Boverhof D R, Fertuck K C, Burgoon L D, Eckel J E, Gennings C, Zacharewski T R
Department of Biochemistry and Molecular Biology, National Food Safety and Toxicology Center, Michigan State University, East Lansing, MI 48824, USA.
Carcinogenesis. 2004 Jul;25(7):1277-91. doi: 10.1093/carcin/bgh114. Epub 2004 Feb 19.
Temporal- and dose-dependent changes in hepatic gene expression were examined in immature ovariectomized C57BL/6 mice gavaged with ethynyl estradiol (EE), an orally active estrogen. For temporal analysis, mice were gavaged every 24 h for 3 days with 100 microg/kg EE or vehicle and liver samples were collected at 2, 4, 8, 12, 24 and 72 h. Gene expression was monitored using custom cDNA microarrays containing 3067 genes/ESTs of which 393 exhibited a change at one or more time points. Functional gene annotation extracted from public databases associated temporal gene expression changes with growth and proliferation, cytoskeletal and extracellular matrix responses, microtubule-based processes, oxidative metabolism and stress, and lipid metabolism and transport. In the dose-response study, hepatic samples were collected 24 h following treatment with 0, 0.1, 1, 10, 100 or 250 microg/kg EE. Thirty-nine of the 79 genes identified as differentially regulated at 24 h in the time course study exhibited a dose-response relationship with an average ED50 value of 47 +/- 3.5 microg/kg. Comparative analysis indicated that many of the identified temporal and dose-dependent hepatic responses are similar to EE-induced uterine responses reported in the literature and in a companion study using the same animals. Results from these studies confirm that the liver is a highly estrogen responsive tissue that exhibits a number of common responses shared with the uterus as well as distinct estrogen-mediated profiles. These data will further aid in the elucidation of the mechanisms of action of estrogens in the liver as well as in other classical and non-classical estrogen responsive tissues.
在未成熟卵巢切除的C57BL/6小鼠中,通过灌胃给予具有口服活性的雌激素乙炔雌二醇(EE),研究了肝脏基因表达的时间和剂量依赖性变化。进行时间分析时,小鼠每隔24小时灌胃一次,连续3天,给予100μg/kg EE或溶剂对照,在2、4、8、12、24和72小时采集肝脏样本。使用定制的cDNA微阵列监测基因表达,该微阵列包含3067个基因/EST,其中393个在一个或多个时间点表现出变化。从公共数据库中提取的功能基因注释将时间性基因表达变化与生长和增殖、细胞骨架和细胞外基质反应、基于微管的过程、氧化代谢和应激以及脂质代谢和转运联系起来。在剂量反应研究中,在给予0、0.1、1、10、100或250μg/kg EE处理24小时后采集肝脏样本。在时间进程研究中确定在24小时差异调节的79个基因中的39个表现出剂量反应关系,平均ED50值为47±3.5μg/kg。比较分析表明,许多已确定的时间和剂量依赖性肝脏反应与文献中报道的以及在使用相同动物的一项配套研究中EE诱导的子宫反应相似。这些研究结果证实,肝脏是一个对雌激素高度敏感的组织,表现出许多与子宫共有的反应以及独特的雌激素介导的特征。这些数据将进一步有助于阐明雌激素在肝脏以及其他经典和非经典雌激素反应组织中的作用机制。