[
Abd El-Hack M.E., Alagawany M., Arif M., Emam M., Saeed M., Arain M.A., Khan R.U. (2018). The uses of microbial phytase as a feed additive in poultry nutrition–a review. Annals Anim. Sci., 18: 639–658.
]Search in Google Scholar
[
Abd El-Hack M.E., Alagawany M., Farag M.R., Tiwari R., Karthik K., Dhama K. (2016). Nutritional, healthical and therapeutic efficacy of black cumin (Nigella sativa) in animals, poultry and humans. Int. J. Pharmacol, 12: 232–248.
]Search in Google Scholar
[
Abd El-Hack M.E., El-Saadony M.T., Shehata A.M., Arif M., Paswan V. K., Elbestawy A.R. (2021). Approaches to prevent and control Campylobacter spp. colonization in broiler chickens: a review. Environ. Sci. Poll. Res., 28: 4989–5004.
]Search in Google Scholar
[
Abd El-Hack M.E., Shafi M.E., Alghamdi W.Y., Abdelnour S.A., Shehata A.M., Ragni M. (2020). Black soldier fly (Hermetia illucens) meal as a promising feed ingredient for poultry: A comprehensive review. Agriculture, 10: 339.
]Search in Google Scholar
[
Abdel-Moneim A.M.E., Shehata A.M., Alzahrani S.O., Shafi M.E., Mesalam N.M., Taha A.E., Abd El-Hack M.E. (2020). The role of polyphenols in poultry nutrition. J. Anim. Physiol. Anim. Nutr., 104: 1851–1866.
]Search in Google Scholar
[
Alagawany M., Abd El-Hack M.E., El-Kholy M.S. (2016). Productive performance, egg quality, blood constituents, immune functions, and antioxidant parameters in laying hens fed diets with different levels of Yucca schidigera extract. Environ. Sci. Poll. Res., 23: 6774–6782.
]Search in Google Scholar
[
Alagawany M., Abd El-Hack M.E., Laudadio V., Tufarelli V. (2014). Effect of low-protein diets with crystalline amino acid supplementation on egg production, blood parameters and nitrogen balance in laying Japanese quails. Avian Biol. Res., 7: 235–243.
]Search in Google Scholar
[
Ameh T., Sayes S.M. (2019). The potential exposure and hazards of copper nanoparticles: a review. Environ. Toxicol. Pharmacol., 71: 103220.
]Search in Google Scholar
[
Blanco J., Lafuente D., Gómez M., García T., Domingo J.L., Sánchez, D.J. (2017). Polyvinyl pyrrolidone-coated silver nanoparticles in a human lung cancer cells: time- and dose-dependent influence over p53 and caspase-3 protein expression and epigenetic effects. Arch. Toxicol., 91: 651–666.
]Search in Google Scholar
[
Brown T.A., Lee J.W., Holian A., Porter V., Fredriksen H., Kim M., Cho Y.H. (2016). Alterations in DNA methylation corresponding with lung inflammation and as a biomarker for disease development after MWCNT exposure. Nanotoxicol., 10: 453–461.
]Search in Google Scholar
[
Brzóska K., Grądzka I., Kruszewski M. (2019). Silver, gold, and iron oxide nanoparticles alter miRNA expression but do not affect DNA methylation in HepG2 cells. Materials., 12: 1038.
]Search in Google Scholar
[
Choudhury S.R, Ordaz J., Lo C.L., Damayanti N.P., Zhou F., Irudayaraj J. (2017). Zinc oxide nanoparticles-induced reactive oxygen species promotes multimodal cyto- and epigenetic toxicity. Toxicol Sci., 156: 261–274.
]Search in Google Scholar
[
Chouke P.B., Potbhare A.K., Meshram N.P., Rai M.M., Dadure K.M., Chaudhary K., ... & Masram D.T. (2022). Bioinspired NiO nanospheres: Exploring in vitro toxicity using Bm-17 and L. rohita liver cells, DNA degradation, docking, and proposed vacuolization mechanism. ACS omega., 7: 6869–6884.
