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Role of p53 and reactive oxygen species in apoptotic response to copper and zinc in epithelial breast cancer cells

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Abstract

Previous studies revealed that cells may differ in their response to metal stress depending on their p53 status; however, the sequence of events leading to copper-induced apoptosis is still unclear. Exposure of copper (10 and 25 μM) and zinc (10 and 25 μ M) caused activation of p53 in ER+/p53+ human epithelial breast cancer MCF7 cells and resulted in up-regulation of p21. Transactivation of p53 in MCF7 cells also led to increase in expression of Bax, proapototic Bcl-2 family member, triggering mitochondrial pore opening, and PIG3 (p53-induced gene 3 product), and also generation of intracellular reactive oxygen species (ROS). The treatment of MCF7 cells with either copper or zinc for 4 h also caused decrease in mitochondrial membrane potential (Δ ψ m ), accompanied by an elevation in the ROS production and redistribution of p53 into mitochondria. The loss of Δ ψ m was correlated with accumulation of Annexin V positive apoptotic cells. However, the release of apoptosis inducing factor (AIF) and its translocation into nucleus was observed only in MCF7 cells treated with copper. In MDA-MB-231 (ER−/p53−) and MCF7-E6 (ER+/p53−) cells, both p53 and p21 protein levels were not altered in the presence of metals. These cells were resistant to metals, and there was no alteration in Δ ψ m . Copper treatment did not result in accumulation of ROS in these cell lines with an inactive p53 even after exposure to 50 μM of copper for 6 h, indicating a key role for p53 in the ROS generation. Pretreatment of MCF7 cells with p53 inhibitor, pifithrin-α, resulted in decrease of copper and zinc induced ROS production to the control level, suppression of both Bax expression and AIF release.

Therefore, the activation of p53 seems to play a crucial role in copper and zinc induced generation of ROS in epithelial breast cancer cells, and expression of downstream targets of p53, such as PIG3 and Bax, responsible for increased generation of the intracellular ROS, as well as disruption of mitochondrial integrity. Our data suggest that copper induces apoptosis in MCF-7 cells with no caspases through the depolarization of mitochondrial membrane with release of AIF and its translocation into the nucleus. The results demonstrate that a functional p53 is required for the execution of apoptosis in epithelial cells.

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References

  1. Michieli P, Chedid M, Lin D, Pierce JH, Mercer WE, Givol D. Induction of WAF1/CIP1 by a p53-independent pathway. Cancer Res 1994; 54: 3391–3395.

    PubMed  CAS  Google Scholar 

  2. Serrano M, Lin AW, McCurrach ME, Beach D, Lowe SW. Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a. Cell 1997; 88: 593–602.

    PubMed  CAS  Google Scholar 

  3. Toyokuni S, Okamoto K, Yodoi J, Hiai H. Persistent oxidative stress in cancer. FEBS Lett 1995; 358: 1–3.

    PubMed  CAS  Google Scholar 

  4. Uberti D, Yavin E, Gil S, Ayasola KR, Goldfinger N, Rotter V. Hydrogen peroxide induces nuclear translocation of p53 and apoptosis in cells of oligodendroglia origin. Brain Res Mol Brain Res 1999; 65: 167–175.

    PubMed  CAS  Google Scholar 

  5. Li PF, Dietz R, von Harsdorf R. p53 regulates mitochondrial membrane potential through reactive oxygen species and induces cytochrome c-independent apoptosis blocked by Bcl-2. EMBO J 1999; 18: 6027–6036.

    Article  CAS  PubMed  Google Scholar 

  6. Miyashita T, Reed JC. Tumor suppressor p53 is a direct transcriptional activator of the human bax gene. Cell 1995; 80: 293–299.

    CAS  PubMed  Google Scholar 

  7. Oda E, Ohki R, Murasawa H, et al. Noxa, a BH3-only member of the Bcl-2 family and candidate mediator of p53-induced apoptosis. Science 2000; 288: 1053–1058.

    PubMed  CAS  Google Scholar 

  8. Yu J, Zhang L, Hwang PM, Kinzler KW, Vogelstein B. PUMA induces the rapid apoptosis of colorectal cancer cells. Mol Cell 2001; 7: 673–682.

    PubMed  CAS  Google Scholar 

  9. Nakano K, Vousden KH. PUMA, a novel proapoptotic gene, is induced by p53. Mol Cell 2001; 7: 683–694.

    PubMed  CAS  Google Scholar 

  10. Miyashita T, Reed JC. Tumor suppressor p53 is a direct transcriptional activator of the human bax gene. Cell 1995; 80: 293–299.

