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Thiol – Disulphide Homeostasis in Polycythemia Vera

Year 2019, Volume: 46 Issue: 2, 315 - 320, 11.06.2019
https://doi.org/10.5798/dicletip.574893

Abstract

Background: Thiol-disulphide homeostasis has vital role in cell signalling mechanisms, regulation of transcription factors and enzymatic activities, signal transduction and regulation of proliferation rate, apoptosis and detoxification and antioxidant protective mechanism. 
Objective: This study aims to demonstrate in Polycythemia Vera (PV) patients the thioldisulphide homeostasis which is known to play a role in cell proliferation, apoptosis and various steps of cell cycle. 
Design: Descriptive prospective cross-sectional study. 
Settings: Yildirim Beyazıt University Hospital Ankara, Turkey between 2016-2018. 
Method: Forty-two PV patients and 43 healthy controls were included in the study. Serum total (–SH + –S–S–) and native (–SH) thiol levels were measured in all subjects. The amount of dynamic disulphide bonds and, the ratio of (–S–S–) and (–S–S–) × 100/(–SH), (–S–S–) × 100/(–SH + –S–S–), and –SH ×100/(–SH + –S–S–) were calculated with automatic method. The data obtained from the patient group were compared with the control group. 
Main outcome measures: The amount of dynamic disulphide bonds and, the ratio of (–S–S–) and (–S–S–) × 100/(–SH), (–S–S–) × 100/(–SH + –S–S–), and –SH ×100/(–SH + –S–S–) were calculated with automatic method in PV patieint and healthy control group. Results: Both groups were similar in terms of age and gender distribution. Compared with the control group, PV group had significantly higher native thiol, total thiol and nativ/total thiol levels.  
Limitation: The generalizability of the study's findings were limited by the small sample size. 
Conclusions: In accordance with the nature of the disease, thiol balance in PV patients was in favor of proliferation. Increased total thiol (–SH + –S–S), native thiol (–SH) levels and native thiol/total thiol ratio might be associated with uncontrolled proliferation. The balance of the thiol-disulphide homeostasis shifted to reductive thiol side in the PV. This change can provocate proliferation status of the disease and/or may be secondary to the disease. 
Conflict of Interest: No conflict of interest was declared by the authors.  

