Natural Products as Farnesoid X Receptor (FXR) Agonists: Their Interactions with FXR Ligand Binding Region

被引:0
|
作者
Lin, Hsiang-Ru [1 ]
机构
[1] Natl Kaohsiung Normal Univ, Coll Sci, Dept Chem, Kaohsiung 82446, Taiwan
关键词
Farnesoid X receptor (FXR); FXR ligand binding region; liver; NAFLD; nuclear receptors; natural product; NUCLEAR RECEPTOR; NONALCOHOLIC STEATOHEPATITIS; CRYPTOCARYA-CHINENSIS; METABOLISM; ACTIVATION; IDENTIFICATION; TRITERPENES; EXPRESSION; ACT;
D O I
10.2174/1570193X13666160401000445
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Nuclear receptors (NRs) are ligand-activated transcription factors modulating significant biological functions including cell growth, lipid metabolism, and glucose homeostasis, so they are frequently to be utilized as important drug targets to develop therapeutic reagents. Farnesoid X receptor (FXR) with bile acids as the natural ligands, plays an essential role in regulation of bile acid and glucose metabolism, and is involved in the pathologies of human diseases including diabetes and chronic liver diseases. Thus, FXR is a promising pharmacological target for these diseases. Synthetic FXR agonists like INT-747 developed by Intercept Pharmaceutical Company is in the clinical trial phase III for non-alcoholic steatohepatitis and can be approved as the treatment of primary biliary cirrhosis in 2016. Due to the promising clinical trial results of INT-747, the naturally occurring FXR ligands may be utilized as the preventive nutraceuticals or treatments of the chronic liver diseases and diabetes. In this review, the natural FXR agonists are summarized and their possible interactions with FXR ligand binding region are discussed.
引用
收藏
页码:97 / 108
页数:12
相关论文
共 50 条
  • [1] Design, synthesis and biological evaluations of novel farnesoid X receptor (FXR) agonists
    Zhu, Yuanju
    Zhang, Jay
    Min, Feng
    Yang, Xinying
    Li, Li
    Zhang, Yan
    Hou, Xuben
    Fang, Hao
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2022, 76
  • [2] Conformationally constrained farnesoid X receptor (FXR) agonists: Alternative replacements of the stilbene
    Akwabi-Ameyaw, Adwoa
    Caravella, Justin A.
    Chen, Lihong
    Creech, Katrina L.
    Deaton, David N.
    Madauss, Kevin P.
    Marr, Harry B.
    Miller, Aaron B.
    Navas, Frank, III
    Parks, Derek J.
    Spearing, Paul K.
    Todd, Dan
    Williams, Shawn P.
    Wisely, Bruce
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (20) : 6154 - 6160
  • [3] Conformationally constrained farnesoid X receptor (FXR) agonists: Heteroaryl replacements of the naphthalene
    Bass, Jonathan Y.
    Caravella, Justin A.
    Chen, Lihong
    Creech, Katrina L.
    Deaton, David N.
    Madauss, Kevin P.
    Marr, Harry B.
    McFadyen, Robert B.
    Miller, Aaron B.
    Mills, Wendy Y.
    Navas, Frank, III
    Parks, Derek J.
    Smalley, Terrence L., Jr.
    Spearing, Paul K.
    Todd, Dan
    Williams, Shawn P.
    Wisely, G. Bruce
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (04) : 1206 - 1213
  • [4] Farnesoid X receptor (FXR): Structures and ligands
    Jiang, Longying
    Zhang, Huajun
    Xiao, Desheng
    Wei, Hudie
    Chen, Yongheng
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2021, 19 : 2148 - 2159
  • [5] SUMOylation of the Farnesoid X Receptor (FXR) Regulates the Expression of FXR Target Genes
    Balasubramaniyan, Natarajan
    Luo, Yuhuan
    Sun, An-Qiang
    Suchy, Frederick J.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (19) : 13850 - 13862
  • [6] Farnesoid X receptor (FXR) agonists induce hepatocellular apoptosis and impair hepatic functions via FXR/SHP pathway
    Tianwei Zhang
    Shanshan Feng
    Jiahuan Li
    Zhitao Wu
    Qiangqiang Deng
    Wei Yang
    Jing Li
    Guoyu Pan
    Archives of Toxicology, 2022, 96 : 1829 - 1843
  • [7] Farnesoid X receptor (FXR) agonists induce hepatocellular apoptosis and impair hepatic functions via FXR/SHP pathway
    Zhang, Tianwei
    Feng, Shanshan
    Li, Jiahuan
    Wu, Zhitao
    Deng, Qiangqiang
    Yang, Wei
    Li, Jing
    Pan, Guoyu
    ARCHIVES OF TOXICOLOGY, 2022, 96 (06) : 1829 - 1843
  • [8] Ligand binding and heterodimerization with retinoid X receptor α (RXRα) induce farnesoid X receptor (FXR) conformational changes affecting coactivator binding
    Wang, Na
    Zou, Qingan
    Xu, Jinxin
    Zhang, Jiancun
    Liu, Jinsong
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (47) : 18180 - 18191
  • [9] Farnesoid X Receptor (FXR) Activation and FXR Genetic Variation in Inflammatory Bowel Disease
    Nijmeijer, Rian M.
    Gadaleta, Raffaella M.
    van Mil, Saskia W. C.
    van Bodegraven, Adriaan A.
    Crusius, J. Bart A.
    Dijkstra, Gerard
    Hommes, Daan W.
    de Jong, Dirk J.
    Stokkers, Pieter C. F.
    Verspaget, Hein W.
    Weersma, Rinse K.
    van der Woude, C. Janneke
    Stapelbroek, Janneke M.
    Schipper, Marguerite E. I.
    Wijmenga, Cisca
    van Erpecum, Karel J.
    Oldenburg, Bas
    PLOS ONE, 2011, 6 (08):
  • [10] Ligand-binding domain of farnesoid X receptor (FXR) had the highest sensitivity and activity among FXR variants in a fluorescence-based assay
    Cho, KH
    Park, JY
    Han, JI
    Jeong, TS
    LIPIDS, 2003, 38 (11) : 1149 - 1156