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Article

Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function

  • Authors:
    • Liangyu Chen
    • Xinxing Li
    • Libo Liu
    • Bo Yu
    • Yixue Xue
    • Yunhui Liu
  • View Affiliations / Copyright

    Affiliations: Department of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, Liaoning, P.R. China, Department of Neurobiology, College of Basic Medicine, China Medical University, Shenyang, Liaoning, P.R. China
  • Pages: 1465-1474
    |
    Published online on: January 13, 2015
       https://doi.org/10.3892/or.2015.3712
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Abstract

Glioblastoma multiforme (GBM) is one of the most common encephalic malignant tumors. Due to a high recurrence rate and a lack of effective treatments, the average survival rate remains low. Temozolomide (TMZ), a class of alkylating agent, is widely used as a first-line therapeutic drug during the adjuvant treatment for GBM patients. However, most patients exhibit a palpable resistance to TMZ treatment. Additionally, the underlying mechanism remains to be clarified. In this study, glutathione (GSH) and reactive oxygen species (ROS) levels were found to be closely associated with the sensitivity of GBM cells to TMZ. We also found that TMZ markedly induced xCT, the subunit of glutamate/cystine transporter system xc- expression, which together with the GSH synthesis was increased while the TMZ-inducible ROS level was decreased in GBM cells. In addition, the cystathionine γ-lyase (CTH) acivity, a key enzyme in the transsulfuration pathway was enhanced by TMZ, which insured a cysteine supply and GSH synthesis in a compensatory manner when xCT was blocked. Thus, the individual inhibition of xCT by siRNA and a pharmacological inhibitor (sulfasalazine) only partially inhibited GSH synthesis and moderately enhanced the GBM cell sensitivity to TMZ. However, the TMZ‑induced cytotoxicity was markedly increased along with a marked decrease in GSH levels as result of co-treatment with erastin, which inhibited cysteine uptake from xCT transporter and suppressed CTH activity, leading to impaired transformation from methionine to cysteine. In conclusion, to GBM therapy with a drug combination of TMZ and erastin may be beneficial.
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1 

Friedman HS, Kerby T and Calvert H: Temozolomide and treatment of malignant glioma. Clin Cancer Res. 6:2585–2597. 2000.PubMed/NCBI

2 

Gunther W, Pawlak E, Damasceno R, Arnold H and Terzis AJ: Temozolomide induces apoptosis and senescence in glioma cells cultured as multicellular spheroids. Br J Cancer. 88:463–469. 2003. View Article : Google Scholar : PubMed/NCBI

3 

Knauth M, Wirtz CR, Tronnier VM, Aras N, Kunze S and Sartor K: Intraoperative MR imaging increases the extent of tumor resection in patients with high-grade gliomas. AJNR Am J Neuroradiol. 20:1642–1646. 1999.PubMed/NCBI

4 

Nakada M, Nakada S, Demuth T, Tran NL, Hoelzinger DB and Berens ME: Molecular targets of glioma invasion. Cell Mol Life Sci. 64:458–478. 2007. View Article : Google Scholar : PubMed/NCBI

5 

Stupp R, Mason WP, van den Bent MJ, et al: Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 352:987–996. 2005. View Article : Google Scholar : PubMed/NCBI

6 

Burnet NG, Jefferies SJ, Benson RJ, Hunt DP and Treasure FP: Years of life lost (YLL) from cancer is an important measure of population burden - and should be considered when allocating research funds. Br J Cancer. 92:241–245. 2005.PubMed/NCBI

7 

Bocangel DB, Finkelstein S, Schold SC, Bhakat KK, Mitra S and Kokkinakis DM: Multifaceted resistance of gliomas to temozolomide. Clin Cancer Res. 8:2725–2734. 2002.PubMed/NCBI

8 

Hegi ME, Diserens A, Gorlia T, et al: MGMT gene silencing and benefit from temozolomide in glioblastoma. New Engl J Med. 352:997–1003. 2005. View Article : Google Scholar : PubMed/NCBI

9 

Conrad M and Sato H: The oxidative stress-inducible cystine/glutamate antiporter, system x (c) (−): cystine supplier and beyond. Amino Acids. 42:231–246. 2012. View Article : Google Scholar

