Literature DB >> 8232285

Diethylglyoxal bis(guanylhydrazone), a potent inhibitor of mammalian S-adenosylmethionine decarboxylase. Effects on cell proliferation and polyamine metabolism in L1210 leukemia cells.

F Svensson1, I Kockum, L Persson.   

Abstract

The polyamines are cell constituents essential for growth and differentiation. S-Adenosylmethionine decarboxylase (AdoMetDC) catalyzes a key step in the polyamine biosynthetic pathway. Methylglyoxal bis(guanylhydrazone) (MGBG) is an anti-leukemic agent with a strong inhibitory effect against AdoMetDC. However, the lack of specificity limits the usefulness of MGBG. In the present report we have used an analog of MGBG, diethylglyoxal bis(guanylhydrazone) (DEGBG), with a much greater specificity and potency against AdoMetDC, to investigate the effects of AdoMetDC inhibition on cell proliferation and polyamine metabolism in mouse L1210 leukemia cells. DEGBG was shown to effectively inhibit AdoMetDC activity in exponentially growing L1210 cells. The inhibition of AdoMetDC was reflected in a marked decrease in the cellular concentrations of spermidine and spermine. The concentration of putrescine, on the other hand, was greatly increased. Treatment with DEGBG resulted in a compensatory increase in the synthesis of AdoMetDC demonstrating an efficient feedback control. Cells seeded in the presence of DEGBG ceased to grow after a lag period of 1-2 days, indicating that the cells contained an excess of polyamines which were sufficient for one or two cell cycles in the absence of polyamine synthesis. The present results indicate that analogs of MGBG, having a greater specificity against AdoMetDC, might be valuable for studies concerning polyamines and cell proliferation.

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Year:  1993        PMID: 8232285     DOI: 10.1007/bf00929206

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  20 in total

1.  Regulation of S-adenosylmethionine decarboxylase in L1210 leukemia cells. Studies using an irreversible inhibitor of the enzyme.

Authors:  R Autelli; L Stjernborg; A R Khomutov; R M Khomutov; L Persson
Journal:  Eur J Biochem       Date:  1991-03-28

2.  Restoration of the polyamine contents in rat hepatoma tissue-culture cells after inhibition of polyamine biosynthesis. Relationship with cell proliferation.

Authors:  E W Gerner; P S Mamont
Journal:  Eur J Biochem       Date:  1986-04-01

3.  Methyl glyoxal bis(guanylhydrazone) as a potent inhibitor of mammalian and yeast S-adenosylmethionine decarboxylases.

Authors:  H G Williams-Ashman; A Schenone
Journal:  Biochem Biophys Res Commun       Date:  1972-01-14       Impact factor: 3.575

4.  Paradoxical enhancement of S-adenosylmethionine decarboxylase in rat tissues following administration of the specific inhibitor methyl glyoxal bis(guanylhydrazone).

Authors:  A E Pegg; A Corti; H G Williams-Ashman
Journal:  Biochem Biophys Res Commun       Date:  1973-05-15       Impact factor: 3.575

5.  S-adenosyl-L-methionine decarboxylase during lymphocyte transformation: decreased degradation in the presence of a specific inhibitor.

Authors:  R H Fillingame; D R Morris
Journal:  Biochem Biophys Res Commun       Date:  1973-06-08       Impact factor: 3.575

Review 6.  Polyamines.

Authors:  C W Tabor; H Tabor
Journal:  Annu Rev Biochem       Date:  1984       Impact factor: 23.643

7.  Irreversible inhibition of the early increase in ornithine decarboxylase activity following growth stimulation is required to block Ehrlich ascites tumor cell proliferation in culture.

Authors:  S Oredsson; S Anehus; O Heby
Journal:  Biochem Biophys Res Commun       Date:  1980-05-14       Impact factor: 3.575

Review 8.  Molecular genetics of polyamine synthesis in eukaryotic cells.

Authors:  O Heby; L Persson
Journal:  Trends Biochem Sci       Date:  1990-04       Impact factor: 13.807

9.  Induction of spermidine/spermine N1-acetyltransferase by methylglyoxal bis(guanylhydrazone).

Authors:  A E Pegg; B G Erwin; L Persson
Journal:  Biochim Biophys Acta       Date:  1985-10-17

Review 10.  Polyamine metabolism and its importance in neoplastic growth and a target for chemotherapy.

Authors:  A E Pegg
Journal:  Cancer Res       Date:  1988-02-15       Impact factor: 12.701

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  3 in total

1.  A novel trans-spliced mRNA from Onchocerca volvulus encodes a functional S-adenosylmethionine decarboxylase.

Authors:  A A Da'Dara; K Henkle-Dührsen; R D Walter
Journal:  Biochem J       Date:  1996-12-01       Impact factor: 3.857

2.  CGP 48664, a potent and specific S-adenosylmethionine decarboxylase inhibitor: effects on regulation and stability of the enzyme.

Authors:  F Svensson; H Mett; L Persson
Journal:  Biochem J       Date:  1997-02-15       Impact factor: 3.857

3.  Spermidine, a sensor for antizyme 1 expression regulates intracellular polyamine homeostasis.

Authors:  Ramesh M Ray; Sujoy Bhattacharya; Mitul N Bavaria; Mary Jane Viar; Leonard R Johnson
Journal:  Amino Acids       Date:  2014-05-14       Impact factor: 3.520

  3 in total

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