Literature DB >> 901422

Polyamines and their biosynthetic enzymes in Ehrlich ascites-carcinoma cells. Modification of tumour polyamine pattern by diamines.

A Kallio, H Pösö, S K Guha, J Jänne.   

Abstract

1. Ehrlich ascites-carcinoma cells contained relatively high concentrations of spermidine and spermine, but the putrescine content of the washed cells was less than 10% of that of higher polyamines. 2. Ascites-tumour cells likewise exhibited high activities of L-ornithine decarboxylase (EC 4.1.1.17), S-adenosyl-L-methionine decarboxylase (EC 4.1.1.50), spermidine synthase (EC 2.5.1.16) and spermine synthase. 3. During the first days after the inoculation, the polyamine pattern of the ascites cells was characterized by a high molar ratio of spermidine to spermine, which markedly decreased on aging of the cells. 4. Various diamines injected into mice bearing ascites cells rapidly and powerfully decreased ornithine decarboxylase activity in the carcinoma cells, apparently through a mechanism that was not a direct inhibition of the enzyme in vitro. Cadaverine (1,5-diaminopentane) and 1,6-diaminohexane were the most potent inhibitors of ornithine decarboxylase among the amines tested. 5. Chronic treatment of the mice with diamines resulted in a virtually complete disappearance of ornithine decarboxylase activity, and after 24h a significant decline in spermidine accumulation. 6. Cadaverine appeared to be an especially suitable compound for use as an inhibitor of the synthesis of higher polyamines, at least in Ehrlich ascites cells, since this diamine also acted as a competitive inhibitor for putrescine in the spermidine synthase reaction without being incorporated into the higher polyamines.

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Year:  1977        PMID: 901422      PMCID: PMC1164960          DOI: 10.1042/bj1660089

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  20 in total

1.  Potent inhibition of ornithine decarboxylase by beta,gamma unsaturated substrate analogs.

Authors:  N Relyea; R R Rando
Journal:  Biochem Biophys Res Commun       Date:  1975-11-03       Impact factor: 3.575

2.  Inhibition of ornithine decarboxylase activity and spermidine accumulation in regenerating rat liver.

Authors:  H Pöso; J Jänne
Journal:  Biochem Biophys Res Commun       Date:  1976-04-19       Impact factor: 3.575

3.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

4.  A rapid assay method for spermidine and spermine synthases. Distribution of polyamine-synthesizing enzymes and methionine adenosyltransferase in rat tissues.

Authors:  A Raina; R L Pajula; T Eloranta
Journal:  FEBS Lett       Date:  1976-09-01       Impact factor: 4.124

5.  Alpha-hydrazino-ornithine blocks net synthesis of putrescine but not of RNA and DNA.

Authors:  S I Harik; M D Hollenberg; S H Snyder
Journal:  Nature       Date:  1974-05-17       Impact factor: 49.962

6.  Dissociation of putrescine-activated decarboxylation of S-adenosyl-L-methionine from the enzymic synthesis of spermidine and spermine by purified prostatic enzyme preparations.

Authors:  J Jänne; H G Williams-Ashman
Journal:  Biochem Biophys Res Commun       Date:  1971-01-22       Impact factor: 3.575

7.  Separation of two proteins required for synthesis of spermidine from S-adenosyl-L-methionine and putrescine in rat prostate.

Authors:  J Jänne; A Schenone; H G Williams-Ashman
Journal:  Biochem Biophys Res Commun       Date:  1971-02-19       Impact factor: 3.575

Review 8.  Biosynthesis and metabolism of 1,4-diaminobutane, spermidine, spermine, and related amines.

Authors:  H Tabor; C W Tabor
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1972

9.  Effect of DL-alpha-hydrazino-delta-aminovaleric acid, an inhibitor of ornithine decarboxylase, on polyamine metabolism in isoproterenol-stimulated mouse parotid glands.

Authors:  H Inoue; Y Kato; M Takigawa; K Adachi; Y Takeda
Journal:  J Biochem       Date:  1975-04       Impact factor: 3.387

10.  Inhibition of polyamine accumulation and deoxyribonucleic acid synthesis in regenerating rat liver.

Authors:  H Pösö; J Jänne
Journal:  Biochem J       Date:  1976-08-15       Impact factor: 3.857

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  9 in total

1.  Specificity of mammalian spermidine synthase and spermine synthase.

Authors:  A E Pegg; K Shuttleworth; H Hibasami
Journal:  Biochem J       Date:  1981-08-01       Impact factor: 3.857

2.  Diamine oxidase and polyamine oxidase activities in normal and transformed cells.

Authors:  G Quash; T Keolouangkhot; L Gazzolo; H Ripoll; S Saez
Journal:  Biochem J       Date:  1979-01-01       Impact factor: 3.857

3.  Effects of diamines on ornithine decarboxylase activity in control and virally transformed mouse fibroblasts.

Authors:  D R Bethell; A E Pegg
Journal:  Biochem J       Date:  1979-04-15       Impact factor: 3.857

4.  Rapid and convenient method for the assay of aminopropyltransferases.

Authors:  H Hibasami; A E Pegg
Journal:  Biochem J       Date:  1978-03-01       Impact factor: 3.857

5.  Diamine-induced inhibition of liver ornithine decarboxylase.

Authors:  A Kallio; M Löfman; H Pösö; J Jänne
Journal:  Biochem J       Date:  1979-01-01       Impact factor: 3.857

6.  Regulation of L-ornithine decarboxylase and S-adenosyl-L-methionine decarboxylase in rat ventral prostate and seminal vesicle.

Authors:  K Piik; P Rajamäki; S K Guha; J Jänne
Journal:  Biochem J       Date:  1977-12-15       Impact factor: 3.857

7.  Inhibition of ornithine decarboxylase of HeLa cells by diamines and polyamines. Effect on cell proliferation.

Authors:  A A Branca; E J Herbst
Journal:  Biochem J       Date:  1980-03-15       Impact factor: 3.857

8.  Role of propylamine transferases in hormone-induced stimulation of polyamine biosynthesis.

Authors:  K Käpyaho; H Pösö; J Jänne
Journal:  Biochem J       Date:  1980-10-15       Impact factor: 3.857

9.  Diamine oxidase activity in human melanoma cell lines with different tumorigenicity in nude mice.

Authors:  N Thomasset; G Quash; J F Doré
Journal:  Br J Cancer       Date:  1982-07       Impact factor: 7.640

  9 in total

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