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Inhibition of DNA damage with the activation of gastric mucosal protection and gastric carcinogenesis

Research Project

Project/Area Number 05671018
Research Category

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

Allocation TypeSingle-year Grants
Research Field General surgery
Research InstitutionKyoto prefectural University of Medicine

Principal Investigator

YAMANE Tetsuro  Kyoto prefectural University of Medicine, 医学部, 教授 (50166766)

Project Period (FY) 1993 – 1995
Project Status Completed (Fiscal Year 1995)
Budget Amount *help
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1995: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1994: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1993: ¥1,000,000 (Direct Cost: ¥1,000,000)
KeywordsGastric mucosal protection / DNA damage / Chemoprevention / Gastric cancer / Cytoprotection / MNNG / ENNG / Rebamipide / 胃発癌抑制
Research Abstract

We hypothesized that gastric carcinogenesis may controlled by the balance of the host defense mechanism and offense by carcinogen like a mechansisms of gastric formation. We tested Rebamipide in ENNG-induced mouse duodenal carcinogenesis. ENNG was administered to the C57B1/6 mice at a concentration of 100 mg/L for 4 weeks. Then, the mice were given Rebamipide (20 or 50mg/kg) for 16 weeks. In the 16th week of the experiment, the mice were killed and the duodenum and stomach were resected. Duodenal tumors were examined by stereomicroscopy, and their incidence and size were recorded. The incidence of duodenal tumors in mice treated with ENNG,ENNG plus 20mg/kg Rebamipide and ENNG plus 50mg/kg Rebamipide was 66.7%, 58.1% and 45.2% respectively. The difference between the group treated with ENNG and the group treated with ENNG plus Rebamipide was not significant.
Male wistar rats were given MNNG at a concentration of 80 mg/L for 28 weeks. Rebamipide was administered. In the 48th week of the expriment, the glandular stomach was examined for macroscopic tumors and histological examination were recorded. The incidence of gastric carcinogenesis in the group treated with MNNG and MNNG plus 20mg/kg Rebamipide was 76.9% and 61.5%, respectively. The incidence between the both groups were not significantly different. In the histological study of gastric tumors, the incidence of carcinoma and adenoma in the MNNG and MNNG Plus Rebamipide treated group were 69.2% and 30.7% respectively. The defference between these groups were significant (p<0.05).

Report

(3 results)
  • 1995 Annual Research Report   Final Research Report Summary
  • 1993 Annual Research Report
  • Research Products

    (24 results)

All Other

All Publications (24 results)

  • [Publications] Kitao,Y.: "Risk analysis of carcinogenesis in the remnant stomach with measurement of ornithine decarboxylase activity" J. Surg. Oncol. 57. 22-24 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Kitao,Y.: "Risk analysis of carcinogenesis in the remnant stomach of rats after oral administration of MNNG." Proceedings of the International Cancer Congress (Ed. by R. S. Rao,M. G. Deo and L. D. Sanghvi). 1639-1644 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Yamane,T.: "Chemoprevention of gastrointestinal carcinogenesis by green tea polyphenols." Proceedings of the International Cancer Congress (Ed. by R. S. Rao,M. G. Deo and L. D. Sanghvi). 1645-1648 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Oya,K.: "Immunohistochemical staining and Activity of Ornithine Decarboxylase in Colorectal Cancer" Cancer Letters. 91. 101-106 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Yamane,T.: "Inhibition of MNNG-induced carcinogenesis by (-)-epigallocatechin gallate in the rat glandular stomach" Cancer Res. 55. 2081-2084 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Inagake,M.: "Inhibition of 1,2-Dimethylhy drazine-induced Oxidative DNA Damage by Green Tea Extract in Rat." Jpn. J. Cancer Res.86. 1106-1111 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Kitao, Y.: "Risk analysis of carcinogenesis in the remnant stomach with measurement of ornithine decarboxylase activity" J.Surg.Oncol.57. 22-24 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Ymane, T.: "Chemoprevention of gastrointestinal carcinogenesis by green tea polyphenols." Proceedings of the International Cancer Congress (Ed.by R.S.Rao, M.G.Deo and L.D.Sanghvi). 1645-1648 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Kitao, Y.: "Risk analysis of carcinogenesis in the remnant stomach of rats after oral administration of MNNG" Proceedings of the International Cancer Congress (Ed.by R.S.Rao, M.G.Deo and L.D.Sanghvi). 1639-1644 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Oya, K.: "Immunohistochemical staining and Activity of Ornithine Decarboxylase in Colorectal Cancer" Cancer Letters. 91. 101-106 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Inagake, M.: "Inhibition of 1,2-Dimethylhydrazine-induced Oxidative DNA Damage by Green Tea Extract in Rat." Jpn.J.Cancer Res.86(11). 1106-1111 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Yaname, T.: "Inhibition of MNNG-induced carcinogenesis by (-)-epigallocatechin gallate in the rat glandular stomach" Cancer Res.55. 2081-2084 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Kitao,Y.: "Risk analysis of carcinogenesis in the remnant stomach of rats after oral administration of MNNG." Proceedings of the International Cancer Congress(Ed.by R.S.Rao,M.G.Deo and L.D.Sanghvi). 1639-1644 (1994)