]Search in Google Scholar
[
Dusinska M., Tulinska J., El Yamani N., Kuricova M., Liskova A., Rollerova E., Rundén-Pran E., Smolkova B. (2017). Immunotoxicity, genotoxicity and epigenetic toxicity of nanomaterials: New strategies for toxicity testing? Food Chem. Toxicol., 109: 797–811.
]Search in Google Scholar
[
Emerce E., Ghosh M., Öner D., Duca R.C., Vanoirbeek J., Bekaert B., Hoet P.M., Godderis L. (2019). Carbon nanotube- and asbestos-induced DNA and RNA methylation changes in bronchial epithelial cells. Chem. Res. Toxicol., 32: 850–860.
]Search in Google Scholar
[
Eom W., Lee E., Lee S.H., Sung T.H., Clancy A.J., Lee W.J., Han T.H. (2021). Carbon nanotube-reduced graphene oxide fiber with high torsional strength from rheological hierarchy control. Nat Commun., 12: 396.
]Search in Google Scholar
[
Fenech M. (2008). Genome health nutrigenomics and nutrigenetics diagnosis and nutritional treatment of genome damage on an individual basis. Food Chem. Toxicol., 46: 1365–1370.
]Search in Google Scholar
[
Fernández-Bertólez N., Costa C., Brandão F., Kiliç G., Duarte J.A., Teixeira J.P., Pásaro E., Valdiglesias V., Laffon B. (2018). Toxicological assessment of silica-coated iron oxide nanoparticles in human astrocytes. Food Chem. Toxicol., 118: 13–23.
]Search in Google Scholar
[
Gado A.R., Ellakany H.F., Elbestawy A.R., Abd El-Hack M.E., Khafaga A.F., Taha A.E., Mahgoub S. A. (2019). Herbal medicine additives as powerful agents to control and prevent avian influenza virus in poultry – a review. Ann. Anim. Sci., 19: 905–935.
]Search in Google Scholar
[
Gao F., Ma N., Zhou H., Wang Q., Zhang H., Wang P., Hou H., Wen H., Li L. (2016). Zinc oxide nanoparticles-induced epigenetic change and G2/M arrest are associated with apoptosis in human epidermal keratinocytes. Int. J. Nanomed., 11: 3859–3874.
]Search in Google Scholar
[
Ghanghas P., Sharma M., Desai D., Raza K., Bhalla A., Kumar P., Narula D., Amin S., Sanyal S.N., Kaushal N. (2022). Selenium-based novel epigenetic regulators offer effective chemotherapeutic alternative with wider safety margins in experimental colorectal cancer. Biol. Trace Elem. Res., 200: 635–646.
]Search in Google Scholar
[
Gharpure S., Akash A., Ankamwar B. (2020). A Review on antimicrobial properties of metal nanoparticles. J. Nanosci. Nanotechnol., 20: 3303–3339.
]Search in Google Scholar
[
Ghosh M., Godderis L., Hoet P. (2022). Epigenetic mechanisms in understanding nanomaterial-induced toxicity. In: Nanotoxicology in Safety Assessment of Nanomaterials, Louro H., Silva M.J. (eds). Advances in Experimental Medicine and Biology, 1357, Springer, Cham.
]Search in Google Scholar
[
Ghosh M., Öner D., Duca R.C., Bekaert B., Vanoirbeek J., Godderis L., Hoet P.M. (2018). Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells. Oncotarget., 9: 20351–20365.
]Search in Google Scholar
[
Ghosh M., Öner D., Poels K., Tabish A.M., Vlaanderen J., Pronk A., Kuijpers E., Lan Q., Vermeulen R., Bekaert B., Hoet P.H., Godderis L. (2017). Changes in DNA methylation induced by multi-walled carbon nanotube exposure in the workplace. Nanotoxicology, 11: 1195–1210.
]Search in Google Scholar
[
Gliga A.R., Di Bucchianico S., Lindvall J., Fadeel B., Karlsson H.L. (2018). RNA-sequencing reveals long-term effects of silver nanoparticles on human lung cells. Sci. Rep., 8: 6668.
