Skip to main content
Erschienen in: Journal of Mammary Gland Biology and Neoplasia 1/2013

01.03.2013

Endocrine Disruptors and the Breast: Early Life Effects and Later Life Disease

verfasst von: Madisa B. Macon, Suzanne E. Fenton

Erschienen in: Journal of Mammary Gland Biology and Neoplasia | Ausgabe 1/2013

Einloggen, um Zugang zu erhalten

Abstract

Breast cancer risk has both heritable and environment/lifestyle components. The heritable component is a small contribution (5–27 %), leaving the majority of risk to environment (e.g., applied chemicals, food residues, occupational hazards, pharmaceuticals, stress) and lifestyle (e.g., physical activity, cosmetics, water source, alcohol, smoking). However, these factors are not well-defined, primarily due to the enormous number of factors to be considered. In both humans and rodent models, environmental factors that act as endocrine disrupting compounds (EDCs) have been shown to disrupt normal mammary development and lead to adverse lifelong consequences, especially when exposures occur during early life. EDCs can act directly or indirectly on mammary tissue to increase sensitivity to chemical carcinogens or enhance development of hyperplasia, beaded ducts, or tumors. Protective effects have also been reported. The mechanisms for these changes are not well understood. Environmental agents may also act as carcinogens in adult rodent models, directly causing or promoting tumor development, typically in more than one organ. Many of the environmental agents that act as EDCs and are known to affect the breast are discussed. Understanding the mechanism(s) of action for these compounds will be critical to prevent their effects on the breast in the future.
Literatur
3.
Zurück zum Zitat American Cancer Society. Breast cancer facts and figures 2011–2012. 2011. American Cancer Society. Breast cancer facts and figures 2011–2012. 2011.
4.
Zurück zum Zitat Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, Koskenvuo M, et al. Environmental and heritable factors in the causation of cancer–analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med. 2000;343(2):78–85. doi:10.1056/NEJM200007133430201.PubMed Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, Koskenvuo M, et al. Environmental and heritable factors in the causation of cancer–analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med. 2000;343(2):78–85. doi:10.​1056/​NEJM200007133430​201.PubMed
5.
Zurück zum Zitat Buttke DE, Sircar K, Martin C. Exposures to endocrine-disrupting chemicals and age of menarche in adolescent girls in NHANES (2003–2008). Environ Heal Perspect. doi:10.1289/ehp.1104748. Buttke DE, Sircar K, Martin C. Exposures to endocrine-disrupting chemicals and age of menarche in adolescent girls in NHANES (2003–2008). Environ Heal Perspect. doi:10.​1289/​ehp.​1104748.
6.
Zurück zum Zitat Diamanti-Kandarakis E, Bourguignon J-P, Giudice LC, Hauser R, Prins GS, Soto AM et al. Endocrine-disrupting chemicals: an endocrine society scientific statement. Endocrine Rev. 2009;30(4):293–342. doi:10.1210/er.2009-0002. Diamanti-Kandarakis E, Bourguignon J-P, Giudice LC, Hauser R, Prins GS, Soto AM et al. Endocrine-disrupting chemicals: an endocrine society scientific statement. Endocrine Rev. 2009;30(4):293–342. doi:10.​1210/​er.​2009-0002.
11.
Zurück zum Zitat Soto AM, Sonnenschein C. The tissue organization field theory of cancer: a testable replacement for the somatic mutation theory. BioEssays: News Rev Mol Cell Dev Biol. 2011;33(5):332–40. doi:10.1002/bies.201100025. Soto AM, Sonnenschein C. The tissue organization field theory of cancer: a testable replacement for the somatic mutation theory. BioEssays: News Rev Mol Cell Dev Biol. 2011;33(5):332–40. doi:10.​1002/​bies.​201100025.
15.
Zurück zum Zitat Knudson AG. Hereditary cancer: two hits revisited. J Cancer Res Clin Oncol. 1996;122(3):135–40.PubMed Knudson AG. Hereditary cancer: two hits revisited. J Cancer Res Clin Oncol. 1996;122(3):135–40.PubMed
16.
Zurück zum Zitat Markey CM, Luque EH, Munoz De Toro M, Sonnenschein C, Soto AM. In utero exposure to bisphenol A alters the development and tissue organization of the mouse mammary gland. Biol Reprod. 2001;65(4):1215–23.PubMed Markey CM, Luque EH, Munoz De Toro M, Sonnenschein C, Soto AM. In utero exposure to bisphenol A alters the development and tissue organization of the mouse mammary gland. Biol Reprod. 2001;65(4):1215–23.PubMed
17.
Zurück zum Zitat Rudel RA, Fenton SE, Ackerman JM, Euling SY, Makris SL. Environmental exposures and mammary gland development: state of the science, public health implications, and research recommendations. Environ Heal Perspect. 2011;119(8):1053–61. doi:10.1289/ehp.1002864. Rudel RA, Fenton SE, Ackerman JM, Euling SY, Makris SL. Environmental exposures and mammary gland development: state of the science, public health implications, and research recommendations. Environ Heal Perspect. 2011;119(8):1053–61. doi:10.​1289/​ehp.​1002864.
19.
21.
Zurück zum Zitat Rouzier R, Perou CM, Symmans WF, Ibrahim N, Cristofanilli M, Anderson K, et al. Breast cancer molecular subtypes respond differently to preoperative chemotherapy. Clin Cancer Res. 2005;11(16):5678–85. doi:10.1158/1078-0432.CCR-04-2421.PubMed Rouzier R, Perou CM, Symmans WF, Ibrahim N, Cristofanilli M, Anderson K, et al. Breast cancer molecular subtypes respond differently to preoperative chemotherapy. Clin Cancer Res. 2005;11(16):5678–85. doi:10.​1158/​1078-0432.​CCR-04-2421.PubMed
22.
Zurück zum Zitat Desmedt C, Haibe-Kains B, Wirapati P, Buyse M, Larsimont D, Bontempi G, et al. Biological processes associated with breast cancer clinical outcome depend on the molecular subtypes. Clin Cancer Res. 2008;14(16):5158–65. doi:10.1158/1078-0432.CCR-07-4756.PubMed Desmedt C, Haibe-Kains B, Wirapati P, Buyse M, Larsimont D, Bontempi G, et al. Biological processes associated with breast cancer clinical outcome depend on the molecular subtypes. Clin Cancer Res. 2008;14(16):5158–65. doi:10.​1158/​1078-0432.​CCR-07-4756.PubMed
23.
Zurück zum Zitat Fenton SE. Endocrine-disrupting compounds and mammary gland development: early exposure and later life consequences. Endocrinology. 2006;147(6 Suppl):S18–24. doi:10.1210/en.2005-1131.PubMed Fenton SE. Endocrine-disrupting compounds and mammary gland development: early exposure and later life consequences. Endocrinology. 2006;147(6 Suppl):S18–24. doi:10.​1210/​en.​2005-1131.PubMed
24.
Zurück zum Zitat Monosson E, Kelce WR, Lambright C, Ostby J, Gray Jr LE. Peripubertal exposure to the antiandrogenic fungicide, vinclozolin, delays puberty, inhibits the development of androgen-dependent tissues, and alters androgen receptor function in the male rat. Toxicol Ind Health. 1999;15(1–2):65–79.PubMed Monosson E, Kelce WR, Lambright C, Ostby J, Gray Jr LE. Peripubertal exposure to the antiandrogenic fungicide, vinclozolin, delays puberty, inhibits the development of androgen-dependent tissues, and alters androgen receptor function in the male rat. Toxicol Ind Health. 1999;15(1–2):65–79.PubMed
25.
Zurück zum Zitat Buckley J, Willingham E, Agras K, Baskin LS. Embryonic exposure to the fungicide vinclozolin causes virilization of females and alteration of progesterone receptor expression in vivo: an experimental study in mice. Environ Health. 2006;5:4. doi:10.1186/1476-069X-5-4.PubMed Buckley J, Willingham E, Agras K, Baskin LS. Embryonic exposure to the fungicide vinclozolin causes virilization of females and alteration of progesterone receptor expression in vivo: an experimental study in mice. Environ Health. 2006;5:4. doi:10.​1186/​1476-069X-5-4.PubMed
26.
Zurück zum Zitat Gray LE, Ostby J, Furr J, Wolf CJ, Lambright C, Parks L, et al. Effects of environmental antiandrogens on reproductive development in experimental animals. Hum Reprod Update. 2001;7(3):248–64.PubMed Gray LE, Ostby J, Furr J, Wolf CJ, Lambright C, Parks L, et al. Effects of environmental antiandrogens on reproductive development in experimental animals. Hum Reprod Update. 2001;7(3):248–64.PubMed
