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Changes in plasma thiol levels induced by different phases of treatment in breast cancer; the role of commercial extract from black chokeberry

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Abstract

Different low-molecular-weight thiols, including glutathione, cysteine, and cysteinylglycine are physiological free radical scavengers. On the other hand, homocysteine may play a role as an oxidant. The aim of our present study was to establish in vitro the effects of the commercial extract of Aronia melanocarpa (Aronox®) on the amount of selected low-molecular-weight thiols and the activity of antioxidative enzymes (superoxide dismutase, glutathione peroxidase, and glutathione reductase) in plasma obtained from patients with invasive breast cancer during different phases of treatment [before or after the surgery and patients after different phases of chemotherapy (doxorubicin and cyclophosphamide)] and from healthy subjects. Patients were hospitalized in Department of Oncological Surgery and Department of Chemotherapy, Medical University of Lodz, Poland. The level of low-molecular-weight thiols was determined by high-performance liquid chromatography. We observed that in the presence of the Aronia extract changes in amount of thiols in plasma from breast cancer patients (at all tested groups) were significantly reduced. Our results showed that tested commercial extract reduced modifications of antioxidative enzymes activity in plasma from patients during different phases of treatment, but this effect was not statistical significant. Our results suggest that the Aronia extract supplementation in breast cancer patients has a beneficial effect on thiols concentration in plasma. Plasma, as reported in this work, could be used as an experimental model to evaluate the beneficial action of plant supplements, including phenolic extracts on thiols or other molecules during different phases of treatment.

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References

  1. Keppler BK (1993) Metal complexes in cancer chemotherapy. General remarks. In: Keppler BK (ed) Metal complexes in cancer chemotherapy. VCH, Weinheim, pp 1–8

    Google Scholar 

  2. Strumberg D, Brugge S, Korn MW, Koeppen S, Ranft J, Scheiber G, Reiners C, Mockel C, Seeber S, Scheulen ME (2002) Evaluation of long-term toxicity in patients after cisplatin-based chemotherapy for non-seminomatous testicular cancer. Ann Oncol 13:229–236

    Article  PubMed  CAS  Google Scholar 

  3. Gonenc A, Erten D, Aslan S, Akinci M, Simsek B, Torun M (2006) Lipid peroxidation and antioxidant status in blood and tissue of malignant breast tumor and benign breast disease. Cell Biol Int 30:376–380

    Article  PubMed  Google Scholar 

  4. Delimaris I, Faviou E, Antonakos G, Stathoulou E, Zachari A, Dioyssiou-Aseriou A (2007) Oxidized LDL, serum oxidizability and serum lipid levels in patients with breast and ovarian cancer. Clin Biochem 40:1129–1134

    Article  PubMed  CAS  Google Scholar 

  5. Erten-Sener D, Goenenc A, Akinci M, Akinci M, Torun M (2007) Lipid peroxidation and total antioxidant status in patients with breast cancer. Cell Biochem Funct 25:377–382

    Article  Google Scholar 

  6. Kasapović J, Pejić S, Todorović A, Stojilijkovic V, Pajovic SB (2008) Antioxidant status and lipid peroxidation on the blood of breast cancer patients in different ages. Cell Biochem Funct 26:723–730

    Article  PubMed  Google Scholar 

  7. Hamo-Mahmood I, Abdullah KS, Abdullah MS (2009) Total antioxidant status in women with breast cancer. Pak J Med Sci 4:609–612

    Google Scholar 

  8. Trachootham D, Alexandre J, Huang P (2009) Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach? Nat Rev Drug Discov 8:579–591

    Article  PubMed  CAS  Google Scholar 

  9. Kędzierska M, Olas B, Wachowicz B, Stochmal A, Oleszek W, Jeziorski A, Piekarski J (2010) The nitrative and oxidative stress in blood platelets isolated from breast cancer patients; the protectory action of Aronia melanocarpa extract. Platelets 21:541–548

    Article  PubMed  Google Scholar 

  10. Kędzierska M, Olas B, Wachowicz B, Jeziorski A, Piekarski J (2012) Relationship between thiol, tyrosine nitration and carbonyl formation as biomarkers of oxidative stress and changes of hemostatic function of plasma isolated from breast cancer patients before surgery. Clin Biochem 45:231–236

    Article  PubMed  Google Scholar 

  11. Yaneva MP, Botushanova AD, Grigorov LA, Kokov JL, Todorova EP, Krachanova MP (2002) Evaluation of the immunomodulatory activity of Aronia in combination with apple pectin in patients with breast cancer undergoing postoperative radiation therapy. Folia Med 44:22–25