]Search in Google Scholar
[
Gong C., Tao G., Yang L., Liu J., Liu Q., Li W., Zhuang Z. (2012). Methylation of PARP-1 promoter involved in the regulation of nano-SiO2-induced decrease of PARP-1 mRNA expression. Toxicol Lett., 209: 264–269.
]Search in Google Scholar
[
Gong C., Tao G., Yang L., Liu J., Liu Q., Zhuang Z. (2010). SiO2 nanoparticles induce global genomic hypomethylation in HaCaT cells. Biochem. Biophys. Res. Commun., 397: 396–400.
]Search in Google Scholar
[
Gupta J., Sharma S., Sharma N.R., Kabra D. (2020). Phytochemicals enriched in spices: a source of natural epigenetic therapy. Arch. Pharm. Res., 43: 171–186.
]Search in Google Scholar
[
Gupta R., Xie H. (2018). Nanoparticles in daily life: applications, toxicity and regulations. J. Environ. Pathol. Toxicol. Oncol., 37: 209–230.
]Search in Google Scholar
[
Hanot-Roy M., Tubeuf E., Guilbert A., Bado-Nilles A., Vigneron P., Trouiller B., Braun A., Lacroix G. (2016). Oxidative stress pathways involved in cytotoxicity and genotoxicity of titanium dioxide (TiO2) nanoparticles on cells constitutive of alveolo-capillary barrier in vitro. Toxicol. In vitro, 33: 125–135.
]Search in Google Scholar
[
Hu J., Lin W., Lin B., Wu K., Fan H., Yu Y. (2019). Persistent DNA methylation changes in zebrafish following graphene quantum dots exposure in surface chemistry-dependent manner. Ecotoxicol. Environ. Saf., 169: 370–375.
]Search in Google Scholar
[
Huang Y., Wu R., Su Z.Y., Guo Y., Zheng X., Yang C.S., Kong A.N. (2017). A naturally occurring mixture of tocotrienols inhibits the growth of human prostate tumor, associated with epigenetic modifications of cyclin-dependent kinase inhibitors p21 and p27. J. Nutr. Biochem., 40: 155–163.
]Search in Google Scholar
[
Jiang Z., Lai Y., Beaver J.M., Tsegay P.S., Zhao M.L., Horton J., Zamora M., Rein H.L., Miralles F., Shaver M., Hutcheson J.D., Agoulnik I., Wilson S.H., Liu Y. (2020). Oxidative DNA damage modulates DNA methylation pattern in human breast cancer 1 (BRCA1) gene via the crosstalk between DNA polymerase β and a de novo DNA methyltransferase. Cells, 9: E225.
]Search in Google Scholar
[
Johansen K.M., Johansen J. (2006). Regulation of chromatin structure by histone H3S10 phosphorylation. Chromosome Res., 14: 393–404.
]Search in Google Scholar
[
Jou Y.J., Chen C.J., Liu Y.C., Way T.D., Lai C.H., Hua C.H., Wang C.Y., Huang S.H., Kao J.Y., Lin C.W. (2015). Quantitative phosphoproteomic analysis reveals γ-bisabolene inducing p53-mediated apoptosis of human oral squamous cell carcinoma via HDAC2 inhibition and ERK1/2 activation. Proteomics, 15: 3296–3309.
]Search in Google Scholar
[
Kalaiarasi A., Sankar R., Anusha C., Saravanan K., Aarthy K., Karthic S., Mathuram T.L., Ravikumar V. (2018). Copper oxide nanoparticles induce anticancer activity in A549 lung cancer cells by inhibition of histone deacetylase. Biotechnol Lett., 40: 249–256.
]Search in Google Scholar
[
Kanwal R., Datt M., Liu X., Gupta S. (2016). Dietary flavones as dual inhibitors of DNA methyltransferases and histone methyltransferases. PLoS One, 11(9):e0162956.
]Search in Google Scholar
[
Khafaga A.F., Abd El-Hack M.E., Taha, A.E., Elnesr S.S., Alagawany M. (2019). The potential modulatory role of herbal additives against Cd toxicity in human, animal, and poultry: a review. Environ. Sci. Poll. Res., 26: 4588–4604.
