Selective Estrogen Receptor Modulation by Larrea nitida on MCF-7 Cell Proliferation and Immature Rat Uterus.
- Author:
Hye Na AHN
1
;
Si Yeon JEONG
;
Gyu Un BAE
;
Minsun CHANG
;
Dongwei ZHANG
;
Xiyuan LIU
;
Yihua PEI
;
Young Won CHIN
;
Joongku LEE
;
Sei Ryang OH
;
Yun Seon SONG
Author Information
1. College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Republic of Korea. yssong@sookmyung.ac.kr
- Publication Type:Original Article
- Keywords:
Larrea nitida;
Lignan;
Phytoestrogen;
Estrogen receptor;
MCF-7 cell;
Uterus
- MeSH:
Animals;
Breast Neoplasms;
Chromatography;
Dysmenorrhea;
Estrogens*;
Female;
Genes, Reporter;
Humans;
Inhibitory Concentration 50;
Larrea*;
MCF-7 Cells*;
Menopause;
Phytoestrogens;
Plants;
Rats*;
Receptors, Progesterone;
Response Elements;
Selective Estrogen Receptor Modulators;
Solvents;
South America;
Uterus*;
Zygophyllaceae
- From:Biomolecules & Therapeutics
2014;22(4):347-354
- CountryRepublic of Korea
- Language:English
-
Abstract:
Larrea nitida is a plant that belongs to the Zygophyllaceae family and is widely used in South America to treat inflammatory diseases, tumors and menstrual pain. However, its pharmacological activity remains unclear. In this study we evaluated the property of selective estrogen receptor modulator (SERM) of Larrea nitida extracts (LNE) as a phytoestrogen that can mimic, modulate or disrupt the actions of endogenous estrogens, depending on the tissue and relative amount of other SERMs. To investigate the property of SERM of LNE, we performed MCF-7 cell proliferation assays, estrogen response element (ERE)-luciferase reporter gene assay, human estrogen receptor (hER) binding assays and in vivo uterotrophic assay. To gain insight into the active principles, we performed a bioassay-guided analysis of LNE employing solvents of various polarities and using classical column chromatography, which yielded 16 fractions (LNs). LNE showed high binding affinities for hERalpha and hERbeta with IC50 values of 1.20x10(-7) g/ml and 1.00x10(-7) g/ml, respectively. LNE induced 17beta-estradiol (E2)-induced MCF-7 cell proliferation, however, it reduced the proliferation in the presence of E2. Furthermore, LNE had an atrophic effect in the uterus of immature rats through reducing the expression level of progesterone receptor (PR) proteins. LN08 and LN10 had more potent affinities for binding on hER alpha and beta than other fractions. Our results indicate that LNE had higher binding affinities for hERbeta than hERalpha, and showed SERM properties in MCF-7 breast cancer cells and the rat uterus. LNE may be useful for the treatment of estrogen-related conditions, such as female cancers and menopause.
