Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 2002 Feb;110(Suppl 1):25–42. doi: 10.1289/ehp.02110s125

Understanding the human health effects of chemical mixtures.

David O Carpenter 1, Kathleen Arcaro 1, David C Spink 1
PMCID: PMC1241145  PMID: 11834461

Abstract

Most research on the effects of chemicals on biologic systems is conducted on one chemical at a time. However, in the real world people are exposed to mixtures, not single chemicals. Although various substances may have totally independent actions, in many cases two substances may act at the same site in ways that can be either additive or nonadditive. Many even more complex interactions may occur if two chemicals act at different but related targets. In the extreme case there may be synergistic effects, in which case the effects of two substances together are greater than the sum of either effect alone. In reality, most persons are exposed to many chemicals, not just one or two, and therefore the effects of a chemical mixture are extremely complex and may differ for each mixture depending on the chemical composition. This complexity is a major reason why mixtures have not been well studied. In this review we attempt to illustrate some of the principles and approaches that can be used to study effects of mixtures. By the nature of the state of the science, this discussion is more a presentation of what we do not know than of what we do know about mixtures. We approach the study of mixtures at three levels, using specific examples. First, we discuss several human diseases in relation to a variety of environmental agents believed to influence the development and progression of the disease. We present results of selected cellular and animal studies in which simple mixtures have been investigated. Finally, we discuss some of the effects of mixtures at a molecular level.

Full Text

The Full Text of this article is available as a PDF (638.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adachi J., Mori Y., Matsui S., Takigami H., Fujino J., Kitagawa H., Miller C. A., 3rd, Kato T., Saeki K., Matsuda T. Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine. J Biol Chem. 2001 Jun 25;276(34):31475–31478. doi: 10.1074/jbc.C100238200. [DOI] [PubMed] [Google Scholar]
  2. Alam J., Stewart D., Touchard C., Boinapally S., Choi A. M., Cook J. L. Nrf2, a Cap'n'Collar transcription factor, regulates induction of the heme oxygenase-1 gene. J Biol Chem. 1999 Sep 10;274(37):26071–26078. doi: 10.1074/jbc.274.37.26071. [DOI] [PubMed] [Google Scholar]
  3. Amaro A. R., Oakley G. G., Bauer U., Spielmann H. P., Robertson L. W. Metabolic activation of PCBs to quinones: reactivity toward nitrogen and sulfur nucleophiles and influence of superoxide dismutase. Chem Res Toxicol. 1996 Apr-May;9(3):623–629. doi: 10.1021/tx950117e. [DOI] [PubMed] [Google Scholar]
  4. Ambrosone C. B., Freudenheim J. L., Graham S., Marshall J. R., Vena J. E., Brasure J. R., Michalek A. M., Laughlin R., Nemoto T., Gillenwater K. A. Cigarette smoking, N-acetyltransferase 2 genetic polymorphisms, and breast cancer risk. JAMA. 1996 Nov 13;276(18):1494–1501. [PubMed] [Google Scholar]
  5. Ames B. N., Gold L. S., Willett W. C. The causes and prevention of cancer. Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5258–5265. doi: 10.1073/pnas.92.12.5258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Apostoli P., Kiss P., Porru S., Bonde J. P., Vanhoorne M. Male reproductive toxicity of lead in animals and humans. ASCLEPIOS Study Group. Occup Environ Med. 1998 Jun;55(6):364–374. doi: 10.1136/oem.55.6.364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Arcaro K. F., O'Keefe P. W., Yang Y., Clayton W., Gierthy J. F. Antiestrogenicity of environmental polycyclic aromatic hydrocarbons in human breast cancer cells. Toxicology. 1999 Apr 15;133(2-3):115–127. doi: 10.1016/s0300-483x(99)00018-9. [DOI] [PubMed] [Google Scholar]
  8. Arcaro K. F., Yi L., Seegal R. F., Vakharia D. D., Yang Y., Spink D. C., Brosch K., Gierthy J. F. 2,2',6,6'-Tetrachlorobiphenyl is estrogenic in vitro and in vivo. J Cell Biochem. 1999 Jan 1;72(1):94–102. [PubMed] [Google Scholar]
  9. Baba T., Mimura J., Gradin K., Kuroiwa A., Watanabe T., Matsuda Y., Inazawa J., Sogawa K., Fujii-Kuriyama Y. Structure and expression of the Ah receptor repressor gene. J Biol Chem. 2001 Jun 21;276(35):33101–33110. doi: 10.1074/jbc.M011497200. [DOI] [PubMed] [Google Scholar]
  10. Bae D. S., Gennings C., Carter W. H., Jr, Yang R. S., Campain J. A. Toxicological interactions among arsenic, cadmium, chromium, and lead in human keratinocytes. Toxicol Sci. 2001 Sep;63(1):132–142. doi: 10.1093/toxsci/63.1.132. [DOI] [PubMed] [Google Scholar]
  11. Baker E. L., Jr, Landrigan P. J., Glueck C. J., Zack M. M., Jr, Liddle J. A., Burse V. W., Housworth W. J., Needham L. L. Metabolic consequences of exposure to polychlorinated biphenyls (PCB) in sewage sludge. Am J Epidemiol. 1980 Oct;112(4):553–563. doi: 10.1093/oxfordjournals.aje.a113024. [DOI] [PubMed] [Google Scholar]
  12. Barker C. W., Fagan J. B., Pasco D. S. Down-regulation of P4501A1 and P4501A2 mRNA expression in isolated hepatocytes by oxidative stress. J Biol Chem. 1994 Feb 11;269(6):3985–3990. [PubMed] [Google Scholar]
  13. Barker C. W., Fagan J. B., Pasco D. S. Interleukin-1 beta suppresses the induction of P4501A1 and P4501A2 mRNAs in isolated hepatocytes. J Biol Chem. 1992 Apr 25;267(12):8050–8055. [PubMed] [Google Scholar]
  14. Barnes P. J., Karin M. Nuclear factor-kappaB: a pivotal transcription factor in chronic inflammatory diseases. N Engl J Med. 1997 Apr 10;336(15):1066–1071. doi: 10.1056/NEJM199704103361506. [DOI] [PubMed] [Google Scholar]
  15. Barrett J. C., Wong A., McLachlan J. A. Diethylstilbestrol induces neoplastic transformation without measurable gene mutation at two loci. Science. 1981 Jun 19;212(4501):1402–1404. doi: 10.1126/science.6262919. [DOI] [PubMed] [Google Scholar]
  16. Bartosiewicz M. J., Jenkins D., Penn S., Emery J., Buckpitt A. Unique gene expression patterns in liver and kidney associated with exposure to chemical toxicants. J Pharmacol Exp Ther. 2001 Jun;297(3):895–905. [PubMed] [Google Scholar]
  17. Bartosiewicz M., Penn S., Buckpitt A. Applications of gene arrays in environmental toxicology: fingerprints of gene regulation associated with cadmium chloride, benzo(a)pyrene, and trichloroethylene. Environ Health Perspect. 2001 Jan;109(1):71–74. doi: 10.1289/ehp.0110971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Bemis J. C., Seegal R. F. Polychlorinated biphenyls and methylmercury act synergistically to reduce rat brain dopamine content in vitro. Environ Health Perspect. 1999 Nov;107(11):879–885. doi: 10.1289/ehp.99107879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ben-Shachar D., Eshel G., Riederer P., Youdim M. B. Role of iron and iron chelation in dopaminergic-induced neurodegeneration: implication for Parkinson's disease. Ann Neurol. 1992;32 (Suppl):S105–S110. doi: 10.1002/ana.410320718. [DOI] [PubMed] [Google Scholar]
  20. Ben-Shachar D., Youdim M. B. Iron, melanin and dopamine interaction: relevance to Parkinson's disease. Prog Neuropsychopharmacol Biol Psychiatry. 1993 Jan;17(1):139–150. doi: 10.1016/0278-5846(93)90038-t. [DOI] [PubMed] [Google Scholar]
  21. Benoff S., Jacob A., Hurley I. R. Male infertility and environmental exposure to lead and cadmium. Hum Reprod Update. 2000 Mar-Apr;6(2):107–121. doi: 10.1093/humupd/6.2.107. [DOI] [PubMed] [Google Scholar]
  22. Bernstein L., Ross R. K. Endogenous hormones and breast cancer risk. Epidemiol Rev. 1993;15(1):48–65. doi: 10.1093/oxfordjournals.epirev.a036116. [DOI] [PubMed] [Google Scholar]
  23. Bhatt M. H., Elias M. A., Mankodi A. K. Acute and reversible parkinsonism due to organophosphate pesticide intoxication: five cases. Neurology. 1999 Apr 22;52(7):1467–1471. doi: 10.1212/wnl.52.7.1467. [DOI] [PubMed] [Google Scholar]
  24. Bjerke D. L., Brown T. J., MacLusky N. J., Hochberg R. B., Peterson R. E. Partial demasculinization and feminization of sex behavior in male rats by in utero and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin is not associated with alterations in estrogen receptor binding or volumes of sexually differentiated brain nuclei. Toxicol Appl Pharmacol. 1994 Aug;127(2):258–267. doi: 10.1006/taap.1994.1160. [DOI] [PubMed] [Google Scholar]
  25. Bjerke D. L., Peterson R. E. Reproductive toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin in male rats: different effects of in utero versus lactational exposure. Toxicol Appl Pharmacol. 1994 Aug;127(2):241–249. doi: 10.1006/taap.1994.1158. [DOI] [PubMed] [Google Scholar]
  26. Bjerke D. L., Sommer R. J., Moore R. W., Peterson R. E. Effects of in utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure on responsiveness of the male rat reproductive system to testosterone stimulation in adulthood. Toxicol Appl Pharmacol. 1994 Aug;127(2):250–257. doi: 10.1006/taap.1994.1159. [DOI] [PubMed] [Google Scholar]
  27. Blanck H. M., Marcus M., Tolbert P. E., Rubin C., Henderson A. K., Hertzberg V. S., Zhang R. H., Cameron L. Age at menarche and tanner stage in girls exposed in utero and postnatally to polybrominated biphenyl. Epidemiology. 2000 Nov;11(6):641–647. doi: 10.1097/00001648-200011000-00005. [DOI] [PubMed] [Google Scholar]
  28. Boll M., Weber L. W., Messner B., Stampfl A. Polychlorinated biphenyls affect the activities of gluconeogenic and lipogenic enzymes in rat liver: is there an interference with regulatory hormone actions? Xenobiotica. 1998 May;28(5):479–492. doi: 10.1080/004982598239407. [DOI] [PubMed] [Google Scholar]
  29. Bolton J. L., Trush M. A., Penning T. M., Dryhurst G., Monks T. J. Role of quinones in toxicology. Chem Res Toxicol. 2000 Mar;13(3):135–160. doi: 10.1021/tx9902082. [DOI] [PubMed] [Google Scholar]
  30. Bradlow H. L., Hershcopf R. J., Martucci C. P., Fishman J. Estradiol 16 alpha-hydroxylation in the mouse correlates with mammary tumor incidence and presence of murine mammary tumor virus: a possible model for the hormonal etiology of breast cancer in humans. Proc Natl Acad Sci U S A. 1985 Sep;82(18):6295–6299. doi: 10.1073/pnas.82.18.6295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Burczynski M. E., Penning T. M. Genotoxic polycyclic aromatic hydrocarbon ortho-quinones generated by aldo-keto reductases induce CYP1A1 via nuclear translocation of the aryl hydrocarbon receptor. Cancer Res. 2000 Feb 15;60(4):908–915. [PubMed] [Google Scholar]
  32. Bush B., Bennett A. H., Snow J. T. Polychlorobiphenyl congeners, p,p'-DDE, and sperm function in humans. Arch Environ Contam Toxicol. 1986 Jul;15(4):333–341. doi: 10.1007/BF01066399. [DOI] [PubMed] [Google Scholar]
  33. Cahill A., Wang X., Hoek J. B. Increased oxidative damage to mitochondrial DNA following chronic ethanol consumption. Biochem Biophys Res Commun. 1997 Jun 18;235(2):286–290. doi: 10.1006/bbrc.1997.6774. [DOI] [PubMed] [Google Scholar]