27.
Zurück zum Zitat Rothschild TC, Boylan ES, Calhoon RE, Vonderhaar BK. Transplacental effects of diethylstilbestrol on mammary development and tumorigenesis in female ACI rats. Cancer Res. 1987;47(16):4508–16.PubMed Rothschild TC, Boylan ES, Calhoon RE, Vonderhaar BK. Transplacental effects of diethylstilbestrol on mammary development and tumorigenesis in female ACI rats. Cancer Res. 1987;47(16):4508–16.PubMed
28.
Zurück zum Zitat Kawaguchi H, Umekita Y, Souda M, Gejima K, Kawashima H, Yoshikawa T, et al. Effects of neonatally administered high-dose diethylstilbestrol on the induction of mammary tumors induced by 7,12-dimethylbenz[a]anthracene in female rats. Vet Pathol. 2009;46(1):142–50. doi:10.1354/vp.46-1-142.PubMed Kawaguchi H, Umekita Y, Souda M, Gejima K, Kawashima H, Yoshikawa T, et al. Effects of neonatally administered high-dose diethylstilbestrol on the induction of mammary tumors induced by 7,12-dimethylbenz[a]anthracene in female rats. Vet Pathol. 2009;46(1):142–50. doi:10.​1354/​vp.​46-1-142.PubMed
29.
Zurück zum Zitat Muto T, Wakui S, Imano N, Nakaaki K, Hano H, Furusato K, et al. In utero and lactational exposure of 3,3′, 4,4′, 5- pentachlorobiphenyl modulate dimenthlben[a]anthracene-induced rat mammary carcinogenesis. J Toxicologica Pathol. 2001;14:213–24. Muto T, Wakui S, Imano N, Nakaaki K, Hano H, Furusato K, et al. In utero and lactational exposure of 3,3′, 4,4′, 5- pentachlorobiphenyl modulate dimenthlben[a]anthracene-induced rat mammary carcinogenesis. J Toxicologica Pathol. 2001;14:213–24.
30.
Zurück zum Zitat Rayner JL, Enoch RR, Fenton SE. Adverse effects of prenatal exposure to atrazine during a critical period of mammary gland growth. Toxicol Sci. 2005;87(1):255–66. doi:10.1093/toxsci/kfi213.PubMed Rayner JL, Enoch RR, Fenton SE. Adverse effects of prenatal exposure to atrazine during a critical period of mammary gland growth. Toxicol Sci. 2005;87(1):255–66. doi:10.​1093/​toxsci/​kfi213.PubMed
32.
Zurück zum Zitat Restum JC, Bursian SJ, Giesy JP, Render JA, Helferich WG, Shipp EB, et al. Multigenerational study of the effects of consumption of PCB-contaminated carp from Saginaw Bay, Lake Huron, on mink. 1. Effects on mink reproduction, kit growth and survival, and selected biological parameters. J Toxicol Environ Health A. 1998;54(5):343–75.PubMed Restum JC, Bursian SJ, Giesy JP, Render JA, Helferich WG, Shipp EB, et al. Multigenerational study of the effects of consumption of PCB-contaminated carp from Saginaw Bay, Lake Huron, on mink. 1. Effects on mink reproduction, kit growth and survival, and selected biological parameters. J Toxicol Environ Health A. 1998;54(5):343–75.PubMed
33.
Zurück zum Zitat Provenzano PP, Inman DR, Eliceiri KW, Knittel JG, Yan L, Rueden CT, et al. Collagen density promotes mammary tumor initiation and progression. BMC Med. 2008;6:11. doi:10.1186/1741-7015-6-11.PubMed Provenzano PP, Inman DR, Eliceiri KW, Knittel JG, Yan L, Rueden CT, et al. Collagen density promotes mammary tumor initiation and progression. BMC Med. 2008;6:11. doi:10.​1186/​1741-7015-6-11.PubMed
34.
Zurück zum Zitat Maffini MV, Soto AM, Calabro JM, Ucci AA, Sonnenschein C. The stroma as a crucial target in rat mammary gland carcinogenesis. J Cell Sci. 2004;117(Pt 8):1495–502. doi:10.1242/jcs.01000.PubMed Maffini MV, Soto AM, Calabro JM, Ucci AA, Sonnenschein C. The stroma as a crucial target in rat mammary gland carcinogenesis. J Cell Sci. 2004;117(Pt 8):1495–502. doi:10.​1242/​jcs.​01000.PubMed
35.
Zurück zum Zitat White SE, Kato K, Jia LT, Basden BJ, Calafat AM, Hines EP, et al. Effect of perfluorooctanoic acid on mouse mammary gland development and differention resulting from cross-foster and restricted gestational exposure. Reprod Toxicol. 2009;27:289–98. doi:10.1016/j.reprotox.2008.11.054.PubMed White SE, Kato K, Jia LT, Basden BJ, Calafat AM, Hines EP, et al. Effect of perfluorooctanoic acid on mouse mammary gland development and differention resulting from cross-foster and restricted gestational exposure. Reprod Toxicol. 2009;27:289–98. doi:10.​1016/​j.​reprotox.​2008.​11.​054.PubMed
36.
Zurück zum Zitat White SE, Calafat AM, Kuklenyik Z, Villanueva L, Zehr RD, Helfant L, et al. Gestational PFOA exposure of mice is associated with altered mammary gland development in dams and female offspring. Toxicol Sci. 2007;96(1):133–44. doi:10.1093/toxsci/kfl177.PubMed White SE, Calafat AM, Kuklenyik Z, Villanueva L, Zehr RD, Helfant L, et al. Gestational PFOA exposure of mice is associated with altered mammary gland development in dams and female offspring. Toxicol Sci. 2007;96(1):133–44. doi:10.​1093/​toxsci/​kfl177.PubMed
37.
Zurück zum Zitat Fertuck KC, Kumar S, Sikka HC, Matthews JB, Zacharewski TR. Interaction of PAH-related compounds with the alpha and beta isoforms of the estrogen receptor. Toxicol Lett. 2001;121(3):167–77.PubMed Fertuck KC, Kumar S, Sikka HC, Matthews JB, Zacharewski TR. Interaction of PAH-related compounds with the alpha and beta isoforms of the estrogen receptor. Toxicol Lett. 2001;121(3):167–77.PubMed
38.
Zurück zum Zitat Archer FL, Orlando R. Morphology, natural history, and enzyme patterns in mammary tumors of the rat induced by 7,12-dimethylbenz(a)anthracene. Cancer Res. 1968;28:217–23.PubMed Archer FL, Orlando R. Morphology, natural history, and enzyme patterns in mammary tumors of the rat induced by 7,12-dimethylbenz(a)anthracene. Cancer Res. 1968;28:217–23.PubMed
39.
Zurück zum Zitat Ito N, Hasegawa R, Sano M, Tamano S, Esumi H, Takayama S, et al. A new colon and mammary carcinogen in cooked food, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP). Carcinogenesis. 1991;12(8):1503–6.PubMed Ito N, Hasegawa R, Sano M, Tamano S, Esumi H, Takayama S, et al. A new colon and mammary carcinogen in cooked food, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP). Carcinogenesis. 1991;12(8):1503–6.PubMed
40.
Zurück zum Zitat Lauber SN, Ali S, Gooderham NJ. The cooked food derived carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine is a potent oestrogen: a mechanistic basis for its tissue-specific carcinogenicity. Carcinogenesis. 2004;25(12):2509–17.PubMed Lauber SN, Ali S, Gooderham NJ. The cooked food derived carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine is a potent oestrogen: a mechanistic basis for its tissue-specific carcinogenicity. Carcinogenesis. 2004;25(12):2509–17.PubMed
41.
Zurück zum Zitat Gooderham NJ, Zhu H, Lauber S, Boyce A, Creton S. Molecular and genetic toxicology of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP). Mutat Res. 2002;507:91–9. Gooderham NJ, Zhu H, Lauber S, Boyce A, Creton S. Molecular and genetic toxicology of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP). Mutat Res. 2002;507:91–9.
42.
Zurück zum Zitat Lightfoot TJ, Coxhead JM, Cupid BC, Nicholson S, Garner RC. Analysis of DNA adducts by accelerator mass spectrometry in human breast tissue after administration of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine and benzo[a]pyrene. Mutat Res. 2000;472(1–2):119–27.PubMed Lightfoot TJ, Coxhead JM, Cupid BC, Nicholson S, Garner RC. Analysis of DNA adducts by accelerator mass spectrometry in human breast tissue after administration of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine and benzo[a]pyrene. Mutat Res. 2000;472(1–2):119–27.PubMed
43.
Zurück zum Zitat Zheng W, Gustafson DR, Sinha R, Cerhan JR, Moore D, Hong CP, et al. Well-done meat intake and the risk of breast cancer. J Natl Canc Inst. 1998;90(22):1724–9. Zheng W, Gustafson DR, Sinha R, Cerhan JR, Moore D, Hong CP, et al. Well-done meat intake and the risk of breast cancer. J Natl Canc Inst. 1998;90(22):1724–9.
44.
Zurück zum Zitat Pottenger LH, Domoradzki JY, Markham DA, Hansen SC, Cagen SZ, Waechter Jr JM. The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration. Toxicol Sci. 2000;54(1):3–18.PubMed Pottenger LH, Domoradzki JY, Markham DA, Hansen SC, Cagen SZ, Waechter Jr JM. The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration. Toxicol Sci. 2000;54(1):3–18.PubMed
45.
Zurück zum Zitat Völkel W, Colnot T, Csanady GA, Filser JG, Dekant W. Metabolism and kinetics of bisphenol a in humans at low doses following oral administration. Chem Res Toxicol. 2002;15(10):1281–7.PubMed Völkel W, Colnot T, Csanady GA, Filser JG, Dekant W. Metabolism and kinetics of bisphenol a in humans at low doses following oral administration. Chem Res Toxicol. 2002;15(10):1281–7.PubMed
46.
47.
Zurück zum Zitat Vandenberg LN, Maffini MV, Schaeberle CM, Ucci AA, Sonnenschein C, Rubin BS, et al. Perinatal exposure to the xenoestrogen bisphenol-A induces mammary intraductal hyperplasias in adult CD-1 mice. Reprod Toxicol. 2008;26(3–4):210–9. doi:10.1016/j.reprotox.2008.09.015.PubMed Vandenberg LN, Maffini MV, Schaeberle CM, Ucci AA, Sonnenschein C, Rubin BS, et al. Perinatal exposure to the xenoestrogen bisphenol-A induces mammary intraductal hyperplasias in adult CD-1 mice. Reprod Toxicol. 2008;26(3–4):210–9. doi:10.​1016/​j.​reprotox.​2008.​09.​015.PubMed
48.
Zurück zum Zitat Naciff JM, Jump ML, Torontali SM, Carr GJ, Tiesman JP, Overmann GJ, et al. Gene expression profile induced by 17alpha-ethynyl estradiol, bisphenol A, and genistein in the developing female reproductive system of the rat. Toxicol Sci. 2002;68(1):184–99.PubMed Naciff JM, Jump ML, Torontali SM, Carr GJ, Tiesman JP, Overmann GJ, et al. Gene expression profile induced by 17alpha-ethynyl estradiol, bisphenol A, and genistein in the developing female reproductive system of the rat. Toxicol Sci. 2002;68(1):184–99.PubMed
51.
Zurück zum Zitat Quignot N, Arnaud M, Robidel F, Lecomte A, Tournier M, Cren-Olive C, et al. Characterization of endocrine-disrupting chemicals based on hormonal balance disruption in male and female adult rats. Reprod Toxicol. 2012;33(3):339–52. doi:10.1016/j.reprotox.2012.01.004.PubMed Quignot N, Arnaud M, Robidel F, Lecomte A, Tournier M, Cren-Olive C, et al. Characterization of endocrine-disrupting chemicals based on hormonal balance disruption in male and female adult rats. Reprod Toxicol. 2012;33(3):339–52. doi:10.​1016/​j.​reprotox.​2012.​01.​004.PubMed
53.
Zurück zum Zitat Munoz-de-Toro M, Markey CM, Wadia PR, Luque EH, Rubin BS, Sonnenschein C, et al. Perinatal exposure to bisphenol-A alters peripubertal mammary gland development in mice. Endocrinology. 2005;146(9):4138–47. doi:10.1210/en.2005-0340.PubMed Munoz-de-Toro M, Markey CM, Wadia PR, Luque EH, Rubin BS, Sonnenschein C, et al. Perinatal exposure to bisphenol-A alters peripubertal mammary gland development in mice. Endocrinology. 2005;146(9):4138–47. doi:10.​1210/​en.​2005-0340.PubMed
54.
Zurück zum Zitat Mori T, Bern HA, Mills KT, Young PN. Long-term effects of neonatal steroid exposure on mammary gland development and tumorigenesis in mice. J Natl Cancer Inst. 1976;57(5):1057–62.PubMed Mori T, Bern HA, Mills KT, Young PN. Long-term effects of neonatal steroid exposure on mammary gland development and tumorigenesis in mice. J Natl Cancer Inst. 1976;57(5):1057–62.PubMed
55.
Zurück zum Zitat Lamartiniere CA, Jenkins S, Betancourt AM, Wang J, Russo J. Exposure to the endocrine disruptor bisphenol A alters susceptibility for mammary cancer. Horm Mol Biol Clin Investig. 2011;5(2):45–52. doi:10.1515/HMBCI.2010.075.PubMed Lamartiniere CA, Jenkins S, Betancourt AM, Wang J, Russo J. Exposure to the endocrine disruptor bisphenol A alters susceptibility for mammary cancer. Horm Mol Biol Clin Investig. 2011;5(2):45–52. doi:10.​1515/​HMBCI.​2010.​075.PubMed
56.
Zurück zum Zitat Tharp AP, Maffini MV, Hunt PA, VandeVoort CA, Sonnenschein C, Soto AM. Bisphenol A alters the development of the rhesus monkey mammary gland. Proc Natl Acad Sci U S A. 2012;109(21):8190–5. doi:10.1073/pnas.1120488109.PubMed Tharp AP, Maffini MV, Hunt PA, VandeVoort CA, Sonnenschein C, Soto AM. Bisphenol A alters the development of the rhesus monkey mammary gland. Proc Natl Acad Sci U S A. 2012;109(21):8190–5. doi:10.​1073/​pnas.​1120488109.PubMed
57.
Zurück zum Zitat Jenkins S, Raghuraman N, Eltoum I, Carpenter M, Russo J, Lamartiniere CA. Oral exposure to bisphenol a increases dimethylbenzanthracene-induced mammary cancer in rats. Environ Heal Perspect. 2009;117(6):910–5. doi:10.1289/ehp.11751. Jenkins S, Raghuraman N, Eltoum I, Carpenter M, Russo J, Lamartiniere CA. Oral exposure to bisphenol a increases dimethylbenzanthracene-induced mammary cancer in rats. Environ Heal Perspect. 2009;117(6):910–5. doi:10.​1289/​ehp.​11751.
58.
Zurück zum Zitat Betancourt AM, Eltoum IA, Desmond RA, Russo J, Lamartiniere CA. In utero exposure to bisphenol A shifts the window of susceptibility for mammary carcinogenesis in the rat. Environ Heal Perspect. 2010;118(11):1614–9. doi:10.1289/ehp.1002148. Betancourt AM, Eltoum IA, Desmond RA, Russo J, Lamartiniere CA. In utero exposure to bisphenol A shifts the window of susceptibility for mammary carcinogenesis in the rat. Environ Heal Perspect. 2010;118(11):1614–9. doi:10.​1289/​ehp.​1002148.
59.
Zurück zum Zitat Doherty LF, Bromer JG, Zhou Y, Aldad TS, Taylor HS. In utero exposure to diethylstilbestrol (DES) or bisphenol-A (BPA) increases EZH2 expression in the mammary gland: an epigenetic mechanism linking endocrine disruptors to breast cancer. Horm Cancer. 2010;1(3):146–55. doi:10.1007/s12672-010-0015-9.PubMed Doherty LF, Bromer JG, Zhou Y, Aldad TS, Taylor HS. In utero exposure to diethylstilbestrol (DES) or bisphenol-A (BPA) increases EZH2 expression in the mammary gland: an epigenetic mechanism linking endocrine disruptors to breast cancer. Horm Cancer. 2010;1(3):146–55. doi:10.​1007/​s12672-010-0015-9.PubMed
60.
Zurück zum Zitat Jenkins S, Wang J, Eltoum I, Desmond R, Lamartiniere CA. Chronic oral exposure to bisphenol A results in a nonmonotonic dose response in mammary carcinogenesis and metastasis in MMTV-erbB2 mice. Environ Heal Perspect. 2011;119(11):1604–9. doi:10.1289/ehp.1103850. Jenkins S, Wang J, Eltoum I, Desmond R, Lamartiniere CA. Chronic oral exposure to bisphenol A results in a nonmonotonic dose response in mammary carcinogenesis and metastasis in MMTV-erbB2 mice. Environ Heal Perspect. 2011;119(11):1604–9. doi:10.​1289/​ehp.​1103850.
61.
Zurück zum Zitat Ogura I, Masunaga S, Nakanishi J. Quantitative source identification of dioxin-like PCBs in Yokohama, Japan, by temperature dependence of their atmospheric concentrations. Environ Sci Technol. 2004;38(12):3279–85.PubMed Ogura I, Masunaga S, Nakanishi J. Quantitative source identification of dioxin-like PCBs in Yokohama, Japan, by temperature dependence of their atmospheric concentrations. Environ Sci Technol. 2004;38(12):3279–85.PubMed
62.
Zurück zum Zitat Safe SH. Modulation of gene expression and endocrine response pathways by 2,3,7,8-tetrachlorodibenzo-p-dioxin and related compounds. Pharmacol Ther. 1995;67(2):247–81.PubMed Safe SH. Modulation of gene expression and endocrine response pathways by 2,3,7,8-tetrachlorodibenzo-p-dioxin and related compounds. Pharmacol Ther. 1995;67(2):247–81.PubMed
63.
Zurück zum Zitat Safe SH. Hazard and risk assessment of chemical mixtures using the toxic equivalency factor approach. Environ Heal Perspect. 1998;106 Suppl 4:1051–8. Safe SH. Hazard and risk assessment of chemical mixtures using the toxic equivalency factor approach. Environ Heal Perspect. 1998;106 Suppl 4:1051–8.
64.
Zurück zum Zitat Chaffin CL, Peterson RE, Hutz RJ. In utero and lactational exposure of female Holtzman rats to 2,3,7,8-tetrachlorodibenzo-p-dioxin: modulation of the estrogen signal. Biol Reprod. 1996;55(1):62–7.PubMed Chaffin CL, Peterson RE, Hutz RJ. In utero and lactational exposure of female Holtzman rats to 2,3,7,8-tetrachlorodibenzo-p-dioxin: modulation of the estrogen signal. Biol Reprod. 1996;55(1):62–7.PubMed
65.
