Epigenetic changes involved in hydroquinone-induced mutations

References

• Allis, C.D. and Jenuwein, T., 2016. The molecular hallmarks of epigenetic control. Nature reviews genetics, 17 (8), 487–500.
   PubMed Web of Science ®Google Scholar
• Becker, A., et al., 2016. Poly(ADP-ribosyl)ation of methyl CpG binding domain protein 2 regulates chromatin structure. Journal of biological chemistry, 291 (10), 4873–4881.
   PubMed Web of Science ®Google Scholar
• Bogdanovic, O. and Lister, R., 2017. DNA methylation and the preservation of cell identity. Current opinion in genetics & development, 46, 9–14.
   PubMed Web of Science ®Google Scholar
• Caruso, L.B., et al., 2018. Poly(ADP-ribose) Polymerase 1, PARP1, modifies EZH2 and inhibits EZH2 histone methyltransferase activity after DNA damage. Oncotarget, 9 (12), 10585–10605.
   PubMedGoogle Scholar
• Chen, S., et al., 2017. Differently expressed long noncoding RNAs and mRNAs in TK6 cells exposed to low dose hydroquinone. Oncotarget, 8 (56), 95554–95567.
   PubMedGoogle Scholar
• Chen, Y.-J. and Chang, L.-S., 2013. Hydroquinone-induced miR-122 down-regulation elicits ADAM17 up-regulation, leading to increased soluble TNF-α production in human leukemia cells with expressed Bcr/Abl. Biochemical pharmacology, 86 (5), 620–631.
   PubMed Web of Science ®Google Scholar
• Chen, Y., et al., 2016. Hydroquinone-induced malignant transformation of TK6 cells by facilitating SIRT1-mediated p53 degradation and up-regulating KRAS. Toxicology letters, 259, 133–142.
   PubMed Web of Science ®Google Scholar
• Chen, Y., et al., 2018. Bcl-2 protects TK6 cells against hydroquinone-induced apoptosis through PARP-1 cytoplasm translocation and stabilizing mitochondrial membrane potential. Environmental and molecular mutagenesis, 59 (1), 49–59.
   PubMed Web of Science ®Google Scholar
• Chen, Y., et al., 2019. A PARP1-BRG1-SIRT1 axis promotes HR repair by reducing nucleosome density at DNA damage sites. Nucleic acids research, 47 (16), 8563–8580.
   PubMed Web of Science ®Google Scholar
• Coulter, J.B., O'Driscoll, C.M., and Bressler, J.P., 2013. Hydroquinone increases 5-hydroxymethylcytosine formation through ten eleven translocation 1 (TET1) 5-methylcytosine dioxygenase. Journal of biological chemistry, 288 (40), 28792–28800.
   PubMed Web of Science ®Google Scholar
• Fenga, C., Gangemi, S., and Costa, C., 2016. Benzene exposure is associated with epigenetic changes (Review). Molecular medicine reports, 13 (4), 3401–3405.
   PubMed Web of Science ®Google Scholar
• Gui, Z., et al., 2019. Poly(ADP-ribose) polymerase-1 promotes expression of miR-155 by the up-regulation of methyl-CpG binding domain protein 2 in TK6 cells exposed to hydroquinone. Toxicology in vitro, 55, 51–57.
   PubMed Web of Science ®Google Scholar
• Hombach, S., and Kretz, M., 2016. Non-coding RNAs: classification, biology and functioning. Advances in experimental medicine and biology, 937, 3–17.
   PubMed Web of Science ®Google Scholar
• Hu, J., et al., 2014. Effects of benzene and its metabolites on global DNA methylation in human normal hepatic L02 cells. Environmental toxicology, 29 (1), 108–116.
   PubMed Web of Science ®Google Scholar
• Ji, J., et al., 2017. Phosphorylated fraction of H2AX as a measurement for DNA damage in cancer cells and potential applications of a novel assay. PLoS one, 12 (2), e0171582.
   PubMed Web of Science ®Google Scholar
• Jiang, R., et al., 2019. Exosomal miR-221 derived from hydroquinone-transformed malignant human bronchial epithelial cells is involved in cell viability of recipient cells. Journal of applied toxicology. 40(2):224–233.