]Search in Google Scholar
[
Kiany T., Pishkar L., Sartipnia N., Iranbakhsh A., Barzin G. (2022). Effects of silicon and titanium dioxide nanoparticles on arsenic accumulation, phytochelatin metabolism, and antioxidant system by rice under arsenic toxicity. Environ. Sci. Pollut. Res. Int., 29: 34725–34737.
]Search in Google Scholar
[
Könen-Adıgüzel S., Ergene S. (2018). In vitro evaluation of the genotoxicity of CeO2 nanoparticles in human peripheral blood lymphocytes using cytokinesis-block micronucleus test, comet assay, and gamma H2AX. Toxicol. Ind. Health., 34: 293–300.
]Search in Google Scholar
[
Kopp B., Dario M., Zalko D., Audebert M. (2018). Assessment of a panel of cellular biomarkers and the kinetics of their induction in comparing genotoxic modes of action in HepG2 cells. Environ. Mol. Mutagen., 59: 516–528.
]Search in Google Scholar
[
Kung M.L., Hsieh S.L., Wu C.C., Chu T.H., Lin Y.C., Yeh B.W., Hsieh S. (2015). Enhanced reactive oxygen species overexpression by CuO nanoparticles in poorly differentiated hepatocellular carcinoma cells. Nanoscale, 7: 1820–1829.
]Search in Google Scholar
[
Lebre F., Chatterjee N., Costa S., Fernández-de-Gortari E., Lopes C., Meneses, J., Ortiz L., Ribeiro A.R., Vilas-Boas V., Alfaro-Moreno E. (2022). Nanosafety: An Evolving Concept to Bring the Safest Possible Nanomaterials to Society and Environment. Nanomaterials, 12: 1810.
]Search in Google Scholar
[
Lee K.S., El-Sayed M.A. (2006). Gold and silver nanoparticles in sensing and imaging: sensitivity of plasmon response to size, shape, and metal composition. J. Phys. Chem. B., 110: 19220–19225.
]Search in Google Scholar
[
Liang Z.Z., Zhang Y.X., Zhu, R.M. Li Y.L., Jiang H.M., Li R.B., Chen Q.X., Wang Q., Tang L.Y., Ren Z.F. (2022). Identification of epigenetic modifications mediating the antagonistic effect of selenium against cadmium-induced breast carcinogenesis. Environ. Sci. Pollut. Res., 29: 22056–22068.
]Search in Google Scholar
[
Liou S.H., Wu W.T., Liao H.Y., Chen C.Y., Tsai C.Y., Jung W.T., Lee H.L. (2017). Global DNA methylation and oxidative stress biomarkers in workers exposed to metal oxide nanoparticles. J. Hazard Mater., 331: 329–335.
]Search in Google Scholar
[
Liu D., Wu D., Zhao L., Yang Y., Ding J., Dong L., Hu L., Wang F., Zhao X., Cai Y., Jin J. (2015). Arsenic trioxide reduces global histone H4 acetylation at lysine 16 through direct binding to histone acetyltransferase hMOF in human cells. PLoS One, 10:e0141014.
]Search in Google Scholar
[
Liu J., Zhao Y., Ge W., Zhang P., Liu X., Zhang W., Hao Y., Yu S., Li L., Chu M., Min L., Zhang H., Shen W. (2017). Oocyte exposure to ZnO nanoparticles inhibits early embryonic development through the γ-H2AX and NF-κB signaling pathways. Oncotarget, 8: 42673–42692.
]Search in Google Scholar
[
Long J., Ma W., Yu Z., Liu H., Cao Y. (2019). Multi-walled carbon nanotubes (MWCNTs) promoted lipid accumulation in THP-1 macrophages through modulation of endoplasmic reticulum (ER) stress. Nanotoxicology, 13: 938–951.
]Search in Google Scholar
[
Lu X., Miousse I.R., Pirela S.V., Melnyk S., Koturbash I., Demokritou P. (2016). Short-term exposure to engineered nanomaterials affects cellular epigenome. Nanotoxicology, 10: 140–150.
]Search in Google Scholar
[
Lu X., Miousse I.R., Pirela S.V., Moore J.K., Melnyk S., Koturbash I., Demokritou P. (2016). In vivo epigenetic effects induced by engineered nanomaterials: A case study of copper oxide and laser printer-emitted engineered nanoparticles. Nanotoxicology, 10: 629–639.
]Search in Google Scholar
[
Lv L., Liu Y., Zhang P., Zhang X., Liu J., Chen T., Su P., Li H., Zhou Y. (2015). The nanoscale geometry of TiO2 nanotubes influences the osteogenic differentiation of human adipose-derived stem cells by modulating H3K4 trimethylation. Biomaterials, 39: 193–205.
]Search in Google Scholar
[
Mira A., Shimizu K. (2015). In vitro cytotoxic activities and molecular mechanisms of angelica shikokiana extract and its isolated compounds. Pharmacogn. Mag., 11(Suppl 4): S564–S569.
]Search in Google Scholar
[
Missaoui W.N., Arnold R.D., Cummings B.S. (2018). Toxicological status of nanoparticles: what we know and what we don’t know. Chem. Biol. Interact., 295: 1–12.
]Search in Google Scholar
[
Mytych J., Zebrowski J., Lewinska A., Wnuk M. (2017). Prolonged effects of silver nanoparticles on p53/p21 pathway-mediated proliferation, DNA damage response, and methylation parameters in HT22 hippocampal neuronal cells. Mol. Neurobiol., 54: 1285–300.
]Search in Google Scholar
[
Ng C.T., Dheen S.T., Yip W.C., Ong C.N., Bay B.H., Yung L.Y.L. (2011). The induction of epigenetic regulation of PROS1 gene in lung fibroblasts by gold nanoparticles and implications for potential lung injury. Biomaterials, 32: 7609–7615.
]Search in Google Scholar
[
Öner D., Ghosh M., Bové H., Moisse M., Boeckx B., Duca R.C., Poels K., Luyts K., Putzeys E., Van Landuydt K., Vanoirbeek J.A., Ameloot M., Lambrechts D., Godderis L., Hoet P.H. (2018). Differences in MWCNT- and SWCNT-induced DNA methylation alterations in association with the nuclear deposition. Part Fibre Toxicol., 15: 11.
]Search in Google Scholar
[
Öner D., Ghosh M., Coorens R., Bové H., Moisse M., Lambrechts D., Ameloot M., Godderis L., Hoet P.M. (2020). Induction and recovery of CpG site specific methylation changes in human bronchial cells after long-term exposure to carbon nanotubes and asbestos. Environ. Int., 137: 105530.
]Search in Google Scholar
[
Öner D., Ghosh M., Coorens R., Bové H., Moisse M., Lambrechts D., Ameloot M., Godderis L., Hoet P.M. (2017). Epigenetic effects of carbon nanotubes in human monocytic cells. Mutagenesis, 32: 181–191.
]Search in Google Scholar
[
Ooi S.K., O’Donnel A.H., Bestor T.H. (2009). Mammalian cytosine methylation at a glance. J. Cell Sci., 122: 2787–2791.
]Search in Google Scholar
[
Pascoal G.L., Novaes G.M., Sobrinho M.P., Hirayama A.B., Castro I.A., Ong T.P. (2022). Selenium supplementation during puberty and young adulthood mitigates obesity-induced metabolic, cellular and epigenetic alterations in male rat physiology. Antioxidants, 11: 895.
]Search in Google Scholar
[
Patil N.A., Gade W.N., Deobagkar D.D. (2016). Epigenetic modulation upon exposure of lung fibroblasts to TiO2 and ZnO nanoparticles: alterations in DNA methylation. Int. J. Nanomedicine, 11: 4509–4519.
]Search in Google Scholar
[
Patil Y.M., Rajpathak S.N., Deobagkar D.D. (2019). Characterization and DNA methylation modulatory activity of gold nanoparticles synthesized by Pseudoalteromonas strain. J. Biosci., 14: 4573–4587.
