Journal of Cancer Research and Clinical Oncology

, Volume 128, Issue 11, pp 589–595

Effects of long-term administration of sulindac on APC mRNA and apoptosis in colons of rats treated with azoxymethane

Authors

  •  Y. Kishimoto
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
  •  K. Yashima
    • Division of Medicine and Clinical Science, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, 36–1 Nishicho, Yonago 683–8504, Japan
  •  T. Morisawa
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
  •  T. Ohishi
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
  •  A. Marumoto
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
  •  A. Sano
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
  •  Y. Idobe-Fujii
    • Division of Medicine and Clinical Science, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, 36–1 Nishicho, Yonago 683–8504, Japan
  •  N. Miura
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
  •  G. Shiota
    • Division of Medicine and Clinical Science, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, 36–1 Nishicho, Yonago 683–8504, Japan
  •  Y. Murawaki
    • Division of Medicine and Clinical Science, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, 36–1 Nishicho, Yonago 683–8504, Japan
  •  J. Hasegawa
    • Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, 86 Nishicho, Yonago 683–8503, Japan
Original Paper

DOI: 10.1007/s00432-002-0384-8

Cite this article as:
Kishimoto, Y., Yashima, K., Morisawa, T. et al. J Cancer Res Clin Oncol (2002) 128: 589. doi:10.1007/s00432-002-0384-8
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Abstract

Purpose. Non-steroidal anti-inflammatory drugs, including sulindac, have been shown to exhibit anti-colon cancer activity; however, the detailed mechanisms concerning continuous long-term administration are still unclear. Therefore, we examined the anti-colon carcinogenesis effects of sulindac after prolonged administration.

Methods. Administration of AOM, a colon-specific carcinogen, induced colonic preneoplastic lesions, which can progress to carcinomas about 40–50 weeks after AOM administration. We studied the effects of sulindac on the incidence of preneoplastic lesions, proliferative activity of colonic cells (AgNORs), tumor suppressor adenomatous polyposis coli (APC) gene expression, and apoptosis using AOM-treated rat colon mucosa at 4 weeks and 40 weeks (early and late stage of colon carcinogenesis, respectively).

Results. Sulindac suppressed the development of preneoplastic lesions induced by AOM at 4 weeks and 40 weeks by about 50% (P<0.01); the proliferative activity of colonic cells increased by AOM was suppressed almost completely. Furthermore, APC expression was significantly increased by sulindac at both the early and late stages (P<0.01). However, apoptosis was clearly increased at the early stage (P<0.01), but not at the late stage.

Conclusions. APC overexpression induced by sulindac can suppress colon carcinogenesis at both the early and late stages, but apoptosis might work as one of anti-cancer mechanisms at the early stage of colon carcinogenesis.

APC Apoptosis Sulindac Colon
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© Springer-Verlag 2002