者の生存率の向上のみならず、生存者の晩期合併症を軽減し、良好な成長発達と充実した社会活動を得ることができる。
胚細胞腫瘍には家族内発生例があることから、患者家族の生殖細胞系列において感受性遺伝子の変異を調べることで、個人の遺伝情報に応じた発症予測が可能となり、スクリーニング検査による早期発見早期治療といった2次予防に活用することができる。

Report

(3 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • Research Products

    (8 results)

All 2020 2019 Other

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

  • [Int'l Joint Research] University of Connecticut(米国)

    • Related Report
      2019 Annual Research Report
  • [Int'l Joint Research] University of Connecticut(米国)

    • Related Report
      2018 Research-status Report
  • [Journal Article] Japan society of clinical oncology/Japanese society of medical oncology-led clinical recommendations on the diagnosis and use of tropomyosin receptor kinase inhibitors in adult and pediatric patients with neurotrophic receptor tyrosine kinase fusion-positive advanced solid tumors, cooperated by the Japanese society of pediatric hematology/oncology2020

    • Author(s)
      Naito Y、Mishima S、Akagi K、Igarashi A、Ikeda M、Okano S、Kato S、Takano T、Tsuchihara K、Terashima K、Nishihara H、Nishiyama H、Hiyama E、Hirasawa A、Hosoi H、Maeda O、Yatabe Y、Okamoto W、Ono S、Kajiyama H、Nagashima F、Hatanaka Y、Miyachi M、Kodera Y、Yoshino T、Taniguchi H
    • Journal Title

      International Journal of Clinical Oncology

      Volume: 25 Issue: 3 Pages: 403-417

    • DOI

      10.1007/s10147-019-01610-y

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors2020

    • Author(s)
      Shirai Ryota、Osumi Tomoo、Terashima Keita、et al
    • Journal Title

      European Journal of Human Genetics

      Volume: 未刊 Issue: 8 Pages: 26-26

    • DOI

      10.1038/s41431-020-0614-z

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas2019

    • Author(s)
      Guerreiro Stucklin AS, Ichimura K, Nagane M, Bouffet E, Taylor M, Tabori U, Hawkins C, et al.
    • Journal Title

      Nature Comm

      Volume: 10(1) Issue: 1 Pages: 4343-4343

    • DOI

      10.1038/s41467-019-12187-5

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] 脳腫瘍の標準治療開発2019

    • Author(s)
      寺島慶太
    • Organizer
      平成30年度がん研究シンポジウム
    • Related Report
      2019 Annual Research Report
    • Invited
  • [Presentation] CNS Germ Cell Tumors: Where do we come from? Where are we going?2019

    • Author(s)
      Terashima K
    • Organizer
      Korean Society for Pediatric Neuro-Oncology Annual Meeting
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research / Invited
  • [Book] 成人・小児進行固形がんにおける臓器横断的ゲノム診療のガイドライン2019

    • Author(s)
      一般社団法人日本癌治療学会、公益社団法人日本臨床腫瘍学会
    • Total Pages
      92
    • Publisher
      金原出版
    • ISBN
      9784307101981
    • Related Report
      2019 Annual Research Report

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Published: 2018-04-23   Modified: 2021-02-19  

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