]Search in Google Scholar
[
Pogribna M., Koonce N.A., Mathew A., Word B., Patri A.K., Lyn-Cook B., Hammons G. (2020). Effect of titanium dioxide nanoparticles on DNA methylation in multiple human cell lines. Nanotoxicology, 14: 534–553.
]Search in Google Scholar
[
Prasad R.Y., Chastain P.D., Nikolaishvili-Feinberg N., Smeester L., Kaufmann W.K., Fry R.C. (2013). Titanium dioxide nanoparticles activate the ATM-Chk2 DNA damage response in human dermal fibroblasts. Nanotoxicology, 7: 1111–1119.
]Search in Google Scholar
[
Qian Y., Zhang J., Hu Q., Xu M., Chen Y., Hu G., Zhao M., Liu S. (2015). Silver nanoparticle-induced hemoglobin decrease involves alteration of histone 3 methylation status. Biomaterials, 70: 12–22.
]Search in Google Scholar
[
Romanek J. (2013). Epigenetic basis of molecular changes in animal cells with particular regard to embryonic development – a review. Ann. Anim. Sci., 13: 675–685.
]Search in Google Scholar
[
Rossner P., Vrbova K., Rossnerova A., Zavodna T., Milcova A., Klema J., Vecera Z., Mikuska P., Coufalik P., Capka L., Krumal K., Docekal B., Holan V., Machala M., Topinka J. (2020). Gene expression and epigenetic changes in mice following inhalation of Copper (II) oxide nanoparticles. Nanomaterials, 10: 550.
]Search in Google Scholar
[
Rossnerova A., Honkova K., Pelclova D., Zdimal V., Hubacek J.A., Chvojkova I., Vrbova K., Rossner P., Topinka J., Vlckova S., Fenclova Z., Lischkova L., Klusackova P., Schwarz J., Ondracek J., Ondrackova L., Kostejn M., Klema J., Dvorackova S. (2020). DNA methylation profiles in a group of workers occupationally exposed to nanoparticles. Int. J. Mol. Sci., 21: 2420.
]Search in Google Scholar
[
Saeed M., Abd El-Hack M.E., Alagawany M., Arain M.A., Arif M., Mirza M.A., Dhama K. (2017). Chicory (cichorium intybus) herb: Chemical composition, pharmacology, nutritional and healthical applications. Inter. J. Pharm., 13: 351–360.
]Search in Google Scholar
[
Saeed M., Abd El-Hack M.E., Arif M., El-Hindawy M.M., Attia A.I., Mahrose K.M., Noreldin A.E. (2017). Impacts of distiller’s dried grains with solubles as replacement of soybean meal plus vitamin E supplementation on production, egg quality and blood chemistry of laying hens. Ann. Anim. Sci., 17: 849–862.
]Search in Google Scholar
[
Saeed M., Yatao, X., Hassan F.U., Arain M.A., Abd El-Hack M.E., Noreldin A.E., Sun C. (2018). Influence of graded levels of l-theanine dietary supplementation on growth performance, carcass traits, meat quality, organs histomorphometry, blood chemistry and immune response of broiler chickens. Inter. J. Mol. Sci., 19: 462.
]Search in Google Scholar
[
Samiec M., Skrzyszowska M. (2018). Can reprogramming of overall epigenetic memory and specific parental genomic imprinting memory within donor cell-inherited nuclear genome be a major hindrance for the somatic cell cloning of mammals? – a review. Ann. Anim. Sci., 18: 623–638.
]Search in Google Scholar
[
Schulte P.A., Leso V., Niang M., Iavicoli I. (2019). Current state of knowledge on the health effects of engineered nanomaterials in workers: a systematic review of human studies and epidemiological investigations. Scand. J. Work Environ. Health, 45: 217–238.
]Search in Google Scholar
[
Seidel C., Kirsch A., Fontana C., Visvikis A., Remy A., Gaté L., Darne C., Guichard Y. (2017). Epigenetic changes in the early stage of silica-induced cell transformation. Nanotoxicology, 11: 923–935.