  34. Calvert G. M., Willie K. K., Sweeney M. H., Fingerhut M. A., Halperin W. E. Evaluation of serum lipid concentrations among U.S. workers exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin. Arch Environ Health. 1996 Mar-Apr;51(2):100–107. doi: 10.1080/00039896.1996.9936001. [DOI] [PubMed] [Google Scholar]
  35. Campbell A. M., Williams E. R., Barltrop D. Motor neurone disease and exposure to lead. J Neurol Neurosurg Psychiatry. 1970 Dec;33(6):877–885. doi: 10.1136/jnnp.33.6.877. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Carpenter D. O., Arcaro K. F., Bush B., Niemi W. D., Pang S., Vakharia D. D. Human health and chemical mixtures: an overview. Environ Health Perspect. 1998 Dec;106 (Suppl 6):1263–1270. doi: 10.1289/ehp.98106s61263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Carpenter D. O., Shen Y., Nguyen T., Le L., Lininger L. L. Incidence of endocrine disease among residents of New York areas of concern. Environ Health Perspect. 2001 Dec;109 (Suppl 6):845–851. doi: 10.1289/ehp.01109s6845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Carpy S. A., Kobel W., Doe J. Health risk of low-dose pesticides mixtures: a review of the 1985-1998 literature on combination toxicology and health risk assessment. J Toxicol Environ Health B Crit Rev. 2000 Jan-Mar;3(1):1–25. doi: 10.1080/109374000281122. [DOI] [PubMed] [Google Scholar]
  39. Carver L. A., LaPres J. J., Jain S., Dunham E. E., Bradfield C. A. Characterization of the Ah receptor-associated protein, ARA9. J Biol Chem. 1998 Dec 11;273(50):33580–33587. doi: 10.1074/jbc.273.50.33580. [DOI] [PubMed] [Google Scholar]
  40. Castro G. D., Delgado de Layño A. M., Costantini M. H., Castro J. A. Cytosolic xanthine oxidoreductase mediated bioactivation of ethanol to acetaldehyde and free radicals in rat breast tissue. Its potential role in alcohol-promoted mammary cancer. Toxicology. 2001 Mar 7;160(1-3):11–18. doi: 10.1016/s0300-483x(00)00433-9. [DOI] [PubMed] [Google Scholar]
  41. Cavalieri E. L., Stack D. E., Devanesan P. D., Todorovic R., Dwivedy I., Higginbotham S., Johansson S. L., Patil K. D., Gross M. L., Gooden J. K. Molecular origin of cancer: catechol estrogen-3,4-quinones as endogenous tumor initiators. Proc Natl Acad Sci U S A. 1997 Sep 30;94(20):10937–10942. doi: 10.1073/pnas.94.20.10937. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Chan W. K., Yao G., Gu Y. Z., Bradfield C. A. Cross-talk between the aryl hydrocarbon receptor and hypoxia inducible factor signaling pathways. Demonstration of competition and compensation. J Biol Chem. 1999 Apr 23;274(17):12115–12123. doi: 10.1074/jbc.274.17.12115. [DOI] [PubMed] [Google Scholar]
  43. Chang C. Y., Puga A. Constitutive activation of the aromatic hydrocarbon receptor. Mol Cell Biol. 1998 Jan;18(1):525–535. doi: 10.1128/mcb.18.1.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Chen C. J., Chiou H. Y., Chiang M. H., Lin L. J., Tai T. Y. Dose-response relationship between ischemic heart disease mortality and long-term arsenic exposure. Arterioscler Thromb Vasc Biol. 1996 Apr;16(4):504–510. doi: 10.1161/01.atv.16.4.504. [DOI] [PubMed] [Google Scholar]
  45. Chen F., Lu Y., Zhang Z., Vallyathan V., Ding M., Castranova V., Shi X. Opposite effect of NF-kappa B and c-Jun N-terminal kinase on p53-independent GADD45 induction by arsenite. J Biol Chem. 2001 Jan 9;276(14):11414–11419. doi: 10.1074/jbc.M011682200. [DOI] [PubMed] [Google Scholar]
  46. Chen Y. C., Guo Y. L., Hsu C. C., Rogan W. J. Cognitive development of Yu-Cheng ("oil disease") children prenatally exposed to heat-degraded PCBs. JAMA. 1992 Dec 9;268(22):3213–3218. [PubMed] [Google Scholar]
  47. Cherng S. H., Lin P., Yang J. L., Hsu S. L., Lee H. Benzo[g,h,i]perylene synergistically transactivates benzo[a]pyrene-induced CYP1A1 gene expression by aryl hydrocarbon receptor pathway. Toxicol Appl Pharmacol. 2001 Jan 1;170(1):63–68. doi: 10.1006/taap.2000.9082. [DOI] [PubMed] [Google Scholar]
  48. Conradi S., Ronnevi L. O., Nise G., Vesterberg O. Abnormal distribution of lead in amyotrophic lateral sclerosis--reestimation of lead in the cerebrospinal fluid. J Neurol Sci. 1980 Dec;48(3):413–418. doi: 10.1016/0022-510x(80)90112-4. [DOI] [PubMed] [Google Scholar]
  49. Cooke P. S., Zhao Y. D., Hansen L. G. Neonatal polychlorinated biphenyl treatment increases adult testis size and sperm production in the rat. Toxicol Appl Pharmacol. 1996 Jan;136(1):112–117. doi: 10.1006/taap.1996.0013. [DOI] [PubMed] [Google Scholar]
  50. Corrigan F. M., Murray L., Wyatt C. L., Shore R. F. Diorthosubstituted polychlorinated biphenyls in caudate nucleus in Parkinson's disease. Exp Neurol. 1998 Apr;150(2):339–342. doi: 10.1006/exnr.1998.6776. [DOI] [PubMed] [Google Scholar]
  51. Corrigan F. M., Wienburg C. L., Shore R. F., Daniel S. E., Mann D. Organochlorine insecticides in substantia nigra in Parkinson's disease. J Toxicol Environ Health A. 2000 Feb 25;59(4):229–234. doi: 10.1080/009841000156907. [DOI] [PubMed] [Google Scholar]
  52. Dalton T. P., Shertzer H. G., Puga A. Regulation of gene expression by reactive oxygen. Annu Rev Pharmacol Toxicol. 1999;39:67–101. doi: 10.1146/annurev.pharmtox.39.1.67. [DOI] [PubMed] [Google Scholar]
  53. Davarinos N. A., Pollenz R. S. Aryl hydrocarbon receptor imported into the nucleus following ligand binding is rapidly degraded via the cytosplasmic proteasome following nuclear export. J Biol Chem. 1999 Oct 1;274(40):28708–28715. doi: 10.1074/jbc.274.40.28708. [DOI] [PubMed] [Google Scholar]
  54. Davidson P. W., Myer G. J., Shamlaye C., Cox C., Gao P., Axtell C., Morris D., Sloane-Reeves J., Cernichiari E., Choi A. Association between prenatal exposure to methylmercury and developmental outcomes in Seychellois children: effect modification by social and environmental factors. Neurotoxicology. 1999 Oct;20(5):833–841. [PubMed] [Google Scholar]
  55. Davis D. L., Bradlow H. L., Wolff M., Woodruff T., Hoel D. G., Anton-Culver H. Medical hypothesis: xenoestrogens as preventable causes of breast cancer. Environ Health Perspect. 1993 Oct;101(5):372–377. doi: 10.1289/ehp.93101372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Denissenko M. F., Pao A., Tang M., Pfeifer G. P. Preferential formation of benzo[a]pyrene adducts at lung cancer mutational hotspots in P53. Science. 1996 Oct 18;274(5286):430–432. doi: 10.1126/science.274.5286.430. [DOI] [PubMed] [Google Scholar]
  57. Dewailly E., Dodin S., Verreault R., Ayotte P., Sauvé L., Morin J., Brisson J. High organochlorine body burden in women with estrogen receptor-positive breast cancer. J Natl Cancer Inst. 1994 Feb 2;86(3):232–234. doi: 10.1093/jnci/86.3.232. [DOI] [PubMed] [Google Scholar]
  58. Dexter D. T., Carter C. J., Wells F. R., Javoy-Agid F., Agid Y., Lees A., Jenner P., Marsden C. D. Basal lipid peroxidation in substantia nigra is increased in Parkinson's disease. J Neurochem. 1989 Feb;52(2):381–389. doi: 10.1111/j.1471-4159.1989.tb09133.x. [DOI] [PubMed] [Google Scholar]
  59. Dey A., Nebert D. W. Markedly increased constitutive CYP1A1 mRNA levels in the fertilized ovum of the mouse. Biochem Biophys Res Commun. 1998 Oct 20;251(2):657–661. doi: 10.1006/bbrc.1998.9519. [DOI] [PubMed] [Google Scholar]
  60. Dorgan J. F., Brock J. W., Rothman N., Needham L. L., Miller R., Stephenson H. E., Jr, Schussler N., Taylor P. R. Serum organochlorine pesticides and PCBs and breast cancer risk: results from a prospective analysis (USA). Cancer Causes Control. 1999 Feb;10(1):1–11. doi: 10.1023/a:1008824131727. [DOI] [PubMed] [Google Scholar]
  61. Du K., Chu S., Xu X. Stimulation of MCF-7 cell proliferation by low concentrations of Chinese domestic polychlorinated biphenyls. J Toxicol Environ Health A. 2000 Oct 13;61(3):201–207. doi: 10.1080/00984100050131341. [DOI] [PubMed] [Google Scholar]
  62. Eadon G., Kaminsky L., Silkworth J., Aldous K., Hilker D., O'Keefe P., Smith R., Gierthy J., Hawley J., Kim N. Calculation of 2,3,7,8-TCDD equivalent concentrations of complex environmental contaminant mixtures. Environ Health Perspect. 1986 Dec;70:221–227. doi: 10.1289/ehp.8670221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Ebright R. H., Wong J. R., Chen L. B. Binding of 2-hydroxybenzo(a)pyrene to estrogen receptors in rat cytosol. Cancer Res. 1986 May;46(5):2349–2351. [PubMed] [Google Scholar]
  64. Elferink C. J., Ge N. L., Levine A. Maximal aryl hydrocarbon receptor activity depends on an interaction with the retinoblastoma protein. Mol Pharmacol. 2001 Apr;59(4):664–673. doi: 10.1124/mol.59.4.664. [DOI] [PubMed] [Google Scholar]
  65. Emmett E. A., Maroni M., Jefferys J., Schmith J., Levin B. K., Alvares A. Studies of transformer repair workers exposed to PCBs: II. Results of clinical laboratory investigations. Am J Ind Med. 1988;14(1):47–62. doi: 10.1002/ajim.4700140107. [DOI] [PubMed] [Google Scholar]
  66. Erren T. C., Jacobsen M., Piekarski C. Synergy between asbestos and smoking on lung cancer risks. Epidemiology. 1999 Jul;10(4):405–411. doi: 10.1097/00001648-199907000-00008. [DOI] [PubMed] [Google Scholar]
  67. Falahatpisheh M. H., Donnelly K. C., Ramos K. S. Antagonistic interactions among nephrotoxic polycyclic aromatic hydrocarbons. J Toxicol Environ Health A. 2001 Apr 6;62(7):543–560. doi: 10.1080/152873901300007833. [DOI] [PubMed] [Google Scholar]
  68. Falck F., Jr, Ricci A., Jr, Wolff M. S., Godbold J., Deckers P. Pesticides and polychlorinated biphenyl residues in human breast lipids and their relation to breast cancer. Arch Environ Health. 1992 Mar-Apr;47(2):143–146. [PubMed] [Google Scholar]
  69. Faux S. P., Francis J. E., Smith A. G., Chipman J. K. Induction of 8-hydroxydeoxyguanosine in Ah-responsive mouse liver by iron and Aroclor 1254. Carcinogenesis. 1992 Feb;13(2):247–250. doi: 10.1093/carcin/13.2.247. [DOI] [PubMed] [Google Scholar]
  70. Feigelson H. S., McKean-Cowdin R., Coetzee G. A., Stram D. O., Kolonel L. N., Henderson B. E. Building a multigenic model of breast cancer susceptibility: CYP17 and HSD17B1 are two important candidates. Cancer Res. 2001 Jan 15;61(2):785–789. [PubMed] [Google Scholar]
  71. Feigelson H. S., Ross R. K., Yu M. C., Coetzee G. A., Reichardt J. K., Henderson B. E. Sex steroid hormones and genetic susceptibility to breast and prostate cancer. Drug Metab Rev. 1998 May;30(2):421–434. doi: 10.3109/03602539808996320. [DOI] [PubMed] [Google Scholar]
  72. Ferraz H. B., Bertolucci P. H., Pereira J. S., Lima J. G., Andrade L. A. Chronic exposure to the fungicide maneb may produce symptoms and signs of CNS manganese intoxication. Neurology. 1988 Apr;38(4):550–553. doi: 10.1212/wnl.38.4.550. [DOI] [PubMed] [Google Scholar]
