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围产期接触己烯雌酚的经验教训。

Lessons learned from perinatal exposure to diethylstilbestrol.

作者信息

Newbold Retha R

机构信息

Developmental Endocrinology Section, Laboratory of Toxicology, Environmental Toxicology Program, Division of Intramural Research, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.

出版信息

Toxicol Appl Pharmacol. 2004 Sep 1;199(2):142-50. doi: 10.1016/j.taap.2003.11.033.

Abstract

The synthetic estrogen diethylstilbestrol (DES) is well documented to be a perinatal carcinogen in both humans and experimental animals. Exposure to DES during critical periods of differentiation permanently alters the programming of estrogen target tissues resulting in benign and malignant abnormalities in the reproductive tract later in life. Using the perinatal DES-exposed rodent model, cellular and molecular mechanisms have been identified that play a role in these carcinogenic effects. Although DES is a potent estrogenic chemical, effects of low doses of the compound are being used to predict health risks of weaker environmental estrogens. Therefore, it is of particular interest that developmental exposure to very low doses of DES has been found to adversely affect fertility and to increase tumor incidence in murine reproductive tract tissues. These adverse effects are seen at environmentally relevant estrogen dose levels. New studies from our lab verify that DES effects are not unique; when numerous environmental chemicals with weak estrogenic activity are tested in the experimental neonatal mouse model, developmental exposure results in an increased incidence of benign and malignant tumors including uterine leiomyomas and adenocarcinomas that are similar to those shown following DES exposure. Finally, growing evidence in experimental animals suggests that some adverse effects can be passed on to subsequent generations, although the mechanisms involved in these trans-generational events remain unknown. Although the complete spectrum of risks to DES-exposed humans are uncertain at this time, the scientific community continues to learn more about cellular and molecular mechanisms by which perinatal carcinogenesis occurs. These advances in knowledge of both genetic and epigenetic mechanisms will be significant in ultimately predicting risks to other environmental estrogens and understanding more about the role of estrogens in normal and abnormal development.

摘要

合成雌激素己烯雌酚(DES)在人类和实验动物中均被充分证明是一种围产期致癌物。在关键分化期接触DES会永久性改变雌激素靶组织的程序,导致日后生殖系统出现良性和恶性异常。利用围产期接触DES的啮齿动物模型,已经确定了在这些致癌作用中起作用的细胞和分子机制。尽管DES是一种强效雌激素化学物质,但该化合物低剂量的影响正被用于预测较弱环境雌激素的健康风险。因此,特别值得关注的是,已发现极低剂量的DES发育暴露会对生育能力产生不利影响,并增加小鼠生殖道组织中的肿瘤发生率。在与环境相关的雌激素剂量水平下可观察到这些不利影响。我们实验室的新研究证实,DES的影响并非独一无二;当在实验性新生小鼠模型中测试多种具有弱雌激素活性的环境化学物质时,发育暴露会导致良性和恶性肿瘤的发生率增加,包括子宫平滑肌瘤和腺癌,与DES暴露后所显示的情况相似。最后,实验动物中越来越多的证据表明,一些不利影响可以传递给后代,尽管这些跨代事件所涉及的机制仍然未知。尽管目前尚不确定接触DES的人类面临的全部风险范围,但科学界仍在不断深入了解围产期致癌发生的细胞和分子机制。这些遗传和表观遗传机制知识的进展对于最终预测其他环境雌激素的风险以及更深入了解雌激素在正常和异常发育中的作用具有重要意义。

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