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Role of SOD in malignant tumor by anti cancer drugs

Research Project

Project/Area Number 06672020
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Surgical dentistry
Research InstitutionShowa University

Principal Investigator

YAGAMI Kimitoshi  Showa University, Dental School, Assistant Professor, 歯学部, 講師 (00210211)

Co-Investigator(Kenkyū-buntansha) SAKAMAKI Hideaki  Showa University, Dental School, Assistant Professor, 歯学部, 助手 (50201520)
Project Period (FY) 1994 – 1995
Project Status Completed (Fiscal Year 1995)
Budget Amount *help
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1995: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1994: ¥1,200,000 (Direct Cost: ¥1,200,000)
KeywordsMalignant tumor / SOD activity / radiation / anti cancer drugs / tumor cell line / xanthin-xanthin oxidase / progressed cancer / sensitivity / Xanthin-Oxidase / Xanthin Oxidase
Research Abstract

Recently, many anti cancer drugs have been shown to produce super oxide anion (O_2^-) and seem to involve O_2^- in their mode of action. Ionizing radiation provokes the decomposition reaction of water, producing a variety of reactive oxygen species including O_2^-. The finding that cancer cells are generally low in SOD activity may offer a theoretical base for radiation therapy and chemotherapy. Thus, intracellular SOD level may be an important factor determining the resistance of cancer cells against anti cancer drugs or radiation.
For this purpose, we analyzes the activity of tumor tissue SOD that probed tumor sample form patient at the first time visit, and at the operation. Treatment with anti cancer drugs or radiation a few increasea of SOD activity in tumor tissue. To analyzes the mechanisms of resistance of cancer cells against anti cancer drugs or radiation, xanthin and xanthin oxidase were employed to some tumor cell line as an O_2^- generating system, and treatment with 5-FU or CDDP or ionizing radiation. Treatment with anti cancer drugs or radiation a few increases of SOD activity in tumor cells. The treatment with TNF or INF-gamma did a small reduction of SOD activity in tumor cells. CuZnSOD, catalase and GSH-px mRNAs were up regulated by O_2^- exposure with in 20 minus.

Report

(3 results)
  • 1995 Annual Research Report   Final Research Report Summary
  • 1994 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] 山口真吾,他: "スーパーオキサイドによるヒト扁平上皮癌細胞におけるCuZnSODとCatalaseのmRNA発現について" 第50回 日本口腔科学会総会,鹿児島,1996. (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Shingo Yamaguchi, et al., Showa University, Dental School: "CuZnSOD and catalase mRNA expression in squamous cell cartinoma of human induced by super oxide" 50th Annual meeting of J.Jpn.Stomatrol.Soc.Kagoshima. (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] 山口真吾,他: "スーパーオキサイドによるヒト偏平上皮癌株化細胞のCuZnSODおよびカタラーゼのmRNA発現" 日本口腔科学会誌. 50回抄録集(発表予定). (1996)

    • Related Report
      1995 Annual Research Report

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Published: 1994-04-01   Modified: 2016-04-21  

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