Zurück zum Zitat Fenton SE, Hamm JT, Birnbaum LS, Youngblood GL. Persistent abnormalities in the rat mammary gland following gestational and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Toxicol Sci. 2002;67(63):63–74.PubMed Fenton SE, Hamm JT, Birnbaum LS, Youngblood GL. Persistent abnormalities in the rat mammary gland following gestational and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Toxicol Sci. 2002;67(63):63–74.PubMed
66.
Zurück zum Zitat Brown NM, Manzolillo PA, Zhang JX, Wang J, Lamartiniere CA. Prenatal TCDD and predisposition to mammary cancer in the rat. Carcinogenesis. 1998;19(9):1623–9.PubMed Brown NM, Manzolillo PA, Zhang JX, Wang J, Lamartiniere CA. Prenatal TCDD and predisposition to mammary cancer in the rat. Carcinogenesis. 1998;19(9):1623–9.PubMed
67.
Zurück zum Zitat Franczak A, Nynca A, Valdez KE, Mizinga KM, Petroff BK. Effects of acute and chronic exposure to the aryl hydrocarbon receptor agonist 2,3,7,8-tetrachlorodibenzo-p-dioxin on the transition to reproductive senescence in female Sprague–Dawley rats. Biol Reprod. 2006;74(1):125–30. doi:10.1095/biolreprod.105.044396.PubMed Franczak A, Nynca A, Valdez KE, Mizinga KM, Petroff BK. Effects of acute and chronic exposure to the aryl hydrocarbon receptor agonist 2,3,7,8-tetrachlorodibenzo-p-dioxin on the transition to reproductive senescence in female Sprague–Dawley rats. Biol Reprod. 2006;74(1):125–30. doi:10.​1095/​biolreprod.​105.​044396.PubMed
68.
Zurück zum Zitat Brown NM, Lamartiniere CA. Xenoestrogens alter mammary gland differentiation and cell proliferation in the rat. Environ Heal Perspect. 1995;103(7–8):708–13. Brown NM, Lamartiniere CA. Xenoestrogens alter mammary gland differentiation and cell proliferation in the rat. Environ Heal Perspect. 1995;103(7–8):708–13.
69.
Zurück zum Zitat Gray Jr LE, Kelce WR, Monosson E, Ostby JS, Birnbaum LS. 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;131(1):108–18. doi:10.1006/taap.1995.1052.PubMed Gray Jr LE, Kelce WR, Monosson E, Ostby JS, Birnbaum LS. 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;131(1):108–18. doi:10.​1006/​taap.​1995.​1052.PubMed
71.
Zurück zum Zitat Warner M, Eskenazi B, Mocarelli P, Gerthoux PM, Samuels S, Needham L, et al. Serum dioxin concentrations and breast cancer risk in the Seveso Women’s Health Study. Environ Heal Perspect. 2002;110(7):625–8. Warner M, Eskenazi B, Mocarelli P, Gerthoux PM, Samuels S, Needham L, et al. Serum dioxin concentrations and breast cancer risk in the Seveso Women’s Health Study. Environ Heal Perspect. 2002;110(7):625–8.
73.
Zurück zum Zitat Manuwald U, Velasco Garrido M, Berger J, Manz A, Baur X. Mortality study of chemical workers exposed to dioxins: follow-up 23 years after chemical plant closure. Occup Environ Med. 2012;69(9):636–42. doi:10.1136/oemed-2012-100682.PubMed Manuwald U, Velasco Garrido M, Berger J, Manz A, Baur X. Mortality study of chemical workers exposed to dioxins: follow-up 23 years after chemical plant closure. Occup Environ Med. 2012;69(9):636–42. doi:10.​1136/​oemed-2012-100682.PubMed
74.
Zurück zum Zitat Van den Berg M, Birnbaum LS, Denison M, De Vito M, Farland W, Feeley M, et al. The 2005 World Health Organization reevaluation of human and Mammalian toxic equivalency factors for dioxins and dioxin-like compounds. Toxicol Sci. 2006;93(2):223–41. doi:10.1093/toxsci/kfl055.PubMed Van den Berg M, Birnbaum LS, Denison M, De Vito M, Farland W, Feeley M, et al. The 2005 World Health Organization reevaluation of human and Mammalian toxic equivalency factors for dioxins and dioxin-like compounds. Toxicol Sci. 2006;93(2):223–41. doi:10.​1093/​toxsci/​kfl055.PubMed
75.
Zurück zum Zitat Muto T, Wakui S, Imano N, Nakaaki K, Takahashi H, Hano H, et al. Mammary gland differentiation in female rats after prenatal exposure to 3,3′,4,4′,5-pentachlorobiphenyl. Toxicology. 2002;177(2–3):197–205.PubMed Muto T, Wakui S, Imano N, Nakaaki K, Takahashi H, Hano H, et al. Mammary gland differentiation in female rats after prenatal exposure to 3,3′,4,4′,5-pentachlorobiphenyl. Toxicology. 2002;177(2–3):197–205.PubMed
77.
Zurück zum Zitat Brody JG, Moysich KB, Humblet O, Attfield KR, Beehler GP, Rudel RA. Environmental pollutants and breast cancer: epidemiologic studies. Cancer. 2007;109(12 Suppl):2667–711. doi:10.1002/cncr.22655.PubMed Brody JG, Moysich KB, Humblet O, Attfield KR, Beehler GP, Rudel RA. Environmental pollutants and breast cancer: epidemiologic studies. Cancer. 2007;109(12 Suppl):2667–711. doi:10.​1002/​cncr.​22655.PubMed
78.
Zurück zum Zitat LeBlanc GA. Endocrine system. In: Hodgson E, editor. A textbook of modern toxicology. 3rd ed. Hoboken: John Wiley & Sons, Inc; 2004. p. 299–315. LeBlanc GA. Endocrine system. In: Hodgson E, editor. A textbook of modern toxicology. 3rd ed. Hoboken: John Wiley & Sons, Inc; 2004. p. 299–315.
80.
Zurück zum Zitat Johnson NA, Ho A, Cline JM, Hughes CL, Foster WG, Davis VL. Accelerated mammary tumor onset in a HER2/Neu mouse model exposed to DDT metabolites locally delivered to the mammary gland. Environ Heal Perspect. 2012;120(8):1170–6. doi:10.1289/ehp.1104327. Johnson NA, Ho A, Cline JM, Hughes CL, Foster WG, Davis VL. Accelerated mammary tumor onset in a HER2/Neu mouse model exposed to DDT metabolites locally delivered to the mammary gland. Environ Heal Perspect. 2012;120(8):1170–6. doi:10.​1289/​ehp.​1104327.
81.
Zurück zum Zitat Robison AK, Sirbasku DA, Stancel GM. DDT supports the growth of an estrogen-responsive tumor. Toxicol Lett. 1985;27(1–3):109–13.PubMed Robison AK, Sirbasku DA, Stancel GM. DDT supports the growth of an estrogen-responsive tumor. Toxicol Lett. 1985;27(1–3):109–13.PubMed
82.
Zurück zum Zitat Cohn BA, Wolff MS, Cirillo PM, Sholtz RI. DDT and breast cancer in young women: new data on the significance of age at exposure. Environ Health Perspect. 2007;115(10):1406–14. doi:10.1289/ehp.10260.PubMed Cohn BA, Wolff MS, Cirillo PM, Sholtz RI. DDT and breast cancer in young women: new data on the significance of age at exposure. Environ Health Perspect. 2007;115(10):1406–14. doi:10.​1289/​ehp.​10260.PubMed
84.
Zurück zum Zitat Rayner JL, Fenton SE. In: Russo J, editor. Atrazine: an environmental endocrine disruptor that alters mammary gland development and tumor susceptibility environment and breast cancer. New York: Springer; 2011. p. 167–83. Rayner JL, Fenton SE. In: Russo J, editor. Atrazine: an environmental endocrine disruptor that alters mammary gland development and tumor susceptibility environment and breast cancer. New York: Springer; 2011. p. 167–83.
86.
Zurück zum Zitat Foradori CD, Hinds LR, Hanneman WH, Handa RJ. Effects of atrazine and its withdrawal on gonadotropin-releasing hormone neuroendocrine function in the adult female Wistar rat. Biol Reprod. 2009;81(6):1099–105. doi:10.1095/biolreprod.109.077453.PubMed Foradori CD, Hinds LR, Hanneman WH, Handa RJ. Effects of atrazine and its withdrawal on gonadotropin-releasing hormone neuroendocrine function in the adult female Wistar rat. Biol Reprod. 2009;81(6):1099–105. doi:10.​1095/​biolreprod.​109.​077453.PubMed
87.
Zurück zum Zitat Stoker TE, Laws SC, Guidici DL, Cooper RL. The effect of atrazine on puberty in male wistar rats: an evaluation in the protocol for the assessment of pubertal development and thyroid function. Toxicol Sci. 2000;58(1):50–9.PubMed Stoker TE, Laws SC, Guidici DL, Cooper RL. The effect of atrazine on puberty in male wistar rats: an evaluation in the protocol for the assessment of pubertal development and thyroid function. Toxicol Sci. 2000;58(1):50–9.PubMed
88.
Zurück zum Zitat Stanko JP, Enoch RR, Rayner JL, Davis CC, Wolf DC, Malarkey DE, et al. Effects of prenatal exposure to a low dose atrazine metabolite mixture on pubertal timing and prostate development of male Long-Evans rats. Reprod Toxicol. 2010;30(4):540–9. doi:10.1016/j.reprotox.2010.07.006.PubMed Stanko JP, Enoch RR, Rayner JL, Davis CC, Wolf DC, Malarkey DE, et al. Effects of prenatal exposure to a low dose atrazine metabolite mixture on pubertal timing and prostate development of male Long-Evans rats. Reprod Toxicol. 2010;30(4):540–9. doi:10.​1016/​j.​reprotox.​2010.​07.​006.PubMed
89.
