Peculiarities of redox status regulation in blood of patients with different types of pancreatic lesions
https://doi.org/10.17709/2409-2231-2020-7-2-3
Abstract
Purpose of the study. A comparative analysis of the intensity of lipid peroxidation and the functioning of various units of the antioxidant system in the blood of patients with malignant pancreatic lesions and with chronic pancreatitis.
Patients and Methods. The content of malondialdehyde (MDA) and diene conjugates, the activity and content of antioxidant enzymes (superoxide dismutase, catalase, glutathione reductase, glutathione peroxidase), the content of reduced glutathione and blood thiol status, as well as the content of vitamins E and A (as indicators of the non-enzymatic link of the antioxidant system), were studied in the blood of 51 patients before treatment and 22 donors. Based on a histological study of tumors, patients were divided into groups: neuroendocrine pancreatic cancer, pancreatic adenocarcinoma, pancreatic adenocarcinoma with a neuroendocrine component; a group of patients with chronic pancreatitis was also identified.
Results. According to most of the studied parameters, neuroendocrine cancer differs from pancreatic adenocarcinoma in a more pronounced imbalance in the functioning of all units of the antioxidant system, which contributes to a greater intensification of free radical processes. Chronic pancreatitis was characterized by a lower content of all the studied antioxidant enzymes, as well as a decrease in the thiol status of the blood as compared with a malignant pancreatic lesion, which was possibly associated with the highest MDA level in the plasma of patients with chronic pancreatitis. At the same time, the content of vitamin E in chronic pancreatitis was significantly higher than for adenocarcinoma and adenocarcinoma with a neuroendocrine component.
Conclusions. The most pronounced violation of oxidative status is one of the metabolic features of neuroendocrine cancer. Differences revealed in patients with neuroendocrine cancer, adenocarcinoma and pancreatitis can be useful both in the diagnosis of different types of pancreatic lesions and for assessing the state of patients during treatment.
About the Authors
I. A. GoroshinskayaRussian Federation
Irina A. Goroshinskaya – Dr. Sci. (Biol.), professor, senior researcher of the laboratory for the study of pathogenesis of malignant tumors
63 14 line str., Rostov-on-Don 344037
Author ID: 79968
ResearcherID: Y-2277-2018
Scopus Author ID: 79968
E. M. Frantsiyants
Russian Federation
Elena M. Frantsiyants – Dr. Sci. (Biol.), professor, deputy director general for science, head of the laboratory for the study of the pathogenesis of malignant tumors
63 14 line str., Rostov-on-Don 344037
SPIN: 9427-9928
Author ID: 462868
ResearcherID: Y-1491-2018
Scopus Author ID: 462868
V. I. Aleynov
Russian Federation
Vyacheslav I. Aleynov – full-time graduate student
63 14 line str., Rostov-on-Don 344037
SPIN: 4731-0642
Author ID: 1054736
Scopus Author ID: 1054736
L. A. Nemashkalova
Russian Federation
Lyidmila A. Nemashkalova – researcher at the laboratory for studying the pathogenesis of malignant tumors
63 14 line str., Rostov-on-Don 344037
SPIN: 1355-8652
Author ID: 734146
Scopus Author ID: 734146
N. D. Cheryarina
Russian Federation
Natalja D. Cheryarina – laboratory doctor at the laboratory for studying the pathogenesis of malignant tumors
63 14 line str., Rostov-on-Don 344037
SPIN: 2189-3404
Author ID: 558243
Scopus Author ID: 558243
A. V. Shaposhnikov
Russian Federation
Aleksandr V. Shaposhnikov – Dr. Sci. (Med.), professor, chief scientific officer of the Department of General Oncology
63 14 line str., Rostov-on-Don 344037
SPIN: 8756-9438
Author ID: 712823
Scopus Author ID: 712823
E. A. Dzhenkova