10 

Sato H, Tamba M, Ishii T and Bannai S: Cloning and expression of a plasma membrane cystine/glutamate exchange transporter composed of two distinct proteins. J Biol Chem. 274:11455–11458. 1999. View Article : Google Scholar : PubMed/NCBI

11 

Okuno S, Sato H, Kuriyama-Matsumura K, et al: Role of cystine transport in intracellular glutathione level and cisplatin resistance in human ovarian cancer cell lines. Br J Cancer. 88:951–956. 2003. View Article : Google Scholar : PubMed/NCBI

12 

Lu SC: Glutathione synthesis. Biochim Biophys Acta. 1830:3143–3153. 2013. View Article : Google Scholar :

13 

Ye P, Mimura J, Okada T, et al: Nrf2- and ATF4-dependent up-regulation of xCT modulates the sensitivity of T24 bladder carcinoma cells to proteasome inhibition. Mol Cell Biol. 34:3421–3434. 2014. View Article : Google Scholar : PubMed/NCBI

14 

Toyoda M, Kaira K, Ohshima Y, et al: Prognostic significance of amino-acid transporter expression (LAT1, ASCT2, and xCT) in surgically resected tongue cancer. Br J Cancer. 110:2506–2513. 2014. View Article : Google Scholar : PubMed/NCBI

15 

Yoshikawa M, Tsuchihashi K, Ishimoto T, et al: xCT inhibition depletes CD44v-expressing tumor cells that are resistant to EGFR-targeted therapy in head and neck squamous cell carcinoma. Cancer Res. 73:1855–1866. 2013. View Article : Google Scholar : PubMed/NCBI

16 

Guo W, Zhao Y, Zhang Z, et al: Disruption of xCT inhibits cell growth via the ROS/autophagy pathway in hepatocellular carcinoma. Cancer Lett. 312:55–61. 2011. View Article : Google Scholar : PubMed/NCBI

17 

Chen RS, Song YM, Zhou ZY, et al: Disruption of xCT inhibits cancer cell metastasis via the caveolin-1/beta-catenin pathway. Oncogene. 28:599–609. 2009. View Article : Google Scholar

18 

Gout PW, Buckley AR, Simms CR and Bruchovsky N: Sulfasalazine, a potent suppressor of lymphoma growth by inhibition of the x(c)- cystine transporter: a new action for an old drug. Leukemia. 15:1633–1640. 2001. View Article : Google Scholar : PubMed/NCBI

19 

Robe PA, Martin DH, Nguyen-Khac MT, et al: Early termination of ISRCTN45828668, a phase 1/2 prospective, randomized study of sulfasalazine for the treatment of progressing malignant gliomas in adults. BMC Cancer. 9:3722009. View Article : Google Scholar : PubMed/NCBI

20 

Takeuchi S, Wada K, Nagatani K, Otani N, Osada H and Nawashiro H: Sulfasalazine and temozolomide with radiation therapy for newly diagnosed glioblastoma. Neurol India. 62:42–47. 2014. View Article : Google Scholar : PubMed/NCBI

21 

Yagoda N, von Rechenberg M, Zaganjor E, et al: RAS-RAF-MEK-dependent oxidative cell death involving voltage-dependent anion channels. Nature. 447:864–868. 2007. View Article : Google Scholar : PubMed/NCBI

22 

Dixon SJ, Lemberg KM, Lamprecht MR, et al: Ferroptosis: an iron-dependent form of nonapoptotic cell death. Cell. 149:1060–1072. PubMed/NCBI

23 

Yang WS, SriRamaratnam R, Welsch ME, et al: Regulation of ferroptotic cancer cell death by GPX4. Cell. 156:317–331. 2014. View Article : Google Scholar : PubMed/NCBI

24 

Giordana L, Mantilla BS, Santana M, Silber AM and Nowicki C: Cystathionine γ-lyase, an enzyme related to the reverse transsulfuration pathway, is functional in Leishmania spp. J Eukaryot Microbiol. 61:204–213. 2014. View Article : Google Scholar : PubMed/NCBI

