Endocrine disruptors in female reproductive tract development and carcinogenesis

被引:66
|
作者
Ma, Liang [1 ,2 ]
机构
[1] Washington Univ, Dept Med, Div Dermatol, St Louis, MO 63110 USA
[2] Washington Univ, Dept Dev Biol, St Louis, MO 63110 USA
来源
基金
美国国家卫生研究院;
关键词
ESTROGEN-RECEPTOR-ALPHA; NEONATAL DIETHYLSTILBESTROL EXPOSURE; DIFFERENTIAL EXPRESSION PATTERNS; UTERINE GENE-EXPRESSION; MULLERIAN DUCT; IN-UTERO; MOUSE UTERUS; EPITHELIAL DIFFERENTIATION; UROGENITAL DEVELOPMENT; BETA-CATENIN;
D O I
10.1016/j.tem.2009.03.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Growing concerns over endocrine disrupting chemicals (EDCs) and their effects on human fetal development and adult health have promoted research into the underlying molecular mechanisms of endocrine disruption. Gene targeting technology has allowed insight into the genetic pathways governing reproductive tract development and how exposure to EDCs during a critical developmental window can alter reproductive tract development, potentially forming the basis for adult diseases. This review primarily uses diethylstilbestrol (DES) as a model agent for EDCs and discusses the recent progress elucidating how DES and other EDCs affect murine female reproductive tract development and cancer at the molecular level.
引用
收藏
页码:357 / 363
页数:7
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