Russian Federation
Elena A. Dzhenkova – Dr. Sci. (Biol.), associate professor, scientific secretary
63 14 line str., Rostov-on-Don 344037
SPIN: 6206-6222
Author ID: 697354
ResearcherID: K-96222014
Scopus Author ID: 697354
References
1. Ferlay J, Colombet M, Soerjomataram I, Dyba T, Randi G, Bettio M, et al. Cancer incidence and mortality patterns in Europe: Estimates for 40 countries and 25 major cancers in 2018. Eur.J. Cancer. 2018; 103: 356–387. https://doi.org/10.1016/j.ejca.2018.07.005
2. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2017. CA: A Cancer Journal for Clinicians. 2017; 67: 7–30. https://doi.org/10.3322/caac.21387
3. Rahib L, Smith BD, Aizenberg R, Rosenzweig AB, Fleshman JM, Matrisian LM. Projecting cancer incidence and deaths to 2030: the unexpected burden of thyroid, liver, and pancreas cancers in the United States. Cancer Res. 2014; 74: 2913–2921. https://doi.org/10.1158/0008–5472.CAN-14–0155
4. Malignant neoplasms in Russia in 2018 (morbidity and mortality). Ed by Kaprin AD, Starinskii VV, Petrova GV. Moscow, 2019. (In Russian). Available at: http://www.oncology.ru/service/statistics/malignant_tumors/2018.pdf
5. Prasad S, Gupta SC, Tyagi AK. Reactive oxygen species (ROS) and cancer: Role of antioxidative nutraceuticals. Cancer Letters. 2017; 387: 95–105. https://doi.org/10.1016/j.canlet.2016.03.042
6. Galadari S, Rahman A, Pallichankandy S, Thayyullathil F. Reactive oxygen species and cancer paradox: To promote or to suppress? Free Radic. Biol. Med. 2017; 104: 144–164. https://doi.org/10.1016/j.freeradbiomed.2017.01.004
7. Helfinger V, Schröder K. Redox control in cancer development and progression. Mol. Aspects Med. 2018; 63: 88–98. https://doi.org/10.1016/j.mam.2018.02.003
8. Bandovkina VA, Neskubina IV, Frantsiyants EM, Tkalja LD, Przhedetskiy YuV. Influence of transplantable В16/F10 melanoma growth on peroxidation system of the lipid in liver of female С57 ВL/6 mice. University News North Caucasus region. Natural Sciences. 2017; 3(2): 4–10. (In Russian). https://doi.org/10.23683/0321–3005–2017–3-2–4-10
9. Kit OI, Frantsiyants EM, Kotieva IM, Surikova EI, Kaplieva IV, Bandovkina VA, et al. The dynamics of the concentration of components of the NO-system during the growth of B16/F10 melanoma with chronic neurogenic pain in female mice. Problems in Oncology. 2019; 65(6): 898–903. (In Russian).
10. Neskubina IV, Frantsiyants EM, Surikova EI, Kaplieva IV, Trepitaki LК, Nemashkalova LА, et al. Actions and effects of malignant tumor growth and chronic neurogenic pain exerted on the glutathione system in cardiac mitochondria in experimental animals. Cardiometry. 2018; 13: 27–34. https://doi.org/10.12710/cardiometry.2018.13.2734
11. He L, He T, Farrar S, Ji L, Liu T, Ma X. Antioxidants Maintain Cellular Redox Homeostasis by Elimination of Reactive Oxygen Species. Cell Physiol Biochem. 2017; 44(2): 532–553. https://doi.org/10.1159/000485089
12. Kalyanaraman B, Cheng G, Hardy M, Ouari O, Bennett B, Zielonka J. Teaching the basics of reactive oxygen species and their relevance to cancer biology: Mitochondrial reactive oxygen species detection, redox signaling, and targeted therapies. Redox Biology. 2018; 15: 347–362. https://doi.org/10.1016/j.redox.2017.12.012
13. Zenkov NK, Kozhin PM, Vcherashnyaya AV, Martinovich GG, Kandalintseva NV, Menshchikova EB. Features of redox regulation in tumor cells. Siberian scientific medical journal. (In Russian). 2019; 39(2): 11–26. https://doi.org/10.15372/SSMJ20190202
14. Wu S, Lu H, Bai Y. Nrf2 in cancers: A double-edged sword. Cancer Med. 2019; 8(5): 2252–2267. https://doi.org/10.1002/cam4.2101
15. Arutyunyan AV, Dubinina EE, Zybina NN. Methods for assessing free radical oxidation and the antioxidant system of the body. Guidelines. S.-Peterburg: 2000, 104 p. (In Russian).
