New potential selective estrogen receptor modulators in traditional Chinese medicine for treating menopausal syndrome

被引:0
作者
Song, Xintong [1 ]
Shen, Lan [1 ]
Contreras, Janine Micahella [2 ]
Liu, Zhiyuan [1 ]
Ma, Kai [1 ]
Ma, Biao [3 ]
Liu, Xiaoling [1 ]
Wang, Dan Ohtan [1 ,2 ]
机构
[1] Shenyang Pharmaceut Univ, Wuya Coll Innovat, Shenyang 110016, Peoples R China
[2] New York Univ Abu Dhabi, Biol Program, Abu Dhabi, U Arab Emirates
[3] RIKEN Ctr Computat Sci, Kobe, Japan
基金
中国国家自然科学基金;
关键词
estrogen receptor; menopausal syndrome; SERM; traditional Chinese medicine; women; HORMONE REPLACEMENT THERAPY; INVASIVE BREAST-CANCER; FACTOR-KAPPA-B; POSTMENOPAUSAL WOMEN; OVARIECTOMIZED RATS; GINSENOSIDE RG1; BONE LOSS; IN-VITRO; ANTIOSTEOPOROTIC ACTIVITY; GENITOURINARY SYNDROME;
D O I
10.1002/ptr.8289
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Women go through several predictable conditions and symptoms during menopause that are caused by age, changes in sex hormone levels, and other factors. Conventional menopause hormone therapy has raised serious concerns about the increased risks of cancers, blood clots, depression, etc. Selective estrogen receptor modulators (SERMs) that can be both agonists and antagonists of estrogen receptors in a tissue-specific manner are being developed to reduce the health concerns associated with menopause hormone therapy. Here, we have searched the Chinese national traditional Chinese medicine (TCM) patent database to identify potential SERM-like compounds with reduced health risks. TCM has been widely used for treating complex symptoms associated with menopause syndrome and thus can be a particularly rich source for pharmaceutical alternatives with SERM properties. After extensive literature review and molecular simulation, we conclude that protopanaxatriol, paeoniflorin, astragalin, catalpol, and hyperoside among others may be particularly promising as SERM-like compounds in treating the menopausal syndrome. Compounds in TCM hold promise in yielding comparable outcomes to hormone therapy but with reduced associated risks, thus presenting promising avenues for their clinical applications.
引用
收藏
页码:4736 / 4756
页数:21
相关论文
共 190 条
[41]   Raloxifene use in clinical practice: efficacy and safety [J].
Goldstein, Steven R. ;
Duvernoy, Claire S. ;
Calaf, Joaquim ;
Adachi, Jonathan D. ;
Mershon, John L. ;
Dowsett, Sherie A. ;
Agnusdei, Donato ;
Stuenkel, Cynthia A. .
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2009, 16 (02) :413-421
[42]   The role of estrogen receptor gene polymorphisms in menopausal symptoms and estradiol levels in perimenopausal women - Findings from the Swiss Perimenopause Study [J].
Grub, Jessica ;
Willi, Jasmine ;
Suss, Hannah ;
Ehlert, Ulrike .
MATURITAS, 2024, 183
[43]   Use of Network Pharmacology and Molecular Docking Technology to Analyze the Mechanism of Action of Velvet Antler in the Treatment of Postmenopausal Osteoporosis [J].
Guo, Kuiting ;
Wang, Tiancheng ;
Luo, Enjing ;
Leng, Xiangyang ;
Yao, Baojin .
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2021, 2021
[44]   Selective estrogen receptor modulators - A new age of estrogens in cardiovascular disease? [J].
Guzzo, JA .
CLINICAL CARDIOLOGY, 2000, 23 (01) :15-17
[45]   Effects of Resveratrol on Receptor Expression and Serum Levels of Estrogen and Progesterone in the Rat Endometritis Model [J].
Han, Sevtap ;
Cicek, Ali Fuat ;
Tokmak, Aytekin ;
Ustun, Tugce Yildirir ;
Gokay, Nilufer Ercan ;
Uludag, Mecit Orhan ;
Demirel, Murside Ayse .
REPRODUCTIVE SCIENCES, 2021, 28 (09) :2610-2622
[46]   Stereospecific lasofoxifene derivatives reveal the interplay between estrogen receptor alpha stability and antagonistic activity in ESR1 mutant breast cancer cells [J].
Hosfield, David J. ;
Weber, Sandra ;
Li, Nan-Sheng ;
Suavage, Madline ;
Joiner, Carstyn F. ;
Hancock, Govinda R. ;
Sullivan, Emily A. ;
Ndukwe, Estelle ;
Han, Ross ;
Cush, Sydney ;
Laine, Muriel ;
Mader, Sylvie C. ;
Greene, Geoffrey L. ;
Fanning, Sean W. .
ELIFE, 2022, 11
[47]  
Huang HL, 2015, INT J CLIN EXP MED, V8, P5103
[48]   Resveratrol Mitigates High-Fat Diet-Induced Vascular Dysfunction by Activating the Akt/eNOS/NO and Sirt1/ER Pathway [J].
Huang, Jiung-Pang ;
Hsu, Sheng-Chieh ;
Li, Dai-Er ;
Chen, Kuan-Hsing ;
Kuo, Chao-Yu ;
Hung, Li-Man .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2018, 72 (05) :231-241
[49]   Emodin and Aloe-Emodin Suppress Breast Cancer Cell Proliferation through ERα Inhibition [J].
Huang, Pao-Hsuan ;
Huang, Chih-Yang ;
Chen, Mei-Chih ;
Lee, Yueh-Tsung ;
Yue, Chia-Herng ;
Wang, Hsin-Yi ;
Lin, Ho .
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2013, 2013
[50]   Factors associated with endometrial pathology during tamoxifen therapy in women with breast cancer: a retrospective analysis of 821 biopsies [J].
Jeon, Jungeun ;
Kim, Sung Eun ;
Lee, Dong-Yun ;
Choi, DooSeok .
BREAST CANCER RESEARCH AND TREATMENT, 2020, 179 (01) :125-130