• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

The 11q13.3 amplicon and mechanisms of bone invasion in in oral cancer

Research Project

Project/Area Number 23792321
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Surgical dentistry
Research InstitutionTokyo Medical and Dental University

Principal Investigator

MORITA Keiichi  東京医科歯科大学, 硬組織疾患ゲノムセンター, 特任講師 (10396971)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Keywords口腔がん / 骨破壊 / ゲノム増幅 / ストレス応答 / 11番染色体
Research Abstract

With the functional analysis of 11q13.3 domain gene centered around FADD, by clarifying the cancer outbreak mechanism using genetically modified mutational molecular forced expression system in the cultured cell derived from oral cancer and also by a comprehensive analysis of the genome structure abnormality the aim was to examine also the gene which was predicted to be of new importance in not only the FADD but in the11q13.3 domain gene.【The influence on the life and death of the forced expression system in the 11q13.3 domain gene】We cloned the full length cDNA of FADD which is one of the 11q13.3 domain gene and sub cloned it to the expression vector. However the protein expression in these vectors was very weak that it could not be confirmed by western blotting so we introduced an adenovirusand carried out sub cloning again. At present the sub cloning to the virus vector has ceased and we are up to confirming the expression.【Gene analysis of 11q13.3 domain using the microarray data】We are confirming the amplification of the 11q13.3 domain by extracting DNA from a formalin fixation paraffin embedded block of the oral cancer excision specimen and carried out a CGH microarray analysis. By increasing the case of CGH microarray analysis the detailed amplification range within the 11q13.3 domain is narrowed down and theoccurrence of cancer and the gene candidate which participated in the property in the11q13.3 domain was identified.

Report

(3 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Research-status Report
  • Research Products

    (6 results)

All 2012 2011

All Presentation (6 results)

  • [Presentation] 口腔扁平上皮癌のFFPE組織を用いたゲノムコピー数異常解析2012

    • Author(s)
      森田圭一,プラディットルシャタムカヤヌント,松川祥,林深,小崎健一,稲澤譲治,小村健
    • Organizer
      第36回日本頭頸部癌学会
    • Place of Presentation
      松江市
    • Related Report
      2012 Annual Research Report 2012 Final Research Report
  • [Presentation] 舌扁平上皮癌後発頸部リンパ節転移症例のFFPE組織を用いたゲノムコピー数異常解析2012

    • Author(s)
      森田圭一,プラディットルシャタムカヤヌント,松川祥,林深,小崎健一,稲澤譲治,小村健
    • Organizer
      第50回日本癌治療学会学術集会
    • Place of Presentation
      横浜市
    • Related Report
      2012 Annual Research Report 2012 Final Research Report
  • [Presentation] 口腔がんにおけるFADDゲノム増幅2011

    • Author(s)
      森田圭一、ルシャタムカヤヌント・プラディット、松川祥、小村健
    • Organizer
      第35回日本頭頸部癌学会
    • Place of Presentation
      名古屋市
    • Related Report
      2012 Final Research Report 2011 Research-status Report
  • [Presentation] 口腔扁平上皮癌におけるEGFRおよびSGLT1の発現解析2011

    • Author(s)
      中島雄介、花畑泰子、森田圭一、柏森高、小村健
    • Organizer
      第35回日本頭頸部癌学会
    • Place of Presentation
      名古屋市
    • Related Report
      2012 Final Research Report
  • [Presentation] 口腔白板症におけるFADDゲノム増幅2011

    • Author(s)
      森田圭一、吉本光洋、松川祥、小村健
    • Organizer
      第49回日本癌治療学会総会
    • Place of Presentation
      名古屋市
    • Related Report
      2012 Final Research Report 2011 Research-status Report
  • [Presentation] 口腔白板症におけるFADDゲノム増幅検出法2011

    • Author(s)
      吉本光洋、森田圭一、小健
    • Organizer
      第76回口腔病学会学術大会
    • Place of Presentation
      東京
    • Related Report
      2012 Final Research Report

URL: 

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

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi