View Item 

Show simple item record

Mercury biomarkers and DNA methylation among michigan dental professionals

dc.contributor.authorGoodrich, Jaclyn M.en_US
dc.contributor.authorBasu, Niladrien_US
dc.contributor.authorFranzblau, Alfreden_US
dc.contributor.authorDolinoy, Dana C.en_US
dc.date.accessioned2013-04-08T20:49:54Z
dc.date.available2014-05-23T15:04:19Zen_US
dc.date.issued2013-04en_US
dc.identifier.citationGoodrich, Jaclyn M.; Basu, Niladri; Franzblau, Alfred; Dolinoy, Dana C. (2013). "Mercury biomarkers and DNA methylation among michigan dental professionals." Environmental and Molecular Mutagenesis 54(3): 195-203. <http://hdl.handle.net/2027.42/97235>en_US
dc.identifier.issn0893-6692en_US
dc.identifier.issn1098-2280en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/97235
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherEpigeneticsen_US
dc.subject.otherOccupational Exposureen_US
dc.subject.otherSelenoproteinsen_US
dc.subject.otherEnvironmental Exposureen_US
dc.titleMercury biomarkers and DNA methylation among michigan dental professionalsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.identifier.pmid23444121en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/97235/1/em21763.pdf
dc.identifier.doi10.1002/em.21763en_US
dc.identifier.sourceEnvironmental and Molecular Mutagenesisen_US
dc.identifier.citedreferencePilsner JR, Lazarus AL, Nam DH, Letcher RJ, Sonne C, Dietz R, Basu N. 2010. Mercury‐associated DNA hypomethylation in polar bear brains via the luminometric methylation assay: A sensitive method to study epigenetics in wildlife. Mol Ecol 19: 307 – 314.en_US
dc.identifier.citedreferenceMcDowell MA, Dillon CF, Osterloh J, Bolger PM, Pellizzari E, Fernando R, Montes de Oca R, Schober SE, Sinks T, Jones RL, Mahaffey KR. 2004. Hair mercury levels in U.S. children and women of childbearing age: Reference range data from NHANES 1999–2000. Environ Health Perspect 112: 1165 – 1171.en_US
dc.identifier.citedreferenceMeplan C, Crosley LK, Nicol F, Beckett GJ, Howie AF, Hill KE, Horgan G, Mathers JC, Arthur JR, Hesketh JE. 2007. Genetic polymorphisms in the human selenoprotein P gene determine the response of selenoprotein markers to selenium supplementation in a gender‐specific manner (the SELGEN study). FASEB J 21: 3063 – 3074.en_US
dc.identifier.citedreferenceMeplan C, Nicol F, Burtle BT, Crosley LK, Arthur JR, Mathers JC, Hesketh JE. 2009. Relative abundance of selenoprotein P isoforms in human plasma depends on genotype, Se intake, and cancer status. Antioxid Redox Signal 11: 2631 – 2640.en_US
dc.identifier.citedreferenceMergler D, Anderson HA, Chan LHM, Mahaffey KR, Murray M, Sakamoto M, Stern AH. 2007. Methylmercury exposure and health effects in humans: A worldwide concern. Ambio 36: 3 – 11.en_US
dc.identifier.citedreferenceMillis RM. 2011. Epigenetics and hypertension. Curr Hypertens Rep 13: 21 – 28.en_US
dc.identifier.citedreferenceMin JL, Lakenberg N, Bakker‐Verweij M, Suchiman E, Boomsma DI, Slagboom PE, Meulenbelt I. 2006. High microsatellite and SNP genotyping success rates established in a large number of genomic DNA samples extracted from mouth swabs and genotypes. Twin Res Hum Genet 9: 501 – 506.en_US
dc.identifier.citedreferenceNam DH, Basu N. 2011. Rapid methods to detect organic mercury and total selenium in biological samples. Chem Cent J 5: 3.en_US
dc.identifier.citedreferenceNohesara S, Ghadirivasfi M, Mostafavi S, Eskandari MR, Ahmadkhaniha H, Thiagalingam S, Abdolmaleky HM. 2011. DNA hypomethylation of MB‐COMT promoter in the DNA derived from saliva in schizophrenia and bipolar disorder. J Psychiatr Res 45: 1432 – 1438.en_US