]Search in Google Scholar
[
Semik-Gurgul E., Ząbek T., Kawecka-Grochocka E., Zalewska M., Kościuczuk E., Bagnicka E. (2022). Epigenetic states of genes controlling immune responsiveness in bovine chronic mastitis. Ann. Anim. Sci., 22: 575–581.
]Search in Google Scholar
[
Setyawati M.I., Khoo P.K., Eng B.H., Xiong S., Zhao X., Das G.K., Tan T.T., Loo J.S., Leong D.T., Ng K.W. (2013). Cytotoxic and genotoxic characterization of titanium dioxide, gadolinium oxide, and poly (lactic-co-glycolic acid) nanoparticles in human fibroblasts. J. Biomed. Mater Res A., 101: 633–640.
]Search in Google Scholar
[
Shyamasundar S., Ng C.T., Yung L.L., Dheen S.T., Bay B.H. (2015). Epigenetic mechanisms in nanomaterial-induced toxicity. Epigenomics, 7: 395–411.
]Search in Google Scholar
[
Sierra M.I., Valdés A., Fernández A.F., Torrecillas R., Fraga M.F. (2016). The effect of exposure to nanoparticles and nanomaterials on the mammalian epigenome. Int. J. Nanomedicine, 11: 6297–6306.
]Search in Google Scholar
[
Sima M., Vrbova K., Zavodna T., Honkova K., Chvojkova I., Ambroz A., Klema J., Rossnerova A., Polakova K., Malina T., Belza J., Topinka J., Rossner P. Jr. (2020). The differential effect of carbon dots on gene expression and DNA methylation of human embryonic lung fibroblasts as a function of surface charge and dose. Int. J. Mol. Sci., 4763.10.3390/ijms21134763736994632635498
]Search in Google Scholar
[
Skrzyszowska M., Samiec M. (2020). Enhancement of in vitro developmental outcome of cloned goat embryos after epigenetic modulation of somatic cell-inherited nuclear genome with trichostatin A. Ann. Anim. Sci., 20: 97–108.
]Search in Google Scholar
[
Smolkova B., Miklikova S., Horvatova K.V., Babelova A., El Yamani N., Zdurencikova M., Fridrichova I., Zmetakova I., Krivulcik T., Kalinkova L., Matuskova M., Kucerova L., Dusinska M. (2016). Global and gene specific DNA methylation in breast cancer cells was not affected during epithelial-to-mesenchymal transition in vitro. Neoplasma, 63: 901–910.
]Search in Google Scholar
[
Sooklert K., Nilyai S., Rojanathanes R., Jindatip D., Sae-Liang N., Kitkumthorn N., Mutirangura A., Sereemaspun A. (2019). N-acetylcysteine reverses the decrease of DNA methylation status caused engineered gold, silicon, and chitosan nanoparticles. Int. J. Nanomedicine, 14: 4573–4587.
]Search in Google Scholar
[
Stoccoro A., Di Bucchianico S., Coppedé F., Ponti J., Uboldi C., Blosi M., Delpivo C., Ortelli S., Costa A.L., Migliore L. (2017). Multiple endpoints to evaluate pristine and remediated titanium dioxide nanoparticles genotoxicity in lung epithelial A549 cells. Toxicol Lett., 276: 48–61.
]Search in Google Scholar
[
Surapaneni S.K., Bashir S., Tikoo K. (2018). Gold nanoparticles-induced cytotoxicity in triple negative breast cancer involves different epigenetic alterations depending upon the surface charge. Sci. Rep., 8: 12295.
]Search in Google Scholar
[
Tabish A.M., Poels K., Byun H.M., Luyts K., Baccarelli A.A., Martens J., Kerkhofs S., Seys S., Hoet P., Godderis L. (2017). Changes in DNA methylation in mouse lungs after a single intra-tracheal administration of nanomaterials. PLoS One, 12:e0169886.
]Search in Google Scholar
[
Tarantini A., Lanceleur R., Mourot A., Lavault M.T., Casterou G., Jarry G., Hogeveen K., Fessard V. (2015). Toxicity, genotoxicity and proinflammatory effects of amorphous nanosilica in the human intestinal Caco-2 cell line. Toxicol In vitro, 29: 398–407.
