Role of mitochondrial DNA in oxidative damage induced by sodium arsenite in human bronchial epithelial cells

References

• Al Shahrani, M., S. Heales, I. Hargreaves, and M. Orford. 2017. Oxidative stress: Mechanistic insights into inherited mitochondrial disorders and Parkinson’s disease. J. Clin. Med. 6:100. doi:10.3390/jcm6110100.
   Web of Science ®Google Scholar
• Aodengqimuge, S. Liu, S. Mai, X. Li, Y. Li, M. Hu, S. Yuan, and L. Song. 2014. AP-1 activation attenuates the arsenite-induced apoptotic response in human bronchial epithelial cells by up-regulating HO-1 expression. Biotechnol. Lett. 36:1927–36. doi:10.1007/s10529-014-1560-z.
   PubMed Web of Science ®Google Scholar
• Azad, N., Y. Rojanasakul, and V. Vallyathan. 2008. Inflammation and lung cancer: Roles of reactive oxygen/nitrogen species. J. Toxicol. Environ. Health B 11:1–15. doi:10.1080/10937400701436460.
   PubMed Web of Science ®Google Scholar
• Barja, G. 2007. Mitochondrial oxygen consumption and reactive oxygen species production are independently modulated: Implications for aging studies. Rejuvenation Res. 10:215–24. doi:10.1089/rej.2006.0516.
   PubMed Web of Science ®Google Scholar
• Bernstam, L., and J. Nriagu. 2000. Molecular aspects of arsenic stress. J. Toxicol. Environ. Health B 3:293–322. doi:10.1080/109374000436355.
   PubMed Web of Science ®Google Scholar
• Evdokimovsky, E. V., T. E. Ushakova, A. A. Kudriavtcev, and A. I. Gaziev. 2011. Alteration of mtDNA copy number, mitochondrial gene expression and extracellular DNA content in mice after irradiation at lethal dose. Radiat. Environ. Biophys. 50:181–88. doi:10.1007/s00411-010-0329-6.
   PubMed Web of Science ®Google Scholar
• Flora, S. J. 2011. Arsenic-induced oxidative stress and its reversibility. Free Radical Biol. Med. 51:257–81. doi:10.1016/j.freeradbiomed.2011.04.008.
   PubMed Web of Science ®Google Scholar
• Guidarelli, A., M. Fiorani, L. Cerioni, M. Scotti, and O. Cantoni. 2017. Arsenite induces DNA damage via mitochondrial ROS and induction of mitochondrial permeability transition. Biofactors 43:673–84. doi:10.1002/biof.v43.5.
   PubMed Web of Science ®Google Scholar
• Guo, H., D. Wen, Z. Liu, Y. Jia, and Q. Guo. 2014. A review of high arsenic groundwater in Mainland and Taiwan, China: Distribution, characteristics and geochemical processes. Appl. Geochem. 41:196–217. doi:10.1016/j.apgeochem.2013.12.016.
   Web of Science ®Google Scholar
• Guo, X., Y. Fujino, S. Kaneko, K. Wu, Y. Xia, and T. Yoshimura. 2001. Arsenic contamination of groundwater and prevalence of arsenical dermatosis in the Hetao plain area, Inner Mongolia, China. Mol. Cell. Biochem. 222:137–40. doi:10.1023/A:1017916826439.
   PubMed Web of Science ®Google Scholar
• Hanahan, D., and R. A. Weinberg. 2011. Hallmarks of cancer: The next generation. Cell 144:646–74. doi:10.1016/j.cell.2011.02.013.
   PubMed Web of Science ®Google Scholar
• He, Q., L. Zong, Y. Sun, P. T. J. Vijayalaxmi, J. Tong, and Y. Cao. 2017. Adaptive response in mouse bone marrow cells exposed to 900 MHz radiofrequency fields: Impact of poly (ADP-ribose) polymerase (PARP). Mutat. Res. 820:19–25. doi:10.1016/j.mrgentox.2017.05.007.
   PubMed Web of Science ®Google Scholar
• Huang, -C.-C., -C.-C. Lee, -H.-H. Lin, M.-C. Chen, -C.-C. Lin, and J.-Y. Chang. 2015. Autophagy-regulated ROS from xanthine oxidase acts as an early effector for triggering late mitochondria-dependent apoptosis in cathepsin S-targeted tumor cells. PLoS ONE 10:1–20.
   Web of Science ®Google Scholar
• IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. 2012. Arsenic, metals, fibres, and dusts. IARC Monogr. Eval. Carcinogenic Risks Humans 100: 11–465.
   PubMedGoogle Scholar
• Indo, H. P., M. Davidson, H.-C. Yen, S. Suenaga, K. Tomita, T. Nishii, M. Higuchi, Y. Koga, T. Ozawa, and H. J. Majima. 2007. Evidence of ROS generation by mitochondria in cells with impaired electron transport chain and mitochondrial DNA damage. Mitochondrion 7:106–18. doi:10.1016/j.mito.2006.11.026.
   PubMed Web of Science ®Google Scholar
• King, M. P., and G. Attardi. 1989. Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation. Science 246:500–03. doi:10.1126/science.2814477.
   PubMed Web of Science ®Google Scholar
• Kleiman, N. J., A. M. Quinn, K. G. Fields, V. Slavkovich, and J. H. Graziano. 2016. Arsenite accumulation in the mouse eye. J. Toxicol. Environ. Health Part A 79:339–41. doi:10.1080/15287394.2016.1151392.
