Literature DB >> 10652244

High concentrations of bisphenol A induce cell growth and prolactin secretion in an estrogen-responsive pituitary tumor cell line.

T Y Chun1, J Gorski.   

Abstract

PR1 cells are a prolactin (PRL)-secreting cell line derived from pituitary lactotroph tumors found in 17beta-estradiol (E(2))-treated female Fischer 344 rats. Recently, we reported that as little as 0. 01 pM E(2) could induce half-maximal cell proliferation, whereas the antiestrogen ICI 182,780 (ICI) inhibited proliferation. Interestingly, the cell proliferation response is 1000-fold more sensitive to E(2) than the PRL response (induction of prolactin protein synthesis), suggesting that there is a distinction between cell proliferation and the PRL response in PR1 cells. Bisphenol A (BPA) is a monomer of plastics and epoxy resins that is widely used in dentistry and the food packaging industry. Although it has low estrogenic activity in somatolactotrophs and breast cancer cell lines, its presence in the environment and its long biological half-life have raised concerns about potential effects in humans. We analyzed the effect of BPA and compared its activity with E(2) in the PR1 cell line. PR1 cells show half-maximal proliferation upon treatment with 10 nM BPA, which is 10,000- to 100,000-fold less active than E(2). BPA-induced PR1 cell proliferation is decreased by the pure antiestrogen ICI, suggesting that BPA-induced PR1 cell proliferation is mediated by the estrogen receptor (ER). The decreased affinity of BPA for the ER is illustrated by the fact that 1 nM of ICI inhibited 100 nM BPA-induced cell proliferation, whereas 100 nM ICI was required to block 1 nM E(2)-induced cell proliferation. The PRL response to BPA required 1000 nM BPA to match the PRL secretion induced by 0.01 nM E(2). A competitive binding assay showed that the K(i) of BPA for the ER in PR1 cells is approximately 30-60 nM, which is 1000- to 2000-fold lower than that of E(2). Our study suggests the PR1 cell line can be used as an in vitro assay system for analyzing the effects of weak estrogens on ER-mediated responses and the activities of various estrogenic compounds present in small amounts in the environment. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10652244     DOI: 10.1006/taap.1999.8840

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  7 in total

1.  Prenatal exposure to low doses of bisphenol A increases pituitary proliferation and gonadotroph number in female mice offspring at birth.

Authors:  Katherine E Brannick; Zelieann R Craig; Ashley D Himes; Jackye R Peretz; Wei Wang; Jodi A Flaws; Lori T Raetzman
Journal:  Biol Reprod       Date:  2012-10-11       Impact factor: 4.285

Review 2.  Estrogenic Endocrine Disrupting Chemicals Influencing NRF1 Regulated Gene Networks in the Development of Complex Human Brain Diseases.

Authors:  Mark Preciados; Changwon Yoo; Deodutta Roy
Journal:  Int J Mol Sci       Date:  2016-12-13       Impact factor: 5.923

3.  Effect of bisphenol a on occurrence and progression of prolactinoma and its underlying mechanisms.

Authors:  Lanxiang Hao; Jing Zhang; Yonghong Zhang; Haitao Hu; Weiwei Shao; Xiaochen Zhang; Chunmei Geng; Yanyan Wang; Ling Jiang
Journal:  Am J Transl Res       Date:  2016-10-15       Impact factor: 4.060

Review 4.  Endocrine disruption via estrogen receptors that participate in nongenomic signaling pathways.

Authors:  Cheryl S Watson; Yow-Jiun Jeng; Jutatip Guptarak
Journal:  J Steroid Biochem Mol Biol       Date:  2011-02-12       Impact factor: 4.292

Review 5.  Endocrine disrupting chemicals: effects on pituitary, thyroid and adrenal glands.

Authors:  Filippo Egalini; Lorenzo Marinelli; Mattia Rossi; Giovanna Motta; Nunzia Prencipe; Ruth Rossetto Giaccherino; Loredana Pagano; Silvia Grottoli; Roberta Giordano
Journal:  Endocrine       Date:  2022-05-23       Impact factor: 3.925

6.  Perinatal exposure to low doses of bisphenol A affects body weight, patterns of estrous cyclicity, and plasma LH levels.

Authors:  B S Rubin; M K Murray; D A Damassa; J C King; A M Soto
Journal:  Environ Health Perspect       Date:  2001-07       Impact factor: 9.031

7.  Alkylphenol xenoestrogens with varying carbon chain lengths differentially and potently activate signaling and functional responses in GH3/B6/F10 somatomammotropes.

Authors:  Mikhail Y Kochukov; Yow-Jiun Jeng; Cheryl S Watson
Journal:  Environ Health Perspect       Date:  2008-12-31       Impact factor: 9.031

  7 in total

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