Zurück zum Zitat Enoch RR, Stanko JP, Greiner SN, Youngblood GL, Rayner JL, Fenton SE. Mammary gland development as a sensitive end point after acute prenatal exposure to an atrazine metabolite mixture in female Long-Evans rats. Environ Heal Perspect. 2007;115(4):541–7. doi:10.1289/ehp.9612. Enoch RR, Stanko JP, Greiner SN, Youngblood GL, Rayner JL, Fenton SE. Mammary gland development as a sensitive end point after acute prenatal exposure to an atrazine metabolite mixture in female Long-Evans rats. Environ Heal Perspect. 2007;115(4):541–7. doi:10.​1289/​ehp.​9612.
90.
Zurück zum Zitat Gammon DW, Aldous CN, Carr Jr WC, Sanborn JR, Pfeifer KF. A risk assessment of atrazine use in California: human health and ecological aspects. Pest Manag Sci. 2005;61(4):331–55. doi:10.1002/ps.1000.PubMed Gammon DW, Aldous CN, Carr Jr WC, Sanborn JR, Pfeifer KF. A risk assessment of atrazine use in California: human health and ecological aspects. Pest Manag Sci. 2005;61(4):331–55. doi:10.​1002/​ps.​1000.PubMed
91.
Zurück zum Zitat Stevens JT, Breckenridge CB, Wetzel L. A risk characterization for atrazine: oncogenicity profile. J Toxicol Environ Health A. 1999;56(2):69–109.PubMed Stevens JT, Breckenridge CB, Wetzel L. A risk characterization for atrazine: oncogenicity profile. J Toxicol Environ Health A. 1999;56(2):69–109.PubMed
92.
Zurück zum Zitat Eldridge JC, Wetzel LT, Stevens JT, Simpkins JW. The mammary tumor response in triazine-treated female rats: a threshold-mediated interaction with strain and species-specific reproductive senescence. Steroids. 1999;64(9):672–8.PubMed Eldridge JC, Wetzel LT, Stevens JT, Simpkins JW. The mammary tumor response in triazine-treated female rats: a threshold-mediated interaction with strain and species-specific reproductive senescence. Steroids. 1999;64(9):672–8.PubMed
93.
Zurück zum Zitat Fukamachi K, Han BS, Kim CK, Takasuka N, Matsuoka Y, Matsuda E, et al. Possible enhancing effects of atrazine and nonylphenol on 7,12-dimethylbenz[a]anthracene-induced mammary tumor development in human c-Ha-ras proto-oncogene transgenic rats. Cancer Sci. 2004;95(5):404–10.PubMed Fukamachi K, Han BS, Kim CK, Takasuka N, Matsuoka Y, Matsuda E, et al. Possible enhancing effects of atrazine and nonylphenol on 7,12-dimethylbenz[a]anthracene-induced mammary tumor development in human c-Ha-ras proto-oncogene transgenic rats. Cancer Sci. 2004;95(5):404–10.PubMed
96.
Zurück zum Zitat Molina-Molina JM, Hillenweck A, Jouanin I, Zalko D, Cravedi JP, Fernandez MF, et al. Steroid receptor profiling of vinclozolin and its primary metabolites. Toxicol Appl Pharmacol. 2006;216(1):44–54. doi:10.1016/j.taap.2006.04.005.PubMed Molina-Molina JM, Hillenweck A, Jouanin I, Zalko D, Cravedi JP, Fernandez MF, et al. Steroid receptor profiling of vinclozolin and its primary metabolites. Toxicol Appl Pharmacol. 2006;216(1):44–54. doi:10.​1016/​j.​taap.​2006.​04.​005.PubMed
97.
Zurück zum Zitat Gray Jr LE, Ostby JS, Kelce WR. Developmental effects of an environmental antiandrogen: the fungicide vinclozolin alters sex differentiation of the male rat. Toxicol Appl Pharmacol. 1994;129(1):46–52. doi:10.1006/taap.1994.1227.PubMed Gray Jr LE, Ostby JS, Kelce WR. Developmental effects of an environmental antiandrogen: the fungicide vinclozolin alters sex differentiation of the male rat. Toxicol Appl Pharmacol. 1994;129(1):46–52. doi:10.​1006/​taap.​1994.​1227.PubMed
98.
Zurück zum Zitat Kelce WR, Monosson E, Gamcsik MP, Laws SC, Gray Jr LE. Environmental hormone disruptors: evidence that vinclozolin developmental toxicity is mediated by antiandrogenic metabolites. Toxicol Appl Pharmacol. 1994;126(2):276–85. doi:10.1006/taap.1994.1117.PubMed Kelce WR, Monosson E, Gamcsik MP, Laws SC, Gray Jr LE. Environmental hormone disruptors: evidence that vinclozolin developmental toxicity is mediated by antiandrogenic metabolites. Toxicol Appl Pharmacol. 1994;126(2):276–85. doi:10.​1006/​taap.​1994.​1117.PubMed
99.
Zurück zum Zitat Anway MD, Leathers C, Skinner MK. Endocrine disruptor vinclozolin induced epigenetic transgenerational adult-onset disease. Endocrinology. 2006;147(12):5515–23.PubMed Anway MD, Leathers C, Skinner MK. Endocrine disruptor vinclozolin induced epigenetic transgenerational adult-onset disease. Endocrinology. 2006;147(12):5515–23.PubMed
100.
Zurück zum Zitat El Sheikh Saad H, Meduri G, Phrakonkham P, Berges R, Vacher S, Djallali M, et al. Abnormal peripubertal development of the rat mammary gland following exposure in utero and during lactation to a mixture of genistein and the food contaminant vinclozolin. Reprod Toxicol. 2011;32(1):15–25. doi:10.1016/j.reprotox.2011.03.001.PubMed El Sheikh Saad H, Meduri G, Phrakonkham P, Berges R, Vacher S, Djallali M, et al. Abnormal peripubertal development of the rat mammary gland following exposure in utero and during lactation to a mixture of genistein and the food contaminant vinclozolin. Reprod Toxicol. 2011;32(1):15–25. doi:10.​1016/​j.​reprotox.​2011.​03.​001.PubMed
101.
Zurück zum Zitat Ozen S, Darcan S, Bayindir P, Karasulu E, Simsek DG, Gurler T. Effects of pesticides used in agriculture on the development of precocious puberty. Environ Monit Assess. 2012;184(7):4223–32. doi:10.1007/s10661-011-2257-6.PubMed Ozen S, Darcan S, Bayindir P, Karasulu E, Simsek DG, Gurler T. Effects of pesticides used in agriculture on the development of precocious puberty. Environ Monit Assess. 2012;184(7):4223–32. doi:10.​1007/​s10661-011-2257-6.PubMed
102.
103.
Zurück zum Zitat Swan SH, Main KM, Liu F, Stewart SL, Kruse RL, Calafat AM, et al. Decrease in anogenital distance among male infants with prenatal phthalate exposure. Environ Heal Perspect. 2005;113(8):1056–61. Swan SH, Main KM, Liu F, Stewart SL, Kruse RL, Calafat AM, et al. Decrease in anogenital distance among male infants with prenatal phthalate exposure. Environ Heal Perspect. 2005;113(8):1056–61.
104.
Zurück zum Zitat Rider CV, Wilson VS, Howdeshell KL, Hotchkiss AK, Furr JR, Lambright CR, et al. Cumulative effects of in utero administration of mixtures of “antiandrogens” on male rat reproductive development. Toxicol Pathol. 2009;37(1):100–13. doi:10.1177/0192623308329478.PubMed Rider CV, Wilson VS, Howdeshell KL, Hotchkiss AK, Furr JR, Lambright CR, et al. Cumulative effects of in utero administration of mixtures of “antiandrogens” on male rat reproductive development. Toxicol Pathol. 2009;37(1):100–13. doi:10.​1177/​0192623308329478​.PubMed
105.
Zurück zum Zitat Mylchreest E, Cattley RC, Foster PM. Male reproductive tract malformations in rats following gestational and lactational exposure to Di(n-butyl) phthalate: an antiandrogenic mechanism? Toxicol Sci. 1998;43(1):47–60. doi:10.1006/toxs.1998.2436.PubMed Mylchreest E, Cattley RC, Foster PM. Male reproductive tract malformations in rats following gestational and lactational exposure to Di(n-butyl) phthalate: an antiandrogenic mechanism? Toxicol Sci. 1998;43(1):47–60. doi:10.​1006/​toxs.​1998.​2436.PubMed
106.
Zurück zum Zitat Gray Jr LE, Ostby J, Furr J, Price M, Veeramachaneni DN, Parks L. Perinatal exposure to the phthalates DEHP, BBP, and DINP, but not DEP, DMP, or DOTP, alters sexual differentiation of the male rat. Toxicol Sci. 2000;58(2):350–65.PubMed Gray Jr LE, Ostby J, Furr J, Price M, Veeramachaneni DN, Parks L. Perinatal exposure to the phthalates DEHP, BBP, and DINP, but not DEP, DMP, or DOTP, alters sexual differentiation of the male rat. Toxicol Sci. 2000;58(2):350–65.PubMed
107.
Zurück zum Zitat Agas D, Sabbieti MG, Capacchietti M, Materazzi S, Menghi G, Materazzi G, et al. Benzyl butyl phthalate influences actin distribution and cell proliferation in rat Py1a osteoblasts. J Cell Biochem. 2007;101(3):543–51. doi:10.1002/jcb.21212.PubMed Agas D, Sabbieti MG, Capacchietti M, Materazzi S, Menghi G, Materazzi G, et al. Benzyl butyl phthalate influences actin distribution and cell proliferation in rat Py1a osteoblasts. J Cell Biochem. 2007;101(3):543–51. doi:10.​1002/​jcb.​21212.PubMed
109.