References

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  • 2. Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014; 47: 326- 32.
  • 3. Turell L, Radi R, Alvarez B. The thiol pool in human plasma: the central contribution of albumin to redox processes. Free Radic Biol Med. 2013; 65: 244-53.
  • 4. Kundi H, Erel Ö, Balun A, et all. Association of thiol/disulfide ratio with syntax score in patients with NSTEMI. Scand Cardiovasc J. 2015; 49: 95-100.
  • 5. Li W, Busu C, Circu ML, Aw TY. Glutathione in cerebral microvascular endothelial biology and pathobiology: implications for brain homeostasis. Int J Cell Biol. 2012: 434971.
  • 6. Wondrak GT. Redox-directed cancer therapeutics: molecular mechanisms and opportunities. Antioxid Redox Signal. 2009; 11: 3013-69.
  • 7. Kundi H, Ates I, Kiziltunc E, et all. A novel oxidative stress marker in acute myocardial infarction; thiol/disulphide homeostasis. Am J Emerg Med. 2015; 33: 1567-71.
  • 8. Ateş İ, Ozkayar N, Altay M, et all. Is disulphide/thiol ratio related to blood pressure in masked hypertension? Clin Exp Hypertens. 2016; 38: 150-4
  • 9. Ates I, Kaplan M, Yuksel M, et all. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine. 2016; 51: 47-51.
  • 10. Korkmaz V, Kurdoglu Z, Alisik M, et all. Impairment of thiol-disulphide homeostasis in preeclampsia. J Matern Fetal Neonatal Med. 2016; 3: 1-6
  • 11. Bektas H, Vural G, Gumusyayla S et all. Dynamic thiol-disulphide homeostasis in acute ischemic stroke patients. Acta Neurol Belg. 2016; 116: 489-94.
  • 12. Prabhu A, Sarcar B, Kahali S, et all. Cysteine catabolism: a novel metabolic pathway contributing to glioblastoma growth. Cancer Res. 2014; 74: 787–96.
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  • 14. Nkabyo YS, Ziegler TR, Gu LH, et all. Glutathione and thioredoxin redox during differentiation in human colon epithelial (Caco-2) cells. Am J Physiol Gastrointest Liver Physiol 2002; 283: 1352–9.
  • 15. Michiels J.J.,Berneman Z.,Schroyens W, et all. Changing Concepts of Diagnostic Criteria of Myeloproliferative Disorders and the Molecular Etiology and Classification of Myeloproliferative Neoplasms: From Dameshek 1950 to Vainchenker 2005 and Beyond, Acta Haematologica. 2015; 133: 36-51.
  • 16. Cao HC, Lin J, Qian J, et all. Detection of the JAK2 mutation in myeloproliferative neoplasms by asymmetric PCR with unlabeled probe and high-resolution melt analysis. J Clin Lab Anal. 2011; 25: 300-4. doi: 10.1002/jcla.20474.
  • 17. Andersen CL, Bjørn ME, McMullin MF, et all l. Circulating YKL-40 in patients with essential thrombocythemia and polycythemia vera treated with the novel histone deacetylase inhibitor vorinostat. Leuk Res. 2014; 38: 816-21.
  • 18. Bjørn ME, Andersen CL, Jensen MK, et all. Circulating YKL-40 in myelofibrosis a potential novel biomarker of disease activity and the inflammatory state. Eur J Haematol. 2014; 93: 224-8.
  • 19. Klampfl T, Gisslinger H, Harutyunyan AS, et all. Somatic mutations of calreticulin in myeloproliferative neoplasms. N Engl J Med. 2013; 369: 2379-90.
  • 20. Bruchova H, Yoon D, Agarwal AM, et all. Erythropoiesis in polycythemia vera is hyper-proliferative and has accelerated maturation. Blood Cells Mol Dis. 2009; 43: 81-7.
  • 21. Laubach JP, Fu P, Jiang X, et all. Polycythemia vera erythroid precursors exhibit increased proliferation and apoptosis resistance associated with abnormal RAS and PI3K pathway activation. Exp Hematol. 2009; 37: 1411-22.
  • 22. Blume KG, Paniker NV, Beutler E. Enzymes of glutathione synthesis in patients with myeloproliferative disorders. Clin Chim Acta. 1973; 45: 281- 5.
  • 23. Ates I, Kaplan M, Yuksel M, et all. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine. 2016; 1: 47-51.
  • 24. Yıldırım F, Sermetow K, Aycicek A, et all. Increased oxidative stress in preschool children exposed to passive smoking. J Pediatr (Rio J). 2011; 87: 523-8.
  • 25. Ozler S, Oztas E, Erel O, et al. Impact of Gestational Diabetes Mellitus and Maternal Obesity on Cord Blood Dynamic Thiol/Disulfide Homeostasis. Fetal Pediatr Pathol. 2017; 36: 8-15. doi: 10.1080/15513815.2016.1223237.
  • 26. Babaoglu E, Kilic H, Hezer H, et all. Comparison of thiol/disulphide homeostasis parameters in patients with COPD, asthma and ACOS. Eur Rev Med Pharmacol Sci. 2016; 20: 1537-43.
  • 27. Hanikoglu F, Hanikoglu A, Kucuksayan E, et al. Dynamic Thiol/Disulphide Homeostasis Before and After Radical Prostatectomy in Patients with Prostate Cancer. Free Radic Res. 2016; 50: S79-S84
  • 28. Dirican N, Dirican A, Sen O, et al. Thiol/disulfide homeostasis: A prognostic biomarker for patients with advanced non-small cell lung cancer? Redox Rep. 2016; 21: 197-203.
  • 29. Guney T, Kanat IF, Alkan A, et al. Assessment of serum thiol/disulfide homeostasis in multiple myeloma patients by a new method. Redox Report. 2017;22: 246- 51. doi: 10.1080/13510002.2016.1180100.
  • 30. Aldemir M, Karaguzel E, Okulu E, et all. Evaluation of oxidative stress status and antioxidant capacity in patients with renal cell carcinoma. Cent European J Urol. 2015; 68: 415-20.
Year 2019, Volume: 46 Issue: 2, 315 - 320, 11.06.2019
https://doi.org/10.5798/dicletip.574893

