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Exposures to Synthetic Estrogens at Different Times During the Life, and Their Effect on Breast Cancer Risk

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Date 2013 Feb 9
PMID 23392570
Citations 26
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Abstract

Women are using estrogens for many purposes, such as to prevent pregnancy or miscarriage, or to treat menopausal symptoms. Estrogens also have been used to treat breast cancer which seems puzzling, since there is convincing evidence to support a link between high lifetime estrogen exposure and increased breast cancer risk. In this review, we discuss the findings that maternal exposure to the synthetic estrogen diethylstilbestrol during pregnancy increases breast cancer risk in both exposed mothers and their daughters. In addition, we review data regarding the use of estrogens in oral contraceptives and as postmenopausal hormone therapy and discuss the opposing effects on breast cancer risk based upon timing of exposure. We place particular emphasis on studies investigating how maternal estrogenic exposures during pregnancy increase breast cancer risk among daughters. New data suggest that these exposures induce epigenetic modifications in the mammary gland and germ cells, thereby causing an inheritable increase in breast cancer risk for multiple generations.

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References
1.
Tomooka Y, Bern H . Growth of mouse mammary glands after neonatal sex hormone treatment. J Natl Cancer Inst. 1982; 69(6):1347-52. View

2.
Heiss G, Wallace R, Anderson G, Aragaki A, Beresford S, Brzyski R . Health risks and benefits 3 years after stopping randomized treatment with estrogen and progestin. JAMA. 2008; 299(9):1036-45. DOI: 10.1001/jama.299.9.1036. View

3.
Hersh A, Stefanick M, Stafford R . National use of postmenopausal hormone therapy: annual trends and response to recent evidence. JAMA. 2004; 291(1):47-53. DOI: 10.1001/jama.291.1.47. View

4.
Martin L, Minkin S, Boyd N . Hormone therapy, mammographic density, and breast cancer risk. Maturitas. 2009; 64(1):20-6. DOI: 10.1016/j.maturitas.2009.07.009. View

5.
Bern H, Edery M, Mills K, Kohrman A, Mori T, Larson L . Long-term alterations in histology and steroid receptor levels of the genital tract and mammary gland following neonatal exposure of female BALB/cCrgl mice to various doses of diethylstilbestrol. Cancer Res. 1987; 47(15):4165-72. View