    CAS  PubMed  Google Scholar 

  11. Stewart ZA, Pietenpol JA. p53 Signaling and cell cycle checkpoints. Chem Res Toxicol 2001; 14: 243–263.

    PubMed  CAS  Google Scholar 

  12. Marchenko ND, Zaika A, Moll UM. Death signal-induced localization of p53 protein to mitochondria. A potential role in apoptotic signaling. J Biol Chem 2000; 275: 16202–16212.

    PubMed  CAS  Google Scholar 

  13. Mihara M, Erster S, Zaika A, et al. p53 has a direct apoptogenic role at the mitochondria. Mol Cell 2003; 11: 577–590.

    Article  CAS  PubMed  Google Scholar 

  14. Dumont P, Leu JI, Della PA, III, George DL, Murphy M. The codon 72 polymorphic variants of p53 have markedly different apoptotic potential. Nat Genet 2003; 33: 357–365.

    Article  CAS  PubMed  Google Scholar 

  15. Schuler M, Bossy-Wetzel E, Goldstein JC, Fitzgerald P, Green DR. p53 induces apoptosis by caspase activation through mitochondrial cytochrome c release. J Biol Chem 2000; 275: 7337–7342.

    Article  CAS  PubMed  Google Scholar 

  16. Chipuk JE, Maurer U, Green DR, Schuler M. Pharmacologic activation of p53 elicits Bax-dependent apoptosis in the absence of transcription. Cancer Cell 2003; 4: 371–381.

    PubMed  CAS  Google Scholar 

  17. Yu SW, Wang H, Poitras MF, et al. Mediation of poly(ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor. Science 2002; 297: 259–263.

    PubMed  CAS  Google Scholar 

  18. Daugas E, Susin SA, Zamzami N, et al. Mitochondrio-nuclear translocation of AIF in apoptosis and necrosis. FASEB J 2000; 14: 729–739.

    PubMed  CAS  Google Scholar 

  19. Arnoult D, Parone P, Martinou JC, Antonsson B, Estaquier J, Ameisen JC. Mitochondrial release of apoptosis-inducing factor occurs downstream of cytochrome c release in response to several proapoptotic stimuli. J Cell Biol 2002; 159: 923–929.

    PubMed  CAS  Google Scholar 

  20. Fonfria E, Dare E, Benelli M, Sunol C, Ceccatelli S. Translocation of apoptosis-inducing factor in cerebellar granule cells exposed to neurotoxic agents inducing oxidative stress. Eur J Neurosci 2002; 16: 2013–2016.

    Article  CAS  PubMed  Google Scholar 

  21. Cregan SP, Fortin A, MacLaurin JG, et al. Apoptosis-inducing factor is involved in the regulation of caspase-independent neuronal cell death. J Cell Biol 2002; 158: 507–517.

    PubMed  CAS  Google Scholar 

  22. Susin SA, Daugas E, Ravagnan L, et al. Two distinct pathways leading to nuclear apoptosis. J Exp Med 2000; 192: 571–580.

    PubMed  CAS  Google Scholar 

  23. Cregan SP, Fortin A, MacLaurin JG, et al. Apoptosis-inducing factor is involved in the regulation of caspase-independent neuronal cell death. J Cell Biol 2002; 158: 507–517.

    PubMed  CAS  Google Scholar 

  24. Fan S, Smith ML, Rivet DJ, et al. Disruption of p53 function sensitizes breast cancer MCF-7 cells to cisplatin and pentoxifylline. Cancer Res 1995; 55: 1649–1654.

    PubMed  CAS  Google Scholar 

  25. Kim HJ, Mun JY, Chun YJ, Choi KH, Kim MY. Bax-dependent apoptosis induced by ceramide in HL-60 cells. FEBS Lett 2001; 505: 264–268.

    PubMed  CAS  Google Scholar 

  26. Skulachev VP. Why are mitochondria involved in apoptosis? Permeability transition pores and apoptosis as selective mechanisms to eliminate superoxide-producing mitochondria and cell. FEBS Lett 1996; 397: 7–10.

    Article  CAS  PubMed  Google Scholar 

  27. Zamzami N, Susin SA, Marchetti P, et al. Mitochondrial control of nuclear apoptosis. J Exp Med 1996; 183: 1533–1544.

    PubMed  CAS  Google Scholar 

  28. Shibata MA, Liu ML, Knudson MC, et al. Haploid loss of bax leads to accelerated mammary tumor development in C3(1)/SV40-TAg transgenic mice: Reduction in protective apoptotic response at the preneoplastic stage. EMBO J 1999; 18: 2692–2701.