25 

Romero I, Téllez J, Yamanaka LE, Steindel M, Romanha AJ and Grisard EC: Transsulfuration is an active pathway for cysteine biosynthesis in Trypanosoma rangeli. Parasit Vectors. 7:1972014. View Article : Google Scholar : PubMed/NCBI

26 

McBean GJ: The transsulfuration pathway: a source of cysteine for glutathione in astrocytes. Amino Acids. 42:199–205. 2012. View Article : Google Scholar

27 

Manna P and Jain SK: Vitamin D up-regulates glucose transporter 4 (GLUT4) translocation and glucose utilization mediated by cystathionine-gamma-lyase (CSE) activation and H2S formation in 3T3L1 adipocytes. J Biol Chem. 287:42324–42332. 2012. View Article : Google Scholar : PubMed/NCBI

28 

Rao AM, Drake MR and Stipanuk MH: Role of the transsulfuration pathway and of gamma-cystathionase activity in the formation of cysteine and sulfate from methionine in rat hepatocytes. J Nutr. 120:837–845. 1990.PubMed/NCBI

29 

Liu G, Casqueiro J, Bañuelos O, Cardoza RE, Gutiérrez S and Martín JF: Targeted inactivation of the mecB gene, encoding cystathionine-gamma-lyase, shows that the reverse transsulfuration pathway is required for high-level cephalosporin biosynthesis in Acremonium chrysogenum C10 but not for methionine induction of the cephalosporin genes. J Bacteriol. 183:1765–1772. 2001. View Article : Google Scholar : PubMed/NCBI

30 

Yang G, Cao K, Wu L and Wang R: Cystathionine gamma-lyase overexpression inhibits cell proliferation via a H2S-dependent modulation of ERK1/2 phosphorylation and p21Cip/WAK-1. J Biol Chem. 279:49199–49205. 2004. View Article : Google Scholar : PubMed/NCBI

31 

Sasaki H, Sato H, Kuriyama-Matsumura K, et al: Electrophile response element-mediated induction of the cystine/glutamate exchange transporter gene expression. J Biol Chem. 277:44765–44771. 2002. View Article : Google Scholar : PubMed/NCBI

32 

Wu G, Fang YZ, Yang S, Lupton JR and Turner ND: Glutathione metabolism and its implications for health. J Nutr. 134:489–492. 2004.PubMed/NCBI

33 

Chung WJ and Sontheimer H: Sulfasalazine inhibits the growth of primary brain tumors independent of nuclear factor-kappaB. J Neurochem. 110:182–193. 2009. View Article : Google Scholar : PubMed/NCBI

34 

Kandil S, Brennan L and McBean GJ: Glutathione depletion causes a JNK and p38MAPK-mediated increase in expression of cystathionine-gamma-lyase and upregulation of the transsulfuration pathway in C6 glioma cells. Neurochem Int. 56:611–619. 2010. View Article : Google Scholar : PubMed/NCBI

35 

Hottinger AF, Aissa AB, Espeli V, et al: Phase I study of sorafenib combined with radiation therapy and temozolomide as first-line treatment of high-grade glioma. Br J Cancer. 110:2655–2661. 2014. View Article : Google Scholar : PubMed/NCBI

36 

Bartels U, Wolff J, Gore L, et al: Phase 2 study of safety and efficacy of nimotuzumab in pediatric patients with progressive diffuse intrinsic pontine glioma. Neuro Oncol. 16:1554–1559. 2014. View Article : Google Scholar : PubMed/NCBI

37 

Margison GP and Santibanez-Koref MF: O6-alkylguanine-DNA alkyltransferase: role in carcinogenesis and chemotherapy. Bioessays. 24:255–266. 2002. View Article : Google Scholar : PubMed/NCBI

38 

Zhang J, Stevens MF and Bradshaw TD: Temozolomide: mechanisms of action, repair and resistance. Curr Mol Pharmacol. 5:102–114. 2012. View Article : Google Scholar

39 

She X, Yu Z, Cui Y, et al: miR-128 and miR-149 enhance the chemosensitivity of temozolomide by Rap1B-mediated cytoskeletal remodeling in glioblastoma. Oncol Rep. 32:957–964. 2014.PubMed/NCBI

