Literature DB >> 15686872

Gene expression changes related to growth and differentiation in the fetal and juvenile reproductive system of the female rat: evaluation of microarray results.

George P Daston1, Jorge M Naciff.   

Abstract

Microarrays make it possible to evaluate the responses of a major fraction of the genome in response to physiological perturbation or exogenous insult. This represents a huge advance in our ability to detect changes in gene expression that may be responsible for physiological or toxicological responses. Our laboratory is interested in the effects of estrogens on female reproductive system development and function. We have evaluated the changes in gene expression in response to estrogens in the female reproductive tract of rats during embryo/fetal development and in the juvenile rat (which is capable of mounting a uterotrophic response). The results of these experiments indicate that a number of genes (dozens to hundreds) are changed in a reproducible, dose-related manner in response to estrogens. These results have been published elsewhere; the purpose of this review is to evaluate, based on information from the literature, the potential role of selected genes on processes of cell proliferation and differentiation, and to suggest plausible relationships among these genes in eliciting responses at the tissue or organ level. We also discuss the utility of gene-expression experiments in elucidating the shape of the dose-response curve at low doses. In particular, we show that the dose-response for gene expression in the juvenile rat uterus is monotonic down to levels a few orders of magnitude below the NOEL for a uterotrophic response, suggesting that gene expression (and by inference higher order responses) do not follow patterns that are unpredictable based on response at higher dosages.

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Year:  2005        PMID: 15686872     DOI: 10.1016/j.reprotox.2004.09.004

Source DB:  PubMed          Journal:  Reprod Toxicol        ISSN: 0890-6238            Impact factor:   3.143


  5 in total

1.  Metabolomics in the assessment of chemical-induced reproductive and developmental outcomes using non-invasive biological fluids: application to the study of butylbenzyl phthalate.

Authors:  Susan Sumner; Rodney Snyder; Jason Burgess; Christina Myers; Rochelle Tyl; Carol Sloan; Timothy Fennell
Journal:  J Appl Toxicol       Date:  2009-11       Impact factor: 3.446

Review 2.  Application of ecotoxicogenomics for studying endocrine disruption in vertebrates and invertebrates.

Authors:  Taisen Iguchi; Hajime Watanabe; Yoshinao Katsu
Journal:  Environ Health Perspect       Date:  2006-04       Impact factor: 9.031

3.  Systemic compensatory response to neonatal estradiol exposure does not prevent depletion of the oocyte pool in the rat.

Authors:  Clémentine Chalmey; Frank Giton; Franck Giton; Frédéric Chalmel; Jean Fiet; Bernard Jégou; Séverine Mazaud-Guittot
Journal:  PLoS One       Date:  2013-12-16       Impact factor: 3.240

4.  Uterine and placental expression of TRPV6 gene is regulated via progesterone receptor- or estrogen receptor-mediated pathways during pregnancy in rodents.

Authors:  Bo-Mi Lee; Geun-Shik Lee; Eui-Man Jung; Kyung-Chul Choi; Eui-Bae Jeung
Journal:  Reprod Biol Endocrinol       Date:  2009-05-21       Impact factor: 5.211

5.  The estrogenicity of methylparaben and ethylparaben at doses close to the acceptable daily intake in immature Sprague-Dawley rats.

Authors:  Libei Sun; Tong Yu; Jilong Guo; Zhaobin Zhang; Ying Hu; Xuan Xiao; Yingli Sun; Han Xiao; Junyu Li; Desheng Zhu; Linlin Sai; Jun Li
Journal:  Sci Rep       Date:  2016-04-28       Impact factor: 4.379

  5 in total

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