Literature DB >> 14976129

Temporal- and dose-dependent hepatic gene expression changes in immature ovariectomized mice following exposure to ethynyl estradiol.

D R Boverhof1, K C Fertuck, L D Burgoon, J E Eckel, C Gennings, T R Zacharewski.   

Abstract

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.

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Year:  2004        PMID: 14976129     DOI: 10.1093/carcin/bgh114

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  9 in total

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Authors:  Y V Sun; D R Boverhof; L D Burgoon; M R Fielden; T R Zacharewski
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2.  Identification of a transcriptional fingerprint of estrogen exposure in rainbow trout liver.

Authors:  Abby D Benninghoff; David E Williams
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Journal:  Mol Endocrinol       Date:  2014-07-03

4.  DNA binding by estrogen receptor-alpha is essential for the transcriptional response to estrogen in the liver and the uterus.

Authors:  Dörthe L Ahlbory-Dieker; Brenda D Stride; Gabriele Leder; Jenny Schkoldow; Susanne Trölenberg; Henrik Seidel; Christiane Otto; Anette Sommer; Malcolm G Parker; Günther Schütz; Tim M Wintermantel
Journal:  Mol Endocrinol       Date:  2009-07-02

5.  Protocols for the assurance of microarray data quality and process control.

Authors:  L D Burgoon; J E Eckel-Passow; C Gennings; D R Boverhof; J W Burt; C J Fong; T R Zacharewski
Journal:  Nucleic Acids Res       Date:  2005-11-04       Impact factor: 16.971

6.  Proteomics Complementation of the Rat Uterotrophic Assay for Estrogenic Endocrine Disruptors: A Roadmap of Advancing High Resolution Mass Spectrometry-Based Shotgun Survey to Targeted Biomarker Quantifications.

Authors:  Laszlo Prokai; Fatima Rahlouni; Khadiza Zaman; Vien Nguyen; Katalin Prokai-Tatrai
Journal:  Int J Mol Sci       Date:  2021-02-08       Impact factor: 5.923

7.  Species-specific regulation of PXR/CAR/ER-target genes in the mouse and rat liver elicited by o, p'-DDT.

Authors:  Naoki Kiyosawa; Joshua C Kwekel; Lyle D Burgoon; Edward Dere; Kurt J Williams; Colleen Tashiro; Brock Chittim; Timothy R Zacharewski
Journal:  BMC Genomics       Date:  2008-10-16       Impact factor: 3.969

8.  Comparative temporal and dose-dependent morphological and transcriptional uterine effects elicited by tamoxifen and ethynylestradiol in immature, ovariectomized mice.

Authors:  Cora J Fong; Lyle D Burgoon; Kurt J Williams; Agnes L Forgacs; Timothy R Zacharewski
Journal:  BMC Genomics       Date:  2007-06-07       Impact factor: 3.969

9.  Estradiol and progesterone exhibit similar patterns of hepatic gene expression regulation in the bovine model.

Authors:  Carla A Piccinato; Guilherme J M Rosa; Alhaji U N'jai; Colin R Jefcoate; Milo C Wiltbank
Journal:  PLoS One       Date:  2013-09-17       Impact factor: 3.240

  9 in total

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