Literature DB >> 25500870

Identification of estrogen-responsive genes based on the DNA binding properties of estrogen receptors using high-throughput sequencing technology.

Kazuhiro Ikeda1, Kuniko Horie-Inoue1, Satoshi Inoue2.   

Abstract

Estrogens are important endocrine hormones that control physiological functions in reproductive organs, and play a pivotal role in the generation and progression of breast cancer. Therapeutic drugs including anti-estrogen and aromatase inhibitors are used to treat patients with breast cancer. The estrogen receptors, ERα and ERβ, function as hormone-dependent transcription factors that directly regulate the expression of their target genes. Therefore, a better understanding of the function and regulation of estrogen-responsive genes provides insight into the gene regulation network associated with breast cancer. Recent technological developments in high-throughput sequencing have enabled the genome-wide identification of estrogen-responsive genes. Further elucidating the estrogen gene cascade is critical for advancements in the diagnosis and treatment of breast cancer.

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Year:  2014        PMID: 25500870      PMCID: PMC4571320          DOI: 10.1038/aps.2014.123

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  82 in total

1.  Genome-wide analysis of estrogen receptor binding sites.

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Journal:  Nat Genet       Date:  2006-10-01       Impact factor: 38.330

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3.  Regulation of vascular endothelial growth factor (VEGF) gene transcription by estrogen receptors alpha and beta.

Authors:  M D Mueller; J L Vigne; A Minchenko; D I Lebovic; D C Leitman; R N Taylor
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

4.  An upstream region of the rat luteinizing hormone beta gene binds estrogen receptor and confers estrogen responsiveness.

Authors:  M A Shupnik; C M Weinmann; A C Notides; W W Chin
Journal:  J Biol Chem       Date:  1989-01-05       Impact factor: 5.157

5.  Estrogen-responsive element of the human pS2 gene is an imperfectly palindromic sequence.

Authors:  M Berry; A M Nunez; P Chambon
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

6.  Repression of estrogen-dependent stimulation of the oxytocin gene by chicken ovalbumin upstream promoter transcription factor I.

Authors:  J P Burbach; S Lopes da Silva; J J Cox; R A Adan; A J Cooney; M J Tsai; S Y Tsai
Journal:  J Biol Chem       Date:  1994-05-27       Impact factor: 5.157

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8.  Identification of an estrogen response element in the 3'-flanking region of the murine c-fos protooncogene.

Authors:  S M Hyder; G M Stancel; Z Nawaz; D P McDonnell; D S Loose-Mitchell
Journal:  J Biol Chem       Date:  1992-09-05       Impact factor: 5.157

Review 9.  The steroid and thyroid hormone receptor superfamily.

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10.  GATA3 acts upstream of FOXA1 in mediating ESR1 binding by shaping enhancer accessibility.

Authors:  Vasiliki Theodorou; Rory Stark; Suraj Menon; Jason S Carroll
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  28 in total

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2.  Family reunion of nuclear hormone receptors: structures, diseases, and drug discovery.

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Journal:  Acta Pharmacol Sin       Date:  2015-01       Impact factor: 6.150

3.  Transcript profiling in the testes and prostates of postnatal day 30 Sprague-Dawley rats exposed prenatally and lactationally to 2-hydroxy-4-methoxybenzophenone.

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5.  The E3 ligase COP1 promotes ERα signaling and suppresses EMT in breast cancer.

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Review 6.  Drug Repurposing by Tumor Tissue Editing.

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7.  Extracellular Matrix-Bound FGF2 Mediates Estrogen Receptor Signaling and Therapeutic Response in Breast Cancer.

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8.  miR-378a-3p modulates tamoxifen sensitivity in breast cancer MCF-7 cells through targeting GOLT1A.

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Review 9.  The UDP-glucose ceramide glycosyltransferase (UGCG) and the link to multidrug resistance protein 1 (MDR1).

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10.  Integrated bioinformatics analysis reveals key candidate genes and pathways in breast cancer.

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Journal:  Mol Med Rep       Date:  2018-04-19       Impact factor: 2.952

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