dc.identifier.citedreferenceOmotayo TI, Rocha JB, Ibukun EO, Kade IJ. 2011. Inorganic mercury interacts with thiols at the nucleotide and cationic binding sites of the ouabain‐sensitive cerebral electrogenic sodium pump. Neurochem Int 58: 776 – 784.en_US
dc.identifier.citedreferenceOnishchenko N, Karpova N, Sabri F, Castren E, Ceccatelli S. 2008. Long‐lasting depression‐like behavior and epigenetic changes of BDNF gene expression induced by perinatal exposure to methylmercury. J Neurochem 106: 1378 – 1387.en_US
dc.identifier.citedreferenceOuellet‐Morin I, Wong CC, Danese A, Pariante CM, Papadopoulos AS, Mill J, Arseneault L. Increase serotonin transporter gene (SERT) DNA methylation is associated with bullying victimization and blunted cortisol response in stress in childhood: A longitudinal study of discordant monozygotic twins. Psychol Med, in press.en_US
dc.identifier.citedreferenceRoman HA, Walsh TL, Coull BA, Dewailly E, Guallar E, Hattis D, Marien K, Schwartz J, Stern AH, Virtanen JK, Rice G. 2011. Evaluation of the cardiovascular effects of methylmercury exposures: current evidence supports development of a dose‐response function for regulatory benefits analysis. Environ Health Perspect 119: 607 – 614.en_US
dc.identifier.citedreferenceRusiecki JA, Baccarelli A, Bollati V, Tarantini L, Moore LE, Bonefeld‐Jorgensen EC. 2008. Global DNA hypomethylation is associated with high serum‐persistent organic pollutants in Greenlandic Inuit. Environ Health Perspect 116: 1547 – 1552.en_US
dc.identifier.citedreferenceSchulz WA, Steinhoff C, Florl AR. 2006. Methylation of endogenous human retroelements in health and disease. Curr Top Microbiol Immunol 310: 211 – 250.en_US
dc.identifier.citedreferenceSwain EB, Jakus PM, Rice G, Lupi F, Maxson PA, Pacyna JM, Penn A, Spiegel SJ, Veiga MM. 2007. Socioeconomic consequences of mercury use and pollution. Ambio 36: 45 – 61.en_US
dc.identifier.citedreferenceThompson RF, Atzmon G, Gheorghe C, Liang HQ, Lowes C, Greally JM, Barzilai N. 2010. Tissue‐specific dysregulation of DNA methylation in aging. Aging Cell 9: 506 – 518.en_US
dc.identifier.citedreferenceVirani S, Dolinoy DC, Halubai S, Jones TR, Domino SE, Rozek LS, Nahar MS, Padmanabhan V. 2012. Delivery type not associated with global methylation at birth. Clin Epigenet 4: 8.en_US
dc.identifier.citedreferenceWaly M, Olteanu H, Banerjee R, Choi SW, Mason JB, Parker BS, Sukumar S, Shim S, Sharma A, Benzecry JM, Power-Charnitsky VA, Deth RC. 2004. Activation of methionine synthase by insulin‐like growth factor‐1 and dopamine: a target for neurodevelopmental toxins and thimerosal. Mol Psychiatr 9: 358 – 370.en_US
dc.identifier.citedreferenceWang Y, Goodrich JM, Gillespie B, Werner R, Basu N, Franzblau A. 2012. An investigation of modifying effects of metallothionein single nucleotide polymorphisms on the association between mercury exposure and biomarker levels. Environ Health Perspect 120: 530 – 534.en_US
dc.identifier.citedreferenceWaterland RA, Kellermayer R, Laritsky E, Rayco‐Solon P, Harris RA, Travisano M, Zhang W, Torskaya MS, Zhang J, Shen L, Manary MJ, Prentice AM. 2010. Season of conception in rural gambia affects DNA methylation at putative human metastable epialleles. PLoS Genet 6: e1001252.en_US
dc.identifier.citedreferenceWeinhouse C, Anderson OS, Jones TR, Kim J, Liberman SA, Nahar MS, Rozek LS, Jirtle RL, Dolinoy DC. 2011. An expression microarray approach for the identification of metastable epialleles in the mouse genome. Epigenetics 6: 1105 – 1113.en_US
