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      Effect of 5‐Fluorouracil and UFT on Experimental Liver Metastasis Model of Colorectal Cancer Using Mouse Colon 26 Cells

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          Abstract

          Effects of 5‐fluorouracil (5‐FU) and UFT on an experimental liver metastasis model were compared at equi‐effective dosage levels against subcutaneous tumor of mouse colon 26. 5‐FU at the dosage level of 40 mg/kg suppressed the subcutaneous tumor growth by 70.0% and 45.0% on day 13 and day 18, respectively, and UFT at 20 mg/kg provided almost equal suppression (63.0% and 48.0%). In the liver metastasis model, 5‐FU at 40 mg/kg showed more potent prevention of the formation of metastatic foci (94.9%) than did UFT (60.4%) at 20 mg/kg. 5‐FU at 40 mg/kg produced a much higher peak serum level of 5‐FU than did UFT at 20 mg/kg and also showed a much higher AUC (area under the curve) level in the portal blood. These results suggest that oral administration of 5‐FU might be useful in prevention of liver metastasis of colorectal cancer.

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          Liver metastasis of colon 26 cells implanted into the superior mesenteric vein in mice.

          The intraportal implantation of mouse transplantable colon adenocarcinoma 26 was investigated as an experimental liver metastasis model of colorectal cancer. CDF1 male mice (5 weeks old) were laparotomized under pentobarbital sodium anesthesia, and colon 26 tumor cells (1 X 10, 1 X 10(3), or 1 X 10(5) cells) were inoculated into the superior mesenteric vein. On day 21 after inoculation, mice inoculated with 1 X 10(3) tumor cells showed five to 12 colonies of liver metastasis (mean, 9.2 colonies; n = 6). The survival time was 27 to 36 days (median, 27 days; n = 5) in these mice. When mitomycin C (MMC) was administered into the superior mesenteric vein 15 min after the inoculation of tumor cells, the number of metastatic foci in the liver was strongly inhibited; 81.1% and 100% inhibitions were observed in the groups given 4 mg/kg and 6 mg/kg of MMC, respectively. The mouse colon 26 model seems to be one of the more useful experimental models for evaluating treatments for the prevention of liver metastases from colorectal cancer.
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            Metabolic studies of 5‐fluorouracil ‐ II. Influence of the route of administration on the dynamics of distribution in man

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              [Quantitative method of 5-fluorouracil and its metabolites in biological samples using high performance liquid chromatography].

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                Author and article information

                Journal
                Jpn J Cancer Res
                Jpn. J. Cancer Res
                10.1111/(ISSN)1349-7006a
                CAS
                Japanese Journal of Cancer Research : Gann
                Blackwell Publishing Ltd (Oxford, UK )
                0910-5050
                1876-4673
                July 1993
                : 84
                : 7 ( doiID: 10.1111/cas.1993.84.issue-7 )
                : 783-786
                Affiliations
                [ 1 ]Department of Surgery, Tokyo Metropolitan Komagome Hospital, 3–18–22 Honkomagome, Bunkyo‐ku, Tokyo 113
                [ 2 ]Department of Internal Medicine, Toyosu Hospital, Showa University School of Medicine, 4–1–18 Toyosu, Koto‐ku, Tokyo 135
                Article
                CAE783
                10.1111/j.1349-7006.1993.tb02044.x
                5919202
                8370653
                9bf2d0c8-77cb-4a4d-95fb-26a32d4644ad
                History
                Page count
                References: 4, Pages: 4
                Categories
                Article
                Custom metadata
                2.0
                July 1993
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.6.9 mode:remove_FC converted:04.11.2015

                colorectal cancer,liver metastasis model,colon 26,5‐fu,uft

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