Influence of redox cyclers on thiol oxidation in the presence of nanoparticles
Abstract
Background: An increase in metabolic rate interconnected with oxidative imbalance are major features of tumor process. Higher ROS (reactive oxygen species) levels make tumor cells more sensitive to oxidative stress compared to normal cells. Therefore, generating additional ROS can lead to cancer cell death. Redox cycling is a crucial process responsible for the production of ROS by various clinical and experimental anticancer agents. Among these compounds are quinones and ascorbic acid, which exhibits a synergistic antitumor effect. Elevated glutathione levels and glutathione-dependent antioxidant enzymes play a key role in protecting cancer cells from intracellular oxidative stress. Nanoparticles with glutathione depletion properties can act as smart chemodynamic agents, disrupting the cellular antioxidant defense system. In this work, inorganic nanoparticles based on rare earth elements are used as catalytic amplifiers of one- electron transfer with the formation of organic and oxygen radicals in the redox cycles of ascorbic acid and vitamin K3.
Objectives: The thiol oxidation was studied in the presence of nanoparticles in combination with redox cyclers.
Materials and methods: As an indicator of the pro-oxidant efficiency of nanoparticles (CeO2 (2 nm, 20 μg/ml) or GdYVO4:Eu3+ (2 nm, 20 μg/ml)) combined with organic compounds (ascorbic acid (100 or 200 µM) and vitamin K3 (4 μM)) changes in the level of thiols (glutathione (200 μM), L-cysteine (200 μM) or dithiothreitol (500 μM)) in the model system were used.
Results: It was shown that GdYVO4:Eu3+ and CeO2 nanoparticles enhances oxidation of thiols under an influence of the redox active molecule as well as their combination. The efficiency of bare nanoceria as well as in redox cyclers combinations was higher compared to respective orthovanadate nanoparticles combinations (including time dynamics) that was especially pronounced in the dithiothreitol oxidation system.
Conclusions: The data obtained indicate the ability of nanoceria to significantly enhance the oxidation of thiols induced by redox cyclers revealing the perspective of this approach in solving the problem of increased thiol level in tumor cells.
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References
Li J, Zuo X, Cheng P, Ren X, Sun S, Xu J, et al. The production of reactive oxygen species enhanced with the reduction of menadione by active thioredoxin reductase. Metallomics. 2019;11(9):1490–97. https://doi.org/10.1039/c9mt00133f
Chaiswing L, St Clair WH, St Clair DK. Redox paradox: a novel approach to therapeutics-resistant cancer. Antioxid Redox Signal. 2018;29(13):1237–72. https://doi.org/10.1089/ars.2017.7485
Trachootham D, Alexandre J, Huang P. Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach? Nat Rev Drug Discov. 2009;8(7):579–91. https://doi.org/10.1038/nrd2803
Khramtsov VV, Gillies RJ. Janus-faced tumor microenvironment and redox. Antioxid Redox Signal. 2014;21(5):723–9. https://doi.org/10.1089/ars.2014.5864
Wondrak GT. Redox-directed cancer therapeutics: molecular mechanisms and opportunities. Antioxid Redox Signal. 2009;11(12):3013–69. https://doi.org/10.1089/ars.2009.2541
Delwar ZM, Avramidis D, Follin E, Hua Y, Siden A, Cruz M, et al. Cytotoxic effect of menadione and sodium orthovanadate in combination on human glioma cells. Invest New Drugs. 2012;30(4):1302–10. https://doi.org/10.1007/s10637-011-9680-y
Jamison JM, Gilloteaux J, Nassiri MR, Venugopal M, Neal DR, Summers JL. Cell cycle arrest and autoschizis in a human bladder carcinoma cell line following vitamin C and vitamin K3 treatment. Biochem Pharmacol. 2004;67(2):337–51. https://doi.org/10.1016/j.bcp.2003.08.040
Jeyachandran S, Srinivasan R, Ramesh T, Parivallal A, Lee J, Sathiyamoorthi E. Recent development and application of "Nanozyme" Artificial Enzymes-A Review. Biomimetics (Basel). 2023;8(5):446. https://doi.org/10.3390/biomimetics8050446
Nikitchenko YV, Klochkov VK, Kavok NS, Averchenko KA, Karpenko NA, Nikitchenko IV, et al. Anti-aging effects of antioxidant rare-earth orthovanadate nanoparticles in Wistar rats. Biol Trace Elem Res. 2021;199:4183–92. https://doi.org/10.1007/s12011-020-02531-y
Kavok N, Klochkov V, Nikitchenko Yu, Sedyh O, Dudetskaya G, Kot Yu, et al. Exposure of prooxidant potential of CeO2 and GdYVO4/Eu3+ nanoparticles in model systems containing low-molecular antioxidants. In 2023 IEEE 13th International Conference “Nanomaterials: Applications & Properties (NAP)ˮ; 2023 September 10–15; Bratislava, Slovakia: IEEE; 2023. p. NRA11-1-NRA11-4. https://doi.org/10.1109/NAP59739.2023.10310986