dc.identifier.citedreferenceWright RO, Schwartz J, Wright RJ, Bollati V, Tarantini L, Park SK, Hu H, Sparrow D, Vokonas P, Baccarelli A. 2010. Biomarkers of lead exposure and DNA methylation within retrotransposons. Environ Health Perspect 118: 790 – 795.en_US
dc.identifier.citedreferenceAnderson OS, Nahar MS, Faulk C, Jones TR, Liao C, Kannan K, Weinhouse C, Rozek LS, Dolinoy DC. 2012. Epigenetic responses following maternal dietary exposure to physiologically relevant levels of bisphenol A. Environ Mol Mutagen 53: 334 – 342.en_US
dc.identifier.citedreferenceArai Y, Ohgane J, Yagi S, Ito R, Iwasaki Y, Saito K, Akutsu K, Takatori S, Ishii R, Hayashi R, Izumi S, Sugino N, Kondo F, Horie M, Nakazawa H, Makino T, Shiota K. 2011. Epigenetic assessment of environmental chemicals detected in maternal peripheral and cord blood samples. J Reprod Dev 57: 507 – 517.en_US
dc.identifier.citedreferenceATSDR. Priority List of Hazardous Substances. 2011. Available at: http://www.atsdr.cdc.gov/SPL/index.html. Accessed September 28, 2012.en_US
dc.identifier.citedreferenceBaccarelli A, Bollati V. 2009. Epigenetics and environmental chemicals. Curr Opin Pediatr 21: 243 – 251.en_US
dc.identifier.citedreferenceBasu N, Head JA, Nam DH, Pilsner JR, Carvan MJ, Chan HM, Goetz FW, Murphy CA, Rouvinen-Watt K, Scheuhammer AM. Effects of methylmercury of epigenetic markers in a mammal, bird, and fish. Submitted Oct 30, 2012 (Comp Biochem Physiol Pt C).en_US
dc.identifier.citedreferenceBerglund M, Lind B, Bjornberg KA, Palm B, Einarsson O, Vahter M. 2005. Inter‐individual variations of human mercury exposure biomarkers: A cross‐sectional assessment. Environ Health 4: 20.en_US
dc.identifier.citedreferenceCenters for Disease Control and Prevention. Fourth National Report on Human Exposure to Environmental Chemicals. 2009. Available at: http://www.cdc.gov/exposurereport/pdf/FourthReport.pdf2009. Accessed November 1, 2010.en_US
dc.identifier.citedreferenceChen C, Yu H, Zhao J, Li B, Qu L, Liu S, Zhang P, Chai Z. 2006. The roles of serum selenium and selenoproteins on mercury toxicity in environmental and occupational exposure. Environ Health Perspect 114: 297 – 301.en_US
dc.identifier.citedreferenceClarkson TW, Magos L. 2006. The toxicology of mercury and its chemical compounds. Crit Rev Toxicol 36: 609 – 662.en_US
dc.identifier.citedreferenceCui H, Cruz‐Correa M, Giardiello FM, Hutcheon DF, Kafonek DR, Brandenberg S, Wu Y, He X, Powe NR, Feinberg AP. 2003. Loss if IGF2 imprinting: a potential marker for colorectal cancer risk. Science 299: 1753--1755.en_US
dc.identifier.citedreferenceDavies MN, Volta M, Pidsley R, Lunnon K, Dixit A, Lovestone S, Coarfa C, Harris RA, Milosavljevic A, Troakes C, Al-Sarraj S, Dobson R, Schalkwyk LC, Mill J. 2012. Functional annotation of the human brain methylome identifies tissue‐specific epigenetic variation across brain and blood. Genome Biol 13: R43.en_US
dc.identifier.citedreferenceDesaulniers D, Xiao GH, Lian H, Feng YL, Zhu J, Nakai J, et al. 2009. Effects of mixtures of polychlorinated biphenyls, methylmercury, and organochlorine pesticides on hepatic DNA methylation in prepubertal female Sprague‐Dawley rats. Int J Toxicol 28: 294 – 307.en_US
dc.identifier.citedreferenceDesplats P, Spencer B, Coffee E, Patel P, Michael S, Patrick C, Adame A, Rockenstein E, Masliah E. 2011. Alpha‐synuclein sequesters Dnmt1 from the nucleus: A novel mechanism for epigenetic alterations in Lewy body diseases. J Biol Chem 286: 9031 – 9037.en_US
dc.identifier.citedreferenceDolinoy DC, Huang D, Jirtle RL. 2007a. Maternal nutrient supplementation counteracts bisphenol A‐induced DNA hypomethylation in early development. Proc Natl Acad Sci 104: 13056 – 13061.en_US
