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What are the motive forces in the development of histological grade in papillary urothelial carcinoma?

Research Project

Project/Area Number 26460430
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Human pathology
Research InstitutionTokyo Metropolitan Geriatric Hospital and Institute of Gerontology

Principal Investigator

IZUMIYAMA Naotaka  地方独立行政法人東京都健康長寿医療センター(東京都健康長寿医療センター研究所), 東京都健康長寿医療センター研究所, 研究助手 (10158751)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords膀胱癌 / テロメア / 染色体分析
Outline of Final Research Achievements

We examined 37 consecutive cases of papillary urothelial neoplasm of the urinary bladder, from which 26 (70.3%) were suitable for karyotype analysis. In the 26, karyotype showed association of diploidy and aneuploidy in 7 tumors by Q-band analysis (61-88 yr). We could measure telomere length in the 7 tumors (total 91 metaphase spreads) by Q-FISH with a software, TFL-Telo version 2. In the Q-FISH samples from the 7 tumors, one tumor showed aneuploidy, alone. In 6 of the 7 tumors, karyotypes with diploidy and aneuploidy were mixed in the same cases. Mean telomere length of diploidy karyotype in each case was significantly longer than that of aneuploidy. Anaphase bridge (AB) analysis revealed that cases with prominent aneuploidy (more than 60 chromosomes) had more frequently AB than those with less than 50. Our data suggest that critically shortened telomeres cause chromosomal instability (aneuploidy) during progression of papillary urothelial neoplasms.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (5 results)

All 2016 2015 Other

All Journal Article (2 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 2 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (2 results) Remarks (1 results)

  • [Journal Article] Changes of telomere status with aging: An update2016

    • Author(s)
      Naoshi Ishikawa, Ken-Ichi Nakamura, Naotaka Izumiyama-Shimomura, Junko Aida, Yoko Matsuda, Tomio Arai and Kaiyo Takubo
    • Journal Title

      Geriatr Gerontol Int

      Volume: 16 Issue: S1 Pages: 30-42

    • DOI

      10.1111/ggi.12772

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Telomere attrition and restoration in the normal teleost Oryzias latipes are linked to growth rate and telomerase activity at each life stage2016

    • Author(s)
      Hatakeyama H, Yamazaki H, Nakamura K, Izumiyama-Shimomura N, Aida J, Suzuki H, Tsuchida S, Matsuura M, Takubo K, Ishikawa N
    • Journal Title

      Aging (Albany NY)

      Volume: Jan;8(1) Pages: 62-76

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Presentation] 上皮小体好酸性細胞は老化細胞か2015

    • Author(s)
      19.相田順子、泉山七生貴、石川直、直井美穂、富田健一郎、長谷川佳代、藤原睦憲、松田陽子、新井冨生、田久保海誉
    • Organizer
      第104回日本病理学会総会
    • Place of Presentation
      名古屋国際会議場(名古屋)
    • Year and Date
      2015-04-30
    • Related Report
      2015 Research-status Report
  • [Presentation] 下垂体細胞のテロメアは加齢で短縮するか? -男女別、前葉、後葉別テロメア長の検討-2015

    • Author(s)
      21.平石直己、藤原睦憲、相田順子、泉山七生貴、仲村賢一、石川直、直井美穂、松田陽子、新井冨生、田久保海誉
    • Organizer
      第104回日本病理学会総会
    • Place of Presentation
      名古屋国際会議場(名古屋)
    • Year and Date
      2015-04-30
    • Related Report
      2015 Research-status Report
  • [Remarks] 高齢者がん研究グループホームページ

    • Related Report
      2015 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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