  73. Fertuck K. C., Kumar S., Sikka H. C., Matthews J. B., Zacharewski T. R. Interaction of PAH-related compounds with the alpha and beta isoforms of the estrogen receptor. Toxicol Lett. 2001 May 19;121(3):167–177. doi: 10.1016/s0378-4274(01)00344-7. [DOI] [PubMed] [Google Scholar]
  74. Fielden M. R., Chen I., Chittim B., Safe S. H., Zacharewski T. R. Examination of the estrogenicity of 2,4,6,2',6'-pentachlorobiphenyl (PCB 104), its hydroxylated metabolite 2,4,6,2',6'-pentachloro-4-biphenylol (HO-PCB 104), and a further chlorinated derivative, 2,4,6,2',4',6'-hexachlorobiphenyl (PCB 155). Environ Health Perspect. 1997 Nov;105(11):1238–1248. doi: 10.1289/ehp.971051238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  75. Fleming L., Mann J. B., Bean J., Briggle T., Sanchez-Ramos J. R. Parkinson's disease and brain levels of organochlorine pesticides. Ann Neurol. 1994 Jul;36(1):100–103. doi: 10.1002/ana.410360119. [DOI] [PubMed] [Google Scholar]
  76. Flesch-Janys D., Berger J., Gurn P., Manz A., Nagel S., Waltsgott H., Dwyer J. H. Exposure to polychlorinated dioxins and furans (PCDD/F) and mortality in a cohort of workers from a herbicide-producing plant in Hamburg, Federal Republic of Germany. Am J Epidemiol. 1995 Dec 1;142(11):1165–1175. doi: 10.1093/oxfordjournals.aje.a117575. [DOI] [PubMed] [Google Scholar]
  77. Fraga C. G., Motchnik P. A., Shigenaga M. K., Helbock H. J., Jacob R. A., Ames B. N. Ascorbic acid protects against endogenous oxidative DNA damage in human sperm. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11003–11006. doi: 10.1073/pnas.88.24.11003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  78. Fraga C. G., Motchnik P. A., Wyrobek A. J., Rempel D. M., Ames B. N. Smoking and low antioxidant levels increase oxidative damage to sperm DNA. Mutat Res. 1996 Apr 13;351(2):199–203. doi: 10.1016/0027-5107(95)00251-0. [DOI] [PubMed] [Google Scholar]
  79. Garruto R. M., Fukatsu R., Yanagihara R., Gajdusek D. C., Hook G., Fiori C. E. Imaging of calcium and aluminum in neurofibrillary tangle-bearing neurons in parkinsonism-dementia of Guam. Proc Natl Acad Sci U S A. 1984 Mar;81(6):1875–1879. doi: 10.1073/pnas.81.6.1875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  80. Gasiewicz T. A., Neal R. A. 2,3,7,8-Tetrachlorodibenzo-p-dioxin tissue distribution, excretion, and effects on clinical chemical parameters in guinea pigs. Toxicol Appl Pharmacol. 1979 Nov;51(2):329–339. doi: 10.1016/0041-008x(79)90475-7. [DOI] [PubMed] [Google Scholar]
  81. Ge N. L., Elferink C. J. A direct interaction between the aryl hydrocarbon receptor and retinoblastoma protein. Linking dioxin signaling to the cell cycle. J Biol Chem. 1998 Aug 28;273(35):22708–22713. doi: 10.1074/jbc.273.35.22708. [DOI] [PubMed] [Google Scholar]
  82. Gerlach M., Ben-Shachar D., Riederer P., Youdim M. B. Altered brain metabolism of iron as a cause of neurodegenerative diseases? J Neurochem. 1994 Sep;63(3):793–807. doi: 10.1046/j.1471-4159.1994.63030793.x. [DOI] [PubMed] [Google Scholar]
  83. Geva E., Bartoov B., Zabludovsky N., Lessing J. B., Lerner-Geva L., Amit A. The effect of antioxidant treatment on human spermatozoa and fertilization rate in an in vitro fertilization program. Fertil Steril. 1996 Sep;66(3):430–434. doi: 10.1016/s0015-0282(16)58514-8. [DOI] [PubMed] [Google Scholar]
  84. Gierthy J. F., Lincoln D. W., 2nd, Roth K. E., Bowser S. S., Bennett J. A., Bradley L., Dickerman H. W. Estrogen-stimulation of postconfluent cell accumulation and foci formation of human MCF-7 breast cancer cells. J Cell Biochem. 1991 Feb;45(2):177–187. doi: 10.1002/jcb.240450209. [DOI] [PubMed] [Google Scholar]
  85. Goldey E. S., Kehn L. S., Lau C., Rehnberg G. L., Crofton K. M. Developmental exposure to polychlorinated biphenyls (Aroclor 1254) reduces circulating thyroid hormone concentrations and causes hearing deficits in rats. Toxicol Appl Pharmacol. 1995 Nov;135(1):77–88. doi: 10.1006/taap.1995.1210. [DOI] [PubMed] [Google Scholar]
  86. Goldin B. R., Adlercreutz H., Gorbach S. L., Woods M. N., Dwyer J. T., Conlon T., Bohn E., Gershoff S. N. The relationship between estrogen levels and diets of Caucasian American and Oriental immigrant women. Am J Clin Nutr. 1986 Dec;44(6):945–953. doi: 10.1093/ajcn/44.6.945. [DOI] [PubMed] [Google Scholar]
  87. Gorelick P. B., Hier D. B., Mangone C., Robbins S., Plioplys A., Kathpalia S. Status of aluminum as a risk factor for dialysis encephalopathy and Alzheimer's disease. Int J Artif Organs. 1991 Feb;14(2):70–73. [PubMed] [Google Scholar]
  88. Gorell J. M., Johnson C. C., Rybicki B. A., Peterson E. L., Richardson R. J. The risk of Parkinson's disease with exposure to pesticides, farming, well water, and rural living. Neurology. 1998 May;50(5):1346–1350. doi: 10.1212/wnl.50.5.1346. [DOI] [PubMed] [Google Scholar]
  89. Gradin K., McGuire J., Wenger R. H., Kvietikova I., fhitelaw M. L., Toftgård R., Tora L., Gassmann M., Poellinger L. Functional interference between hypoxia and dioxin signal transduction pathways: competition for recruitment of the Arnt transcription factor. Mol Cell Biol. 1996 Oct;16(10):5221–5231. doi: 10.1128/mcb.16.10.5221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  90. Graham D. G. On the origin and significance of neuromelanin. Arch Pathol Lab Med. 1979 Jul;103(7):359–362. [PubMed] [Google Scholar]
  91. Grandjean P., Weihe P., White R. F., Debes F. Cognitive performance of children prenatally exposed to "safe" levels of methylmercury. Environ Res. 1998 May;77(2):165–172. doi: 10.1006/enrs.1997.3804. [DOI] [PubMed] [Google Scholar]
  92. Gray D. L., Warshawsky D., Xue W., Nines R., Wang Y., Yao R., Stoner G. D. The effects of a binary mixture of benzo(a)pyrene and 7H-dibenzo(c,g)carbazole on lung tumors and K-ras oncogene mutations in strain A/J mice. Exp Lung Res. 2001 Apr-May;27(3):245–253. doi: 10.1080/019021401300054000. [DOI] [PubMed] [Google Scholar]
  93. Gray L. E., Jr, Kelce W. R., Monosson E., Ostby J. S., Birnbaum L. S. Exposure to TCDD during development permanently alters reproductive function in male Long Evans rats and hamsters: reduced ejaculated and epididymal sperm numbers and sex accessory gland weights in offspring with normal androgenic status. Toxicol Appl Pharmacol. 1995 Mar;131(1):108–118. doi: 10.1006/taap.1995.1052. [DOI] [PubMed] [Google Scholar]
  94. Gray L. E., Jr Xenoendocrine disrupters: laboratory studies on male reproductive effects. Toxicol Lett. 1998 Dec 28;102-103:331–335. doi: 10.1016/s0378-4274(98)00327-0. [DOI] [PubMed] [Google Scholar]
  95. Gray L. E., Ostby J. S., Kelce W. R. A dose-response analysis of the reproductive effects of a single gestational dose of 2,3,7,8-tetrachlorodibenzo-p-dioxin in male Long Evans Hooded rat offspring. Toxicol Appl Pharmacol. 1997 Sep;146(1):11–20. doi: 10.1006/taap.1997.8223. [DOI] [PubMed] [Google Scholar]
  96. Guengerich F. P., Dannan G. A., Wright S. T., Martin M. V., Kaminsky L. S. Purification and characterization of liver microsomal cytochromes p-450: electrophoretic, spectral, catalytic, and immunochemical properties and inducibility of eight isozymes isolated from rats treated with phenobarbital or beta-naphthoflavone. Biochemistry. 1982 Nov 9;21(23):6019–6030. doi: 10.1021/bi00266a045. [DOI] [PubMed] [Google Scholar]
  97. Guillette E. A., Meza M. M., Aquilar M. G., Soto A. D., Garcia I. E. An anthropological approach to the evaluation of preschool children exposed to pesticides in Mexico. Environ Health Perspect. 1998 Jun;106(6):347–353. doi: 10.1289/ehp.98106347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  98. Guo Y. L., Yu M. L., Hsu C. C., Rogan W. J. Chloracne, goiter, arthritis, and anemia after polychlorinated biphenyl poisoning: 14-year follow-Up of the Taiwan Yucheng cohort. Environ Health Perspect. 1999 Sep;107(9):715–719. doi: 10.1289/ehp.99107715. [DOI] [PMC free article] [PubMed] [Google Scholar]
  99. Güttes S., Failing K., Neumann K., Kleinstein J., Georgii S., Brunn H. Chlororganic pesticides and polychlorinated biphenyls in breast tissue of women with benign and malignant breast disease. Arch Environ Contam Toxicol. 1998 Jul;35(1):140–147. doi: 10.1007/s002449900361. [DOI] [PubMed] [Google Scholar]
  100. Haake-McMillan J. M., Safe S. H. Neonatal exposure to Aroclor 1254: effects on adult hepatic testosterone hydroxylase activities. Xenobiotica. 1991 Apr;21(4):481–489. doi: 10.3109/00498259109039488. [DOI] [PubMed] [Google Scholar]
  101. Haavik J., Almås B., Flatmark T. Generation of reactive oxygen species by tyrosine hydroxylase: a possible contribution to the degeneration of dopaminergic neurons? J Neurochem. 1997 Jan;68(1):328–332. doi: 10.1046/j.1471-4159.1997.68010328.x. [DOI] [PubMed] [Google Scholar]
  102. Hansen L. G. Stepping backward to improve assessment of PCB congener toxicities. Environ Health Perspect. 1998 Feb;106 (Suppl 1):171–189. doi: 10.1289/ehp.98106s1171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  103. Hany J., Lilienthal H., Sarasin A., Roth-Härer A., Fastabend A., Dunemann L., Lichtensteiger W., Winneke G. Developmental exposure of rats to a reconstituted PCB mixture or aroclor 1254: effects on organ weights, aromatase activity, sex hormone levels, and sweet preference behavior. Toxicol Appl Pharmacol. 1999 Aug 1;158(3):231–243. doi: 10.1006/taap.1999.8710. [DOI] [PubMed] [Google Scholar]
  104. Hassoun E. A., Wilt S. C., Devito M. J., Van Birgelen A., Alsharif N. Z., Birnbaum L. S., Stohs S. J. Induction of oxidative stress in brain tissues of mice after subchronic exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin. Toxicol Sci. 1998 Mar;42(1):23–27. doi: 10.1006/toxs.1997.2411. [DOI] [PubMed] [Google Scholar]
  105. Hastings T. G., Lewis D. A., Zigmond M. J. Role of oxidation in the neurotoxic effects of intrastriatal dopamine injections. Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):1956–1961. doi: 10.1073/pnas.93.5.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  106. Hennig B., Slim R., Toborek M., Robertson L. W. Linoleic acid amplifies polychlorinated biphenyl-mediated dysfunction of endothelial cells. J Biochem Mol Toxicol. 1999;13(2):83–91. doi: 10.1002/(sici)1099-0461(1999)13:2<83::aid-jbt4>3.0.co;2-7. [DOI] [PubMed] [Google Scholar]
  107. Henriksen G. L., Ketchum N. S., Michalek J. E., Swaby J. A. Serum dioxin and diabetes mellitus in veterans of Operation Ranch Hand. Epidemiology. 1997 May;8(3):252–258. doi: 10.1097/00001648-199705000-00005. [DOI] [PubMed] [Google Scholar]
  108. Hirose K., Morita M., Ema M., Mimura J., Hamada H., Fujii H., Saijo Y., Gotoh O., Sogawa K., Fujii-Kuriyama Y. cDNA cloning and tissue-specific expression of a novel basic helix-loop-helix/PAS factor (Arnt2) with close sequence similarity to the aryl hydrocarbon receptor nuclear translocator (Arnt). Mol Cell Biol. 1996 Apr;16(4):1706–1713. doi: 10.1128/mcb.16.4.1706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  109. Hirsch E. C., Brandel J. P., Galle P., Javoy-Agid F., Agid Y. Iron and aluminum increase in the substantia nigra of patients with Parkinson's disease: an X-ray microanalysis. J Neurochem. 1991 Feb;56(2):446–451. doi: 10.1111/j.1471-4159.1991.tb08170.x. [DOI] [PubMed] [Google Scholar]