Abstract

References

  • 1. Ruben A. Mesa, Murray N. Silverstein, et all. Population-based incidence and survival figures in essential thrombocythemia and agnogenic myeloid metaplasia: an Olmsted County Study, 1976-1995. Am J Hematol. 1999; 61: 10-5.
  • 2. Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014; 47: 326- 32.
  • 3. Turell L, Radi R, Alvarez B. The thiol pool in human plasma: the central contribution of albumin to redox processes. Free Radic Biol Med. 2013; 65: 244-53.
  • 4. Kundi H, Erel Ö, Balun A, et all. Association of thiol/disulfide ratio with syntax score in patients with NSTEMI. Scand Cardiovasc J. 2015; 49: 95-100.
  • 5. Li W, Busu C, Circu ML, Aw TY. Glutathione in cerebral microvascular endothelial biology and pathobiology: implications for brain homeostasis. Int J Cell Biol. 2012: 434971.
  • 6. Wondrak GT. Redox-directed cancer therapeutics: molecular mechanisms and opportunities. Antioxid Redox Signal. 2009; 11: 3013-69.
  • 7. Kundi H, Ates I, Kiziltunc E, et all. A novel oxidative stress marker in acute myocardial infarction; thiol/disulphide homeostasis. Am J Emerg Med. 2015; 33: 1567-71.
  • 8. Ateş İ, Ozkayar N, Altay M, et all. Is disulphide/thiol ratio related to blood pressure in masked hypertension? Clin Exp Hypertens. 2016; 38: 150-4
  • 9. Ates I, Kaplan M, Yuksel M, et all. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine. 2016; 51: 47-51.
  • 10. Korkmaz V, Kurdoglu Z, Alisik M, et all. Impairment of thiol-disulphide homeostasis in preeclampsia. J Matern Fetal Neonatal Med. 2016; 3: 1-6
  • 11. Bektas H, Vural G, Gumusyayla S et all. Dynamic thiol-disulphide homeostasis in acute ischemic stroke patients. Acta Neurol Belg. 2016; 116: 489-94.
  • 12. Prabhu A, Sarcar B, Kahali S, et all. Cysteine catabolism: a novel metabolic pathway contributing to glioblastoma growth. Cancer Res. 2014; 74: 787–96.
  • 13. Kirlin WG, Cai J, Thompson SA, et all. Glutathione redox potential in response to differentiation and enzyme inducers. Free Radic Biol Med. 1999; 27: 1208–18.
  • 14. Nkabyo YS, Ziegler TR, Gu LH, et all. Glutathione and thioredoxin redox during differentiation in human colon epithelial (Caco-2) cells. Am J Physiol Gastrointest Liver Physiol 2002; 283: 1352–9.
  • 15. Michiels J.J.,Berneman Z.,Schroyens W, et all. Changing Concepts of Diagnostic Criteria of Myeloproliferative Disorders and the Molecular Etiology and Classification of Myeloproliferative Neoplasms: From Dameshek 1950 to Vainchenker 2005 and Beyond, Acta Haematologica. 2015; 133: 36-51.
  • 16. Cao HC, Lin J, Qian J, et all. Detection of the JAK2 mutation in myeloproliferative neoplasms by asymmetric PCR with unlabeled probe and high-resolution melt analysis. J Clin Lab Anal. 2011; 25: 300-4. doi: 10.1002/jcla.20474.
  • 17. Andersen CL, Bjørn ME, McMullin MF, et all l. Circulating YKL-40 in patients with essential thrombocythemia and polycythemia vera treated with the novel histone deacetylase inhibitor vorinostat. Leuk Res. 2014; 38: 816-21.
  • 18. Bjørn ME, Andersen CL, Jensen MK, et all. Circulating YKL-40 in myelofibrosis a potential novel biomarker of disease activity and the inflammatory state. Eur J Haematol. 2014; 93: 224-8.
  • 19. Klampfl T, Gisslinger H, Harutyunyan AS, et all. Somatic mutations of calreticulin in myeloproliferative neoplasms. N Engl J Med. 2013; 369: 2379-90.
  • 20. Bruchova H, Yoon D, Agarwal AM, et all. Erythropoiesis in polycythemia vera is hyper-proliferative and has accelerated maturation. Blood Cells Mol Dis. 2009; 43: 81-7.
  • 21. Laubach JP, Fu P, Jiang X, et all. Polycythemia vera erythroid precursors exhibit increased proliferation and apoptosis resistance associated with abnormal RAS and PI3K pathway activation. Exp Hematol. 2009; 37: 1411-22.
  • 22. Blume KG, Paniker NV, Beutler E. Enzymes of glutathione synthesis in patients with myeloproliferative disorders. Clin Chim Acta. 1973; 45: 281- 5.
  • 23. Ates I, Kaplan M, Yuksel M, et all. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine. 2016; 1: 47-51.
  • 24. Yıldırım F, Sermetow K, Aycicek A, et all. Increased oxidative stress in preschool children exposed to passive smoking. J Pediatr (Rio J). 2011; 87: 523-8.
  • 25. Ozler S, Oztas E, Erel O, et al. Impact of Gestational Diabetes Mellitus and Maternal Obesity on Cord Blood Dynamic Thiol/Disulfide Homeostasis. Fetal Pediatr Pathol. 2017; 36: 8-15. doi: 10.1080/15513815.2016.1223237.
  • 26. Babaoglu E, Kilic H, Hezer H, et all. Comparison of thiol/disulphide homeostasis parameters in patients with COPD, asthma and ACOS. Eur Rev Med Pharmacol Sci. 2016; 20: 1537-43.
  • 27. Hanikoglu F, Hanikoglu A, Kucuksayan E, et al. Dynamic Thiol/Disulphide Homeostasis Before and After Radical Prostatectomy in Patients with Prostate Cancer. Free Radic Res. 2016; 50: S79-S84
  • 28. Dirican N, Dirican A, Sen O, et al. Thiol/disulfide homeostasis: A prognostic biomarker for patients with advanced non-small cell lung cancer? Redox Rep. 2016; 21: 197-203.
  • 29. Guney T, Kanat IF, Alkan A, et al. Assessment of serum thiol/disulfide homeostasis in multiple myeloma patients by a new method. Redox Report. 2017;22: 246- 51. doi: 10.1080/13510002.2016.1180100.
  • 30. Aldemir M, Karaguzel E, Okulu E, et all. Evaluation of oxidative stress status and antioxidant capacity in patients with renal cell carcinoma. Cent European J Urol. 2015; 68: 415-20.
There are 30 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Original Articles
Authors