   PubMed Web of Science ®Google Scholar
• Li, B., X. Li, B. Zhu, X. Zhang, Y. Wang, Y. Xu, H. Wang, Y. Hou, Q. Zheng, and G. Sun. 2013. Sodium arsenite induced reactive oxygen species generation, nuclear factor (erythroid‐2 related) factor 2 activation, heme oxygenase‐1 expression, and glutathione elevation in Chang human hepatocytes. Environ. Toxicol. 28:401–10. doi:10.1002/tox.20731.
   PubMed Web of Science ®Google Scholar
• Li, B. Y., J. Sun, H. Wei, Y. Z. Cheng, L. Xue, Z. H. Cheng, J. M. Wan, A. Q. Wang, T. K. Hei, and J. Tong. 2012. Radon-induced reduced apoptosis in human bronchial epithelial cells with knockdown of mitochondria DNA. J. Toxicol. Environ. Health Part A 75:1111–19. doi:10.1080/15287394.2012.699841.
   PubMed Web of Science ®Google Scholar
• Ram, A. K. S. S., P. K. Reddy, P. Girish, S. Ch, and S. P. Reddy. 2018. Arsenic aggravated reproductive toxicity in male rats exposed to lead during perinatal period. Toxicol. Res. 7:1191–204. doi:10.1039/C8TX00146D.
   Web of Science ®Google Scholar
• Schipper, H. M., W. Song, H. Zukor, J. R. Hascalovici, and D. Zeligman. 2009. Heme oxygenase‐1 and neurodegeneration: Expanding frontiers of engagement. J. Neurochem. 110:469–85. doi:10.1111/j.1471-4159.2009.06160.x.
   PubMed Web of Science ®Google Scholar
• Smith, A. H., and C. M. Steinmaus. 2009. Health effects of arsenic and chromium in drinking water: Recent human findings. Annu. Rev. Public Health 30:107–22. doi:10.1146/annurev.publhealth.031308.100143.
   PubMed Web of Science ®Google Scholar
• Souza, A. C., S. C. Marchesi, R. P. Ferraz, G. D. Lima, J. A. de Oliveira, and M. Machado-Neves. 2016. Effects of sodium arsenate and arsenite on male reproductive functions in Wistar rats. J. Toxicol. Environ. Health Part A 79:274–86. doi:10.1080/15287394.2016.1150926.
   PubMed Web of Science ®Google Scholar
• Sun, Y. L., L. Zong, Z. Gao, S. X. Zhu, J. Tong, and Y. Cao. 2017. Mitochondrial DNA damage and oxidative damage in HL-60 cells exposed to 900 MHz radiofrequency fields. Mutat. Res. 797:7–14. doi:10.1016/j.mrfmmm.2017.03.001.
   PubMed Web of Science ®Google Scholar
• Takeda, T. A., M. Sasai, Y. Adachi, K. Ohnishi, J. I. Fujisawa, S. Izawa, and S. Taketani. 2017. Potential role of heme metabolism in the inducible expression of heme oxygenase-1. Biochim. Biophys. Acta 1861:1813–24. doi:10.1016/j.bbagen.2017.03.018.
   Web of Science ®Google Scholar
• Tang, J., H. Yamazaki, T. Inoue, M. Koizumi, K. Yoshida, and S. Ozeki. 1999. Mitochondrial DNA influences radiation sensitivity and induction of apoptosis in human fibroblasts. Anticancer Res. 19:4959–64.
   PubMed Web of Science ®Google Scholar
• Thornton, C., B. Leaw, C. Mallard, S. Nair, M. Jinnai, and H. Hagberg. 2017. Cell death in the developing brain after hypoxia-ischemia. Front. Cell. Neurosci. 11:248. doi:10.3389/fncel.2017.00248.
   PubMed Web of Science ®Google Scholar
• Trachootham, D., J. Alexandre, and P. Huang. 2009. Targeting cancer cells by ROS-mediated mechanisms: A radical therapeutic approach? Nat. Rev. Drug Discovery 8:579–91. doi:10.1038/nrd2803.
   PubMed Web of Science ®Google Scholar
• Yang, C.-Y. 2006. Does arsenic exposure increase the risk of development of peripheral vascular diseases in humans? J. Toxicol. Environ. Health Part A 69:1797–804. doi:10.1080/15287390600630237.
   PubMed Web of Science ®Google Scholar
• Yang, X., D. Wang, Y. Ma, X. Xu, Z. Zhu, X. Wang, H. Deng, C. Li, M. Chen, and J. Tong. 2015. Continuous activation of Nrf2 and its target antioxidant enzymes leads to arsenite-induced malignant transformation of human bronchial epithelial cells. Toxicol. Appl. Pharmacol. 289:231–39. doi:10.1016/j.taap.2015.09.020.
   PubMed Web of Science ®Google Scholar
• Yu, H., M. Kuang, Y. Wang, S. Rodeni, Q. Wei, W. Wang, and D. Mao. 2018. Sodium arsenite injection induces ovarian oxidative stress and affects steroidogenesis in rats. Biol. Trace Elem. Res. doi:10.1007/s12011-018-1467-y.
   Web of Science ®Google Scholar
• Zeng, Q., H. Yi, L. Huang, Q. An, and H. Wang. 2018. Long-term arsenite exposure induces testicular toxicity by redox imbalance, G2/M cell arrest and apoptosis in mice. Toxicology. doi:10.1016/j.tox.2018.09.010.
   Web of Science ®Google Scholar
• Zhu, X. X., X. F. Yao, L. P. Jiang, C. Y. Geng, L. F. Zhong, G. Yang, B. L. Zheng, and X. C. Sun. 2014. Sodium arsenite induces ROS-dependent autophagic cell death in pancreatic β-cells. Food Chem. Toxicol. 70:144–50. doi:10.1016/j.fct.2014.05.006.
   PubMed Web of Science ®Google Scholar