]Search in Google Scholar
[
Torres I.O., Fudjimori D.G. (2015). Functional coupling between writers, erasers and readers of histone and DNA methylation. Curr. Opin. Struct. Biol., 25: 68–75.
]Search in Google Scholar
[
Valinluck V., Sowers L.C. (2007). Inflammation-mediated cytosine damage: a mechanistic link between inflammation and the epigenetic alterations in human cancers. Cancer Res., 67: 5583–5586.
]Search in Google Scholar
[
Valinluck V., Tsai H.H., Rogstad D.K., Burdzy A., Bird A., Sowers L.C. (2004). Oxidative damage to methyl-CpG sequences inhibits the binding of the methyl-CpG binding domain (MBD) of methyl-CpG binding protein 2 (MeCP2). Nucleic Acids Res., 32: 4100–4108.
]Search in Google Scholar
[
Wan R., Mo Y., Feng L., Chien S., Tollerud D.J., Zhang Q. (2012). DNA damage caused by metal nanoparticles: involvement of oxidative stress and activation of ATM. Chem. Res. Toxicol., 25: 1402–1411.
]Search in Google Scholar
[
Wu X., Zhang Y. (2017). TET-mediated active DNA demethylation: mechanism, function and beyond. Nat. Rev. Genet., 18: 517–534.
]Search in Google Scholar
[
Xiaoli F., Qiyue C., Weihong G., Yaqing Z., Chen H., Junrong W., Longquan S. (2020). Toxicology data of graphene-family nanomaterials: an update. Arch. Toxicol., 94: 1915–1939.
]Search in Google Scholar
[
Zhang L., Han B., Xiang J., Liu K., Dong H., Gao X. (2018). Silica nanoparticle releases SIRT6-induced epigenetic silencing of follistatin. Int. J. Biochem. Cell Biol., 95: 27–34.
]Search in Google Scholar
[
Zhang T., Du E., Liu Y., Cheng J., Zhang Z., Xu Y., Qi S., Chen Y. (2020). Anticancer effects of zinc oxide nanoparticles through altering the methylation status of histone on bladder cancer cells. Int. J. Nanomed., 15: 1457–1468.
]Search in Google Scholar
[
Zhao X., Rao Y., Liang J., Lin S., Wang X., Li Z., Huang J. (2019). Silver Nanoparticle-Induced Phosphorylation of Histone H3 at Serine 10 Involves MAPK Pathways. Biomolecules, 9: 78.
]Search in Google Scholar
[
Zhao X., Takabayashi F., Ibuki Y. (2016). Coexposure to silver nanoparticles and ultraviolet A synergistically enhances the phosphorylation of histone H2AX. J. Photochem. Photobiol. B., 162: 213–222.
]Search in Google Scholar
[
Zhao X., Toyooka T., Ibuki Y. (2017). Silver nanoparticle-induced phosphorylation of histone H3 at serine 10 is due to dynamic changes in actin filaments and the activation of Aurora kinases. Toxicol. Lett., 276: 39–47.
]Search in Google Scholar
[
Zhou W., Tian D., He J., Yan X., Zhao J., Yuan X., Peng S. (2019). Prolonged exposure to carbon nanoparticles induced methylome remodeling and gene expression in zebrafish heart. J. Appl. Toxicol., 39: 322–332.
]Search in Google Scholar
[
Zou Y., Li Q., Jiang L., Guo C., Li Y., Yu Y., Li Y., Duan J., Sun Z. (2016). DNA hypermethylation of CREB3L1 and Bcl-2 associated with the mitochondrial-mediated apoptosis via PI3K/Akt pathway in human BEAS-2B cells exposure to silica nanoparticles. PLoS One, 11:e0158475.
]Search in Google Scholar
[
Zuo Q., Wu R., Xiao X Yang C., Yang Y., Wang C., Lin L., Kong A.N. (2018). The dietary flavone luteolin epigenetically activates the Nrf2 pathway and blocks cell transformation in human colorectal cancer HCT116 cells. J. Cell Biochem., 119: 9573–9582.
]Search in Google Scholar