    • Related Report
      1995 Annual Research Report
  • [Publications] Yamane,T.: "Chemoprevention of gastrointestinal carcinogenesis by green tea polyphenols." Proceedings of the International Cancer Congress(Ed.by R.S.Rao,M.G.Deo and L.D.Sanghvi). 1645-1648 (1994)

    • Related Report
      1995 Annual Research Report
  • [Publications] Kitao,Y.: "Risk analysis of carcinogenesis in the remnant stomach with measurement of ornithine decarboxylase activity" J.Surg.Oncol.57. 22-24 (1994)

    • Related Report
      1995 Annual Research Report
  • [Publications] Oya,K.: "Immunohistochemical staining and Activity of Ornithine Decarboxylase in Colorectal Cancer" Cancer Letters. 91. 101-106 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Inagake,M.: "Inhibition of 1,2-Dimethylhydrazine-induced Oxidative DNA Damage by Green Ter Extract in Rat." Jpn.J.Cancer Res.86. 1106-1111 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Yamane,T.: "Inhibition of MNNG-induced carcinogenesis by(-)-epigallocatechin gallate in the rat glandular stomach" Cancer Res. 55. 2081-2084 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Okuzumi.,Yamane T.,et al.: "Inhibitory effects of fucoxanthin,a natural carotenoid,on N-etyl-N′-nitro-N-nitrosoguanidine-induced mouse duodenal carcinogenesis" Cancer Letters. 68. 159-168 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 奥山 晃,山根哲郎,他: "Green Tea Extractによるマウス十二指腸発癌の抑制について" 消化器癌の発生と進展. 5. 77-80 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 稲掛雅男,山根哲郎,他: "家族性大腸腺腫症の大腸粘膜オルニチン脱炭酸酵素活性" 消化器癌の発生と進展. 5. 179-181 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 大矢和彦,山根哲郎,他: "抗ヒトオルニチン脱炭酸酵素(ODC)モノクローナル抗体を用いた大腸癌組織ODCの染色性と組織内ODC活性について" 消化器癌の発生と進展. 5. 343-346 (1993)

    • Related Report
      1993 Annual Research Report
  • [Publications] 山根哲郎、高橋俊雄: "ポリフェノール化合物による消化器発癌の予防" Oncologia. 27. 29-33 (1994)

    • Related Report
      1993 Annual Research Report
  • [Publications] Inagake M.,Yamane T.,et al.: "Recent Advances in Manegement of Digestive Cancers" Inhibitory effect of green tea extract against azoxymethane induced colon carcinogenesis in rat, 474-476 (1993)

    • Related Report
      1993 Annual Research Report

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Published: 1993-04-01   Modified: 2016-04-21  

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