2013, Number 2
<< Back Next >>
Ann Hepatol 2013; 12 (2)
A metal mixture induces transformation upon antioxidant depletion in a hepatic cell line
Sánchez-Valle V, Valverde M, Carrizales L, Mejía J, Zepeta N, Rojas E
Language: English
References: 53
Page: 315-324
PDF size: 494.43 Kb.
ABSTRACT
Introduction. Metals are ubiquitous soil, air, and water pollutants. A mixture of arsenic cadmium and lead, in particular, has commonly been found in the vicinity of smelter areas. The mixture of As-Cd-Pb has been shown to be carcinogenic, and transforming potential and oxidative stress have been proposed as principal mechanisms involved in this process. The aim of this work was to explore the role of the antioxidant barrier in the establishment of cell transformation upon chronic exposure to a metal mixture containing 2 µM NaAsO
2, 2 µM. CdCl
2, and 5 µM Pb(C
2H
3O
2)
2·3H
2O in WRL-68 cells-a non-transformed human hepatic cell line.
Material and methods. In this study, we used a WRL-68 cell model of human embryonic hepatic origin treated with antioxidant inhibitors (L-Buthionine-sulfoxamine and aminotriazole) to test the role of the antioxidant barrier in the establishment of cell transformation upon chronic exposure to a metal mixture of As-Cd-Pb (2 µM NaAsO
2, 2 µM CdCl2 and 5 µM Pb(C
2H
3O
2)
2·3H
2O). We evaluated oxidative damage markers, including reactive oxygen species, lipid peroxidation, and genotoxicity, as well as antioxidant response markers, including glutathione concentration, catalase activity, and superoxide dismutase activity, wich promote morphological transformation, which can be quantified by foci formation.
Results. As expected, we found an increase in the intracellular concentration of the metals after treatment with the metal mixture. In addition, treatment with the metal mixture in addition to inhibitors resulted in a large increase in the intracellular concentration of cadmium and lead. Our results describe the generation of reactive oxygen species, cytotoxicity, genotoxicity, and oxidative damage to macromolecules that occurred exclusively in cells that were morphologically transformed upon exposure to a metal mixture and antioxidant barrier inhibition.
Conclusion. Our results show the importance of the antioxidant barrier role in the protection of cellular integrity and the transformation potential of this metal mixture via free radicals.
REFERENCES
Carrizales L, Razo I, Tellez-Hernandez JI, Torres-Nerio R, Torres A, Batres LE, Cubillas AC, et al. Exposure to arsenic and lead of children living near a copper-smelter in San Luis Potosi, Mexico: Importance of soil contamination for exposure of children. Environ Res 2006: 101: 1-10.
Wang G, Fowler BA. Roles of biomarkers in evaluating interactions among mixtures of lead, cadmium and arsenic. Toxicol Appl Pharmacol 2008: 233: 92-9.
ATSDR (Agency for Toxic Substances and Disease Registry). 2007. Primary known toxic pollutants list from and possible technology advances to harness, sequester or fix the air and water pollution caused by them-new technologies and possible solutions.
IARC 2006. Monographs on the Evaluation of Carcinogenic Risks to Humans. Inorganic and Organic Lead Compounds. Vol. 87.
Madden EF, Fowler BA. Mechanisms of nephrotoxicity from metal combinations: a review. Drug Chem Toxicol 2000; 23: 1-12.
Banerjee S, Flores-Rozas H. Cadmium inhibits mismatch repair by blocking the ATPase activity of the MSH2-MSH6 complex. Nucleic Acids Res 2005; 33: 1410-9.
Clark AB, Kuntel TA. Cadmium inhibits the functions of eukaryotic MutS complex. J Biol Chem 2004; 279: 52903-6.
Giaginis C, Gatzidou E, Theocharis S. DNA repair systems as targets of cadmium toxicity. Toxicol Appl Pharmacol 2006; 213: 282-90.
Kopera E, Schwerdtle T, Hartwig A, Bal W. Co(II) and Cd(II) substitute for Zn(II) in the zinc finger derived from the DNA repair protein XPA, demonstrating a variety of potential mechanisms of toxicity. Chem Res Toxicol 2004; 17: 1452-8.
Leonard SS, Harris GK, Shi X. Metal-induced oxidative stress and signal transduction. Free Radic Biol Med 2004; 37: 1921-42.
McNeill DR, Narayana A, Wong HK, Wilson DM 3rd. Inhibition of Ape1 nuclease activity by lead, iron, and cadmium. Environ Health Perspect 2004; 112: 799-804.
Witkiewicz-Kucharczyk A, Bal W. Damage of zinc fingers in DNA repair proteins, a novel molecular mechanism in carcinogenesis. Toxicol Lett 2006; 162: 29-42.
