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Influence of pH on the modification of thiols by carbamoylating agents and effects on glutathione levels in normal and neoplastic cells

  • Original Articles
  • Carbamoylation, Glutathione, Thiols
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Summary

In previous studies, we have suggested that the selective inhibitory effect of sodium cyanate (NaOCN) on hepatoma metabolism may be due to the lower pH observed in tumors relative to normal tissues. Lower pH might enhance the action of NaOCN by increasing the formation of isocyanic acid and carbamoylation of sulfhydryl groups. In the present work, studies were conducted on the effect of pH on the carbamoylation of sulfhydryl groups. The data indicated that carbamoylation of the sulfhydryl group of glutathione by NaOCN was enhanced by decreasing the pH from 7.4 to 6.6. A less pH-dependent response was observed with organic isocyanates. However, all reactions were reversible after the pH was increased by the addition of base. Kinetic studies showed that the rate of the reaction is very rapid, a maximal effect occurring within the first 10 min. Dose-dependent modifications of cellular glutathione by NaOCN and organic isocyanates were observed in human HT29 colon tumor cells, rat HTC hepatoma cells, and rat hepatocytes. The rate of carbamoylation of the glutathione sulfhydryl group in cells was similar to that of pure glutathione (GSH). The effect of buthionine sulfoximine on GSH levels in cells was at least as great as that of sodium cyanate, but only the latter showed inhibitory effects on macromolecular synthesis; these were very rapid, pH-dependent, and reversible in tumor cells. Our results suggest that cellular sulfhydryl group(s) other than that of GSH might be involved in the effect of NaOCN on macromolecular synthesis.

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References

  1. Alexander NM (1958) Spectrophotometric assay for sulfhydryl groups using N-ethylmaleimide. Anal Chem 30: 1292

    Google Scholar 

  2. Arrick BA, Nathan CF (1984) Glutathione metabolism as a determinant of therapeutic efficacy: a review. Cancer Res 44: 4224

    Google Scholar 

  3. Babson JR, Reed DJ (1978) Inactivation of glutathione reductase by 2-chloroethyl nitrosourea derived isocyanates. Biochem Biophys Res Commun 83: 754

    Google Scholar 

  4. Babson JR, Abell NS, Reed DJ (1981) Protective role of the glutathione redox cycle against Adriamycin-mediated toxicity in isolated hepatocytes. Biochem Pharmacol 30: 2299

    Google Scholar 

  5. Begleiter A, Grover J Froese E, Goldenberg GJ (1983) Membrane transport, sulfhydryl levels and DNA cross-linking in Chinese hamster ovary cell mutants sensitive and resistant to melphalan. Biochem Pharmacol 32: 293

    Google Scholar 

  6. Carreras J, Chabas A, Diederich D (1976) Physiological and clinical implications of protein carbamoylation. In: Grisolia S, Baguena R, Mayor F (eds) The urea cycle John Wiley & Sons, New York, p 501

    Google Scholar 

  7. Fisher JM, Nauzokaitis AS, Uehara Y, Rabinovitz M (1983) Evidence for a membrane sulfhydryl associated with resistance to melphalan in a murine L1210 leukemia line. Biochem Biophys Res Commun 117: 670

    Google Scholar 

  8. Freedman ML, Schiffman FJ, Geraghty M (1974) Studies on the mechanism of cyanate inhibition of reticulocyte protein synthesis. Br J Haematol 27: 303

    Google Scholar 

  9. Glader BE, Conrad ME (1972) Cyanate inhibition of erythrocyte glucose-6-phosphate dehydrogenase. Nature 237: 336

    Google Scholar 

  10. Griffith OW (1980) Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal Biochem 106: 207

    Google Scholar 

  11. Gullino PM (1966) The internal milieu of tumors. Prog Exp Tumor Res 8: 1

    Google Scholar 

  12. Herrera-Ornelas L, Petrelli NJ, Madajewicz S, Mittelman A, Allfrey VG (1985) Phase-I clinical trial of sodium cyanate in patients with advanced colorectal carcinoma. Oncology 42: 236

    Google Scholar 

  13. Hu JJ, Luke A, Chellani M, Zirvi KA, Lea MA (1988) pH-related effects of sodium cyanate on macromolecular synthesis and tumor cell division. Biochem Pharmacol 37: 2256

    Google Scholar 

  14. Lea MA (1983) Decreased sensitivity to colchicine-mediated inhibition of metabolite uptake in isolated hepatoma cells. J Natl Cancer Inst 71: 1073

    Google Scholar 

  15. Lea MA (1987) Effects of carbamoylating agents on tumor metabolism. Crit Rev Oncol Hemotol 7: 329

    Google Scholar 

  16. Machiedo G, Ghuman S, Rush BF, Draven T, Dikdan G (1981) The effect of ATP-MgCl2 infusion on hepatic cell permeability and metabolism following hemorrhagic shock. Surgery 90: 328

    Google Scholar 

  17. Rotin D, Wan P, Grinstein S, Tannock I (1987) Cytotoxicity of compounds that interfere with the regulation of intracellular pH: a potential new class of anticancer drugs. Cancer Res 47: 1497

    Google Scholar 

  18. Russo A, Carmichael J, Friedman N, Degraff W, Tochner Z, Glatstein E, Mitchell JB (1986) The roles of intracellular glutathione in antineoplastic chemotherapy. Int J Radiat Oncol Biol Phys 12: 1347

    Google Scholar 

  19. Shaw JP, Chou I-N (1986) Elevation of intracellular glutathione content associated with mitogenic stimulation of quiescent fibroblasts. J Cell Physiol 129: 193

    Google Scholar 

  20. Stark GR (1964) On the reversible reaction of cyanate with sulfhydryl groups and the determination of NH2-terminal cysteine and cysteine in proteins. J Biol Chem 239: 1411

    Google Scholar 

  21. Stark GR (1967) Modification of proteins with cyanate. In: Hirs CHW, Timashef SN (eds) Methods in enzymology, vol 11. Academic, New York, p 590

    Google Scholar 

  22. Tew KD, Kyle G, Johnson A, Wang AL (1985) Carbamoylation of glutathione reductase and changes in cellular and chromosome morphology in a rat cell line resistant to nitrogen mustards but collaterally sensitive to nitrosoureas. Cancer Res 45: 2326

    Google Scholar 

  23. Tew KD, Woodworth A, Stearns ME (1986) Relationship of glutathione depletion and inhibition of glutathione-S-transferase activity to the antimitotic properties of estramustine. Cancer Treat Rep 70: 715

    Google Scholar 

  24. Wike-Hooley JL, Haveman J, Reinhold HS (1984) The relevance of tumour pH to the treatment of malignant disease (review article). Radiother Oncol 2: 343

    Google Scholar 

  25. Wolf CR, Lewis AD, Carmichael J, Adams DJ, Allan SG, Ansell DJ (1987) The role of glutathione in determining the response of normal and tumor cells by depletion of intracellular glutathione. Science 217: 544

    Google Scholar 

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Hu, J.J., Dimaira, M.J., Zirvi, K.A. et al. Influence of pH on the modification of thiols by carbamoylating agents and effects on glutathione levels in normal and neoplastic cells. Cancer Chemother. Pharmacol. 24, 95–101 (1989). https://doi.org/10.1007/BF00263127

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  • DOI: https://doi.org/10.1007/BF00263127

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