40 

Lin CJ, Lee CC, Shih YL, et al: Resveratrol enhances the therapeutic effect of temozolomide against malignant glioma in vitro and in vivo by inhibiting autophagy. Free Radic Biol Med. 52:377–391. 2012. View Article : Google Scholar

41 

Yin H, Zhou Y, Wen C, et al: Curcumin sensitizes glioblastoma to temozolomide by simultaneously generating ROS and disrupting AKT/mTOR signaling. Oncol Rep. 32:1610–1616. 2014.PubMed/NCBI

42 

Dai L, Cao Y, Chen Y, Parsons C and Qin Z: Targeting xCT, a cystine-glutamate transporter induces apoptosis and tumor regression for KSHV/HIV-associated lymphoma. J Hematol Oncol. 7:302014. View Article : Google Scholar : PubMed/NCBI

43 

Doxsee DW, Gout PW, Kurita T, et al: Sulfasalazine-induced cystine starvation: potential use for prostate cancer therapy. Prostate. 67:162–171. 2007. View Article : Google Scholar

44 

Ehren JL and Maher P: Concurrent regulation of the transcription factors Nrf2 and ATF4 mediates the enhancement of glutathione levels by the flavonoid fisetin. Biochem Pharmacol. 85:1816–1826. 2013. View Article : Google Scholar : PubMed/NCBI

45 

Dickhout JG, Carlisle RE, Jerome DE, et al: Integrated stress response modulates cellular redox state via induction of cystathionine gamma-lyase: cross-talk between integrated stress response and thiol metabolism. J Biol Chem. 287:7603–7614. 2012. View Article : Google Scholar : PubMed/NCBI

46 

Yang BC, Wang YS, Liu HS and Lin SJ: Ras signaling is involved in the expression of Fas-L in glioma. Lab Invest. 80:529–537. 2000. View Article : Google Scholar : PubMed/NCBI

47 

Bermano G, Smyth E, Goua M, Heys SD and Wahle KW: Impaired expression of glutathione peroxidase-4 gene in peripheral blood mononuclear cells: a biomarker of increased breast cancer risk. Cancer Biomark. 7:39–46. 2010.PubMed/NCBI

48 

Schneider M, Wortmann M, Mandal PK, et al: Absence of Absence of glutathione peroxidase 4 affects tumor angiogenesis through increased 12/15-lipoxygenase activity. Neoplasia. 12:254–263. 2010.PubMed/NCBI

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Copy and paste a formatted citation
Spandidos Publications style
Chen L, Li X, Liu L, Yu B, Xue Y and Liu Y: Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function. Oncol Rep 33: 1465-1474, 2015.
APA
Chen, L., Li, X., Liu, L., Yu, B., Xue, Y., & Liu, Y. (2015). Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function. Oncology Reports, 33, 1465-1474. https://doi.org/10.3892/or.2015.3712
MLA
Chen, L., Li, X., Liu, L., Yu, B., Xue, Y., Liu, Y."Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function". Oncology Reports 33.3 (2015): 1465-1474.
Chicago
Chen, L., Li, X., Liu, L., Yu, B., Xue, Y., Liu, Y."Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function". Oncology Reports 33, no. 3 (2015): 1465-1474. https://doi.org/10.3892/or.2015.3712
Copy and paste a formatted citation
x
Spandidos Publications style
Chen L, Li X, Liu L, Yu B, Xue Y and Liu Y: Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function. Oncol Rep 33: 1465-1474, 2015.
APA
Chen, L., Li, X., Liu, L., Yu, B., Xue, Y., & Liu, Y. (2015). Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function. Oncology Reports, 33, 1465-1474. https://doi.org/10.3892/or.2015.3712
MLA
Chen, L., Li, X., Liu, L., Yu, B., Xue, Y., Liu, Y."Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function". Oncology Reports 33.3 (2015): 1465-1474.
Chicago
Chen, L., Li, X., Liu, L., Yu, B., Xue, Y., Liu, Y."Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-γ-lyase function". Oncology Reports 33, no. 3 (2015): 1465-1474. https://doi.org/10.3892/or.2015.3712
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