  110. Hirvonen A. Polymorphisms of xenobiotic-metabolizing enzymes and susceptibility to cancer. Environ Health Perspect. 1999 Feb;107 (Suppl 1):37–47. doi: 10.1289/ehp.99107s137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  111. Ho S. C., Woo J., Lee C. M. Epidemiologic study of Parkinson's disease in Hong Kong. Neurology. 1989 Oct;39(10):1314–1318. doi: 10.1212/wnl.39.10.1314. [DOI] [PubMed] [Google Scholar]
  112. Honkakoski P., Negishi M. Regulation of cytochrome P450 (CYP) genes by nuclear receptors. Biochem J. 2000 Apr 15;347(Pt 2):321–337. doi: 10.1042/0264-6021:3470321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  113. Hooiveld M., Heederik D. J., Kogevinas M., Boffetta P., Needham L. L., Patterson D. G., Jr, Bueno-de-Mesquita H. B. Second follow-up of a Dutch cohort occupationally exposed to phenoxy herbicides, chlorophenols, and contaminants. Am J Epidemiol. 1998 May 1;147(9):891–901. doi: 10.1093/oxfordjournals.aje.a009543. [DOI] [PubMed] [Google Scholar]
  114. House A. O., Abbott R. J., Davidson D. L., Ferguson I. T., Lenman J. A. Response to penicillamine of lead concentrations in CSF and blood in patients with motor neurone disease. Br Med J. 1978 Dec 16;2(6153):1684–1684. doi: 10.1136/bmj.2.6153.1684. [DOI] [PMC free article] [PubMed] [Google Scholar]
  115. Hsu P. C., Hsu C. C., Liu M. Y., Chen L. Y., Guo Y. L. Lead-induced changes in spermatozoa function and metabolism. J Toxicol Environ Health A. 1998 Sep 11;55(1):45–64. doi: 10.1080/009841098158610. [DOI] [PubMed] [Google Scholar]
  116. Hsu P. C., Liu M. Y., Hsu C. C., Chen L. Y., Guo Y. L. Lead exposure causes generation of reactive oxygen species and functional impairment in rat sperm. Toxicology. 1997 Sep 26;122(1-2):133–143. doi: 10.1016/s0300-483x(97)00090-5. [DOI] [PubMed] [Google Scholar]
  117. Hu H., Aro A., Payton M., Korrick S., Sparrow D., Weiss S. T., Rotnitzky A. The relationship of bone and blood lead to hypertension. The Normative Aging Study. JAMA. 1996 Apr 17;275(15):1171–1176. [PubMed] [Google Scholar]
  118. Hunter D. J., Hankinson S. E., Laden F., Colditz G. A., Manson J. E., Willett W. C., Speizer F. E., Wolff M. S. Plasma organochlorine levels and the risk of breast cancer. N Engl J Med. 1997 Oct 30;337(18):1253–1258. doi: 10.1056/NEJM199710303371801. [DOI] [PubMed] [Google Scholar]
  119. Hussain R. J., Gyori J., DeCaprio A. P., Carpenter D. O. In vivo and in vitro exposure to PCB 153 reduces long-term potentiation. Environ Health Perspect. 2000 Sep;108(9):827–831. doi: 10.1289/ehp.00108827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  120. Hussain R. J., Parsons P. J., Carpenter D. O. Effects of lead on long-term potentiation in hippocampal CA3 vary with age. Brain Res Dev Brain Res. 2000 Jun 30;121(2):243–252. doi: 10.1016/s0165-3806(00)00051-1. [DOI] [PubMed] [Google Scholar]
  121. Ishii T., Itoh K., Takahashi S., Sato H., Yanagawa T., Katoh Y., Bannai S., Yamamoto M. Transcription factor Nrf2 coordinately regulates a group of oxidative stress-inducible genes in macrophages. J Biol Chem. 2000 May 26;275(21):16023–16029. doi: 10.1074/jbc.275.21.16023. [DOI] [PubMed] [Google Scholar]
  122. Jacobs J. M., Nichols C. E., Andrew A. S., Marek D. E., Wood S. G., Sinclair P. R., Wrighton S. A., Kostrubsky V. E., Sinclair J. F. Effect of arsenite on induction of CYP1A, CYP2B, and CYP3A in primary cultures of rat hepatocytes. Toxicol Appl Pharmacol. 1999 May 15;157(1):51–59. doi: 10.1006/taap.1999.8659. [DOI] [PubMed] [Google Scholar]
  123. Jacobson J. L., Jacobson S. W. Intellectual impairment in children exposed to polychlorinated biphenyls in utero. N Engl J Med. 1996 Sep 12;335(11):783–789. doi: 10.1056/NEJM199609123351104. [DOI] [PubMed] [Google Scholar]
  124. Jansen H. T., Cooke P. S., Porcelli J., Liu T. C., Hansen L. G. Estrogenic and antiestrogenic actions of PCBs in the female rat: in vitro and in vivo studies. Reprod Toxicol. 1993 May-Jun;7(3):237–248. doi: 10.1016/0890-6238(93)90230-5. [DOI] [PubMed] [Google Scholar]
  125. Jenner P., Schapira A. H., Marsden C. D. New insights into the cause of Parkinson's disease. Neurology. 1992 Dec;42(12):2241–2250. doi: 10.1212/wnl.42.12.2241. [DOI] [PubMed] [Google Scholar]
  126. Jeyapaul J., Jaiswal A. K. Nrf2 and c-Jun regulation of antioxidant response element (ARE)-mediated expression and induction of gamma-glutamylcysteine synthetase heavy subunit gene. Biochem Pharmacol. 2000 Jun 1;59(11):1433–1439. doi: 10.1016/s0006-2952(00)00256-2. [DOI] [PubMed] [Google Scholar]
  127. Jones L. C., Whitlock J. P., Jr Dioxin-inducible transactivation in a chromosomal setting. Analysis of the acidic domain of the Ah receptor. J Biol Chem. 2001 May 11;276(27):25037–25042. doi: 10.1074/jbc.M102910200. [DOI] [PubMed] [Google Scholar]
  128. Jones R., Mann T., Sherins R. Peroxidative breakdown of phospholipids in human spermatozoa, spermicidal properties of fatty acid peroxides, and protective action of seminal plasma. Fertil Steril. 1979 May;31(5):531–537. doi: 10.1016/s0015-0282(16)43999-3. [DOI] [PubMed] [Google Scholar]
  129. Jones S. A., Moore L. B., Shenk J. L., Wisely G. B., Hamilton G. A., McKee D. D., Tomkinson N. C., LeCluyse E. L., Lambert M. H., Willson T. M. The pregnane X receptor: a promiscuous xenobiotic receptor that has diverged during evolution. Mol Endocrinol. 2000 Jan;14(1):27–39. doi: 10.1210/mend.14.1.0409. [DOI] [PubMed] [Google Scholar]
  130. Jordan V. C. Effect of tamoxifen (ICI 46,474) on initiation and growth of DMBA-induced rat mammary carcinomata. Eur J Cancer. 1976 Jun;12(6):419–424. doi: 10.1016/0014-2964(76)90030-x. [DOI] [PubMed] [Google Scholar]
  131. Jordan V. C. Laboratory models of breast cancer to aid the elucidation of antiestrogen action. J Lab Clin Med. 1987 Mar;109(3):267–277. [PubMed] [Google Scholar]
  132. Jówik M., Jówik M., Kuczyński W., Szamatowicz M. Nonenzymatic antioxidant activity of human seminal plasma. Fertil Steril. 1997 Jul;68(1):154–157. doi: 10.1016/s0015-0282(97)81493-8. [DOI] [PubMed] [Google Scholar]
  133. Kapahi P., Takahashi T., Natoli G., Adams S. R., Chen Y., Tsien R. Y., Karin M. Inhibition of NF-kappa B activation by arsenite through reaction with a critical cysteine in the activation loop of Ikappa B kinase. J Biol Chem. 2000 Nov 17;275(46):36062–36066. doi: 10.1074/jbc.M007204200. [DOI] [PubMed] [Google Scholar]
  134. Kapaki E., Segditsa J., Zournas C., Xenos D., Papageorgiou C. Determination of cerebrospinal fluid and serum lead levels in patients with amyotrophic lateral sclerosis and other neurological diseases. Experientia. 1989 Dec 1;45(11-12):1108–1110. doi: 10.1007/BF01950171. [DOI] [PubMed] [Google Scholar]
  135. Kapitulnik J., Wislocki P. G., Levin W., Yagi H., Jerina D. M., Conney A. H. Tumorigenicity studies with diol-epoxides of benzo(a)pyrene which indicate that (+/-)-trans-7beta,8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo(a)pyrene is an ultimate carcinogen in newborn mice. Cancer Res. 1978 Feb;38(2):354–358. [PubMed] [Google Scholar]
  136. Ke S., Rabson A. B., Germino J. F., Gallo M. A., Tian Y. Mechanism of suppression of cytochrome P-450 1A1 expression by tumor necrosis factor-alpha and lipopolysaccharide. J Biol Chem. 2001 Jul 24;276(43):39638–39644. doi: 10.1074/jbc.M106286200. [DOI] [PubMed] [Google Scholar]
  137. Keith B., Adelman D. M., Simon M. C. Targeted mutation of the murine arylhydrocarbon receptor nuclear translocator 2 (Arnt2) gene reveals partial redundancy with Arnt. Proc Natl Acad Sci U S A. 2001 May 29;98(12):6692–6697. doi: 10.1073/pnas.121494298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  138. Kelce W. R., Stone C. R., Laws S. C., Gray L. E., Kemppainen J. A., Wilson E. M. Persistent DDT metabolite p,p'-DDE is a potent androgen receptor antagonist. Nature. 1995 Jun 15;375(6532):581–585. doi: 10.1038/375581a0. [DOI] [PubMed] [Google Scholar]
  139. Key T. J., Chen J., Wang D. Y., Pike M. C., Boreham J. Sex hormones in women in rural China and in Britain. Br J Cancer. 1990 Oct;62(4):631–636. doi: 10.1038/bjc.1990.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  140. Kim J. H., Stansbury K. H., Walker N. J., Trush M. A., Strickland P. T., Sutter T. R. Metabolism of benzo[a]pyrene and benzo[a]pyrene-7,8-diol by human cytochrome P450 1B1. Carcinogenesis. 1998 Oct;19(10):1847–1853. doi: 10.1093/carcin/19.10.1847. [DOI] [PubMed] [Google Scholar]
  141. Kledzik G. S., Bradley C. J., Marshall S., Campbell G. A., Meites J. Effects of high hoses of estrogen on prolactin-binding activity and growth of carcinogen-induced mammary cancers in rats. Cancer Res. 1976 Sep;36(9 PT1):3265–3268. [PubMed] [Google Scholar]
  142. Klinge C. M., Jernigan S. C., Risinger K. E., Lee J. E., Tyulmenkov V. V., Falkner K. C., Prough R. A. Short heterodimer partner (SHP) orphan nuclear receptor inhibits the transcriptional activity of aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT). Arch Biochem Biophys. 2001 Jun 1;390(1):64–70. doi: 10.1006/abbi.2001.2366. [DOI] [PubMed] [Google Scholar]
  143. Kodama H., Yamaguchi R., Fukuda J., Kasai H., Tanaka T. Increased oxidative deoxyribonucleic acid damage in the spermatozoa of infertile male patients. Fertil Steril. 1997 Sep;68(3):519–524. doi: 10.1016/s0015-0282(97)00236-7. [DOI] [PubMed] [Google Scholar]
  144. Koller W., Vetere-Overfield B., Gray C., Alexander C., Chin T., Dolezal J., Hassanein R., Tanner C. Environmental risk factors in Parkinson's disease. Neurology. 1990 Aug;40(8):1218–1221. doi: 10.1212/wnl.40.8.1218. [DOI] [PubMed] [Google Scholar]
  145. Kolluri S. K., Weiss C., Koff A., Göttlicher M. p27(Kip1) induction and inhibition of proliferation by the intracellular Ah receptor in developing thymus and hepatoma cells. Genes Dev. 1999 Jul 1;13(13):1742–1753. doi: 10.1101/gad.13.13.1742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  146. Kopp S. J., Barron J. T., Tow J. P. Cardiovascular actions of lead and relationship to hypertension: a review. Environ Health Perspect. 1988 Jun;78:91–99. doi: 10.1289/ehp.887891. [DOI] [PMC free article] [PubMed] [Google Scholar]
  147. Korach K. S., Sarver P., Chae K., McLachlan J. A., McKinney J. D. Estrogen receptor-binding activity of polychlorinated hydroxybiphenyls: conformationally restricted structural probes. Mol Pharmacol. 1988 Jan;33(1):120–126. [PubMed] [Google Scholar]
  148. Kovacević R., Vojinović-Miloradov M., Teodorović I., Andrić S. Effect of PCBs on androgen production by suspension of adult rat Leydig cells in vitro. J Steroid Biochem Mol Biol. 1995 Jun;52(6):595–597. doi: 10.1016/0960-0760(95)00060-d. [DOI] [PubMed] [Google Scholar]