    Google Scholar 

  12. Valko M, Rhodes CJ, Moncol J, Izakovic M, Mazur M (2006) Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem Biol Interact 160:1–40

    Article  PubMed  CAS  Google Scholar 

  13. Savouret JF, Quesne M (2002) Resveratrol and cancer: a review. Biomed Pharmacother 56:84–87

    Article  PubMed  CAS  Google Scholar 

  14. Malik M, Zhao C, Schoene N, Guisti MM, Moyer MP, Magnuson BA (2003) Anthocyanin-rich extract from Aronia melanocarpa E induces a cell cycle block in colon cancer but not normal colonic cells. Nutr Cancer 46:186–196

    Article  PubMed  CAS  Google Scholar 

  15. Lala G, Mailk M, Zhao C, He J, Kwon Y, Giusti MM, Magnuson BA (2006) Anthocyanin-rich extracts inhibit multiple biomarkers of colon cancer in rats. Nutr Cancer 54:84–93

    Article  PubMed  CAS  Google Scholar 

  16. Kędzierska M, Olas B, Wachowicz B, Stochmal A, Oleszek W, Jeziorski A, Piekarski J, Głowacki R (2009) An extract from berries of Aronia melanocarpa modulates the generation of superoxide anion radicals in blood platelets from breast cancer patients. Planta Med 75:1405–1409

    Article  PubMed  Google Scholar 

  17. Olas B, Wachowicz B, Nowak P, Kędzierska M, Tomczak A, Stochmal A, Oleszek W, Jeziorski A, Piekarski J (2008) Studies on antioxidant properties of polyphenol-rich extract from berries of Aronia melanocarpa on blood platelets. J Physiol Pharmacol 59:823–835

    PubMed  CAS  Google Scholar 

  18. Ryszawa N, Kawczynska-Drozdz A, Pryjma J, Czesnikiewicz-Guzik M, Adamek-Guzik T, Naruszewicz M et al (2006) Effects of novel plant antioxidants on platelet superoxide production and aggregation in arteriosclerosis. J Physiol Pharmacol 57:611–626

    PubMed  CAS  Google Scholar 

  19. Glowacki R, Bald E (2009) Fully automated method for simultaneous determination of cysteine, cysteinylglycine, glutathione and homocysteine in plasma by high performance liquid chromatography. J Chromatogr B 877:3400–3404

    Article  CAS  Google Scholar 

  20. Bald E, Chwatko G, Glowacki R, Kusmierek K (2004) Analysis of plasma thiols by high-performance liquid chromatography with ultraviolet detection. J Chromatogr 1032:109–115

    Article  CAS  Google Scholar 

  21. Olas B, Kędzierska M, Wachowicz B, Stochmal A, Oleszek W, Jeziorski A, Piekarski J, Glowacki R (2010) Effect of aronia on thiol levels in plasma of breast cancer patients. Central Eur J Biol 5:38–46

    Article  Google Scholar 

  22. Kedzierska M, Olas B, Wachowicz B, Glowacki R, Bald E, Czernek U, Szydłowska-Pazera K, Potemski P, Piekarski J, Jeziorski A (2012) Effects of the commercial extract of aronia on oxidative stress in blood platelets isolated from breast cancer patients after the surgery and various phases of the chemotherapy. Fitoterapia 83:310–317

    Article  PubMed  CAS  Google Scholar 

  23. Engin A (1995) Elevated glutathione levels in erythrocyte of human with gastrointestinal adenocarcinoma. Hacettepe Bull Med Surg 8:66

    Google Scholar 

  24. Kumar A, Sharma S, Pundir CS, Sharma A (1995) Decreased plasma glutathione in cancer of the utefne cervix. Cancer Lett 94:107–110

    Article  PubMed  CAS  Google Scholar 

  25. Della Rovere F, Granata A, Saija A, Broccio M, Tomaino A, Zirilli A, De Caridi G, Broccio G (2000) SH groups and glutathione in cancer patient’s blood. Anticancer Res 20:1595–1598

    PubMed  CAS  Google Scholar 

  26. Jordan J, d’Arcy Doherty M, Cohen GM (1987) Effects of glutathione depletion on the cytotoxicity of agents toward a human colonic tumour cell line. Br J Cancer 55:627–631

    Article  PubMed  CAS  Google Scholar 

  27. Calvert P, Yao KS, Hamilton TC, O’Dwyer PJ (1988) Clinical studies of reversal of drug resistance based on glutathione. Chem Biol Interact 111–112:213–224