Zurück zum Zitat Crinnion WJ. Toxic effects of the easily avoidable phthalates and parabens. Alternative Med Rev: J Clin Ther. 2010;15(3):190–6. Crinnion WJ. Toxic effects of the easily avoidable phthalates and parabens. Alternative Med Rev: J Clin Ther. 2010;15(3):190–6.
110.
Zurück zum Zitat Moral R, Wang R, Russo IH, Mailo DA, Lamartiniere CA, Russo J. The plasticizer butyl benzyl phthalate induces genomic changes in rat mammary gland after neonatal/prepubertal exposure. BMC Genom. 2007;8:453. doi:10.1186/1471-2164-8-453. Moral R, Wang R, Russo IH, Mailo DA, Lamartiniere CA, Russo J. The plasticizer butyl benzyl phthalate induces genomic changes in rat mammary gland after neonatal/prepubertal exposure. BMC Genom. 2007;8:453. doi:10.​1186/​1471-2164-8-453.
111.
Zurück zum Zitat Moral R, Santucci-Pereira J, Wang R, Russo IH, Lamartiniere CA, Russo J. In utero exposure to butyl benzyl phthalate induces modifications in the morphology and the gene expression profile of the mammary gland: an experimental study in rats. Environ Health. 2011;10(1):5. doi:10.1186/1476-069X-10-5.PubMed Moral R, Santucci-Pereira J, Wang R, Russo IH, Lamartiniere CA, Russo J. In utero exposure to butyl benzyl phthalate induces modifications in the morphology and the gene expression profile of the mammary gland: an experimental study in rats. Environ Health. 2011;10(1):5. doi:10.​1186/​1476-069X-10-5.PubMed
112.
Zurück zum Zitat Dewitt JC, Copeland CB, Strynar MJ, Luebke RW. Perfluorooctanoic acid-induced immunomodulation in adult C57BL/6J or C57BL/6N female mice. Environ Heal Perspect. 2008;116(5):644–50. doi:10.1289/ehp.10896. Dewitt JC, Copeland CB, Strynar MJ, Luebke RW. Perfluorooctanoic acid-induced immunomodulation in adult C57BL/6J or C57BL/6N female mice. Environ Heal Perspect. 2008;116(5):644–50. doi:10.​1289/​ehp.​10896.
113.
Zurück zum Zitat National Toxicology Program, NTP Toxicology and Carcinogenesis Studies of Butyl Benzyl Phthalate (CAS No. 85-68-7) in F344/N Rats (Feed Studies). National Toxicology Program, NTP Toxicology and Carcinogenesis Studies of Butyl Benzyl Phthalate (CAS No. 85-68-7) in F344/N Rats (Feed Studies).
114.
Zurück zum Zitat Lopez-Carrillo L, Hernandez-Ramirez RU, Calafat AM, Torres-Sanchez L, Galvan-Portillo M, Needham LL, et al. Exposure to phthalates and breast cancer risk in northern Mexico. Environ Health Perspect. 2010;118(4):539–44. doi:10.1289/ehp.0901091.PubMed Lopez-Carrillo L, Hernandez-Ramirez RU, Calafat AM, Torres-Sanchez L, Galvan-Portillo M, Needham LL, et al. Exposure to phthalates and breast cancer risk in northern Mexico. Environ Health Perspect. 2010;118(4):539–44. doi:10.​1289/​ehp.​0901091.PubMed
115.
116.
Zurück zum Zitat Kim IY, Han SY, Moon A. Phthalates inhibit tamoxifen-induced apoptosis in MCF-7 human breast cancer cells. J Toxic Environ Health A. 2004;67(23–24):2025–35. doi:10.1080/15287390490514750. Kim IY, Han SY, Moon A. Phthalates inhibit tamoxifen-induced apoptosis in MCF-7 human breast cancer cells. J Toxic Environ Health A. 2004;67(23–24):2025–35. doi:10.​1080/​1528739049051475​0.
117.
Zurück zum Zitat Calafat AM, Kuklenyik Z, Reidy JA, Caudill SP, Tully JS, Needham LL. Serum concentrations of 11 polyfluoroalkyl compounds in the US population: data from the National Health and Nutrition Examination Survey (NHANES) 1999–2000. Environ Sci Technol. 2007;41:2237–42.PubMed Calafat AM, Kuklenyik Z, Reidy JA, Caudill SP, Tully JS, Needham LL. Serum concentrations of 11 polyfluoroalkyl compounds in the US population: data from the National Health and Nutrition Examination Survey (NHANES) 1999–2000. Environ Sci Technol. 2007;41:2237–42.PubMed
118.
Zurück zum Zitat Calafat AM, Wong LY, Kuklenyik Z, Reidy JA, Needham LL. Polyfluoroalkyl chemicals in the U.S. population: data from the National Health and Nutrition Examination Survey (NHANES) 2003–2004 and comparisons with NHANES 1999–2000. Environ Health Perspect. 2007;115(11):1596–602.PubMed Calafat AM, Wong LY, Kuklenyik Z, Reidy JA, Needham LL. Polyfluoroalkyl chemicals in the U.S. population: data from the National Health and Nutrition Examination Survey (NHANES) 2003–2004 and comparisons with NHANES 1999–2000. Environ Health Perspect. 2007;115(11):1596–602.PubMed
119.
Zurück zum Zitat Olsen GW, Burris JM, Ehresman DJ, Froehlich JW, Seacat AM, Butenhoff JL, et al. Half-life of serum elimination of perfluorooctanesulfonate, perfluorohexanesulfonate, and perfluorooctanoate in retired fluorochemical production workers. Environ Health Perspect. 2007;115(9):1298–305.PubMed Olsen GW, Burris JM, Ehresman DJ, Froehlich JW, Seacat AM, Butenhoff JL, et al. Half-life of serum elimination of perfluorooctanesulfonate, perfluorohexanesulfonate, and perfluorooctanoate in retired fluorochemical production workers. Environ Health Perspect. 2007;115(9):1298–305.PubMed
121.
Zurück zum Zitat Henry ND, Fair PA. Comparison of in vitro cytotoxicity, estrogenicity and anti-estrogenicity of triclosan, perfluorooctane sulfonate and perfluorooctanoic acid. J Appl Toxicol. 2011. doi:10.1002/jat.1736. Henry ND, Fair PA. Comparison of in vitro cytotoxicity, estrogenicity and anti-estrogenicity of triclosan, perfluorooctane sulfonate and perfluorooctanoic acid. J Appl Toxicol. 2011. doi:10.​1002/​jat.​1736.
122.
Zurück zum Zitat Lau C, Thibodeaux JR, Hanson RG, Narotsky MG, Rogers JM, Lindstrom AB, et al. Effects of perfluorooctanoic acid exposure during pregnancy in the mouse. Toxicol Sci. 2006;90(2):510–8. doi:10.1093/toxsci/kfj105.PubMed Lau C, Thibodeaux JR, Hanson RG, Narotsky MG, Rogers JM, Lindstrom AB, et al. Effects of perfluorooctanoic acid exposure during pregnancy in the mouse. Toxicol Sci. 2006;90(2):510–8. doi:10.​1093/​toxsci/​kfj105.PubMed
123.
Zurück zum Zitat Yang C, Tan YS, Harkema JR, Haslam SZ. Differential effect of peripubertal exposure to perfluorooctanoic acid on mammary gland development in C57Bl/6 and Balb/c mouse strains. Reprod Toxicol. 2009;27(3–4):299–306. doi:10.1016/j.reprotox.2008.10.003.PubMed Yang C, Tan YS, Harkema JR, Haslam SZ. Differential effect of peripubertal exposure to perfluorooctanoic acid on mammary gland development in C57Bl/6 and Balb/c mouse strains. Reprod Toxicol. 2009;27(3–4):299–306. doi:10.​1016/​j.​reprotox.​2008.​10.​003.PubMed
124.
Zurück zum Zitat Macon MB, Villanueva LR, Tatum-Gibbs K, Zehr RD, Strynar M, Stanko JP, et al. Prenatal perfluorooctanoic acid exposure in CD-1 mice: low dose developmental effects and internal dosimetry. Toxicol Sci. 2011;122(1):134–45.PubMed Macon MB, Villanueva LR, Tatum-Gibbs K, Zehr RD, Strynar M, Stanko JP, et al. Prenatal perfluorooctanoic acid exposure in CD-1 mice: low dose developmental effects and internal dosimetry. Toxicol Sci. 2011;122(1):134–45.PubMed
125.
Zurück zum Zitat Dixon D, Reed CE, Moore AB, Gibbs-Flournoy EA, Hines EP, Wallace EA, et al. Histopathologic changes in the uterus, cervix and vagina of immature CD-1 mice exposed to low doses of perfluorooctanoic acid (PFOA) in a uterotrophic assay. Reprod Toxicol. 2012;33(4):506–12.PubMed Dixon D, Reed CE, Moore AB, Gibbs-Flournoy EA, Hines EP, Wallace EA, et al. Histopathologic changes in the uterus, cervix and vagina of immature CD-1 mice exposed to low doses of perfluorooctanoic acid (PFOA) in a uterotrophic assay. Reprod Toxicol. 2012;33(4):506–12.PubMed
126.
Zurück zum Zitat Biegel LB, Liu RC, Hurtt ME, Cook JC. Effects of ammonium perfluorooctanoate on Leydig cell function: in vitro, in vivo, and ex vivo studies. Toxicol Appl Pharmacol. 1995;134(1):18–25. doi:10.1006/taap.1995.1164.PubMed Biegel LB, Liu RC, Hurtt ME, Cook JC. Effects of ammonium perfluorooctanoate on Leydig cell function: in vitro, in vivo, and ex vivo studies. Toxicol Appl Pharmacol. 1995;134(1):18–25. doi:10.​1006/​taap.​1995.​1164.PubMed
127.
Zurück zum Zitat Sibinski L. Two-year oral (diet) toxicity/oncogenicity study of fluorochemical FC-143 in rats.: Riker Laboratories Inc/3m Company1987. Sibinski L. Two-year oral (diet) toxicity/oncogenicity study of fluorochemical FC-143 in rats.: Riker Laboratories Inc/3m Company1987.