  149. Kreiss K. Studies on populations exposed to polychlorinated biphenyls. Environ Health Perspect. 1985 May;60:193–199. doi: 10.1289/ehp.8560193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  150. Krieger N., Wolff M. S., Hiatt R. A., Rivera M., Vogelman J., Orentreich N. Breast cancer and serum organochlorines: a prospective study among white, black, and Asian women. J Natl Cancer Inst. 1994 Apr 20;86(8):589–599. doi: 10.1093/jnci/86.8.589. [DOI] [PubMed] [Google Scholar]
  151. Kumar M. B., Tarpey R. W., Perdew G. H. Differential recruitment of coactivator RIP140 by Ah and estrogen receptors. Absence of a role for LXXLL motifs. J Biol Chem. 1999 Aug 6;274(32):22155–22164. doi: 10.1074/jbc.274.32.22155. [DOI] [PubMed] [Google Scholar]
  152. Laden F., Collman G., Iwamoto K., Alberg A. J., Berkowitz G. S., Freudenheim J. L., Hankinson S. E., Helzlsouer K. J., Holford T. R., Huang H. Y. 1,1-Dichloro-2,2-bis(p-chlorophenyl)ethylene and polychlorinated biphenyls and breast cancer: combined analysis of five U.S. studies. J Natl Cancer Inst. 2001 May 16;93(10):768–776. doi: 10.1093/jnci/93.10.768. [DOI] [PubMed] [Google Scholar]
  153. Lancranjan I., Popescu H. I., GAvănescu O., Klepsch I., Serbănescu M. Reproductive ability of workmen occupationally exposed to lead. Arch Environ Health. 1975 Aug;30(8):396–401. doi: 10.1080/00039896.1975.10666733. [DOI] [PubMed] [Google Scholar]
  154. Li M. H., Hansen L. G. Enzyme induction and acute endocrine effects in prepubertal female rats receiving environmental PCB/PCDF/PCDD mixtures. Environ Health Perspect. 1996 Jul;104(7):712–722. doi: 10.1289/ehp.96104712. [DOI] [PMC free article] [PubMed] [Google Scholar]
  155. Li M. H., Hansen L. G. Uterotropic and enzyme induction effects of 2,2',5-trichlorobiphenyl. Bull Environ Contam Toxicol. 1995 Apr;54(4):494–500. doi: 10.1007/BF00192590. [DOI] [PubMed] [Google Scholar]
  156. Li N., Karin M. Is NF-kappaB the sensor of oxidative stress? FASEB J. 1999 Jul;13(10):1137–1143. [PubMed] [Google Scholar]
  157. Liehr J. G. Dual role of oestrogens as hormones and pro-carcinogens: tumour initiation by metabolic activation of oestrogens. Eur J Cancer Prev. 1997 Feb;6(1):3–10. doi: 10.1097/00008469-199702000-00002. [DOI] [PubMed] [Google Scholar]
  158. Liehr J. G. Genotoxicity of the steroidal oestrogens oestrone and oestradiol: possible mechanism of uterine and mammary cancer development. Hum Reprod Update. 2001 May-Jun;7(3):273–281. doi: 10.1093/humupd/7.3.273. [DOI] [PubMed] [Google Scholar]
  159. Liehr J. G. Is estradiol a genotoxic mutagenic carcinogen? Endocr Rev. 2000 Feb;21(1):40–54. doi: 10.1210/edrv.21.1.0386. [DOI] [PubMed] [Google Scholar]
  160. Liu P. C., Matsumura F. Differential effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin on the "adipose- type" and "brain-type" glucose transporters in mice. Mol Pharmacol. 1995 Jan;47(1):65–73. [PubMed] [Google Scholar]
  161. Liu S. X., Athar M., Lippai I., Waldren C., Hei T. K. Induction of oxyradicals by arsenic: implication for mechanism of genotoxicity. Proc Natl Acad Sci U S A. 2001 Feb 6;98(4):1643–1648. doi: 10.1073/pnas.031482998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  162. Long D. J., 2nd, Waikel R. L., Wang X. J., Perlaky L., Roop D. R., Jaiswal A. K. NAD(P)H:quinone oxidoreductase 1 deficiency increases susceptibility to benzo(a)pyrene-induced mouse skin carcinogenesis. Cancer Res. 2000 Nov 1;60(21):5913–5915. [PubMed] [Google Scholar]
  163. Long D. J., 2nd, Waikel R. L., Wang X. J., Roop D. R., Jaiswal A. K. NAD(P)H:quinone oxidoreductase 1 deficiency and increased susceptibility to 7,12-dimethylbenz[a]-anthracene-induced carcinogenesis in mouse skin. J Natl Cancer Inst. 2001 Aug 1;93(15):1166–1170. doi: 10.1093/jnci/93.15.1166. [DOI] [PubMed] [Google Scholar]
  164. Lovell M. A., Robertson J. D., Teesdale W. J., Campbell J. L., Markesbery W. R. Copper, iron and zinc in Alzheimer's disease senile plaques. J Neurol Sci. 1998 Jun 11;158(1):47–52. doi: 10.1016/s0022-510x(98)00092-6. [DOI] [PubMed] [Google Scholar]
  165. López-Carrillo L., Blair A., López-Cervantes M., Cebrián M., Rueda C., Reyes R., Mohar A., Bravo J. Dichlorodiphenyltrichloroethane serum levels and breast cancer risk: a case-control study from Mexico. Cancer Res. 1997 Sep 1;57(17):3728–3732. [PubMed] [Google Scholar]
  166. Ma Q., Baldwin K. T. 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced degradation of aryl hydrocarbon receptor (AhR) by the ubiquitin-proteasome pathway. Role of the transcription activaton and DNA binding of AhR. J Biol Chem. 2000 Mar 24;275(12):8432–8438. doi: 10.1074/jbc.275.12.8432. [DOI] [PubMed] [Google Scholar]
  167. Ma Q., Whitlock J. P., Jr A novel cytoplasmic protein that interacts with the Ah receptor, contains tetratricopeptide repeat motifs, and augments the transcriptional response to 2,3,7,8-tetrachlorodibenzo-p-dioxin. J Biol Chem. 1997 Apr 4;272(14):8878–8884. [PubMed] [Google Scholar]
  168. Ma Q., Whitlock J. P., Jr The aromatic hydrocarbon receptor modulates the Hepa 1c1c7 cell cycle and differentiated state independently of dioxin. Mol Cell Biol. 1996 May;16(5):2144–2150. doi: 10.1128/mcb.16.5.2144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  169. Mably T. A., Bjerke D. L., Moore R. W., Gendron-Fitzpatrick A., Peterson R. E. In utero and lactational exposure of male rats to 2,3,7,8-tetrachlorodibenzo-p-dioxin. 3. Effects on spermatogenesis and reproductive capability. Toxicol Appl Pharmacol. 1992 May;114(1):118–126. doi: 10.1016/0041-008x(92)90103-y. [DOI] [PubMed] [Google Scholar]
  170. Mably T. A., Moore R. W., Goy R. W., Peterson R. E. In utero and lactational exposure of male rats to 2,3,7,8-tetrachlorodibenzo-p-dioxin. 2. Effects on sexual behavior and the regulation of luteinizing hormone secretion in adulthood. Toxicol Appl Pharmacol. 1992 May;114(1):108–117. doi: 10.1016/0041-008x(92)90102-x. [DOI] [PubMed] [Google Scholar]
  171. Mably T. A., Moore R. W., Peterson R. E. In utero and lactational exposure of male rats to 2,3,7,8-tetrachlorodibenzo-p-dioxin. 1. Effects on androgenic status. Toxicol Appl Pharmacol. 1992 May;114(1):97–107. doi: 10.1016/0041-008x(92)90101-w. [DOI] [PubMed] [Google Scholar]
  172. Machala M., Neca J., Drábek P., Ulrich R., Sabatová V., Nezveda K., Raszyk J., Gajdusková V. Effects of chronic exposure to PCBs on cytochrome P450 systems and steroidogenesis in liver and testis of bulls (Bos taurus). Comp Biochem Physiol A Mol Integr Physiol. 1998 May;120(1):65–70. doi: 10.1016/s1095-6433(98)10011-9. [DOI] [PubMed] [Google Scholar]
  173. Maier A., Dalton T. P., Puga A. Disruption of dioxin-inducible phase I and phase II gene expression patterns by cadmium, chromium, and arsenic. Mol Carcinog. 2000 Aug;28(4):225–235. [PubMed] [Google Scholar]
  174. Maltepe E., Schmidt J. V., Baunoch D., Bradfield C. A., Simon M. C. Abnormal angiogenesis and responses to glucose and oxygen deprivation in mice lacking the protein ARNT. Nature. 1997 Mar 27;386(6623):403–407. doi: 10.1038/386403a0. [DOI] [PubMed] [Google Scholar]
  175. Marchlewicz M., Protasowicki M., Rózewicka L., Piasecka M., Laszczyńska M. Effect of long-term exposure to lead on testis and epididymis in rats. Folia Histochem Cytobiol. 1993;31(2):55–62. [PubMed] [Google Scholar]
  176. Marston C. P., Pereira C., Ferguson J., Fischer K., Hedstrom O., Dashwood W. M., Baird W. M. Effect of a complex environmental mixture from coal tar containing polycyclic aromatic hydrocarbons (PAH) on the tumor initiation, PAH-DNA binding and metabolic activation of carcinogenic PAH in mouse epidermis. Carcinogenesis. 2001 Jul;22(7):1077–1086. doi: 10.1093/carcin/22.7.1077. [DOI] [PubMed] [Google Scholar]
  177. Martyn C. N., Barker D. J., Osmond C., Harris E. C., Edwardson J. A., Lacey R. F. Geographical relation between Alzheimer's disease and aluminum in drinking water. Lancet. 1989 Jan 14;1(8629):59–62. [PubMed] [Google Scholar]
  178. Matikainen T., Perez G. I., Jurisicova A., Pru J. K., Schlezinger J. J., Ryu H. Y., Laine J., Sakai T., Korsmeyer S. J., Casper R. F. Aromatic hydrocarbon receptor-driven Bax gene expression is required for premature ovarian failure caused by biohazardous environmental chemicals. Nat Genet. 2001 Aug;28(4):355–360. doi: 10.1038/ng575. [DOI] [PubMed] [Google Scholar]
  179. Mayes B. A., McConnell E. E., Neal B. H., Brunner M. J., Hamilton S. B., Sullivan T. M., Peters A. C., Ryan M. J., Toft J. D., Singer A. W. Comparative carcinogenicity in Sprague-Dawley rats of the polychlorinated biphenyl mixtures Aroclors 1016, 1242, 1254, and 1260. Toxicol Sci. 1998 Jan;41(1):62–76. doi: 10.1093/toxsci/41.1.62. [DOI] [PMC free article] [PubMed] [Google Scholar]
  180. McGivern R. F., Sokol R. Z., Berman N. G. Prenatal lead exposure in the rat during the third week of gestation: long-term behavioral, physiological, and anatomical effects associated with reproduction. Toxicol Appl Pharmacol. 1991 Sep 1;110(2):206–215. doi: 10.1016/s0041-008x(05)80003-1. [DOI] [PubMed] [Google Scholar]
  181. Meerts I. A., Letcher R. J., Hoving S., Marsh G., Bergman A., Lemmen J. G., van der Burg B., Brouwer A. In vitro estrogenicity of polybrominated diphenyl ethers, hydroxylated PDBEs, and polybrominated bisphenol A compounds. Environ Health Perspect. 2001 Apr;109(4):399–407. doi: 10.1289/ehp.01109399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  182. Mendez D., Warner K. E., Courant P. N. Effects of radon mitigation vs smoking cessation in reducing radon-related risk of lung cancer. Am J Public Health. 1998 May;88(5):811–812. doi: 10.2105/ajph.88.5.811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  183. Mergler D., Bélanger S., Larribe F., Panisset M., Bowler R., Baldwin M., Lebel J., Hudnell K. Preliminary evidence of neurotoxicity associated with eating fish from the Upper St. Lawrence River Lakes. Neurotoxicology. 1998 Aug-Oct;19(4-5):691–702. [PubMed] [Google Scholar]
  184. Michalek J. E., Ketchum N. S., Akhtar F. Z. Postservice mortality of US Air Force veterans occupationally exposed to herbicides in Vietnam: 15-year follow-up. Am J Epidemiol. 1998 Oct 15;148(8):786–792. doi: 10.1093/oxfordjournals.aje.a009699. [DOI] [PubMed] [Google Scholar]
  185. Millikan R., DeVoto E., Duell E. J., Tse C. K., Savitz D. A., Beach J., Edmiston S., Jackson S., Newman B. Dichlorodiphenyldichloroethene, polychlorinated biphenyls, and breast cancer among African-American and white women in North Carolina. Cancer Epidemiol Biomarkers Prev. 2000 Nov;9(11):1233–1240. [PubMed] [Google Scholar]
  186. Minassian E. S., Terner C. Biosynthesis of lipids by human and fish spermatozoa. Am J Physiol. 1966 Mar;210(3):615–618. doi: 10.1152/ajplegacy.1966.210.3.615. [DOI] [PubMed] [Google Scholar]
