Literature DB >> 8636001

Prevention by methionine of enhancement of hepatocarcinogenesis by coadministration of a choline-deficient L-amino acid-defined diet and ethionine in rats.

T Tsujiuchi1, E Kobayashi, D Nakae, Y Mizumoto, N Andoh, H Kitada, K Ohashi, T Fukuda, A Kido, M Tsutsumi.   

Abstract

The effects of methionine on hepatocarcinogenesis induced by coadministration of a choline-deficient L-amino acid-defined (CDAA) diet and ethionine were examined. F344 male rats were divided into 4 experimental groups. Groups 1 and 2 received the CDAA diet and a choline-supplemented L-amino acid-defined (CSAA)++ diet, respectively. Group 3 received the CDAA diet containing 0.05% ethionine, and group 4 the CDAA diet containing 0.05% ethionine and 0.47% methionine. Animals were killed after 12 weeks of treatment. Histologically, the CDAA diet induced intracellular fat accumulation and foci. In contrast, ethionine caused not only foci, but also hyperplastic nodules, cholangiofibrosis and the proliferation of oval cells without such fat accumulation. Methionine abolished the development of all of the liver lesions induced by coadministration of the CDAA diet and ethionine. To investigate the effects of methionine on induction of c-myc and c-Ha-ras expression, as well as generation of 8-hydroxyguanine (8-OHGua) and 2-thiobarbituric acid-reacting substances (TBARS), by coadministration of the CDAA diet and ethionine, subgroups of 3 to 5 animals were killed at 2, 4, 8, or 11 days after the beginning of the experiment. Coadministration of the CDAA diet and ethionine markedly enhanced the level of expression of c-myc and c-Ha-ras, 8-OHGua formation and TBARS generation as compared with the CDAA or CSAA diet within 11 days, and methionine blocks these actions. These results indicate that addition of methionine prevents the induction of c-myc and c-Ha-ras expression, 8-OHGua formation and TBARS generation, as well as hepatocellular lesions, by coadministration of the CDAA diet and ethionine in rats, and suggest a possible involvement of oxidative stress and gene expression in hepatocarcinogenesis by these agents.

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Year:  1995        PMID: 8636001      PMCID: PMC5920662          DOI: 10.1111/j.1349-7006.1995.tb03306.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


semipurified choline‐deficient diet; a choline‐deficient L‐amino acid‐defined diet; a choline‐supplemented L‐amino acid‐defined diet; 8‐hydroxyguanine; 8‐hydroxydeoxy‐guanosine; deoxyguanosine; 2‐thiobarbituric acid‐reacting substances malondialdehyde; γ‐glutamyltransferase
  35 in total

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Authors:  D Nakae; K Yamamoto; H Yoshiji; T Kinugasa; H Maruyama; J L Farber; Y Konishi
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4.  A method for isolation of intact, translationally active ribonucleic acid.

Authors:  G Cathala; J F Savouret; B Mendez; B L West; M Karin; J A Martial; J D Baxter
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5.  Application of quantitative stereology to the evaluation of enzyme-altered foci in rat liver.

Authors:  H A Campbell; H C Pitot; V R Potter; B A Laishes
Journal:  Cancer Res       Date:  1982-02       Impact factor: 12.701

6.  Reversibility of changes in nucleic acid methylation and gene expression induced in rat liver by severe dietary methyl deficiency.

Authors:  J K Christman; G Sheikhnejad; M Dizik; S Abileah; E Wainfan
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7.  Formation of 8-hydroxydeoxyguanosine (8-OH-dG) in rat kidney DNA after intraperitoneal administration of ferric nitrilotriacetate (Fe-NTA).

Authors:  T Umemura; K Sai; A Takagi; R Hasegawa; Y Kurokawa
Journal:  Carcinogenesis       Date:  1990-02       Impact factor: 4.944

8.  High incidence of hepatocellular carcinomas induced by a choline deficient L-amino acid defined diet in rats.

Authors:  D Nakae; H Yoshiji; Y Mizumoto; K Horiguchi; K Shiraiwa; K Tamura; A Denda; Y Konishi
Journal:  Cancer Res       Date:  1992-09-15       Impact factor: 12.701

9.  Hepatocarcinogenesis in rats fed methyl-deficient, amino acid-defined diets.

Authors:  Y B Mikol; K L Hoover; D Creasia; L A Poirier
Journal:  Carcinogenesis       Date:  1983-12       Impact factor: 4.944

10.  A novel combination of K-ras and myc amplification accompanied by point mutational activation of K-ras in a human lung cancer.

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  3 in total

1.  Ethionine regulates cell motile activity through LPA receptor-3 in liver epithelial WB-F344 cells.

Authors:  Serina Inoue; Eriko Tanabe; Ayano Shibata; Miku Hirane; Mutsumi Araki; Yan Dong; Nobuyuki Fukushima; Toshifumi Tsujiuchi
Journal:  Mol Cell Biochem       Date:  2013-07-19       Impact factor: 3.396

2.  Hot-spot mutations in the p53 gene of liver nodules induced in rats fed DL-ethionine with a methyl-deficient diet.

Authors:  T Tsujiuchi; L Yeleswarapu; Y Konishi; B Lombardi
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

3.  Hypomethylation of CpG sites and c-myc gene overexpression in hepatocellular carcinomas, but not hyperplastic nodules, induced by a choline-deficient L-amino acid-defined diet in rats.

Authors:  T Tsujiuchi; M Tsutsumi; Y Sasaki; M Takahama; Y Konishi
Journal:  Jpn J Cancer Res       Date:  1999-09
  3 in total

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