Evidence map›Paper›PMID 23892277›Full record

ArticleJournal of molecular endocrinology2013

Estradiol and tamoxifen regulate NRF-1 and mitochondrial function in mouse mammary gland and uterus.

Margarita M Ivanova, Brandie N Radde, Jieun Son, Fabiola F Mehta, Sang-Hyuk Chung, Carolyn M Klinge

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Postnatal maternal care impacts hypothalamicbioRxiv : the preprint server for biology · 2025
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  4. Review
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  6. Review
  7. Article
  8. Mitochondrial Quality Control in Age-Related Pulmonary Fibrosis.International journal of molecular sciences · 2020
    Review
  9. Article
  10. Article
  11. Estrogens regulate life and death in mitochondria.Journal of bioenergetics and biomembranes · 2017
    Review
  12. Article
  13. Article
  14. Age, APOE and sex: Triad of risk of Alzheimer's disease.The Journal of steroid biochemistry and molecular biology · 2016
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Margarita M IvanovaDepartment of Biochemistry and Molecular Biology, Center for Genetics and Molecular Medicine, University of Louisville School of Medicine, Louisville, Kentucky 40292, USA Department of Biology and Biochemistry, Center for Nuclear Receptors and Cell Signaling, University of Houston, 3605 Cullen Blvd, Houston, Texas 77204, USA.
Brandie N Radde
Jieun Son
Fabiola F Mehta
Sang-Hyuk Chung
Carolyn M Klinge
University of Louisville Hospital · USUniversity of Houston · US

Funding

DNA SEQUENCES IMPACT ESTROGEN AND ANTIESTROGEN ACTIVITYR01DK053220 · NIDDK · UNIVERSITY OF LOUISVILLE · PI KLINGE, CAROLYN M. · 1998 to 2011
$2.8M
NIDDK NIH HHS R01 DK053220
6 · The paper itself

Abstract

Nuclear respiratory factor-1 (NRF-1) stimulates the transcription of nuclear-encoded genes that regulate mitochondrial (mt) genome transcription and biogenesis. We reported that estradiol (E2) and 4-hydroxytamoxifen (4-OHT) stimulate NRF-1 transcription in an estrogen receptor α (ERα)- and ERβ-dependent manner in human breast cancer cells. The aim of this study was to determine whether E2 and 4-OHT increase NRF-1 in vivo. Here, we report that E2 and 4-OHT increase NRF-1 expression in mammary gland (MG) and uterus of ovariectomized C57BL/6 mice in a time-dependent manner. E2 increased NRF-1 protein in the uterus and MG; however, in MG, 4-OHT increased Nrf1 mRNA but not protein. Chromatin immunoprecipitation assays revealed increased in vivo recruitment of ERα to the Nrf1 promoter and intron 3 in MG and uterus 6 h after E2 and 4-OHT treatment, commensurate with increased NRF-1 expression. E2- and 4-OHT-induced increases in NRF-1 and its target genes Tfam, Tfb1m, and Tfb2m were coordinated in MG but not in uterus due to uterine-selective inhibition of the expression of the NRF-1 coactivators Ppargc1a and Ppargc1b by E2 and 4-OHT. E2 transiently increased NRF-1 and PGC-1α nuclear staining while reducing PGC-1α in uterus. E2, not 4-OHT, activates mt biogenesis in MG and uterus in a time-dependent manner. E2 increased mt outer membrane Tomm40 protein levels in MG and uterus whereas 4-OHT increased Tomm40 only in uterus. These data support the hypothesis of tissue-selective regulation of NRF-1 and its downstream targets by E2 and 4-OHT in vivo.

Indexed as

AnimalsDNA-Binding ProteinsElectron Transport Complex IVEstradiolEstrogen Receptor alphaFemaleGene Expression RegulationHigh Mobility Group ProteinsMammary Glands, AnimalMembrane Transport ProteinsMiceMitochondriaNuclear Respiratory Factor 1Organ SpecificityPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPromoter Regions, GeneticDNA-Binding ProteinsElectron Transport Complex IVEstradiolEstrogen Receptor alphaHigh Mobility Group ProteinsMembrane Transport ProteinsNuclear Respiratory Factor 1Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseTamoxifenTfam protein, mouseTranscription Factorsestrogen receptormitochondriamousenuclear respiratory factor-1

Identifiers

PMID23892277
PMCPMC3772954
OpenAlexW2128772105

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.