128.
Zurück zum Zitat Lou I, Wambaugh JF, Lau C, Hanson RG, Lindstrom AB, Strynar MJ, et al. Modeling single and repeated dose pharmacokinetics of PFOA in mice. Toxicol Sci. 2009;107(2):331–41. doi:10.1093/toxsci/kfn234.PubMed Lou I, Wambaugh JF, Lau C, Hanson RG, Lindstrom AB, Strynar MJ, et al. Modeling single and repeated dose pharmacokinetics of PFOA in mice. Toxicol Sci. 2009;107(2):331–41. doi:10.​1093/​toxsci/​kfn234.PubMed
129.
Zurück zum Zitat Lopez-Espinosa M, Fletcher T, Armstrong B, Genser B, Dhatariya K, Mondal D, et al. Association of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) with age of puberty among children living near a chemical plant. Environ Sci Technol. 2011. doi:10.1021/es1038694. Lopez-Espinosa M, Fletcher T, Armstrong B, Genser B, Dhatariya K, Mondal D, et al. Association of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) with age of puberty among children living near a chemical plant. Environ Sci Technol. 2011. doi:10.​1021/​es1038694.
130.
Zurück zum Zitat Knox SS, Jackson T, Javins B, Frisbee SJ, Shankar A, Ducatman AM. Implications of early menopause in women exposed to perfluorocarbons. J Clin Endocrinol Metab. 2011;96(6):1747–53. doi:10.1210/jc.2010-2401.PubMed Knox SS, Jackson T, Javins B, Frisbee SJ, Shankar A, Ducatman AM. Implications of early menopause in women exposed to perfluorocarbons. J Clin Endocrinol Metab. 2011;96(6):1747–53. doi:10.​1210/​jc.​2010-2401.PubMed
131.
Zurück zum Zitat Innes KE, Byers TE. Preeclampsia and breast cancer risk. Epidemiology. 1999;10(6):722–32.PubMed Innes KE, Byers TE. Preeclampsia and breast cancer risk. Epidemiology. 1999;10(6):722–32.PubMed
132.
Zurück zum Zitat Bonefeld-Jorgensen EC, Long M, Bossi R, Ayotte P, Asmund G, Kruger T, et al. Perfluorinated compounds are related to breast cancer risk in Greenlandic Inuit: a case control study. Environ Health. 2011;10:88. doi:10.1186/1476-069X-10-88.PubMed Bonefeld-Jorgensen EC, Long M, Bossi R, Ayotte P, Asmund G, Kruger T, et al. Perfluorinated compounds are related to breast cancer risk in Greenlandic Inuit: a case control study. Environ Health. 2011;10:88. doi:10.​1186/​1476-069X-10-88.PubMed
133.
Zurück zum Zitat White SS, Stanko JP, Kato K, Calafat AM, Hines EP, Fenton SE. Gestational and chronic low-dose PFOA exposures and mammary gland growth and differentiation in three generations of CD-1 mice. Environ Heal Perspect. 2011;119(8):1070–6. doi:10.1289/ehp.1002741. White SS, Stanko JP, Kato K, Calafat AM, Hines EP, Fenton SE. Gestational and chronic low-dose PFOA exposures and mammary gland growth and differentiation in three generations of CD-1 mice. Environ Heal Perspect. 2011;119(8):1070–6. doi:10.​1289/​ehp.​1002741.
134.
Zurück zum Zitat Frisbee SJ, Brooks ABJ, Maher A, Flensborg P, Arnold S, Fletcher T, et al. The C8 health project: design, methods, and participants. Environ Heal Perspect. 2009;117:1873–82. Frisbee SJ, Brooks ABJ, Maher A, Flensborg P, Arnold S, Fletcher T, et al. The C8 health project: design, methods, and participants. Environ Heal Perspect. 2009;117:1873–82.
135.
Zurück zum Zitat Zhao Y, Tan YS, Strynar MJ, Perez G, Haslam SZ, Yang C. Perfluorooctanoic acid effects on ovaries mediate its inhibition of peripubertal mammary gland development in Balb/c and C57Bl/6 mice. Reprod Toxicol. 2012;33(4):563–76. doi:10.1016/j.reprotox.2012.02.004.PubMed Zhao Y, Tan YS, Strynar MJ, Perez G, Haslam SZ, Yang C. Perfluorooctanoic acid effects on ovaries mediate its inhibition of peripubertal mammary gland development in Balb/c and C57Bl/6 mice. Reprod Toxicol. 2012;33(4):563–76. doi:10.​1016/​j.​reprotox.​2012.​02.​004.PubMed
136.
Zurück zum Zitat Zhao Y, Tan YS, Haslam SZ, Yang C. Perfluorooctanoic acid effects on steroid hormone and growth factor levels mediate stimulation of peripubertal mammary gland development in C57Bl/6 mice. Toxicol Sci. 2010;115(1):214–24. doi:10.1093/toxsci/kfq030.PubMed Zhao Y, Tan YS, Haslam SZ, Yang C. Perfluorooctanoic acid effects on steroid hormone and growth factor levels mediate stimulation of peripubertal mammary gland development in C57Bl/6 mice. Toxicol Sci. 2010;115(1):214–24. doi:10.​1093/​toxsci/​kfq030.PubMed
137.
Zurück zum Zitat Zhao G, Wang J, Wang X, Chen S, Zhao Y, Gu F, et al. Mutegenicity of PFOA in mammalian cells: role of mitochondtia-dependent reactive oxygem species. Environ Sci Technol. 2011;45:1638–44. doi:10.1021/es1026129. Zhao G, Wang J, Wang X, Chen S, Zhao Y, Gu F, et al. Mutegenicity of PFOA in mammalian cells: role of mitochondtia-dependent reactive oxygem species. Environ Sci Technol. 2011;45:1638–44. doi:10.​1021/​es1026129.
138.
Zurück zum Zitat Lipworth L, Hsieh CC, Wide L, Ekbom A, Yu SZ, Yu GP, et al. Maternal pregnancy hormone levels in an area with a high incidence (Boston, USA) and in an area with a low incidence (Shanghai, China) of breast cancer. Br J Cancer. 1999;79(1):7–12. doi:10.1038/sj.bjc.6690003.PubMed Lipworth L, Hsieh CC, Wide L, Ekbom A, Yu SZ, Yu GP, et al. Maternal pregnancy hormone levels in an area with a high incidence (Boston, USA) and in an area with a low incidence (Shanghai, China) of breast cancer. Br J Cancer. 1999;79(1):7–12. doi:10.​1038/​sj.​bjc.​6690003.PubMed
139.
Zurück zum Zitat Bray F, McCarron P, Parkin DM. The changing global patterns of female breast cancer incidence and mortality. Breast Cancer Res. 2004;6(6):229–39. doi:10.1186/bcr932.PubMed Bray F, McCarron P, Parkin DM. The changing global patterns of female breast cancer incidence and mortality. Breast Cancer Res. 2004;6(6):229–39. doi:10.​1186/​bcr932.PubMed
142.
Zurück zum Zitat Wu AH, Wan P, Hankin J, Tseng CC, Yu MC, Pike MC. Adolescent and adult soy intake and risk of breast cancer in Asian-Americans. Carcinogenesis. 2002;23(9):1491–6.PubMed Wu AH, Wan P, Hankin J, Tseng CC, Yu MC, Pike MC. Adolescent and adult soy intake and risk of breast cancer in Asian-Americans. Carcinogenesis. 2002;23(9):1491–6.PubMed
144.
Zurück zum Zitat Su Y, Eason RR, Geng Y, Till SR, Badger TM, Simmen RC. In utero exposure to maternal diets containing soy protein isolate, but not genistein alone, protects young adult rat offspring from NMU-induced mammary tumorigenesis. Carcinogenesis. 2007;28(5):1046–51. doi:10.1093/carcin/bgl240.PubMed Su Y, Eason RR, Geng Y, Till SR, Badger TM, Simmen RC. In utero exposure to maternal diets containing soy protein isolate, but not genistein alone, protects young adult rat offspring from NMU-induced mammary tumorigenesis. Carcinogenesis. 2007;28(5):1046–51. doi:10.​1093/​carcin/​bgl240.PubMed
145.
Zurück zum Zitat Hakkak R, Korourian S, Shelnutt SR, Lensing S, Ronis MJ, Badger TM. Diets containing whey proteins or soy protein isolate protect against 7,12-dimethylbenz(a)anthracene-induced mammary tumors in female rats. Cancer Epidemiol Biomarkers Prev. 2000;9(1):113–7.PubMed Hakkak R, Korourian S, Shelnutt SR, Lensing S, Ronis MJ, Badger TM. Diets containing whey proteins or soy protein isolate protect against 7,12-dimethylbenz(a)anthracene-induced mammary tumors in female rats. Cancer Epidemiol Biomarkers Prev. 2000;9(1):113–7.PubMed
146.
Zurück zum Zitat Pei RJ, Sato M, Yuri T, Danbara N, Nikaido Y, Tsubura A. Effect of prenatal and prepubertal genistein exposure on N-methyl-N-nitrosourea-induced mammary tumorigenesis in female Sprague–Dawley rats. In Vivo. 2003;17(4):349–57.PubMed Pei RJ, Sato M, Yuri T, Danbara N, Nikaido Y, Tsubura A. Effect of prenatal and prepubertal genistein exposure on N-methyl-N-nitrosourea-induced mammary tumorigenesis in female Sprague–Dawley rats. In Vivo. 2003;17(4):349–57.PubMed
147.
148.
Zurück zum Zitat Fritz WA, Coward L, Wang J, Lamartiniere CA. Dietary genistein: perinatal mammary cancer prevention, bioavailability and toxicity testing in the rat. Carcinogenesis. 1998;19(12):2151–8.PubMed Fritz WA, Coward L, Wang J, Lamartiniere CA. Dietary genistein: perinatal mammary cancer prevention, bioavailability and toxicity testing in the rat. Carcinogenesis. 1998;19(12):2151–8.PubMed
149.
Zurück zum Zitat Lamartiniere CA. Timing of exposure and mammary cancer risk. J Mammary Gland Biol Neoplasia. 2002;7(1):67–76.PubMed Lamartiniere CA. Timing of exposure and mammary cancer risk. J Mammary Gland Biol Neoplasia. 2002;7(1):67–76.PubMed
151.
Zurück zum Zitat Molzberger AF, Vollmer G, Hertrampf T, Moller FJ, Kulling S, Diel P. In utero and postnatal exposure to isoflavones results in a reduced responsivity of the mammary gland towards estradiol. Mol Nutr food Res. 2012;56(3):399–409. doi:10.1002/mnfr.201100371.PubMed Molzberger AF, Vollmer G, Hertrampf T, Moller FJ, Kulling S, Diel P. In utero and postnatal exposure to isoflavones results in a reduced responsivity of the mammary gland towards estradiol. Mol Nutr food Res. 2012;56(3):399–409. doi:10.​1002/​mnfr.​201100371.PubMed
152.
Zurück zum Zitat Latendresse JR, Bucci TJ, Olson G, Mellick P, Weis CC, Thorn B, et al. Genistein and ethinyl estradiol dietary exposure in multigenerational and chronic studies induce similar proliferative lesions in mammary gland of male Sprague–Dawley rats. Reprod Toxicol. 2009;28(3):342–53. doi:10.1016/j.reprotox.2009.04.006.PubMed Latendresse JR, Bucci TJ, Olson G, Mellick P, Weis CC, Thorn B, et al. Genistein and ethinyl estradiol dietary exposure in multigenerational and chronic studies induce similar proliferative lesions in mammary gland of male Sprague–Dawley rats. Reprod Toxicol. 2009;28(3):342–53. doi:10.​1016/​j.​reprotox.​2009.​04.​006.PubMed
153.
Zurück zum Zitat Juan ME, Vinardell MP, Planas JM. The daily oral administration of high doses of trans-resveratrol to rats for 28 days is not harmful. J Nutr. 2002;132(2):257–60.PubMed Juan ME, Vinardell MP, Planas JM. The daily oral administration of high doses of trans-resveratrol to rats for 28 days is not harmful. J Nutr. 2002;132(2):257–60.PubMed
154.
Zurück zum Zitat Levi F, Pasche C, Lucchini F, Ghidoni R, Ferraroni M, La Vecchia C. Resveratrol and breast cancer risk. Eur J Canc Prev. 2005;14(2):139–42. Levi F, Pasche C, Lucchini F, Ghidoni R, Ferraroni M, La Vecchia C. Resveratrol and breast cancer risk. Eur J Canc Prev. 2005;14(2):139–42.
156.
Zurück zum Zitat Henry LA, Witt DM. Effects of neonatal resveratrol exposure on adult male and female reproductive physiology and behavior. Dev Neurosci. 2006;28(3):186–95. doi:10.1159/000091916.PubMed Henry LA, Witt DM. Effects of neonatal resveratrol exposure on adult male and female reproductive physiology and behavior. Dev Neurosci. 2006;28(3):186–95. doi:10.​1159/​000091916.PubMed
157.
Zurück zum Zitat Nikaido Y, Yoshizawa K, Danbara N, Tsujita-Kyutoku M, Yuri T, Uehara N, et al. Effects of maternal xenoestrogen exposure on development of the reproductive tract and mammary gland in female CD-1 mouse offspring. Reprod Toxicol. 2004;18(6):803–11. doi:10.1016/j.reprotox.2004.05.002.PubMed Nikaido Y, Yoshizawa K, Danbara N, Tsujita-Kyutoku M, Yuri T, Uehara N, et al. Effects of maternal xenoestrogen exposure on development of the reproductive tract and mammary gland in female CD-1 mouse offspring. Reprod Toxicol. 2004;18(6):803–11. doi:10.​1016/​j.​reprotox.​2004.​05.​002.PubMed
158.
Zurück zum Zitat Provinciali M, Re F, Donnini A, Orlando F, Bartozzi B, Di Stasio G, et al. Effect of resveratrol on the development of spontaneous mammary tumors in HER-2/neu transgenic mice. Int J Cancer. 2005;115(1):36–45. doi:10.1002/ijc.20874.PubMed Provinciali M, Re F, Donnini A, Orlando F, Bartozzi B, Di Stasio G, et al. Effect of resveratrol on the development of spontaneous mammary tumors in HER-2/neu transgenic mice. Int J Cancer. 2005;115(1):36–45. doi:10.​1002/​ijc.​20874.PubMed
159.
Zurück zum Zitat Bhat KP, Lantvit D, Christov K, Mehta RG, Moon RC, Pezzuto JM. Estrogenic and antiestrogenic properties of resveratrol in mammary tumor models. Cancer Res. 2001;61(20):7456–63.PubMed Bhat KP, Lantvit D, Christov K, Mehta RG, Moon RC, Pezzuto JM. Estrogenic and antiestrogenic properties of resveratrol in mammary tumor models. Cancer Res. 2001;61(20):7456–63.PubMed
160.
Zurück zum Zitat Jang M, Cai L, Udeani GO, Slowing KV, Thomas CF, Beecher CW, et al. Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. Science. 1997;275(5297):218–20.PubMed Jang M, Cai L, Udeani GO, Slowing KV, Thomas CF, Beecher CW, et al. Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. Science. 1997;275(5297):218–20.PubMed
162.
Zurück zum Zitat Kuiper-Goodman T, Scott PM, Watanabe H. Risk assessment of the mycotoxin zearalenone. Regul Toxicol Pharmacol: RTP. 1987;7(3):253–306.PubMed Kuiper-Goodman T, Scott PM, Watanabe H. Risk assessment of the mycotoxin zearalenone. Regul Toxicol Pharmacol: RTP. 1987;7(3):253–306.PubMed
163.
Zurück zum Zitat Hilakivi-Clarke L, Onojafe I, Raygada M, Cho E, Skaar T, Russo I, et al. Prepubertal exposure to zearalenone or genistein reduces mammary tumorigenesis. Br J Cancer. 1999;80(11):1682–8. doi:10.1038/sj.bjc.6690584.PubMed Hilakivi-Clarke L, Onojafe I, Raygada M, Cho E, Skaar T, Russo I, et al. Prepubertal exposure to zearalenone or genistein reduces mammary tumorigenesis. Br J Cancer. 1999;80(11):1682–8. doi:10.​1038/​sj.​bjc.​6690584.PubMed
164.
Zurück zum Zitat Hilakivi-Clarke L, Cho E, Onojafe I, Raygada M, Clarke R. Maternal exposure to genistein during pregnancy increases carcinogen-induced mammary tumorigenesis in female rat offspring. Oncol Rep. 1999;6(5):1089–95.PubMed Hilakivi-Clarke L, Cho E, Onojafe I, Raygada M, Clarke R. Maternal exposure to genistein during pregnancy increases carcinogen-induced mammary tumorigenesis in female rat offspring. Oncol Rep. 1999;6(5):1089–95.PubMed
165.
Zurück zum Zitat Yuri T, Tsukamoto R, Miki K, Uehara N, Matsuoka Y, Tsubura A. Biphasic effects of zeranol on the growth of estrogen receptor-positive human breast carcinoma cells. Oncol Rep. 2006;16(6):1307–12.PubMed Yuri T, Tsukamoto R, Miki K, Uehara N, Matsuoka Y, Tsubura A. Biphasic effects of zeranol on the growth of estrogen receptor-positive human breast carcinoma cells. Oncol Rep. 2006;16(6):1307–12.PubMed
166.
Zurück zum Zitat Saenz de Rodriguez CA, Bongiovanni AM, Conde de Borrego L. An epidemic of precocious development in Puerto Rican children. J Pediatr. 1985;107(3):393–6.PubMed Saenz de Rodriguez CA, Bongiovanni AM, Conde de Borrego L. An epidemic of precocious development in Puerto Rican children. J Pediatr. 1985;107(3):393–6.PubMed
167.
Zurück zum Zitat Fara GM, Del Corvo G, Bernuzzi S, Bigatello A, Di Pietro C, Scaglioni S, et al. Epidemic of breast enlargement in an Italian school. Lancet. 1979;2(8137):295–7.PubMed Fara GM, Del Corvo G, Bernuzzi S, Bigatello A, Di Pietro C, Scaglioni S, et al. Epidemic of breast enlargement in an Italian school. Lancet. 1979;2(8137):295–7.PubMed
Metadaten
Titel
Endocrine Disruptors and the Breast: Early Life Effects and Later Life Disease
verfasst von
Madisa B. Macon
Suzanne E. Fenton
Publikationsdatum
01.03.2013
Verlag
Springer US
Erschienen in
Journal of Mammary Gland Biology and Neoplasia / Ausgabe 1/2013
Print ISSN: 1083-3021
Elektronische ISSN: 1573-7039
DOI
https://doi.org/10.1007/s10911-013-9275-7

Weitere Artikel der Ausgabe 1/2013

Journal of Mammary Gland Biology and Neoplasia 1/2013 Zur Ausgabe

Preface

Preface

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

15% bedauern gewählte Blasenkrebs-Therapie

29.05.2024 Urothelkarzinom Nachrichten

Ob Patienten und Patientinnen mit neu diagnostiziertem Blasenkrebs ein Jahr später Bedauern über die Therapieentscheidung empfinden, wird einer Studie aus England zufolge von der Radikalität und dem Erfolg des Eingriffs beeinflusst.

Erhöhtes Risiko fürs Herz unter Checkpointhemmer-Therapie

28.05.2024 Nebenwirkungen der Krebstherapie Nachrichten

Kardiotoxische Nebenwirkungen einer Therapie mit Immuncheckpointhemmern mögen selten sein – wenn sie aber auftreten, wird es für Patienten oft lebensgefährlich. Voruntersuchung und Monitoring sind daher obligat.

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.