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Study of the molecular mechanism underlying genomic alterations during Helicobacter pylori-associated gastric carcinogenesis.

Research Project

Project/Area Number 22890089
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Gastroenterology
Research InstitutionKyoto University

Principal Investigator

MATSUMOTO Yuko  京都大学, 医学研究科, 助教 (20452360)

Project Period (FY) 2010 – 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥3,419,000 (Direct Cost: ¥2,630,000、Indirect Cost: ¥789,000)
Fiscal Year 2011: ¥1,469,000 (Direct Cost: ¥1,130,000、Indirect Cost: ¥339,000)
Fiscal Year 2010: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywordsヘリコバクター・ピロリ / 胃癌 / ゲノム異常 / AID / 遺伝子異変 / 染色体異常 / 遺伝子変異
Research Abstract

With persistent infection of Helicobacter pylori(H. pylori), gastric cancer develops by a multistep process occurring through the accumulation of genetic alterations in gastric epithelial cells. The mechanisms how the gastric epithelial cells with H. pylori infection and the resultant inflammatory response acquire the genetic changes leading to malignant transformation, however, remain unknown. Activation-induced cytidine deaminase(AID) induces somatic mutations in various host genes of non-lymphoid tissues, thereby contributing to carcinogenesis. Indeed, we demonstrated that H. pylori infection induced aberrant AID expression in gastric epithelial cells, resulting in the accumulation of p53 tumor suppressor gene mutations. Our findings suggested the novel link among H. pylori infection, accumulation of genetic changes and human gastric cancer development. The process of accumulation of genetic alterations induced by AID activity, however, have not yet been clarified.
We plan to investigate the role of AID in the occurrence of genetic alterations, including somatic mutations and chromosomal changes. We clarify the overall genetic alterations induced by aberrant AID activity using the genome-wide array comparative genomic hybridization(CGH) analyses as well as the comprehensive mutation assays. The results are also assessed in mouse models with the oral challenge of H. pylori and in AID transgenic mice to investigate whether aberrant AID expression induced by H. pylori infection in vivo could contribute to the occurrence of tumor-promoting genetic changes, leading to the gastric cancer development. A successful outcome of this research project would provide the novel insight into the molecular mechanisms of infection-and inflammation-associated carcinogenesis.

Report

(3 results)
  • 2011 Annual Research Report   Final Research Report ( PDF )
  • 2010 Annual Research Report
  • Research Products

    (7 results)

All 2012 2011 2010

All Journal Article (6 results) (of which Peer Reviewed: 6 results) Presentation (1 results)

  • [Journal Article] Excessive activity of apolipoproteinB mRNA editing enzyme catalyticpolypeptide 2 (APOBEC2) contiributes toliver and lung tumorigenesis.2012

    • Author(s)
      Okuyama S, Marusawa H, Matsumoto T, UedaY, Matsumoto Y, Endo Y, Takai A, ChibaT.
    • Journal Title

      Int Jcancer

      Volume: 130 Issue: 6 Pages: 1294-1301

    • DOI

      10.1002/ijc.26114

    • Related Report
      2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Bileacid-induced expression ofactivation-induced cytidine deaminaseduring the development of Barrett'soesophageal adenocarcinoma.2011

    • Author(s)
      Morita S, Matsumoto Y, Okuyama S, Ono K,Kitamura Y, Tomori A, Oyama T, Amano Y,Kinoshita Y, Chiba T, Marusawa H.
    • Journal Title

      Carcinogenesis

      Volume: 32 Issue: 11 Pages: 1706-1712

    • DOI

      10.1093/carcin/bgr194

    • Related Report
      2011 Annual Research Report 2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Excessive activity of apolipoprotein B mRNA editing enzyme catalytic polypeptide 2(APOBEC2) contributes to liver and lung tumorigenesis.2011

    • Author(s)
      Shunsuke Okuyama, Hiroyuki Marusawa, Tomonori Matsumoto, Yoshihide Ueda, Yuko Matsumoto, Yoko Endo, Atsushi Takai and Tsutomu Chiba.
    • Journal Title

      Int J Cancer

      Volume: 130(6) Pages: 1294-301

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Up-regulation of Activation-Induced Cytidine Deaminase Causes Genetic Aberrations at the CDKN2b-CDKN2a in Gastric Cancer.2010

    • Author(s)
      Yuko Matsumoto, Hiroyuki Marusawa, Kazuo Kinoshita, Yoko Niwa, Yoshiharu Sakai and Tsutomu Chiba.
    • Journal Title

      Gastroenterology

      Volume: 139(6) Pages: 1984-1994

    • NAID

      120002696051

    • Related Report
      2011 Final Research Report 2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Nucleotide-binding Oligomerization Domain 1 Contributes to Host Defense against Helicobacter pylori via Induction of Type I IFN and Activation of the IFN-stimulated Gene Factor 3 Signaling Pathway.2010

    • Author(s)
      Tomohiro Watanabe, Naoki Asano, Stefan Fichtner-Feigl, Peter L. Gorelick, Yoshihisa Tsuji, Yuko Matsumoto, Tsutomu Chiba, Ivan J. Fuss, Atsushi Kitani and Warren Strober
    • Journal Title

      J Clin Invest

      Volume: 120(5) Pages: 1645-62

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Nucleotide-binding Oligomerization Domain 1 Contributes to Host Defense against Helicobacter pylori via Induction of Type I IFN and Activation of the IFN-stimulated Gene Factor 3 Signaling Pathway.2010

    • Author(s)
      Tomohiro Watanabe, Yuko Matsumoto, et al.
    • Journal Title

      J Clin Invest

      Volume: 120(5) Pages: 1645-1662

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Presentation] 胃発癌過程におけるactivation-induced cytidine deaminaseを介した癌抑制遺伝子領域の変異生成の分子機構2010

    • Author(s)
      松本裕子、丸澤宏之Hiroyuki Marusawa, Tomonori Matsumoto, 千葉勉
    • Organizer
      日本ヘリコバクター学会
    • Place of Presentation
      京都
    • Year and Date
      2010-06-24
    • Related Report
      2011 Final Research Report 2010 Annual Research Report

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Published: 2010-08-27   Modified: 2016-04-21  

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