   PubMed Web of Science ®Google Scholar
• Kraus, W.L. and Hottiger, M.O., 2013. PARP-1 and gene regulation: progress and puzzles. Molecular aspects of medicine, 34 (6), 1109–1123.
   PubMed Web of Science ®Google Scholar
• Li, J., et al., 2018. Enhanced H3K4me3 modifications are involved in the transactivation of DNA damage responsive genes in workers exposed to low-level benzene. Environmental pollution, 234, 127–135.
   PubMed Web of Science ®Google Scholar
• Li, Y., et al., 2013. Changes in DNA methylation of erythroid-specific genes in K562 cells exposed to phenol and hydroquinone. Toxicology, 312, 108–114.
   PubMed Web of Science ®Google Scholar
• Liang, B., et al., 2018. Down-regulation of miRNA-451a and miRNA-486-5p involved in benzene-induced inhibition on erythroid cell differentiation in vitro and in vivo. Archives of toxicology, 92 (1), 259–272.
   PubMed Web of Science ®Google Scholar
• Ling, X.X., et al., 2016. Poly(ADP-ribosyl)ation of apoptosis antagonizing transcription factor involved in hydroquinone-induced dna damage response. Biomedical and environmental sciences, 29, 80–84.
   PubMed Web of Science ®Google Scholar
• Liu, J., et al., 2017a. PARP1 may be involved in hydroquinone induced apoptosis by poly ADP ribosylation of ZO2. Molecular medicine reports, 16 (6), 8076–8084.
   PubMed Web of Science ®Google Scholar
• Liu, L., et al., 2012. Hypomethylation mediated by decreased DNMTs involves in the activation of proto-oncogene MPL in TK6 cells treated with hydroquinone. Toxicology letters., 209 (3), 239–245.
   PubMed Web of Science ®Google Scholar
• Liu, L., et al., 2015. Poly(ADP-ribosyl)ation enhances H-RAS protein stability and causes abnormal cell cycle progression in human TK6 lymphoblastoid cells treated with hydroquinone. Chemico-biological interactions, 238, 1–8.
   PubMed Web of Science ®Google Scholar
• Liu, L., et al., 2017b. Rb silencing mediated by the down-regulation of MeCP2 is involved in cell transformation induced by long-term exposure to hydroquinone. Molecular carcinogenesis, 56 (2), 651–663.
   PubMed Web of Science ®Google Scholar
• Luo, H., et al., 2017. Hydroquinone induces TK6 cell growth arrest and apoptosis through PARP-1/p53 regulatory pathway. Environmental toxicology, 32 (9), 2163–2171.
   PubMed Web of Science ®Google Scholar
• Luo, H., et al., 2018. miR-7-5p overexpression suppresses cell proliferation and promotes apoptosis through inhibiting the ability of DNA damage repair of PARP-1 and BRCA1 in TK6 cells exposed to hydroquinone. Chemico-biological interactions, 283, 84–90.
   PubMed Web of Science ®Google Scholar
• Mancini, M., et al., 2017. In vitro hydroquinone–induced instauration of histone bivalent mark on human retroelements (LINE-1) in HL60 cells. Toxicology in vitro, 40, 1–10.
   PubMed Web of Science ®Google Scholar
• Moore, S., et al., 2019. The CHD6 chromatin remodeler is an oxidative DNA damage response factor. Nature communications, 10 (1), 241.
   PubMedGoogle Scholar
• Nagelkerke, A. and Span, P.N., 2016. Staining against phospho-H2AX (gamma-H2AX) as a marker for DNA damage and genomic instability in cancer tissues and cells. Advances in experimental medicine and biology, 899, 1–10.
   PubMed Web of Science ®Google Scholar
• Peng, C., et al., 2013. Genotoxicity of hydroquinone in A549 cells. Cell biology and toxicology, 29 (4), 213–227.
   PubMed Web of Science ®Google Scholar
• Rauch, P.J., et al., 2016. MPL expression on AML blasts predicts peripheral blood neutropenia and thrombocytopenia. Blood, 128 (18), 2253–2257.
   PubMed Web of Science ®Google Scholar
• Rota, F., et al., 2018. Epigenetic and transcriptional modifications in repetitive elements in petrol station workers exposed to benzene and MTBE. International journal of environmental research and public health, 15, E735.