    PubMed  CAS  Google Scholar 

  29. Polyak K, Xia Y, Zweier JL, Kinzler KW, Vogelstein B. A model for p53-induced apoptosis. Nature 1997; 389: 300–305.

    Article  CAS  PubMed  Google Scholar 

  30. Susin SA, Zamzami N, Kroemer G. Mitochondria as regulators of apoptosis: Doubt no more. Biochim Biophys Acta 1998; 1366: 151–165.

    PubMed  CAS  Google Scholar 

  31. Green DR, Reed JC. Mitochondria and apoptosis. Science 1998; 281: 1309–1312.

    Article  CAS  PubMed  Google Scholar 

  32. Janicke RU, Sprengart ML, Wati MR, Porter AG. Caspase-3 is required for DNA fragmentation and morphological changes associated with apoptosis. J Biol Chem 1998; 273: 9357–9360.

    Article  CAS  PubMed  Google Scholar 

  33. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular characterization of mitochondrial apoptosis-inducing factor. Nature 1999; 397: 441–446.

    Article  CAS  PubMed  Google Scholar 

  34. Daugas E, Nochy D, Ravagnan L, et al. Apoptosis-inducing factor (AIF): A ubiquitous mitochondrial oxidoreductase involved in apoptosis. FEBS Lett 2000; 476: 118–123.

    PubMed  CAS  Google Scholar 

  35. Fan LZ, Cherian MG. Potential role of p53 on metallothionein induction in human epithelial breast cancer cells. Br J Cancer 2002; 87: 1019–1026.

    PubMed  CAS  Google Scholar 

  36. Fan L, Cherian MG. Toxicology 2002; 36: 154

    Google Scholar 

  37. Ostrakhovitch EA, Cherian MG. Differential regulation of signal transduction pathways in wild type and mutated p53 breast cancer epithelial cells by copper and zinc. Arch Biochem Biophys 2004; 423: 351–361.

    PubMed  CAS  Google Scholar 

  38. Pourahmad J, O’Brien PJ. A comparison of hepatocyte cytotoxic mechanisms for Cu2+ and Cd2+. Toxicology 2000; 143: 263–273.

    PubMed  CAS  Google Scholar 

  39. Luza SC, Speisky HC. Liver copper storage and transport during development: Implications for cytotoxicity. Am J Clin Nutr 1996; 63: 812S–820S.

    PubMed  CAS  Google Scholar 

  40. Gyulkhandanyan AV, Feeney CJ, Pennefather PS. Modulation of mitochondrial membrane potential and reactive oxygen species production by copper in astrocytes. J Neurochem 2003; 87: 448–460.

    PubMed  CAS  Google Scholar 

  41. Barbieri D, Troiano L, Grassilli E, et al. Inhibition of apoptosis by zinc: A reappraisal. Biochem Biophys Res Commun 1992; 187: 1256–1261.

    PubMed  CAS  Google Scholar 

  42. Szuster-Ciesielska A, Stachura A, Slotwinska M, et al. The inhibitory effect of zinc on cadmium-induced cell apoptosis and reactive oxygen species (ROS) production in cell cultures. Toxicology 2000; 145: 159–171.

    PubMed  CAS  Google Scholar 

  43. Kondoh M, Tasaki E, Araragi S, et al. Requirement of caspase and p38MAPK activation in zinc-induced apoptosis in human leukemia HL-60 cells. Eur J Biochem 2002; 269: 6204–6211.

    PubMed  CAS  Google Scholar 

  44. Liang JY, Liu YY, Zou J, Franklin RB, Costello LC, Feng P. Inhibitory effect of zinc on human prostatic carcinoma cell growth. Prostate 1999; 40: 200–207.

    PubMed  CAS  Google Scholar 

  45. Telford WG, Fraker PJ. Preferential induction of apoptosis in mouse CD4+CD8+ alpha beta TCRloCD3 epsilon lo thymocytes by zinc. J Cell Physiol 1995; 164: 259–270.

    PubMed  CAS  Google Scholar 

  46. Cohen JJ, Duke RC. Glucocorticoid activation of a calcium-dependent endonuclease in thymocyte nuclei leads to cell death. J Immunol 1984; 132: 38–42.

    PubMed  CAS  Google Scholar 

  47. Fraker PJ, Telford WG. A reappraisal of the role of zinc in life and death decisions of cells. Proc Soc Exp Biol Med 1997; 215: 229–236.

