Literature DB >> 7327375

Effects of various chemicals including bile acids and chemical carcinogens on the inhibition of metabolic cooperation.

K Noda, M Umeda, T Ono.   

Abstract

The effects of various chemicals, such as bile acids, a lectin, polyamines and chemical carcinogens, on metabolic cooperation in the hypoxanthine-guanine phosphoribosyl transferase system were surveyed. Among bile acids, lithocholic acid, chenodeoxycholic acid and ursodeoxycholic acid inhibited metabolic cooperation. However, cholic acid, deoxycholic acid and dehydrocholic acid did not. There was a structure-activity relationship among these compounds for the inhibition of metabolic cooperation. The metabolic cooperation was not inhibited by such chemicals as phytohemagglutinin, three polyamines, 7, 12-dimethylbenz [a] anthracene, N-methyl-N'-nitro-N-nitrosoguanidine, 4-nitro-quinolone 1-oxide and three biphenyl compounds. These results should be useful in relation to studies on the mechanism of inhibition of metabolic cooperation and on the relationship between this inhibitory activity and the tumor-promoting activity of various chemicals.

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Year:  1981        PMID: 7327375

Source DB:  PubMed          Journal:  Gan        ISSN: 0016-450X


  10 in total

1.  The effect of complete carcinogens on intercellular transfer of lucifer yellow in fibroblast culture.

Authors:  I V Budunova; L A Mittelman; G A Belitsky
Journal:  Cell Biol Toxicol       Date:  1990-01       Impact factor: 6.691

2.  Cytotoxic, mutagenic, and cell-cell communication inhibitory properties of DDT, lindane, and chlordane on Chinese hamster cells in vitro.

Authors:  G Tsushimoto; C C Chang; J E Trosko; F Matsumura
Journal:  Arch Environ Contam Toxicol       Date:  1983-11       Impact factor: 2.804

3.  Inhibition of metabolic cooperation by cigarette smoke condensate and its fractions in V-79 Chinese hamster lung fibroblasts.

Authors:  T G Hartman; J D Rosen
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

4.  Nongenomic steroid action: Inhibiting effects on cell-to-cell communication between rat ventricular myocytes.

Authors:  F Verrecchia; D Sarrouilhe; J C Hervé
Journal:  Exp Clin Cardiol       Date:  2001

5.  Effects of tumor promoters, genotoxic carcinogens and hepatocytotoxins on mouse hepatocyte intercellular communication.

Authors:  R J Ruch; J E Klaunig
Journal:  Cell Biol Toxicol       Date:  1986-12       Impact factor: 6.691

6.  Bile acids promote carcinogenesis in the remnant stomach of rats.

Authors:  A Kuwahara; T Saito; M Kobayashi
Journal:  J Cancer Res Clin Oncol       Date:  1989       Impact factor: 4.553

Review 7.  Effects of fatty acids on gap junctional communication: possible role in tumor promotion by dietary fat.

Authors:  C F Aylsworth; C W Welsch; J J Kabara; J E Trosko
Journal:  Lipids       Date:  1987-06       Impact factor: 1.880

Review 8.  Multistage carcinogenesis: implications for risk estimation.

Authors:  H Yamasaki
Journal:  Cancer Metastasis Rev       Date:  1988-04       Impact factor: 9.264

Review 9.  Cell culture assays for chemicals with tumor-promoting or tumor-inhibiting activity based on the modulation of intercellular communication.

Authors:  I V Budunova; G M Williams
Journal:  Cell Biol Toxicol       Date:  1994-04       Impact factor: 6.691

10.  The carcinogen benzo(e)pyrene is metabolized by DM15 cells without an uncoupling effect on their gap junctions.

Authors:  I V Budunova; L A Mittleman; R D Safaev; G A Belitsky
Journal:  Cell Biol Toxicol       Date:  1993 Apr-Jun       Impact factor: 6.691

  10 in total

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