   PubMed Web of Science ®Google Scholar
• Sha, Y., et al., 2014. Role of poly (ADP-ribose) polymerase 1 in DNA methylation changes induced by hydroquinone in human bronchial epithelial cell. Chinese journal of industrial hygiene and occupational diseases, 32 (3), 181–185.
   Google Scholar
• Shen, J., et al., 2017. Global DNA hypomethylation in leukocytes associated with glioma risk. Oncotarget, 8 (38), 63223–63231.
   PubMedGoogle Scholar
• Shibata, M.A., et al., 1991. Induction of renal cell tumors in rats and mice, and enhancement of hepatocellular tumor development in mice after long-term hydroquinone treatment. Japanese journal of cancer research, 82 (11), 1211–1219.
   PubMedGoogle Scholar
• Souyri, M., 1998. MPL: from an acute myeloproliferative virus to the isolation of the long sought thrombopoietin. Seminars in hematology, 35 (3), 222–231.
   PubMed Web of Science ®Google Scholar
• Stillman, B., 2018. Histone modifications: insights into their influence on gene expression. Cell, 175 (1), 6–9.
   PubMed Web of Science ®Google Scholar
• Tabish, A.M., et al., 2012. Epigenetic factors in cancer risk: effect of chemical carcinogens on global DNA methylation pattern in human TK6 cells. PLoS one, 7 (4), e34674.
   PubMed Web of Science ®Google Scholar
• Tan, Q., et al., 2018. E4F1 silencing inhibits the cell growth through cell-cycle arrest in malignant transformed cells induced by hydroquinone. Journal of biochemical and molecular toxicology, 33, e22269.
   PubMed Web of Science ®Google Scholar
• Tang, K.Y., et al., 2016. Long-term exposure of K562 cells to benzene metabolites inhibited erythroid differentiation and elevated methylation in erythroid specific genes. Toxicology research, 5 (5), 1284–1297.
   Web of Science ®Google Scholar
• Teras, L.R., et al., 2019. Residential ambient benzene exposure in the United States and subsequent risk of hematologic malignancies. International journal of cancer. 145(10):2647–2660.
   PubMed Web of Science ®Google Scholar
• Wang, L., et al., 2015. Inhibition of poly(ADP-ribose) polymerase 1 protects against acute myeloid leukemia by suppressing the myeloproliferative leukemia virus oncogene. Oncotarget, 6 (29), 27490–27504.
   PubMedGoogle Scholar
• Wendling, F., et al., 1986. MPLV: a retrovirus complex inducing an acute myeloproliferative leukemic disorder in adult mice. Virology, 149 (2), 242–246.
   PubMed Web of Science ®Google Scholar
• Wirbisky-Hershberger, S.E., et al., 2017. Atrazine exposure decreases the activity of DNMTs, global DNA methylation levels, and DNMT expression. Food and chemical toxicology, 109, 727–734.
   PubMed Web of Science ®Google Scholar
• Xu, L., et al., 2017. Inhibition of autophagy enhances hydroquinone-induced TK6 cell death. Toxicology in vitro., 41, 123–132.
   PubMed Web of Science ®Google Scholar
• Yang, X., et al., 2019. Benzene metabolite hydroquinone promotes DNA homologous recombination repair via the NF-kappaB pathway. Carcinogenesis, 40 (8), 1021–1030.
   PubMed Web of Science ®Google Scholar
• Yuan, Q., et al., 2020. Regulatory loop between lncRNA FAS-AS1 and DNMT3b controls FAS expression in hydroquinone-treated TK6 cells and benzene-exposed workers. Environmental pollution, 261, 114147.
   PubMed Web of Science ®Google Scholar
• Yuan, W.-X., et al., 2014. Hydroquinone inhibited the differentiation of HL-60 cells through MIRNA-146A mediation. Toxicology letters, 229, S87–S88.
   Web of Science ®Google Scholar
• Zhang, H., et al., 2020. Up-regulation of DNMT3b contributes to HOTAIRM1 silencing via DNA hypermethylation in cells transformed by long-term exposure to hydroquinone and workers exposed to benzene. Toxicology letters, 322, 12–19.
   PubMed Web of Science ®Google Scholar