  187. Mocarelli P., Gerthoux P. M., Ferrari E., Patterson D. G., Jr, Kieszak S. M., Brambilla P., Vincoli N., Signorini S., Tramacere P., Carreri V. Paternal concentrations of dioxin and sex ratio of offspring. Lancet. 2000 May 27;355(9218):1858–1863. doi: 10.1016/S0140-6736(00)02290-X. [DOI] [PubMed] [Google Scholar]
  188. Moore L. B., Parks D. J., Jones S. A., Bledsoe R. K., Consler T. G., Stimmel J. B., Goodwin B., Liddle C., Blanchard S. G., Willson T. M. Orphan nuclear receptors constitutive androstane receptor and pregnane X receptor share xenobiotic and steroid ligands. J Biol Chem. 2000 May 19;275(20):15122–15127. doi: 10.1074/jbc.M001215200. [DOI] [PubMed] [Google Scholar]
  189. Moore R. W., Peterson R. E. Androgen catabolism and excretion in 2,3,7,8-tetrachlorodibenzo-p-dioxin-treated rats. Biochem Pharmacol. 1988 Feb 1;37(3):560–562. doi: 10.1016/0006-2952(88)90232-8. [DOI] [PubMed] [Google Scholar]
  190. Moore R. W., Potter C. L., Theobald H. M., Robinson J. A., Peterson R. E. Androgenic deficiency in male rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin. Toxicol Appl Pharmacol. 1985 Jun 15;79(1):99–111. doi: 10.1016/0041-008x(85)90372-2. [DOI] [PubMed] [Google Scholar]
  191. Morel Y., Barouki R. Down-regulation of cytochrome P450 1A1 gene promoter by oxidative stress. Critical contribution of nuclear factor 1. J Biol Chem. 1998 Oct 9;273(41):26969–26976. doi: 10.1074/jbc.273.41.26969. [DOI] [PubMed] [Google Scholar]
  192. Morrison H. I., Villeneuve P. J., Lubin J. H., Schaubel D. E. Radon-progeny exposure and lung cancer risk in a cohort of Newfoundland fluorspar miners. Radiat Res. 1998 Jul;150(1):58–65. [PubMed] [Google Scholar]
  193. Moysich K. B., Shields P. G., Freudenheim J. L., Schisterman E. F., Vena J. E., Kostyniak P., Greizerstein H., Marshall J. R., Graham S., Ambrosone C. B. Polychlorinated biphenyls, cytochrome P4501A1 polymorphism, and postmenopausal breast cancer risk. Cancer Epidemiol Biomarkers Prev. 1999 Jan;8(1):41–44. [PubMed] [Google Scholar]
  194. Nebert D. W., Ingelman-Sundberg M., Daly A. K. Genetic epidemiology of environmental toxicity and cancer susceptibility: human allelic polymorphisms in drug-metabolizing enzyme genes, their functional importance, and nomenclature issues. Drug Metab Rev. 1999 May;31(2):467–487. doi: 10.1081/dmr-100101931. [DOI] [PubMed] [Google Scholar]
  195. Needleman H. L., Gunnoe C., Leviton A., Reed R., Peresie H., Maher C., Barrett P. Deficits in psychologic and classroom performance of children with elevated dentine lead levels. N Engl J Med. 1979 Mar 29;300(13):689–695. doi: 10.1056/NEJM197903293001301. [DOI] [PubMed] [Google Scholar]
  196. Needleman H. L., Schell A., Bellinger D., Leviton A., Allred E. N. The long-term effects of exposure to low doses of lead in childhood. An 11-year follow-up report. N Engl J Med. 1990 Jan 11;322(2):83–88. doi: 10.1056/NEJM199001113220203. [DOI] [PubMed] [Google Scholar]
  197. Newbold R. Cellular and molecular effects of developmental exposure to diethylstilbestrol: implications for other environmental estrogens. Environ Health Perspect. 1995 Oct;103 (Suppl 7):83–87. doi: 10.1289/ehp.95103s783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  198. Nguyen P. V., Abel T., Kandel E. R., Bourtchouladze R. Strain-dependent differences in LTP and hippocampus-dependent memory in inbred mice. Learn Mem. 2000 May-Jun;7(3):170–179. doi: 10.1101/lm.7.3.170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  199. Ni Z. Y., Liu Y. Q., Shen H. M., Chia S. E., Ong C. N. Does the increase of 8-hydroxydeoxyguanosine lead to poor sperm quality? Mutat Res. 1997 Nov 19;381(1):77–82. doi: 10.1016/s0027-5107(97)00151-6. [DOI] [PubMed] [Google Scholar]
  200. Nie M., Blankenship A. L., Giesy J. P. Interactions between aryl hydrocarbon receptor (AhR) and hypoxia signaling pathways. Environ Toxicol Pharmacol. 2001 Jun;10(1-2):17–27. doi: 10.1016/s1382-6689(01)00065-5. [DOI] [PubMed] [Google Scholar]
  201. Niemi W. D., Slivinski K., Audi J., Rej R., Carpenter D. O. Propylthiouracil treatment reduces long-term potentiation in area CA1 of neonatal rat hippocampus. Neurosci Lett. 1996 May 31;210(2):127–129. doi: 10.1016/0304-3940(96)12676-8. [DOI] [PubMed] [Google Scholar]
  202. Nutter L. M., Ngo E. O., Abul-Hajj Y. J. Characterization of DNA damage induced by 3,4-estrone-o-quinone in human cells. J Biol Chem. 1991 Sep 5;266(25):16380–16386. [PubMed] [Google Scholar]
  203. Oakley G. G., Devanaboyina U., Robertson L. W., Gupta R. C. Oxidative DNA damage induced by activation of polychlorinated biphenyls (PCBs): implications for PCB-induced oxidative stress in breast cancer. Chem Res Toxicol. 1996 Dec;9(8):1285–1292. doi: 10.1021/tx960103o. [DOI] [PubMed] [Google Scholar]
  204. Okino S. T., Whitlock J. P., Jr Dioxin induces localized, graded changes in chromatin structure: implications for Cyp1A1 gene transcription. Mol Cell Biol. 1995 Jul;15(7):3714–3721. doi: 10.1128/mcb.15.7.3714. [DOI] [PMC free article] [PubMed] [Google Scholar]
  205. Park J. Y., Shigenaga M. K., Ames B. N. Induction of cytochrome P4501A1 by 2,3,7,8-tetrachlorodibenzo-p-dioxin or indolo(3,2-b)carbazole is associated with oxidative DNA damage. Proc Natl Acad Sci U S A. 1996 Mar 19;93(6):2322–2327. doi: 10.1073/pnas.93.6.2322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  206. Patterson D. G., Jr, Todd G. D., Turner W. E., Maggio V., Alexander L. R., Needham L. L. Levels of non-ortho-substituted (coplanar), mono- and di-ortho-substituted polychlorinated biphenyls, dibenzo-p-dioxins, and dibenzofurans in human serum and adipose tissue. Environ Health Perspect. 1994 Jan;102 (Suppl 1):195–204. doi: 10.1289/ehp.94102s1195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  207. Payne J., Scholze M., Kortenkamp A. Mixtures of four organochlorines enhance human breast cancer cell proliferation. Environ Health Perspect. 2001 Apr;109(4):391–397. doi: 10.1289/ehp.01109391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  208. Pennie W. D., Woodyatt N. J., Aldridge T. C., Orphanides G. Application of genomics to the definition of the molecular basis for toxicity. Toxicol Lett. 2001 Mar 31;120(1-3):353–358. doi: 10.1016/s0378-4274(01)00322-8. [DOI] [PubMed] [Google Scholar]
  209. Perera F. P. Environment and cancer: who are susceptible? Science. 1997 Nov 7;278(5340):1068–1073. doi: 10.1126/science.278.5340.1068. [DOI] [PubMed] [Google Scholar]
  210. Perera F. P. Molecular epidemiology: insights into cancer susceptibility, risk assessment, and prevention. J Natl Cancer Inst. 1996 Apr 17;88(8):496–509. doi: 10.1093/jnci/88.8.496. [DOI] [PubMed] [Google Scholar]
  211. Pesatori A. C., Zocchetti C., Guercilena S., Consonni D., Turrini D., Bertazzi P. A. Dioxin exposure and non-malignant health effects: a mortality study. Occup Environ Med. 1998 Feb;55(2):126–131. doi: 10.1136/oem.55.2.126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  212. Pines A., Cucos S., Ever-Handani P., Ron M. Some organochlorine insecticide and polychlorinated biphenyl blood residues in infertile males in the general Israeli population of the middle 1980's. Arch Environ Contam Toxicol. 1987 Sep;16(5):587–597. doi: 10.1007/BF01055815. [DOI] [PubMed] [Google Scholar]
  213. Prendergast M. A., Terry A. V., Jr, Buccafusco J. J. Effects of chronic, low-level organophosphate exposure on delayed recall, discrimination, and spatial learning in monkeys and rats. Neurotoxicol Teratol. 1998 Mar-Apr;20(2):115–122. doi: 10.1016/s0892-0362(97)00098-6. [DOI] [PubMed] [Google Scholar]
  214. Prince M. Is chronic low-level lead exposure in early life an etiologic factor in Alzheimer's disease? Epidemiology. 1998 Nov;9(6):618–621. [PubMed] [Google Scholar]
  215. Puga A., Barnes S. J., Dalton T. P., Chang C. y., Knudsen E. S., Maier M. A. Aromatic hydrocarbon receptor interaction with the retinoblastoma protein potentiates repression of E2F-dependent transcription and cell cycle arrest. J Biol Chem. 2000 Jan 28;275(4):2943–2950. doi: 10.1074/jbc.275.4.2943. [DOI] [PubMed] [Google Scholar]
  216. Rajapakse N., Ong D., Kortenkamp A. Defining the impact of weakly estrogenic chemicals on the action of steroidal estrogens. Toxicol Sci. 2001 Apr;60(2):296–304. doi: 10.1093/toxsci/60.2.296. [DOI] [PubMed] [Google Scholar]
  217. Rice D. C. Behavioral effects of lead: commonalities between experimental and epidemiologic data. Environ Health Perspect. 1996 Apr;104 (Suppl 2):337–351. doi: 10.1289/ehp.96104s2337. [DOI] [PMC free article] [PubMed] [Google Scholar]
  218. Rice D. C. Behavioral impairment produced by low-level postnatal PCB exposure in monkeys. Environ Res. 1999 Feb;80(2 Pt 2):S113–S121. doi: 10.1006/enrs.1998.3917. [DOI] [PubMed] [Google Scholar]
  219. Rier S. E., Turner W. E., Martin D. C., Morris R., Lucier G. W., Clark G. C. Serum levels of TCDD and dioxin-like chemicals in Rhesus monkeys chronically exposed to dioxin: correlation of increased serum PCB levels with endometriosis. Toxicol Sci. 2001 Jan;59(1):147–159. doi: 10.1093/toxsci/59.1.147. [DOI] [PubMed] [Google Scholar]
  220. Robertson J. A. Consent and privacy in pharmacogenetic testing. Nat Genet. 2001 Jul;28(3):207–209. doi: 10.1038/90032. [DOI] [PubMed] [Google Scholar]
  221. Rogan W. J., Gladen B. C. Neurotoxicology of PCBs and related compounds. Neurotoxicology. 1992 Spring;13(1):27–35. [PubMed] [Google Scholar]
  222. Romero D. L., Mounho B. J., Lauer F. T., Born J. L., Burchiel S. W. Depletion of glutathione by benzo(a)pyrene metabolites, ionomycin, thapsigargin, and phorbol myristate in human peripheral blood mononuclear cells. Toxicol Appl Pharmacol. 1997 May;144(1):62–69. doi: 10.1006/taap.1997.8113. [DOI] [PubMed] [Google Scholar]
  223. Ronis M. J., Gandy J., Badger T. Endocrine mechanisms underlying reproductive toxicity in the developing rat chronically exposed to dietary lead. J Toxicol Environ Health A. 1998 May 22;54(2):77–99. doi: 10.1080/009841098158935. [DOI] [PubMed] [Google Scholar]
  224. Rosen J. F., Mushak P. Primary prevention of childhood lead poisoning--the only solution. N Engl J Med. 2001 May 10;344(19):1470–1471. doi: 10.1056/NEJM200105103441910. [DOI] [PubMed] [Google Scholar]
  225. Rowlands J. C., Gustafsson J. A. Aryl hydrocarbon receptor-mediated signal transduction. Crit Rev Toxicol. 1997 Mar;27(2):109–134. doi: 10.3109/10408449709021615. [DOI] [PubMed] [Google Scholar]
  226. Rubin B. S., Murray M. K., Damassa D. A., King J. C., Soto A. M. Perinatal exposure to low doses of bisphenol A affects body weight, patterns of estrous cyclicity, and plasma LH levels. Environ Health Perspect. 2001 Jul;109(7):675–680. doi: 10.1289/ehp.01109675. [DOI] [PMC free article] [PubMed] [Google Scholar]
  227. Rundle A., Tang D., Hibshoosh H., Estabrook A., Schnabel F., Cao W., Grumet S., Perera F. P. The relationship between genetic damage from polycyclic aromatic hydrocarbons in breast tissue and breast cancer. Carcinogenesis. 2000 Jul;21(7):1281–1289. [PubMed] [Google Scholar]
