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Increased chemosensitivity and elevated reactive oxygen species are mediated by glutathione reduction in glutamine deprived neuroblastoma cells

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Abstract

Purpose

Glutamine is an essential amino acid for the synthesis of glutathione (GSH), the major endogenous antioxidant which protects cells from oxidative injury. To evaluate the effects of glutamine concentrations, cell growth, GSH levels, oxidative stress, and chemosensitivity were evaluated in neuroblastoma cell lines.

Methods

Three human neuroblastoma cell lines (SMS-KCNR, SMS-KANR, SMS-LHN) were cultured with different concentrations of glutamine (2, 0.2 and 0 mM) under hypoxic (5% O2) or normoxic (20% O2) condition. Cell proliferation and chemosensitivity were determined by MTT assay, and the levels of intracellular GSH were measured by DTNB-GSSG reductase method. Cellular reactive oxidative species (ROS) were quantified by flow cytometry.

Results

There was a significant decrease of cell growth in low glutamine (0.2 and 0 mM) compared with control (2 mM) in all three cell lines (P < 0.01), while adding GSH partially restored the reduced cell proliferation by low glutamine. The levels of GSH in neuroblastoma cells decreased significantly in low glutamine compared with the levels of control cells cultured in 2 mM glutamine (P < 0.05), and the accumulation of cellular ROS was significantly higher in 0 mM glutamine compared to the control. Moreover, glutamine deprivation significantly enhanced cytotoxicity of L-PAM in all three cell lines, which was abolished after addition of GSH.

Conclusion

Glutamine deprivation decreased cell proliferation and enhances cell chemosensitivity in neuroblastoma, which is presumably associated with GSH depletion.

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References

  • Anderson CP, Tsai JM, Chan W, Park CK, Tian L, Lui RM, Forman HJ, Reynolds CP (1997) Buthionine sulfoximine alone and in combination with melphalan (L-PAM) is highly cytotoxic for human neuroblastoma cell lines. Eur J Cancer 33:2016–2019

    Article  PubMed  CAS  Google Scholar 

  • Anderson CP, Seeger RC, Matthay KK et al (1998) Pilot study of buthionine sulfoximine (BSO) and melphalan (L-PAM) in children with recurrent neuroblastoma. Proc Am Soc Clin Oncol 17:531

    Google Scholar 

  • Anderson CP, Tsai JM, Meek WE, Liu RM, Tang Y, Forman HJ, Reynolds CP (1999) Depletion of glutathione by buthionine sulfoxine is cytotoxic for human neuroblastoma cell lines via apoptosis. Exp Cell Res 246:183–192

    Article  PubMed  CAS  Google Scholar 

  • Benlloch M, Mena S, Ferrer P, Obrador E, Aseni M, Pellicer JA, Carretero J, Ortega A, Estrela JM (2006) Bcl-2 and Mn-SOD antisense oligodeoxynucleotides and a glutamine-enriched diet facilitate elimination of highly resistant B16 melanoma cells by tumor necrosis factor- and chemotherapy. J Biol Chem 281:69–79

    Article  PubMed  CAS  Google Scholar 

  • Carretero J, Obrador E, Pellicer JA, Pascual A, Estrela JM (2000) Mitochondrial glutathione depletion by glutamine in growing tumor cells. Free Radical Biol Med 29:913–923

    Article  CAS  Google Scholar 

  • Chang WK, Yang KD, Shaio MF (1999) Lymphocyte proliferation modulated by glutamine: involved in the endogenous redox reaction. Clin Exp Immunol 117:482–488

    Article  PubMed  CAS  Google Scholar 

  • Curi R, Lagranha CJ, Doi SQ, Sellitti DF, Procopio J, Pithon-Curi TC (2005) Glutamine-dependent changes in gene expression and protein activity. Cell Biochem Funct 23:77–84

    Article  PubMed  CAS  Google Scholar 

  • Fernandes RS, Cotter TG (1994) Apoptosis or necrosis: intracellular levels of glutathione influence mode of cell death. Biochem Pharmacol 48:675–681

    Article  PubMed  CAS  Google Scholar 

  • Frenkel K, Gleichauf C (1991) Hydrogen peroxide formation by cells treated with a tumor promoter. Free Radic Res Commun 12–13(Pt 2):783–794

    Article  PubMed  Google Scholar 

  • Fuchs BC, Bode BP (2006) Stressing out over survival: glutamine as an apoptotic modulator. J Surg Res 131:26–40

    Article  PubMed  CAS  Google Scholar 

  • Green JA, Vistica DT, Young RC, Hamilton TC, Rogan AM, Ozols RF (1984) Potentiation of melphalan cytotoxicity in human ovarian cancer cell lines by glutathione depletion. Cancer Res 44:5427–5431

    PubMed  CAS  Google Scholar 

  • Gurney JG, Ross JA, Wall DA, Bleyer WA, Severson RK, Robison LL (1997) Infant cancer in the U.S.: histology-specific incidence and trends, 1973 to 1992. J Pediatr Hematol Oncol 19:428–443

    Article  PubMed  CAS  Google Scholar 

  • Herrlich P, Bohmer FD (2000) Redox regulation of signal transduction in mammalian cells. Biochem Pharmacol 59:35–41

    Article  PubMed  CAS  Google Scholar 

  • Jögi A, Øra I, Nilsson H, Lindeheim A, Makino Y, Poellinger L, Axelson H, Påhlman S (2002) Hypoxia alters gene expression in human neuroblastoma cell lines toward an immature and neural crest-like phenotype. Proc Natl Acad Sci USA 99:7021–7026

    Article  PubMed  CAS  Google Scholar 

  • Jögi A, Øra I, Nilsson H, Poellinger L, Axelson H, Påhlman S (2003) Hypoxia-induced dedifferentiation in neuroblastoma cells. Cancer Lett 197:145–150

    Article  PubMed  Google Scholar 

  • Kang YJ (1993) Buthionine sulfoximine spares intracellular glutamate: a possible mechanism for cell growth stimulation. Cell Mol Biol Res 39:675–684

    PubMed  CAS  Google Scholar 

  • Kang YJ, Freng Y, Hatcher EL (1994) Glutathione stimulates A549 cell proliferation in glutamine-deficient culture: the effect of glutamate supplementation. J Cell Physiol 161:589–596

    Article  PubMed  CAS  Google Scholar 

  • Meister A (1991) Glutathione deficiency produced by inhibition of its synthesis, and its reversal; applications in research and therapy. Pharmacol Ther 51:155–194

    Article  PubMed  CAS  Google Scholar 

  • Neu J, Shenoy V, Chakrabarti R (1996) Glutamine nutrition and metabolism: where do we go from here? FASEB J 10:829–837

    PubMed  CAS  Google Scholar 

  • Oehler R, Roth E (2003) Regulative capacity of glutamine. Curr Opin Clin Nutr Metab Care 6:277–282

    Article  PubMed  CAS  Google Scholar 

  • Roth ER, Oehler R, Manahart N, Exner R, Wessner B, Strasser E, Spittler A (2002) Regulative potential of glutamine-relation to glutathione metabolism. Nutrition 18:217–221

    Article  PubMed  CAS  Google Scholar 

  • Schroder CP, Godwin AK, O’Dwyer PJ, Tew KD, Forman HJ, Reynolds CP (1996) Glutathione and drug resistance. Cancer Investig 14:158–168

    Article  CAS  Google Scholar 

  • Soh H, Wasa M, Wang HS, Fukuzawa M (2005) Glutamine regulates acid transport and glutathione levels in a human neuroblastoma cell line. Pediatr Surg Int 21:29–33

    Article  PubMed  Google Scholar 

  • Tew KD, Houghton PJ, Houghton JA (1993) Preclinical and clinical modulation of anticancer drugs. CRC, Boca Raton, pp 13–17

    Google Scholar 

  • Todorova VK, Harms SA, Kaufmann Y, Luo S, Luo KO, Babb K, Klimberg VS (2004) Effect of dietary glutamine on tumor glutathione levels and apoptosis-related proteins in DMBA-induced breast cancer of rats. Breast Cancer Res Treat 88:247–256

    Article  PubMed  CAS  Google Scholar 

  • Vandeputte C, Guizon I, Genestie-Denis I, Vannier B, Lorenzon G (1994) A microtiter plate assay for total glutathione and glutathione disulfide contents in cultured/isolated cells: performance study of a new miniaturized protocol. Cell Biol Toxicol 10:415–421

    Article  PubMed  CAS  Google Scholar 

  • Wasa M, Bode BP, Abcouwer SF, Collins CL, Tanabe KK, Souba WW (1996) Glutamine as a regulator of DNA and protein biosynthesis in human solid tumor cell lines. Ann Surg 224:189–197

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Sakurako Izaki.

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Izaki, S., Goto, H. & Yokota, S. Increased chemosensitivity and elevated reactive oxygen species are mediated by glutathione reduction in glutamine deprived neuroblastoma cells. J Cancer Res Clin Oncol 134, 761–768 (2008). https://doi.org/10.1007/s00432-007-0338-2

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  • DOI: https://doi.org/10.1007/s00432-007-0338-2

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