dc.identifier.citedreferenceDolinoy DC, Weidman JR, Jirtle RL. 2007b. Epigenetic gene regulation: Linking early developmental environment to adult disease. Reprod Toxicol 23: 297 – 330.en_US
dc.identifier.citedreferenceFranzblau A, d'Arcy H, Ishak MB, Werner RA, Gillespie BW, Albers JW, Hamann C, Gruninger SE, Chou HN, Meyer DM. 2012. Low‐level mercury exposure and peripheral nerve function. Neurotoxicology 33: 299 – 306.en_US
dc.identifier.citedreferenceFrasco MF, Colletier JP, Weik M, Carvalho F, Guilhermino L, Stojan J, Fournier D. 2007. Mechanisms of cholinesterase inhibition by inorganic mercury. FEBS J 274: 1849 – 1861.en_US
dc.identifier.citedreferenceGadhia SR, Calabro AR, Barile FA. 2012. Trace metals alter DNA repair and histone modification pathways concurrently in mouse embryonic stem cells. Toxicol Lett 212: 169 – 177.en_US
dc.identifier.citedreferenceGlover CN, Zheng D, Jayashankar S, Sales GD, Hogstrand C, Lundebye AK. 2009. Methylmercury speciation influences brain gene expression and behavior in gestationally‐exposed mice pups. Toxicol Sci 110: 389 – 400.en_US
dc.identifier.citedreferenceGonzalo S. 2010. Epigenetic alterations in aging. J Appl Physiol 109: 586 – 597.en_US
dc.identifier.citedreferenceGoodrich JM, Wang Y, Gillespie B, Werner R, Franzblau A, Basu N. 2011. Glutathione enzyme and selenoprotein polymorphisms associate with mercury biomarker levels in Michigan dental professionals. Toxicol Appl Pharmacol 257: 301 – 308.en_US
dc.identifier.citedreferenceGoodrich JM, Wang Y, Gillespie B, Werner R, Franzblau A, Basu N. Methylmercury and elemental mercury differentially associate with blood pressure among dental professionals. Int J Hyg Environ Health, in press.en_US
dc.identifier.citedreferenceGrandjean P, Satoh H, Murata K, Eto K. 2010. Adverse effects of methylmercury: Environmental health research implications. Environ Health Perspect 118: 1137 – 1145.en_US
dc.identifier.citedreferenceGrunau C, Clark SJ, Rosenthal A. 2001. Bisulfite genomic sequencing: Systematic investigation of critical experimental parameters. Nucleic Acids Res 29: E65.en_US
dc.identifier.citedreferenceGuallar E, Sanz‐Gallardo MI, van't Veer P, Bode P, Aro A, Gomez‐Aracena J, Kark JD, Riemersma RA, Martin-Moreno JM, Kok FJ. 2002. Mercury, fish oils, and the risk of myocardial infarction. N Engl J Med 347: 1747 – 1754.en_US
dc.identifier.citedreferenceHanna CW, Bloom MS, Robinson WP, Kim D, Parsons PJ, Vom Saal FS, Taylor JA, Saal FS, Steuerwald AJ, Fujimoto VY. DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian stimulation for IVF. Hum Reprod, in press.en_US
dc.identifier.citedreferenceKaragas MR, Choi AL, Oken E, Horvat M, Schoeny R, Kamai E, Cowell W, Grandjean P, Korrick S. 2012. Evidence on the human health effects of low‐level methylmercury exposure. Environ Health Perspect 120: 799 – 806.en_US
dc.identifier.citedreferenceKhan MA, Wang F. 2009. Mercury‐selenium compounds and their toxicological significance: Toward a molecular understanding of the mercury‐selenium antagonism. Environ Toxicol Chem 28: 1567 – 1577.en_US
dc.identifier.citedreferenceKim YJ, Chai YG, Ryu JC. 2005. Selenoprotein W as molecular target of methylmercury in human neuronal cells is down‐regulated by GSH depletion. Biochem Biophys Res Commun 330: 1095 – 1102.en_US
dc.identifier.citedreferenceLander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, et al. 2001. Initial sequencing and analysis of the human genome. Nature 409: 860 – 921.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
em21763.pdf
Size:
156.9KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.