Literature DB >> 1473227

Cell kinetic analysis of the mucosal epithelium and assay of ornithine decarboxylase activity during the process of 1-hydroxyanthraquinone-induced large bowel carcinogenesis in rats.

H Mori1, Y Mori, T Tanaka, N Yoshimi, S Sugie, T Kawamori, T Narisawa.   

Abstract

Cell kinetics and activity of ornithine decarboxylase (ODC) were studied during the process of 1-hydroxyanthraquinone (1-HA)-induced intestinal carcinogenesis in rats. Starting at 6 weeks of age, a total of 37 male ACI/N rats were divided into two groups and treated as follows: group I (18 rats) received diet containing 1% 1-HA for 12 months; group II (19 rats) was given the basal diet alone. Sub-groups of 5-7 rats were sequentially killed at 4, 8 and 12 months for evaluation of the length, cell numbers and 5-bromo-2'-deoxyuridine (BrDU) labeling indices of large bowel crypts together with ODC activity. All kinetic and ODC data indicated increased DNA synthesis and proliferation at all time points. Morphological observation of the intestines also revealed melanosis, crypt abscesses and erosion, becoming more pronounced with length of exposure to the anthraquinone. The data thus suggest that cell proliferation in the crypts of the cecum or colon is important for 1-HA-induced intestinal carcinogenesis.

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Year:  1992        PMID: 1473227     DOI: 10.1093/carcin/13.12.2217

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  4 in total

1.  Does senna extract promote growth of aberrant crypt foci and malignant tumors in rat colon?

Authors:  N Mascolo; E Mereto; F Borrelli; P Orsi; D Sini; A A Izzo; B Massa; M Boggio; F Capasso
Journal:  Dig Dis Sci       Date:  1999-11       Impact factor: 3.199

Review 2.  Bromodeoxyuridine: a diagnostic tool in biology and medicine, Part II: Oncology, chemotherapy and carcinogenesis.

Authors:  F Dolbeare
Journal:  Histochem J       Date:  1995-12

3.  Chemopreventive effect of N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide (NS-398), a selective cyclooxygenase-2 inhibitor, in rat colon carcinogenesis induced by azoxymethane.

Authors:  N Yoshimi; M Shimizu; K Matsunaga; Y Yamada; K Fujii; A Hara; H Mori
Journal:  Jpn J Cancer Res       Date:  1999-04

4.  Inhibitory effect of NS-398, a selective cyclooxygenase-2 inhibitor, on azoxymethane-induced aberrant crypt foci in colon carcinogenesis of F344 rats.

Authors:  N Yoshimi; K Kawabata; A Hara; K Matsunaga; Y Yamada; H Mori
Journal:  Jpn J Cancer Res       Date:  1997-11
  4 in total

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