Del Carmen EM, Souza V, Bucio L, Hernández E, Damián-Matsumura P, Zaga V, Gutiérrez-Ruiz MC. Cadmium induces alpha(1)collagen (I) and metallothionein II gene and alters the antioxidant system in rat hepatic stellate cells. Toxicology 2002; 170: 63-73.
Valverde M, Trejo C, Rojas E. Is the capacity of lead acetate and cadmium chloride to induce genotoxic damage due to direct DNA-metal interaction? Mutagenesis 2001; 16: 265-70.
Cooper KL, Liu KJ, Hudson LG. Enhanced ROS production and redox signaling with combined arsenite and UVA exposure: contribution of NADPH oxidase. Free Radic Biol Med 2009; 47: 381-8.
Valko M, Rhodes CJ, Moncol J, Izakovic M, Mazur M. Free radicals, metals and antioxidants in oxidative stressinduced cancer. Chem Biol Interact 2006; 160: 1-40.
Liu J, Qu W, Kadiiska MB. Role of oxidative stress in cadmium toxicity and carcinogenesis. Toxicol Appl Pharmacol 2009; 238: 209-14.
Ahamed M, Singh S, Behari JR, Kumar A, Siddiqui MK. Interaction of lead with some essential trace metals in the blood of anemic children from Lucknow, India. Clin Chim Acta 2007; 377: 92-7.
Noguchi N, Watanabe A, Shi H. Diverse functions of antioxidants. Free Radic Res 2000; 33: 809-17.
Cicchetti R, Argentin G. The role of oxidative stress in the in vitro induction of micronuclei by pesticides in mouse lung fibroblasts. Mutagenesis 2003; 18: 127-32.
Gutierrez-Ruiz MC, Bucio L, Souza V, Gomez JJ, Campos C, Carabez A. Expression of some hepatocyte-like functional properties of WRL-68 cells in culture. In Vitro Cell Dev Biol Anim 1994; 30A: 366-71.
Silva Aguilar M, Rojas E, Valverde M. Role of oxidative stress in transformation induced by metal mixture. Oxid Med Cell Longev 2011; 2011: 935160.
Merzenich H, Hartwig A, Ahrens W, Beyersmann D, Schlepegrell R, Scholze M, Timm J, et al. Biomonitoring on carcinogenic metals and oxidative DNA damage in a cross-sectional study. Cancer Epidemiol Biomarkers Prev 2001; 10: 515-22.
Palus J, Rydzynski K, Dziubaltowska E, Wyszynska K, Natarajan AT, Nilsson R. Genotoxic effects of occupational exposure to lead and cadmium. Mutat Res 2003; 540: 19-28.
De la Fuente H, Portales-Perez D, Baranda L, Díaz-Barriga F, Saavedra-Alanís V, Layseca E, González-Amaro R. Effect of arsenic, cadmium and lead on the induction of apoptosis of normal human mononuclear cells. Clin Exp Immunol 2002; 129: 69-77.
Hartmann A, Speit G. Genotoxic effects of chemicals in the single cell gel (SCG) test with human blood cells in relation to the induction of sister-chromatid exchanges (SCE). Mutat Res 1995; 346: 49-56.
Lee VM, Quinn PA, Jennings SC, Ng LL. NADPH oxidase activity in preeclampsia with immortalized lymphoblasts used as models. Hypertension 2003; 41: 925-31.
Aebi H. Catalase in vitro. Methods Enzymol 1984; 105: 121-6.
Sun Y, Oberley LW, Li Y. A simple method for clinical assay of superoxide dismutase. Clin Chem 1988; 34: 497-500.
Bouaicha N, Maatouk I. Microcystin-LR and nodularin induce intracellular glutathione alteration, reactive oxygen species production and lipid peroxidation in primary cultured rat hepatocytes. Toxicol Lett 2004; 148: 53-63.
Vega L, Valverde M, Elizondo G, Leyva JF, Rojas E. Diethylthiophosphate and diethyldithiophosphate induce genotoxicity in hepatic cell lines when activated by further biotransformation via Cytochrome P450. Mutat Res 2009; 679: 39-43.
IARC/NCI/EPA Working Group. Cellular and molecular mechanisms of cell transformation and standardization of transformation assays of established cell lines for the prediction of carcinogenic chemicals: overview and recommended protocols. Cancer Res 1985; 45: 2395-9.
Kajiwara Y, Ajimi S. Verification of the BALB/c 3T3 cell transformation assay after improvement by using an ITESmedium. Toxicol In Vitro 2003; 17: 489-96.