  228. Rundle A., Tang D., Zhou J., Cho S., Perera F. The association between glutathione S-transferase M1 genotype and polycyclic aromatic hydrocarbon-DNA adducts in breast tissue. Cancer Epidemiol Biomarkers Prev. 2000 Oct;9(10):1079–1085. [PubMed] [Google Scholar]
  229. Safe S. H. Interactions between hormones and chemicals in breast cancer. Annu Rev Pharmacol Toxicol. 1998;38:121–158. doi: 10.1146/annurev.pharmtox.38.1.121. [DOI] [PubMed] [Google Scholar]
  230. Safe S. H. Polychlorinated biphenyls (PCBs): environmental impact, biochemical and toxic responses, and implications for risk assessment. Crit Rev Toxicol. 1994;24(2):87–149. doi: 10.3109/10408449409049308. [DOI] [PubMed] [Google Scholar]
  231. Safe S. Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and related compounds: environmental and mechanistic considerations which support the development of toxic equivalency factors (TEFs). Crit Rev Toxicol. 1990;21(1):51–88. doi: 10.3109/10408449009089873. [DOI] [PubMed] [Google Scholar]
  232. Sallmén M., Lindbohm M. L., Nurminen M. Paternal exposure to lead and infertility. Epidemiology. 2000 Mar;11(2):148–152. doi: 10.1097/00001648-200003000-00011. [DOI] [PubMed] [Google Scholar]
  233. Salonen J. T., Seppänen K., Nyyssönen K., Korpela H., Kauhanen J., Kantola M., Tuomilehto J., Esterbauer H., Tatzber F., Salonen R. Intake of mercury from fish, lipid peroxidation, and the risk of myocardial infarction and coronary, cardiovascular, and any death in eastern Finnish men. Circulation. 1995 Feb 1;91(3):645–655. doi: 10.1161/01.cir.91.3.645. [DOI] [PubMed] [Google Scholar]
  234. Sarkar D. K., Liehr J. G., Singletary K. W. Role of estrogen in alcohol promotion of breast cancer and prolactinomas. Alcohol Clin Exp Res. 2001 May;25(5 Suppl ISBRA):230S–236S. doi: 10.1097/00000374-200105051-00037. [DOI] [PubMed] [Google Scholar]
  235. Savolainen K. M., Loikkanen J., Eerikäinen S., Naarala J. Interactions of excitatory neurotransmitters and xenobiotics in excitotoxicity and oxidative stress: glutamate and lead. Toxicol Lett. 1998 Dec 28;102-103:363–367. doi: 10.1016/s0378-4274(98)00233-1. [DOI] [PubMed] [Google Scholar]
  236. Schantz S. L., Bowman R. E. Learning in monkeys exposed perinatally to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Neurotoxicol Teratol. 1989 Jan-Feb;11(1):13–19. doi: 10.1016/0892-0362(89)90080-9. [DOI] [PubMed] [Google Scholar]
  237. Schantz S. L., Gasior D. M., Polverejan E., McCaffrey R. J., Sweeney A. M., Humphrey H. E., Gardiner J. C. Impairments of memory and learning in older adults exposed to polychlorinated biphenyls via consumption of Great Lakes fish. Environ Health Perspect. 2001 Jun;109(6):605–611. doi: 10.1289/ehp.01109605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  238. Schilter B., Andersen M. R., Acharya C., Omiecinski C. J. Activation of cytochrome P450 gene expression in the rat brain by phenobarbital-like inducers. J Pharmacol Exp Ther. 2000 Sep;294(3):916–922. [PubMed] [Google Scholar]
  239. Schmidt J. V., Su G. H., Reddy J. K., Simon M. C., Bradfield C. A. Characterization of a murine Ahr null allele: involvement of the Ah receptor in hepatic growth and development. Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6731–6736. doi: 10.1073/pnas.93.13.6731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  240. Schneider J., Kinne D., Fracchia A., Pierce V., Anderson K. E., Bradlow H. L., Fishman J. Abnormal oxidative metabolism of estradiol in women with breast cancer. Proc Natl Acad Sci U S A. 1982 May;79(9):3047–3051. doi: 10.1073/pnas.79.9.3047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  241. Schuetz E. G., Brimer C., Schuetz J. D. Environmental xenobiotics and the antihormones cyproterone acetate and spironolactone use the nuclear hormone pregnenolone X receptor to activate the CYP3A23 hormone response element. Mol Pharmacol. 1998 Dec;54(6):1113–1117. doi: 10.1124/mol.54.6.1113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  242. Schulte P. A., Burnett C. A., Boeniger M. F., Johnson J. Neurodegenerative diseases: occupational occurrence and potential risk factors, 1982 through 1991. Am J Public Health. 1996 Sep;86(9):1281–1288. doi: 10.2105/ajph.86.9.1281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  243. Seed J., Brown R. P., Olin S. S., Foran J. A. Chemical mixtures: current risk assessment methodologies and future directions. Regul Toxicol Pharmacol. 1995 Aug;22(1):76–94. doi: 10.1006/rtph.1995.1071. [DOI] [PubMed] [Google Scholar]
  244. Sharpe R. M., Skakkebaek N. E. Are oestrogens involved in falling sperm counts and disorders of the male reproductive tract? Lancet. 1993 May 29;341(8857):1392–1395. doi: 10.1016/0140-6736(93)90953-e. [DOI] [PubMed] [Google Scholar]
  245. Shen H. M., Chia S. E., Ni Z. Y., New A. L., Lee B. L., Ong C. N. Detection of oxidative DNA damage in human sperm and the association with cigarette smoking. Reprod Toxicol. 1997 Sep-Oct;11(5):675–680. doi: 10.1016/s0890-6238(97)00032-4. [DOI] [PubMed] [Google Scholar]
  246. Shertzer H. G., Nebert D. W., Puga A., Ary M., Sonntag D., Dixon K., Robinson L. J., Cianciolo E., Dalton T. P. Dioxin causes a sustained oxidative stress response in the mouse. Biochem Biophys Res Commun. 1998 Dec 9;253(1):44–48. doi: 10.1006/bbrc.1998.9753. [DOI] [PubMed] [Google Scholar]
  247. Shimada T., Gillam E. M., Oda Y., Tsumura F., Sutter T. R., Guengerich F. P., Inoue K. Metabolism of benzo[a]pyrene to trans-7,8-dihydroxy-7, 8-dihydrobenzo[a]pyrene by recombinant human cytochrome P450 1B1 and purified liver epoxide hydrolase. Chem Res Toxicol. 1999 Jul;12(7):623–629. doi: 10.1021/tx990028s. [DOI] [PubMed] [Google Scholar]
  248. Shimada T., Hayes C. L., Yamazaki H., Amin S., Hecht S. S., Guengerich F. P., Sutter T. R. Activation of chemically diverse procarcinogens by human cytochrome P-450 1B1. Cancer Res. 1996 Jul 1;56(13):2979–2984. [PubMed] [Google Scholar]
  249. Shimizu H., Ross R. K., Bernstein L., Pike M. C., Henderson B. E. Serum oestrogen levels in postmenopausal women: comparison of American whites and Japanese in Japan. Br J Cancer. 1990 Sep;62(3):451–453. doi: 10.1038/bjc.1990.316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  250. Shin R. W., Lee V. M., Trojanowski J. Q. Aluminum modifies the properties of Alzheimer's disease PHF tau proteins in vivo and in vitro. J Neurosci. 1994 Nov;14(11 Pt 2):7221–7233. doi: 10.1523/JNEUROSCI.14-11-07221.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  251. Slim R., Toborek M., Robertson L. W., Hennig B. Antioxidant protection against PCB-mediated endothelial cell activation. Toxicol Sci. 1999 Dec;52(2):232–239. doi: 10.1093/toxsci/52.2.232. [DOI] [PubMed] [Google Scholar]
  252. Smith A. B., Schloemer J., Lowry L. K., Smallwood A. W., Ligo R. N., Tanaka S., Stringer W., Jones M., Hervin R., Glueck C. J. Metabolic and health consequences of occupational exposure to polychlorinated biphenyls. Br J Ind Med. 1982 Nov;39(4):361–369. doi: 10.1136/oem.39.4.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  253. Smith K. R., Corvalán C. F., Kjellström T. How much global ill health is attributable to environmental factors? Epidemiology. 1999 Sep;10(5):573–584. [PubMed] [Google Scholar]
  254. Sokol R. Z., Madding C. E., Swerdloff R. S. Lead toxicity and the hypothalamic-pituitary-testicular axis. Biol Reprod. 1985 Oct;33(3):722–728. doi: 10.1095/biolreprod33.3.722. [DOI] [PubMed] [Google Scholar]
  255. Soto A. M., Sonnenschein C., Chung K. L., Fernandez M. F., Olea N., Serrano F. O. The E-SCREEN assay as a tool to identify estrogens: an update on estrogenic environmental pollutants. Environ Health Perspect. 1995 Oct;103 (Suppl 7):113–122. doi: 10.1289/ehp.95103s7113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  256. Spina M. B., Cohen G. Dopamine turnover and glutathione oxidation: implications for Parkinson disease. Proc Natl Acad Sci U S A. 1989 Feb;86(4):1398–1400. doi: 10.1073/pnas.86.4.1398. [DOI] [PMC free article] [PubMed] [Google Scholar]
  257. Spink D. C., Lincoln D. W., 2nd, Dickerman H. W., Gierthy J. F. 2,3,7,8-Tetrachlorodibenzo-p-dioxin causes an extensive alteration of 17 beta-estradiol metabolism in MCF-7 breast tumor cells. Proc Natl Acad Sci U S A. 1990 Sep;87(17):6917–6921. doi: 10.1073/pnas.87.17.6917. [DOI] [PMC free article] [PubMed] [Google Scholar]
  258. Spivack S. D., Fasco M. J., Walker V. E., Kaminsky L. S. The molecular epidemiology of lung cancer. Crit Rev Toxicol. 1997 Jul;27(4):319–365. doi: 10.3109/10408449709089898. [DOI] [PubMed] [Google Scholar]
  259. Spivack S. D., Hurteau G. J., Reilly A. A., Aldous K. M., Ding X., Kaminsky L. S. CYP1B1 expression in human lung. Drug Metab Dispos. 2001 Jun;29(6):916–922. [PubMed] [Google Scholar]
  260. Stehr-Green P. A., Welty E., Steele G., Steinberg K. Evaluation of potential health effects associated with serum polychlorinated biphenyl levels. Environ Health Perspect. 1986 Dec;70:255–259. doi: 10.1289/ehp.8670255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  261. Stewart P., Reihman J., Lonky E., Darvill T., Pagano J. Prenatal PCB exposure and neonatal behavioral assessment scale (NBAS) performance. Neurotoxicol Teratol. 2000 Jan-Feb;22(1):21–29. doi: 10.1016/s0892-0362(99)00056-2. [DOI] [PubMed] [Google Scholar]
  262. Stober T., Stelte W., Kunze K. Lead concentrations in blood, plasma, erythrocytes, and cerebrospinal fluid in amyotrophic lateral sclerosis. J Neurol Sci. 1983 Sep;61(1):21–26. doi: 10.1016/0022-510x(83)90051-5. [DOI] [PubMed] [Google Scholar]
  263. Stohs S. J. Oxidative stress induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Free Radic Biol Med. 1990;9(1):79–90. doi: 10.1016/0891-5849(90)90052-k. [DOI] [PubMed] [Google Scholar]
  264. Strickland D., Smith S. A., Dolliff G., Goldman L., Roelofs R. I. Amyotrophic lateral sclerosis and occupational history. A pilot case-control study. Arch Neurol. 1996 Aug;53(8):730–733. doi: 10.1001/archneur.1996.00550080044011. [DOI] [PubMed] [Google Scholar]
  265. Suchar L. A., Chang R. L., Thomas P. E., Rosen R. T., Lech J., Conney A. H. Effects of phenobarbital, dexamethasone, and 3-methylcholanthrene administration on the metabolism of 17 beta-estradiol by liver microsomes from female rats. Endocrinology. 1996 Feb;137(2):663–676. doi: 10.1210/endo.137.2.8593816. [DOI] [PubMed] [Google Scholar]
  266. Sueyoshi T., Kawamoto T., Zelko I., Honkakoski P., Negishi M. The repressed nuclear receptor CAR responds to phenobarbital in activating the human CYP2B6 gene. J Biol Chem. 1999 Mar 5;274(10):6043–6046. doi: 10.1074/jbc.274.10.6043. [DOI] [PubMed] [Google Scholar]
