Dioxin and Endometrial Progesterone Resistance

被引:51
作者
Bruner-Tran, Kaylon L. [1 ]
Ding, Tianbing [1 ]
Osteen, Kevin G. [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Obstet & Gynecol, Womens Reprod Hlth Res Ctr, Nashville, TN 37232 USA
关键词
Endometriosis; TCDD; developmental exposure; MATRIX-METALLOPROTEINASE EXPRESSION; DRUG-METABOLIZING-ENZYMES; ARYL-HYDROCARBON RECEPTOR; HUMAN IMPLANTATION; GROWTH-FACTORS; EMBRYONIC-DEVELOPMENT; ENDOCRINE DISRUPTION; CYCLING ENDOMETRIUM; REPRODUCTIVE-CYCLE; PRENATAL EXPOSURE;
D O I
10.1055/s-0029-1242995
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Development of endometriosis likely requires multiple, interactive mechanisms involving both the endocrine and immune systems. Environmental toxicants, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), are of particular interest as potential contributory agents in the development of this disease because they can disrupt both systems. Nevertheless, defining the potential role that environmental exposure to TCDD plays in the development of endometriosis requires a better understanding of how this toxicant affects the biological processes that promote the disease. Although the disease mechanism(s) responsible for progesterone resistance in the endometrium of endometriosis patients remains speculative, our studies indicate that developmental exposure of mice to TCDD leads to a progesterone-resistant phenotype in adult animals that can persist for several generations. These studies and others underscore the importance of developing a greater understanding of the mechanisms of TCDD action that relate to reproductive disorders such as endometriosis.
引用
收藏
页码:59 / 68
页数:10
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