Tsuchiya T, Tanaka-Kagawa T, Jinno H, Tokunaga H, Sakimoto K, Ando M, Umeda M. Inorganic arsenic compounds and methylated metabolites induce morphological transformation in two-stage BALB/c 3T3 cell assay and inhibit metabolic cooperation in V79 cell assay. Toxicol Sci 2005; 84: 344-51.
Yoo SM, Antonyak MA, Cerione RA. The adaptor protein and Arf GTPase-activating protein Cat-1/Git-1 is required for cellular transformation. J Biol Chem 2012; 37: 31462-70.
De Rosa CT, Johnson BL, Fay M, Hansen H, Mumtaz MM. Public health implications of hazardous waste sites: findings, assessment and research. Food Chem Toxicol 1996; 34: 1131-8.
Fay RM, Mumtaz MM. Development of a priority list of chemical mixtures occurring at 1188 hazardous waste sites, using the HazDat database. Food Chem Toxicol 1996; 34: 1163-5.
Hwua YS, Yang JL. Effect of 3-aminotriazole on anchorage independence and mutagenicity in cadmium- and leadtreated diploid human fibroblasts. Carcinogenesis 1998; 19: 881-8.
Kowaltowski AJ, Vercesi AE, Rhee SG, Netto LE. Catalases and thioredoxin peroxidase protect Saccharomyces cerevisiae against Ca(2+)-induced mitochondrial membrane permeabilization and cell death. FEBS Lett 2000; 473: 177-82.
Doroshenko N, Doroshenko P. The glutathione reductase inhibitor carmustine induces an influx of Ca2+ in PC12 cells. Eur J Pharmacol 2004; 497: 17-24.
Lee M, Cho T, Jantaratnotai N, Wang YT, McGeer E, Mc-Geer PL. Depletion of GSH in glial cells induces neurotoxicity: relevance to aging and degenerative neurological diseases. FASEB J 2010; 24: 2533-45.
Hinkle PM, Shanshala ED 2nd, Nelson EJ. Measurement of intracellular cadmium with fluorescent dyes. Further evidence for the role of calcium channels in cadmium uptake. J Biol Chem 1992; 267: 25553-9.
Lou M, Garay R, Alda JO. Cadmium uptake through the anion exchanger in human red blood cells. J Physiol 1991; 443: 123-36.
Reiners JJ Jr, Thai G, Rupp T, Cantu AR. Assessment of the antioxidant/prooxidant status of murine skin following topical treatment with 12-O-tetradecanoylphorbol-13-acetate and throughout the ontogeny of skin cancer. Part I: Quantitation of superoxide dismutase, catalase, glutathione peroxidase and xanthine oxidase. Carcinogenesis 1991;12: 2337-43.
Wei L, Wei H, Frenkel K. Sensitivity to tumor promotion of SENCAR and C57BL/6J mice correlates with oxidative events and DNA damage. Carcinogenesis 1993; 14: 841-7.
Gupta A, Butts B, Kwei KA, Dvorakova K, Stratton SP, Briehl MM, Bowden GT. Attenuation of catalase activity in the malignant phenotype plays a functional role in an in vitro model for tumor progression. Cancer Lett 2001; 173: 115-25.
Wilhelm D, Bender K, Knebel A, Angel P. The level of intracellular glutathione is a key regulator for the induction of stress-activated signal transduction pathways including Jun N-terminal protein kinases and p38 kinase by alkylating agents. Mol Cell Biol 1997; 17: 4792-800.
Lu SC. Regulation of glutathione synthesis. Mol Aspects Med 2009; 30: 42-59.
Croute F, Beau B, Murat JC, Vincent C, Komatsu H, Obata F, Soleilhavoup JP. Expression of stress-related genes in a cadmium-resistant A549 human cell line. J Toxicol Environ Health A 2005; 68: 703-18.
Hartwig A, Schwerdtle T. Interactions by carcinogenic metal compounds with DNA repair processes: toxicological implications. Toxicol Lett 2002; 127: 47-54.
Kenney NJ, Saeki T, Gottardis M, Kim N, Garcia-Morales P, Martin MB, Normanno N, et al. Expression of transforming growth factor alpha antisense mRNA inhibits the estrogeninduced production of TGF alpha and estrogen-induced proliferation of estrogen-responsive human breast cancer cells. J Cell Physiol 1993; 156: 497-514.
Ciardiello F, Pepe S, Bianco C, Baldassarre G, Ruggiero A, Bianco C, Selvam MP, et al. Down-regulation of RI alpha subunit of cAMP-dependent protein kinase induces growth inhibition of human mammary epithelial cells transformed by c-Ha-ras and c-erbB-2 proto-oncogenes. Int J Cancer 1993; 53: 438-43.
Wiseman H, Halliwell B. Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer. Biochem J 1996; 313 (Pt. 1): 17-29.