Rollin-Genetet F, Seidel C, Artells E, Auffan M, Thiéry A, Vidaud C. Redox reactivity of cerium oxide nanoparticles induces the formation of disulfide bridges in thiol-containing biomolecules. Chem Res Toxicol. 2015;28(12):2304–12. https://doi.org/10.1021/acs.chemrestox.5b00319
Pešić M, Podolski-Renić A, Stojković S, Matović B, Zmejkoski D, Kojić V, et al. Anti-cancer effects of cerium oxide nanoparticles and its intracellular redox activity. Chem Biol Interact. 2015;232:85–93. https://doi.org/10.1016/j.cbi.2015.03.013
Goltsev AN, Babenko NN, Gaevskaya YA, Bondarovich NA, Dubrava TG, Ostankov MV, et al. Nanotechniques inactivate cancer stem cells. Nanoscale Res Lett. 2017;12(1):415. https://doi.org/10.1186/s11671-017-2175-9
Klochkov VK, Malyshenko AI, Sedykh OO, Malyukin YV. Wet chemical synthesis and characterization of luminescent colloidal nanoparticles: ReVO4:Eu3+ (Re = La, Gd, Y) with rod-like and spindle-like shape. Funct Mater. 2011;18(1):111–5. http://dspace.nbuv.gov.ua/handle/123456789/135437
Klochkov VK, Grigorova AV, Sedyh OO, Malyukin YV. The influence of agglomeration of nanoparticles on their superoxide dismutase-mimetic activity. Colloids Surf. A: Physicochem. Eng. Asp. 2012;409:176–82. https://doi.org/10.1016/j.colsurfa.2012.06.019
Bates JT, Fang T, Verma V, Zeng L, Weber RJ, Tolbert PE, et al. Review of acellular assays of ambient particulate matter oxidative potential: methods and relationships with composition, sources, and health effects. Environ Sci Technol. 2019;53(8):4003–19. https://doi.org/10.1021/acs.est.8b03430
Charrier JG, Anastasio C. On dithiothreitol (DTT) as a measure of oxidative potential for ambient particles: evidence for the importance of soluble transition metals, atmos. Chem. Phys. 2012;12:9321–33. https://doi.org/10.5194/acp-12-9321-2012
Juchau MR, Fantel AG, Harris C, Beyer BK. The potential role of redox cycling as a mechanism for chemical teratogenesis. Environ. Health Perspect. 1986;70:131–36. http://doi.org/10.2307/3430349
Elman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959;82(1):70–7. https://doi.org/10.1016/0003-9861(59)90090-6
Bakalova R, Semkova S, Ivanova D, Zhelev Z, Miller T, Takeshima T, et al. Selective targeting of cancerous mitochondria and suppression of tumor growth using redox‐active treatment adjuvant. Oxid Med Cell Longev. 2020; Article ID 6212935, 30 pages. https://doi.org/10.1155/2020/6212935
Semkova S, Zhelev Z, Miller T, Sugaya K, Aoki I, Higashi T, et al. Menadione/ascorbate induces overproduction of mitochondrial superoxide and impairs mitochondrial function in cancer: comparative study on cancer and normal cells of the same origin. Anticancer Research. 2020;40(4):1963–72. https://doi.org/10.21873/anticanres.14151
Sumiyoshi A, Shibata S, Lazarova D, Zhelev Z, Aoki I, Bakalova R. Tolerable treatment of glioblastoma with redox-cycling ‘mitocans': a comparative study in vivo. Redox Report. 2023;28(1), 2220531. https://doi.org/10.1080/13510002.2023.2220531
Amaldoss MJN, Mehmood R, Yang J L, Koshy P, Kumar N, Unnikrishnan A. Anticancer therapeutic effect of cerium-based nanoparticles: known and unknown molecular mechanisms. Biomater. Sci. 2022;10(14):3671–94. https://doi.org/10.1039/D2BM00334A
Datta A, Mishra S, Manna K, Saha KD, Mukherjee S, Roy S. Pro-oxidant therapeutic activities of cerium oxide nanoparticles in colorectal carcinoma cells. ACS Omega. 2020;5(17):9714–23. https://doi.org/10.1021/acsomega.9b04006
Lu H, Xiang Z, Ren Q. Sensitive and highly selective biosensor based on innovative V2O5 nanoparticles for detection of glutathione. Asia‐Pac J Chem Eng. 2024;19(4):e3081.https://doi.org/10.1002/apj.3081
Luna-Velasco A, Field JA, Cobo-Curiel A, Sierra-Alvarez R. Inorganic nanoparticles enhance the production of reactive oxygen species (ROS) during the autoxidation of l-3,4-dihydroxyphenylalanine (l-dopa). Chemosphere. 2011;85(1):19–25. https://doi.org/10.1016/j.chemosphere.2011.06.053
Hayat A, Andreescu D, Bulbul G, Andreescu S. Redox reactivity of cerium oxide nanoparticles against dopamine. J Colloid Interface Sci. 2014;418:240–45. https://doi.org/10.1016/j.jcis.2013.12.007
Othman A, Norton L, Finny AS, Andreescu S. Easy-to-use and inexpensive sensors for assessing the quality and traceability of cosmetic antioxidants. Talanta. 2020;208:120473. https://doi.org/10.1016/j.talanta.2019.120473
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