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<datestamp>2017-12-21</datestamp>
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<title lang=en>Glyceollins trigger anti-proliferative effects through estradiol-dependent and independent pathways in breast cancer cells</title>
<creator>Lecomte, Sylvain</creator>
<creator>Chalmel, Frédéric</creator>
<creator>Ferrière, François</creator>
<creator>Percevault, Frédéric</creator>
<creator>Plu, Nicolas</creator>
<creator>Saligaut, Christian</creator>
<creator>Surel, Claire</creator>
<creator>Lelong, Marie</creator>
<creator>Efstathiou, Théo</creator>
<creator>Pakdel, Farzad</creator>
<contributor>Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )</contributor>
<contributor>Analyses et Recherche ; Nutrinov</contributor>
<contributor>This work was funded by FUI mVolio, Région Bretagne and Rennes Métropole.</contributor>
<description>International audience</description>
<source>ISSN: 1478-811X</source>
<source>Cell Communication and Signaling</source>
<publisher>BioMed Central</publisher>
<identifier>hal-01560288</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01560288</identifier>
<source>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01560288</source>
<source>Cell Communication and Signaling, BioMed Central, 2017, 15, pp.26. 〈10.1186/s12964-017-0182-1〉</source>
<identifier>DOI : 10.1186/s12964-017-0182-1</identifier>
<relation>info:eu-repo/semantics/altIdentifier/doi/10.1186/s12964-017-0182-1</relation>
<identifier>PUBMED : 28666461</identifier>
<relation>info:eu-repo/semantics/altIdentifier/pmid/28666461</relation>
<language>en</language>
<subject lang=en>Breast Cancer</subject>
<subject lang=en> Cell Proliferation</subject>
<subject lang=en> Estrogen receptors</subject>
<subject lang=en> Gene Expression</subject>
<subject lang=en> Glyceollins</subject>
<subject lang=en> Transcriptomic</subject>
<subject>[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie</subject>
<type>info:eu-repo/semantics/article</type>
<type>Journal articles</type>
<description lang=en>BACKGROUND: Estrogen receptors (ER) α and β are found in both women and men in many tissues, where they have different functions, including having roles in cell proliferation and differentiation of the reproductive tract. In addition to estradiol (E2), a natural hormone, numerous compounds are able to bind ERs and modulate their activities. Among these compounds, phytoestrogens such as isoflavones, which are found in plants, are promising therapeutics for several pathologies. Glyceollins are second metabolites of isoflavones that are mainly produced in soybean in response to an elicitor. They have potentially therapeutic actions in breast cancer by reducing the proliferation of cancer cells. However, the molecular mechanisms driving these effects remain elusive. METHODS: First, to determine the proliferative or anti-proliferative effects of glyceollins, in vivo and in vitro approaches were used. The length of epithelial duct in mammary gland as well as uterotrophy after treatment by E2 and glyceollins and their effect on proliferation of different breast cell line were assessed. Secondly, the ability of glyceollin to activate ER was assessed by luciferase assay. Finally, to unravel molecular mechanisms involved by glyceollins, transcriptomic analysis was performed on MCF-7 breast cancer cells. RESULTS: In this study, we show that synthetic versions of glyceollin I and II exert anti-proliferative effects in vivo in mouse mammary glands and in vitro in different ER-positive and ER-negative breast cell lines. Using transcriptomic analysis, we produce for the first time an integrated view of gene regulation in response to glyceollins and reveal that these phytochemicals act through at least two major pathways. One pathway involving FOXM1 and ERα is directly linked to proliferation. The other involves the HIF family and reveals that stress is a potential factor in the anti-proliferative effects of glyceollins due to its role in increasing the expression of REDD1, an mTORC1 inhibitor. CONCLUSION: Overall, our study clearly shows that glyceollins exert anti-proliferative effects by reducing the expression of genes encoding cell cycle and mitosis-associated factors and biomarkers overexpressed in cancers and by increasing the expression of growth arrest-related genes. These results reinforce the therapeutic potential of glyceollins for breast cancer.</description>
<date>2017</date>
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