  267. Sueyoshi T., Negishi M. Phenobarbital response elements of cytochrome P450 genes and nuclear receptors. Annu Rev Pharmacol Toxicol. 2001;41:123–143. doi: 10.1146/annurev.pharmtox.41.1.123. [DOI] [PubMed] [Google Scholar]
  268. Telisman S., Cvitković P., Jurasović J., Pizent A., Gavella M., Rocić B. Semen quality and reproductive endocrine function in relation to biomarkers of lead, cadmium, zinc, and copper in men. Environ Health Perspect. 2000 Jan;108(1):45–53. doi: 10.1289/ehp.0010845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  269. Thoreux-Manlay A., Le Goascogne C., Segretain D., Jégou B., Pinon-Lataillade G. Lead affects steroidogenesis in rat Leydig cells in vivo and in vitro. Toxicology. 1995 Nov 20;103(1):53–62. doi: 10.1016/0300-483x(95)03107-q. [DOI] [PubMed] [Google Scholar]
  270. Tian Y., Ke S., Denison M. S., Rabson A. B., Gallo M. A. Ah receptor and NF-kappaB interactions, a potential mechanism for dioxin toxicity. J Biol Chem. 1999 Jan 1;274(1):510–515. doi: 10.1074/jbc.274.1.510. [DOI] [PubMed] [Google Scholar]
  271. Toborek M., Barger S. W., Mattson M. P., Espandiari P., Robertson L. W., Hennig B. Exposure to polychlorinated biphenyls causes endothelial cell dysfunction. J Biochem Toxicol. 1995 Aug;10(4):219–226. doi: 10.1002/jbt.2570100406. [DOI] [PubMed] [Google Scholar]
  272. Tomita S., Sinal C. J., Yim S. H., Gonzalez F. J. Conditional disruption of the aryl hydrocarbon receptor nuclear translocator (Arnt) gene leads to loss of target gene induction by the aryl hydrocarbon receptor and hypoxia-inducible factor 1alpha. Mol Endocrinol. 2000 Oct;14(10):1674–1681. doi: 10.1210/mend.14.10.0533. [DOI] [PubMed] [Google Scholar]
  273. Toniolo P. G. Endogenous estrogens and breast cancer risk: the case for prospective cohort studies. Environ Health Perspect. 1997 Apr;105 (Suppl 3):587–592. doi: 10.1289/ehp.97105s3587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  274. Toppari J., Larsen J. C., Christiansen P., Giwercman A., Grandjean P., Guillette L. J., Jr, Jégou B., Jensen T. K., Jouannet P., Keiding N. Male reproductive health and environmental xenoestrogens. Environ Health Perspect. 1996 Aug;104 (Suppl 4):741–803. doi: 10.1289/ehp.96104s4741. [DOI] [PMC free article] [PubMed] [Google Scholar]
  275. Trottier E., Belzil A., Stoltz C., Anderson A. Localization of a phenobarbital-responsive element (PBRE) in the 5'-flanking region of the rat CYP2B2 gene. Gene. 1995 Jun 9;158(2):263–268. doi: 10.1016/0378-1119(94)00916-g. [DOI] [PubMed] [Google Scholar]
  276. Tseng C. H., Tai T. Y., Chong C. K., Tseng C. P., Lai M. S., Lin B. J., Chiou H. Y., Hsueh Y. M., Hsu K. H., Chen C. J. Long-term arsenic exposure and incidence of non-insulin-dependent diabetes mellitus: a cohort study in arseniasis-hyperendemic villages in Taiwan. Environ Health Perspect. 2000 Sep;108(9):847–851. doi: 10.1289/ehp.00108847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  277. Tsutsui T., Suzuki N., Fukuda S., Sato M., Maizumi H., McLachlan J. A., Barrett J. C. 17beta-Estradiol-induced cell transformation and aneuploidy of Syrian hamster embryo cells in culture. Carcinogenesis. 1987 Nov;8(11):1715–1719. doi: 10.1093/carcin/8.11.1715. [DOI] [PubMed] [Google Scholar]
  278. Twaroski T. P., O'Brien M. L., Robertson L. W. Effects of selected polychlorinated biphenyl (PCB) congeners on hepatic glutathione, glutathione-related enzymes, and selenium status: implications for oxidative stress. Biochem Pharmacol. 2001 Aug 1;62(3):273–281. doi: 10.1016/s0006-2952(01)00668-2. [DOI] [PubMed] [Google Scholar]
  279. Unger M., Kiaer H., Blichert-Toft M., Olsen J., Clausen J. Organochlorine compounds in human breast fat from deceased with and without breast cancer and in a biopsy material from newly diagnosed patients undergoing breast surgery. Environ Res. 1984 Jun;34(1):24–28. doi: 10.1016/0013-9351(84)90072-0. [DOI] [PubMed] [Google Scholar]
  280. Ursin G., Wilson M., Henderson B. E., Kolonel L. N., Monroe K., Lee H. P., Seow A., Yu M. C., Stanczyk F. Z., Gentzschein E. Do urinary estrogen metabolites reflect the differences in breast cancer risk between Singapore Chinese and United States African-American and white women? Cancer Res. 2001 Apr 15;61(8):3326–3329. [PubMed] [Google Scholar]
  281. Vaarala O., Hyöty H., Akerblom H. K. Environmental factors in the aetiology of childhood diabetes. Diabetes Nutr Metab. 1999 Apr;12(2):75–85. [PubMed] [Google Scholar]
  282. Vakharia D. D., Liu N., Pause R., Fasco M., Bessette E., Zhang Q. Y., Kaminsky L. S. Effect of metals on polycyclic aromatic hydrocarbon induction of CYP1A1 and CYP1A2 in human hepatocyte cultures. Toxicol Appl Pharmacol. 2001 Jan 15;170(2):93–103. doi: 10.1006/taap.2000.9087. [DOI] [PubMed] [Google Scholar]
  283. Vayssier-Taussat M., Camilli T., Aron Y., Meplan C., Hainaut P., Polla B. S., Weksler B. Effects of tobacco smoke and benzo[a]pyrene on human endothelial cell and monocyte stress responses. Am J Physiol Heart Circ Physiol. 2001 Mar;280(3):H1293–H1300. doi: 10.1152/ajpheart.2001.280.3.H1293. [DOI] [PubMed] [Google Scholar]
  284. Vena J., Boffetta P., Becher H., Benn T., Bueno-de-Mesquita H. B., Coggon D., Colin D., Flesch-Janys D., Green L., Kauppinen T. Exposure to dioxin and nonneoplastic mortality in the expanded IARC international cohort study of phenoxy herbicide and chlorophenol production workers and sprayers. Environ Health Perspect. 1998 Apr;106 (Suppl 2):645–653. doi: 10.1289/ehp.98106645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  285. Venitt S. Mechanisms of carcinogenesis and individual susceptibility to cancer. Clin Chem. 1994 Jul;40(7 Pt 2):1421–1425. [PubMed] [Google Scholar]
  286. Waxman D. J. P450 gene induction by structurally diverse xenochemicals: central role of nuclear receptors CAR, PXR, and PPAR. Arch Biochem Biophys. 1999 Sep 1;369(1):11–23. doi: 10.1006/abbi.1999.1351. [DOI] [PubMed] [Google Scholar]
  287. Wei P., Zhang J., Egan-Hafley M., Liang S., Moore D. D. The nuclear receptor CAR mediates specific xenobiotic induction of drug metabolism. Nature. 2000 Oct 19;407(6806):920–923. doi: 10.1038/35038112. [DOI] [PubMed] [Google Scholar]
  288. Whitlock J. P., Jr, Okino S. T., Dong L., Ko H. P., Clarke-Katzenberg R., Ma Q., Li H. Cytochromes P450 5: induction of cytochrome P4501A1: a model for analyzing mammalian gene transcription. FASEB J. 1996 Jun;10(8):809–818. doi: 10.1096/fasebj.10.8.8666157. [DOI] [PubMed] [Google Scholar]
  289. Wijeweera J. B., Gandolfi A. J., Parrish A., Lantz R. C. Sodium arsenite enhances AP-1 and NFkappaB DNA binding and induces stress protein expression in precision-cut rat lung slices. Toxicol Sci. 2001 Jun;61(2):283–294. doi: 10.1093/toxsci/61.2.283. [DOI] [PubMed] [Google Scholar]
  290. Willett K. L., Randerath K., Zhou G. D., Safe S. H. Inhibition of CYP1A1-dependent activity by the polynuclear aromatic hydrocarbon (PAH) fluoranthene. Biochem Pharmacol. 1998 Mar 15;55(6):831–839. doi: 10.1016/s0006-2952(97)00561-3. [DOI] [PubMed] [Google Scholar]
  291. Wolff M. S., Toniolo P. G. Environmental organochlorine exposure as a potential etiologic factor in breast cancer. Environ Health Perspect. 1995 Oct;103 (Suppl 7):141–145. doi: 10.1289/ehp.95103s7141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  292. Wolff M. S., Toniolo P. G., Lee E. W., Rivera M., Dubin N. Blood levels of organochlorine residues and risk of breast cancer. J Natl Cancer Inst. 1993 Apr 21;85(8):648–652. doi: 10.1093/jnci/85.8.648. [DOI] [PubMed] [Google Scholar]
  293. Wood A. W., Levin W., Lu A. Y., Yagi H., Hernandez O., Jerina D. M., Conney A. H. Metabolism of benzo(a)pyrene and benzo (a)pyrene derivatives to mutagenic products by highly purified hepatic microsomal enzymes. J Biol Chem. 1976 Aug 25;251(16):4882–4890. [PubMed] [Google Scholar]
  294. Wormhoudt L. W., Commandeur J. N., Vermeulen N. P. Genetic polymorphisms of human N-acetyltransferase, cytochrome P450, glutathione-S-transferase, and epoxide hydrolase enzymes: relevance to xenobiotic metabolism and toxicity. Crit Rev Toxicol. 1999 Jan;29(1):59–124. doi: 10.1080/10408449991349186. [DOI] [PubMed] [Google Scholar]
  295. Wölfle D. Interactions between 2,3,7,8-TCDD and PCBs as tumor promoters: limitations of TEFs. Teratog Carcinog Mutagen. 1997;17(4-5):217–224. doi: 10.1002/(sici)1520-6866(1997)17:4/5<217::aid-tcm4>3.3.co;2-n. [DOI] [PubMed] [Google Scholar]
  296. Xie W., Barwick J. L., Simon C. M., Pierce A. M., Safe S., Blumberg B., Guzelian P. S., Evans R. M. Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CAR. Genes Dev. 2000 Dec 1;14(23):3014–3023. doi: 10.1101/gad.846800. [DOI] [PMC free article] [PubMed] [Google Scholar]
  297. Yasui M., Yase Y., Ota K., Garruto R. M. Aluminum deposition in the central nervous system of patients with amyotrophic lateral sclerosis from the Kii Peninsula of Japan. Neurotoxicology. 1991 Fall;12(3):615–620. [PubMed] [Google Scholar]
  298. Yoshinari K., Sueyoshi T., Moore R., Negishi M. Nuclear receptor CAR as a regulatory factor for the sexually dimorphic induction of CYB2B1 gene by phenobarbital in rat livers. Mol Pharmacol. 2001 Feb;59(2):278–284. doi: 10.1124/mol.59.2.278. [DOI] [PubMed] [Google Scholar]
  299. Yu M. L., Hsu C. C., Guo Y. L., Lai T. J., Chen S. J., Luo J. M. Disordered behavior in the early-born Taiwan Yucheng children. Chemosphere. 1994 Nov-Dec;29(9-11):2413–2422. doi: 10.1016/0045-6535(94)90410-3. [DOI] [PubMed] [Google Scholar]
  300. Yu R., Chen C., Mo Y. Y., Hebbar V., Owuor E. D., Tan T. H., Kong A. N. Activation of mitogen-activated protein kinase pathways induces antioxidant response element-mediated gene expression via a Nrf2-dependent mechanism. J Biol Chem. 2000 Dec 22;275(51):39907–39913. doi: 10.1074/jbc.M004037200. [DOI] [PubMed] [Google Scholar]
  301. Zecca L., Pietra R., Goj C., Mecacci C., Radice D., Sabbioni E. Iron and other metals in neuromelanin, substantia nigra, and putamen of human brain. J Neurochem. 1994 Mar;62(3):1097–1101. doi: 10.1046/j.1471-4159.1994.62031097.x. [DOI] [PubMed] [Google Scholar]
  302. Zeevalk G. D., Bernard L. P., Nicklas W. J. Role of oxidative stress and the glutathione system in loss of dopamine neurons due to impairment of energy metabolism. J Neurochem. 1998 Apr;70(4):1421–1430. doi: 10.1046/j.1471-4159.1998.70041421.x. [DOI] [PubMed] [Google Scholar]
  303. el-Masri H. A., Reardon K. F., Yang R. S. Integrated approaches for the analysis of toxicologic interactions of chemical mixtures. Crit Rev Toxicol. 1997 Mar;27(2):175–197. doi: 10.3109/10408449709021618. [DOI] [PubMed] [Google Scholar]
  304. van't Veer P., Lobbezoo I. E., Martín-Moreno J. M., Guallar E., Gómez-Aracena J., Kardinaal A. F., Kohlmeier L., Martin B. C., Strain J. J., Thamm M. DDT (dicophane) and postmenopausal breast cancer in Europe: case-control study. BMJ. 1997 Jul 12;315(7100):81–85. doi: 10.1136/bmj.315.7100.81. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES