Phytochemicals Targeting Estrogen Receptors: Beneficial Rather Than Adverse Effects?

被引:123
作者
Lecomte, Sylvain [1 ]
Demay, Florence [1 ]
Ferriere, Francois [1 ]
Pakdel, Farzad [1 ]
机构
[1] Univ Rennes 1, UMR 1085, INSERM, IRSET,TREC Team, F-35000 Rennes, France
关键词
estrogen receptor; ligand; xenoestrogens; selective estrogen receptor modulators; transcription; epigenetic regulation; cell signaling; cancer; BREAST-CANCER CELLS; TUMOR-SUPPRESSOR GENE; PROSTATE-CANCER; SOY ISOFLAVONES; DIETARY FLAVONOIDS; MCF-7; CELLS; IN-VITRO; NEONATAL EXPOSURE; BETA EXPRESSION; KAPPA-B;
D O I
10.3390/ijms18071381
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammals, the effects of estrogen are mainly mediated by two different estrogen receptors, ER alpha and ER beta. These proteins are members of the nuclear receptor family, characterized by distinct structural and functional domains, and participate in the regulation of different biological processes, including cell growth, survival and differentiation. The two estrogen receptor (ER) subtypes are generated from two distinct genes and have partially distinct expression patterns. Their activities are modulated differently by a range of natural and synthetic ligands. Some of these ligands show agonistic or antagonistic effects depending on ER subtype and are described as selective ER modulators (SERMs). Accordingly, a few phytochemicals, called phytoestrogens, which are synthesized from plants and vegetables, show low estrogenic activity or anti-estrogenic activity with potentially anti-proliferative effects that offer nutraceutical or pharmacological advantages. These compounds may be used as hormonal substitutes or as complements in breast cancer treatments. In this review, we discuss and summarize the in vitro and in vivo effects of certain phytoestrogens and their potential roles in the interaction with estrogen receptors.
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页数:19
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