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Article . 2009
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Breast Cancer Research and Treatment
Article . 2009 . Peer-reviewed
License: Springer TDM
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SOX9 mediates the retinoic acid-induced HES-1 gene expression in human breast cancer cells

Authors: Müller, Patrick; Crofts, Justin D.; Newman, Ben S.; Bridgewater, Laura C.; Lin, Chin-Yo; Gustafsson, Jan-Åke; Ström, Anders;

SOX9 mediates the retinoic acid-induced HES-1 gene expression in human breast cancer cells

Abstract

We have previously shown that the anti-proliferative effect of retinoic acid in human breast cancer cell line MCF-7 is dependent on HES-1 expression. Here we show that retinoic acid induces HES-1 expression via upregulation of transcription factor SOX9. By expressing a dominant negative form of SOX9, disrupting endogenous SOX9 activity, the retinoic acid-induced HES-1 mRNA expression was inhibited. We found an enhancer regulating HES-1 expression: two SOX9 binding sites upstream of the HES-1 gene that were capable of binding SOX9 in vitro. By performing chromatin immunoprecipitation, we showed that SOX9 binding to the HES-1 enhancer was induced by retinoic acid in vivo. In reporter assays, transfection of a SOX9 expression plasmid increased the activity of the HES-1 enhancer. The enhancer responded to retinoic acid; furthermore, the expression of a dominant negative SOX9 abolished this response. Taken together, we present here a novel transcriptional mechanism in regulating hormone-dependent cancer cell proliferation.

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Keywords

Homeodomain Proteins, Reverse Transcriptase Polymerase Chain Reaction, Proliferation, Blotting, Western, Antineoplastic Agents, Breast Neoplasms, Electrophoretic Mobility Shift Assay, SOX9 Transcription Factor, Tretinoin, Transfection, Gene Expression Regulation, Neoplastic, Enhancer Elements, Genetic, atRA, HES-1, Cell Line, Tumor, Basic Helix-Loop-Helix Transcription Factors, Humans, Immunoprecipitation, Transcription Factor HES-1, Female, RNA, Messenger, SOX9

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    popularity
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    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
42
Top 10%
Top 10%
Top 10%
Green
Related to Research communities
Cancer Research