Aysun Şentürk Yıkılmaz This is me 0000-0001-5281-5955

Şule Mine Bakanay This is me 0000-0003-3941-0368

Sema Akinci This is me 0000-0003-4237-3342

Senem Maral This is me 0000-0003-4766-1861

Fuad Mustafayev This is me

Murat Alisik This is me 0000-0003-0434-3206

Özcan Erel This is me 0000-0002-2996-3236

İmdat Dilek This is me

Publication Date June 11, 2019
Submission Date December 13, 2018
Published in Issue Year 2019 Volume: 46 Issue: 2

Cite

APA Şentürk Yıkılmaz, A., Bakanay, Ş. M., Akinci, S., Maral, S., et al. (2019). Thiol – Disulphide Homeostasis in Polycythemia Vera. Dicle Tıp Dergisi, 46(2), 315-320. https://doi.org/10.5798/dicletip.574893
AMA Şentürk Yıkılmaz A, Bakanay ŞM, Akinci S, Maral S, Mustafayev F, Alisik M, Erel Ö, Dilek İ. Thiol – Disulphide Homeostasis in Polycythemia Vera. diclemedj. June 2019;46(2):315-320. doi:10.5798/dicletip.574893
Chicago Şentürk Yıkılmaz, Aysun, Şule Mine Bakanay, Sema Akinci, Senem Maral, Fuad Mustafayev, Murat Alisik, Özcan Erel, and İmdat Dilek. “Thiol – Disulphide Homeostasis in Polycythemia Vera”. Dicle Tıp Dergisi 46, no. 2 (June 2019): 315-20. https://doi.org/10.5798/dicletip.574893.
EndNote Şentürk Yıkılmaz A, Bakanay ŞM, Akinci S, Maral S, Mustafayev F, Alisik M, Erel Ö, Dilek İ (June 1, 2019) Thiol – Disulphide Homeostasis in Polycythemia Vera. Dicle Tıp Dergisi 46 2 315–320.
IEEE A. Şentürk Yıkılmaz, Ş. M. Bakanay, S. Akinci, S. Maral, F. Mustafayev, M. Alisik, Ö. Erel, and İ. Dilek, “Thiol – Disulphide Homeostasis in Polycythemia Vera”, diclemedj, vol. 46, no. 2, pp. 315–320, 2019, doi: 10.5798/dicletip.574893.
ISNAD Şentürk Yıkılmaz, Aysun et al. “Thiol – Disulphide Homeostasis in Polycythemia Vera”. Dicle Tıp Dergisi 46/2 (June 2019), 315-320. https://doi.org/10.5798/dicletip.574893.
JAMA Şentürk Yıkılmaz A, Bakanay ŞM, Akinci S, Maral S, Mustafayev F, Alisik M, Erel Ö, Dilek İ. Thiol – Disulphide Homeostasis in Polycythemia Vera. diclemedj. 2019;46:315–320.
MLA Şentürk Yıkılmaz, Aysun et al. “Thiol – Disulphide Homeostasis in Polycythemia Vera”. Dicle Tıp Dergisi, vol. 46, no. 2, 2019, pp. 315-20, doi:10.5798/dicletip.574893.
Vancouver Şentürk Yıkılmaz A, Bakanay ŞM, Akinci S, Maral S, Mustafayev F, Alisik M, Erel Ö, Dilek İ. Thiol – Disulphide Homeostasis in Polycythemia Vera. diclemedj. 2019;46(2):315-20.