16. Proskurnina EV. Methods for assessing free radical blood homeostasis. Abstract of dissertation. Moscow, 2018. (In Russian).
17. Goroshinskaya IA, Frantsiyants EM, Aleynov VI, Nemashkalova LA, Cheryarina ND, Kit OI. Parameters of oxidative metabolism in the blood of patients with pancreatic tumors of various histotype. Modern problems of science and education. 2020; 2. (In Russian). https://doi.org/10.17513/spno.29548
18. Menshchikova EB, Zenkov NK, Lankin VZ, Bondar' IA, Trufakin VA. Oxidative stress. Pathological conditions and diseases. Novosibirsk: Siberian University Edition, 2017, 284 p. (In Russian).
19. Gerasimenko MN, Zukov RA, Titova NM, Dyhno JuA, Modestov AA, Popov DV. Antioxidant system and markers of oxidative stress in kidney cancer. Siberian journal of oncology. 2012; 25(5): 39–43. (In Russian).
20. Sies H, Berndt C, Jones DP. Oxidative Stress. Annual Review of Biochemistry. 2017; 86: 715–748. https://doi.org/10.1146/annurev-biochem-061516–045037
21. Rusetskaya NY, Fedotov IV, Koftina VA, Borodulin VB. Selenium compounds in redox regulation of inflammation and apoptosis. Biomedical chemistry. 2019; 65(3): 165–179. (In Russian). https://doi.org/10.18097/PBMC20196503165
22. Mironczuk-Chodakowska I, Witkowska AM, Zujko ME. Endogenous non-enzymatic antioxidantsin the human body. Advancesin Medical Sciences. 2018; 63: 68–78. https://doi.org/10.1016/j.advms.2017.05.005
23. Corso CR, Acco A. Glutathione system in animal model of solid tumors: From regulation to therapeutic target. Crit Rev Oncol Hematol. 2018; 128: 43–57. https://doi.org/10.1016/j.critrevonc.2018.05.014
24. Andrisic L, Dudzika D, Barbasa C, Milkovicb L, Grunec T, Zarkovic N. Short overview on metabolomics approach to study pathophysiology of oxidative stress in cancer. Redox Biology. 2018; 14: 47–58. https://doi.org/10.1016/j.redox.2017.08.009
25. Sirota TV. Effect of the sulfur-containing compounds on the quinoid process of adrenaline autoxidation; potential neuroprotectors. Biomeditsinskaya khimiya. 2019; 65(4): 316–323. (In Russian). https://doi.org/10.18097/PBMC20196504316
26. Goroshinskaya IA, Surikova EI, Frantsiyants EM, Neskubina IV, Pogorelova YuA, Medvedeva DE, et al. Redox forms of glutathione mark the aggressiveness of stomach cancer. Annals of Oncology. 2018; 29 (Suppl5): v3–v4. https://doi.org/10.1093/annonc/mdy151.010
27. Goroshinskaya IA, Surikova EI, Shalashnaya EV, Nerodo GA, Maksimova NA, Men'shenina AP, et al. State of free radical processes in ovarian cancer with different prevalence and course of the disease. University News North Caucasus region. Natural Sciences. 2017; 4(2): 10–19. (In Russian). https://doi.org/10.23683/0321–3005–2017–4-2–10–19
28. Goroshinskaya I, Popova N, Menshenina A, Nemashkalova L, Shikhlyarova A, Frantsiyants E, et al. Free radical processes in the blood of patients with cervical cancer receiving various postoperative treatment modalities. International Journal of Gynecologic Cancer. 2019; 29 (Suppl 4): A218. https://doi.org/10.1136/ijgc-2019-ESGO.362
29. Rozenko LJa, Sidorenko JuS, Frantsiyants EM. Does the tumor volume affect the state of antioxidant defense of the body? Problems in Oncology. 1999; 45(5): 538–541. (In Russian).
Review
For citations:
Goroshinskaya I.A., Frantsiyants E.M., Aleynov V.I., Nemashkalova L.A., Cheryarina N.D., Shaposhnikov A.V., Dzhenkova E.A. Peculiarities of redox status regulation in blood of patients with different types of pancreatic lesions. Research and Practical Medicine Journal. 2020;7(2):30-46. (In Russ.) https://doi.org/10.17709/2409-2231-2020-7-2-3