Literature DB >> 1968749

Multidrug resistance gene expression is controlled by steroid hormones in the secretory epithelium of the uterus.

R J Arceci1, F Baas, R Raponi, S B Horwitz, D Housman, J M Croop.   

Abstract

The multidrug resistance (mdr) gene family has been shown to encode a membrane glycoprotein, termed the P-glycoprotein, which functions as a drug efflux pump with broad substrate specificity. This multigene family is expressed in a tissue-specific fashion in a wide variety of normal and neoplastic tissues. The regulation of mdr gene expression in normal tissues is not understood. We have recently shown that mdr mRNA and the P-glycoprotein increases dramatically in the secretory luminal and glandular epithelium of the gravid murine uterus. This observation has suggested that mdr gene expression in the uterus is controlled by the physiologic changes associated with pregnancy. This report now demonstrates that mdr mRNA and P-glycoprotein are induced at high levels in the uterine secretory epithelium by the combination of estrogen and progesterone, the major steroid hormones of pregnancy. This regulation of mdr gene expression in the uterus does not require any other contribution from the fetus or placenta. The data indicate that this gene locus is hormonally responsive to estrogen and progesterone in the uterine secretory epithelium, suggesting an important and physiologically regulated role during pregnancy.

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Year:  1990        PMID: 1968749     DOI: 10.1002/mrd.1080250202

Source DB:  PubMed          Journal:  Mol Reprod Dev        ISSN: 1040-452X            Impact factor:   2.609


  22 in total

1.  The E23 early gene of Drosophila encodes an ecdysone-inducible ATP-binding cassette transporter capable of repressing ecdysone-mediated gene activation.

Authors:  T Hock; T Cottrill; J Keegan; D Garza
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-15       Impact factor: 11.205

2.  Cell-specific activity of cis-acting regulatory elements in the promoter of the mouse multidrug resistance gene mdr1.

Authors:  M Raymond; P Gros
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

3.  P-glycoprotein structure and evolutionary homologies.

Authors:  I Bosch; J M Croop
Journal:  Cytotechnology       Date:  1998-09       Impact factor: 2.058

4.  Functional analysis of chimeric genes obtained by exchanging homologous domains of the mouse mdr1 and mdr2 genes.

Authors:  E Buschman; P Gros
Journal:  Mol Cell Biol       Date:  1991-02       Impact factor: 4.272

Review 5.  The biology of the P-glycoproteins.

Authors:  C R Leveille-Webster; I M Arias
Journal:  J Membr Biol       Date:  1995-01       Impact factor: 1.843

Review 6.  P-glycoprotein structure and evolutionary homologies.

Authors:  J M Croop
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

7.  Effect of mdr1a P-glycoprotein gene disruption, gender, and substrate concentration on brain uptake of selected compounds.

Authors:  C Dagenais; J Zong; J Ducharme; G M Pollack
Journal:  Pharm Res       Date:  2001-07       Impact factor: 4.200

Review 8.  P-glycoprotein, multidrug resistance and tumor progression.

Authors:  G Bradley; V Ling
Journal:  Cancer Metastasis Rev       Date:  1994-06       Impact factor: 9.264

9.  Changes in the placental glucocorticoid barrier during rat pregnancy: impact on placental corticosterone levels and regulation by progesterone.

Authors:  Peter J Mark; Sheldon Augustus; Jessica L Lewis; Damien P Hewitt; Brendan J Waddell
Journal:  Biol Reprod       Date:  2009-02-04       Impact factor: 4.285

10.  Stage-specific distribution of P-glycoprotein in first-trimester and full-term human placenta.

Authors:  A MacFarland; D R Abramovich; S W Ewen; C K Pearson
Journal:  Histochem J       Date:  1994-05
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