    Google Scholar 

  28. Estrela JM, Ortega A, Obrador E (2006) Glutathione in cancer biology and therapy. Crit Rev Clin Lab Sci 43:143–181

    Article  PubMed  CAS  Google Scholar 

  29. Mena S, Benlloch M, Ortega A, Carretero J, Obrador E, Asensi M, Petchen I, Brown BD, Estrela JM (2007) Bcl-2 and glutathione depletion sensitizes B16 melanoma to combination therapy and eliminates metastatic disease. Clin Cancer Res 13:2658–2666

    Article  PubMed  CAS  Google Scholar 

  30. Jakubowski H (1997) Metabolism of homocysteine thiolactone in human cell cultures. J Biol Chem 272:1935–1940

    PubMed  CAS  Google Scholar 

  31. Gatt A, Makris A, Cladd H, Burcombe RJ, Smith JM, Cooper P, Thomson D, Makris M (2008) Hyperhomocysteinemia in women with advanced breast cancer. Int J Lab Hematol 29:421–425

    Article  Google Scholar 

  32. Kędzierska M, Malinowska J, Glowacki R, Olas B, Bald E, Jeziorski A, Piekarski J (2011) The elevated homocysteine stimulates changes of hemostatic function of plasma isolated from breast cancer patients. Mol Cell Biochem 355:193–199

    Article  PubMed  Google Scholar 

  33. Chrubasik C, Li G, Chrubasik S (2010) The clinical effectiveness of chokeberry: a systematic review. Phytother Res 24:1107–1114

    PubMed  CAS  Google Scholar 

  34. Greenlee H, Hershman DL, Jacobson JS (2009) Use of antioxidant supplements during breast cancer treatment: a comprehensive review. Breast Cancer Res Treat 115:437–452

    Article  PubMed  CAS  Google Scholar 

  35. Rockenbach G, Di Pietro PF, Ambrosi C, Boaventura BC, Vieira FG, Crippa CG, Da Silva EL, Fausto MA (2011) Dietary intake and oxidative stress in breast cancer: before and after treatments. Nutr Hosp 26:737–744

    PubMed  CAS  Google Scholar 

  36. Sharhar S, Normah H, Fatimah A, Fadilah RN, Rohi GA, Amin I, Cham BG, Rizal RM, Fairulnizal MN (2008) Antioxidant intake and status, and oxidative stress in relation to breast cancer risk: a case-control study. Asian Pac J Cancer Prev 9:343–350

    PubMed  Google Scholar 

  37. Hakimuddin F, Paliyath G, Meckling K (2004) Selective cytotoxicity of a red grape wine flavonoid fraction against MCF-7 cells. Breast Cancer Res Treat 85:5–79

    Article  Google Scholar 

  38. Kulling SE, Rawel HM (2008) Chokeberry (Aronia melanocarpa): a review on the characteristic components and potential health effects. Planta Med 74:1625–1634

    Article  PubMed  CAS  Google Scholar 

  39. Skoczynska A, Jedrychowska I, Poreba R, Affelska-Jercha A, Turczyn B, Wojakowska A (2007) Influence of chokeberry juice on arteria blood pressure and lipid parameters in men with mild hypercholesterolemia. Pharmacol Rep 59:177–180

    Google Scholar 

  40. Kowalczyk E, Fijalkowski P, Kura M, Krzesinski P, Blaszczyk J, Kowalski J, Smigielski J, Rutkowski M, Kopff M (2005) The influence of anthocyanins from Aronia melanocarpa on selected parameters of oxidative stress and microelements contents in men with hypercholesterolemia. Pol Merkur Lekarski 19:651–653

    PubMed  Google Scholar 

  41. Manach C, Scalbert A, Morand C, Remesy C, Jimenez L (2004) Polyphenols: food sources and bioavailability. Am J Clin Nutr 89:727–747

    Google Scholar 

  42. Manach C, Williamson G, Morand C, Scalbert A, Remesy C (2005) Bioavailability and bioefficacy of polyphenols in humans. I. Review of 97 bioavailability studies. Am J Clin Nutr 81:230–242

    Google Scholar 

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Acknowledgments

Supported by the Grant 506/810 from University of Lodz, Poland.

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Correspondence to Beata Olas.

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Kędzierska, M., Głowacki, R., Czernek, U. et al. Changes in plasma thiol levels induced by different phases of treatment in breast cancer; the role of commercial extract from black chokeberry. Mol Cell Biochem 372, 47–55 (2013). https://doi.org/10.1007/s11010-012-1444-2

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  • DOI: https://doi.org/10.1007/s11010-012-1444-2

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