    PubMed  CAS  Google Scholar 

  48. Sunderman FW, Jr. The influence of zinc on apoptosis. Ann Clin Lab Sci 1995; 25: 134–142.

    CAS  PubMed  Google Scholar 

  49. Sensi SL, Yin HZ, Carriedo SG, Rao SS, Weiss JH. Preferential Zn2+ influx through Ca2+-permeable AMPA/kainate channels triggers prolonged mitochondrial superoxide production. Proc Natl Acad Sci USA 1999; 96: 2414–2419.

    PubMed  CAS  Google Scholar 

  50. Gazaryan IG, Krasnikov BF, Ashby GA, Thorneley RN, Kristal BS, Brown AM. Zinc is a potent inhibitor of thiol oxidoreductase activity and stimulates reactive oxygen species production by lipoamide dehydrogenase. J Biol Chem 2002; 277: 10064–10072.

    PubMed  CAS  Google Scholar 

  51. Skulachev VP, Chistyakov VV, Jasaitis AA, Smirnova EG. Inhibition of the respiratory chain by zinc ions. Biochem Biophys Res Commun 1967; 26: 1–6.

    PubMed  CAS  Google Scholar 

  52. Lorusso M, Cocco T, Sardanelli AM, Minuto M, Bonomi F, Papa S. Interaction of Zn2+ with the bovine-heart mitochondrial bc1 complex. Eur J Biochem 1991; 197: 555–561.

    PubMed  CAS  Google Scholar 

  53. Dineley KE, Votyakova TV, Reynolds IJ. Zinc inhibition of cellular energy production: Implications for mitochondria and neurodegeneration. J Neurochem 2003; 85: 563–570.

    Article  PubMed  CAS  Google Scholar 

  54. Berry EA, Zhang Z, Bellamy HD, Huang L. Crystallographic location of two Zn(2+)-binding sites in the avian cytochrome bc(1) complex. Biochim Biophys Acta 2000; 1459: 440– 448.

    PubMed  CAS  Google Scholar 

  55. Ye J, Wang S, Leonard SS, et al. Role of reactive oxygen species and p53 in chromium(VI)-induced apoptosis. J Biol Chem 1999; 274: 34974–34980.

    PubMed  CAS  Google Scholar 

  56. el Deiry WS, Tokino T, Velculescu VE, et al. WAF1, a potential mediator of p53 tumor suppression. Cell 1993; 75: 817–825.

    PubMed  CAS  Google Scholar 

  57. Contente A, Dittmer A, Koch MC, Roth J, Dobbelstein M. A polymorphic microsatellite that mediates induction of PIG3 by p53. Nat Genet 2002; 30: 315–320.

    PubMed  Google Scholar 

  58. Fleming JA, Lightcap ES, Sadis S, Thoroddsen V, Bulawa CE, Blackman RK. Complementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341. Proc Natl Acad Sci USA 2002; 99: 1461–1466.

    PubMed  CAS  Google Scholar 

  59. Martinou JC. Apoptosis. Key to the mitochondrial gate. Nature 1999; 399: 411–412.

    PubMed  CAS  Google Scholar 

  60. Marzo I, Brenner C, Zamzami N, et al. Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis. Science 1998; 281: 2027–2031.

    PubMed  CAS  Google Scholar 

  61. Shimizu S, Narita M, Tsujimoto Y. Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC. Nature 1999; 399: 483–487.

    Article  CAS  PubMed  Google Scholar 

  62. Brenner C, Cadiou H, Vieira HL, et al. Bcl-2 and Bax regulate the channel activity of the mitochondrial adenine nucleotide translocator. Oncogene 2000; 19: 329–336.

    PubMed  CAS  Google Scholar 

  63. Zamzami N, Marchetti P, Castedo M, et al. Reduction in mitochondrial potential constitutes an early irreversible step of programmed lymphocyte death in vivo. J Exp Med 1995; 181: 1661–1672.

    Article  CAS  PubMed  Google Scholar 

  64. Martinou JC, Desagher S, Antonsson B. Cytochrome c release from mitochondria: All or nothing. Nat Cell Biol 2000; 2: E41–E43.

    PubMed  CAS  Google Scholar 

  65. Garcia N, Zazueta C, Carrillo R, Correa F, Chavez E. Copper sensitizes the mitochondrial permeability transition to carboxytractyloside and oleate. Mol Cell Biochem 2000; 209: 119–123.

    PubMed  CAS  Google Scholar 

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Ostrakhovitch, E.A., Cherian, M.G. Role of p53 and reactive oxygen species in apoptotic response to copper and zinc in epithelial breast cancer cells. Apoptosis 10, 111–121 (2005). https://doi.org/10.1007/s10495-005-6066-7

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