Results 1 to 10 of about 40,710 (290)

SIRT1 activation synergizes with FXR agonism in hepatoprotection via governing nucleocytoplasmic shuttling and degradation of FXR

open access: yesActa Pharmaceutica Sinica B, 2023
Farnesoid X receptor (FXR) is widely accepted as a promising target for various liver diseases; however, panels of ligands in drug development show limited clinical benefits, without a clear mechanism.
Shuang Cui, Guangji Wang, Haiping Hao
exaly   +6 more sources

Effect of different bile acids on the intestine through enterohepatic circulation based on FXR

open access: yesGut Microbes, 2021
Farnesoid X receptor (FXR) is a nuclear receptor for bile acids (BAs) that is widely expressed in the intestine, liver and kidney. FXR has important regulatory impacts on a wide variety of metabolic pathways (such as glucose, lipid, and sterol metabolism)
Chengcheng Zhang, Yan Bai, Hua Cao
exaly   +3 more sources

Recent advances on FXR-targeting therapeutics

open access: yesMolecular and Cellular Endocrinology, 2022
The bile acid receptor FXR has emerged as a bona fide drug target for chronic cholestatic and metabolic liver diseases, ahead of all non-alcoholic fatty liver disease (NAFLD).
Gernot Zöllner   +2 more
exaly   +4 more sources

FXR activation protects against NAFLD via bile-acid-dependent reductions in lipid absorption

open access: yesCell Metabolism, 2021
FXR agonists are used to treat non-alcoholic fatty liver disease (NAFLD), in part because they reduce hepatic lipids. Here, we show that FXR activation with the FXR agonist GSK2324 controls hepatic lipids via reduced absorption and selective decreases in
William D Barshop   +2 more
exaly   +2 more sources

Tissue specific induction of p62/Sqstm1 by farnesoid X receptor. [PDF]

open access: yesPLoS ONE, 2012
BackgroundFarnesoid X Receptor (FXR) is a member of the nuclear receptor superfamily and is a ligand-activated transcription factor essential for maintaining liver and intestinal homeostasis.
Jessica A Williams   +8 more
doaj   +8 more sources

FXR and liver carcinogenesis [PDF]

open access: yesActa Pharmacologica Sinica, 2014
Farnesoid X receptor (FXR) is a member of the nuclear receptor family and a ligand-modulated transcription factor. In the liver, FXR has been considered a multi-functional cell protector and a tumor suppressor. FXR can suppress liver carcinogenesis via different mechanisms: 1) FXR maintains the normal liver metabolism of bile acids, glucose and lipids;
Xiong-fei, Huang   +2 more
exaly   +3 more sources

FXR Regulates Intestinal Cancer Stem Cell Proliferation

open access: yesCell, 2019
SUMMARY Increased levels of intestinal bile acids (BAs) are a risk factor for colorectal cancer (CRC). Here we show that the convergence of dietary factors (high-fat diet) and dysregulated WNT signaling (APC mutation) alters BA profiles to drive ...
Eiji Yoshihara   +2 more
exaly   +2 more sources

FXR in liver physiology: Multiple faces to regulate liver metabolism

open access: yesBiochimica Et Biophysica Acta - Molecular Basis of Disease, 2021
The liver is the central metabolic hub which coordinates nutritional inputs and metabolic outputs. Food intake releases bile acids which can be sensed by the bile acid receptor FXR in the liver and the intestine.
Martin Wagner
exaly   +2 more sources

FXR: a metabolic regulator and cell protector [PDF]

open access: yesCell Research, 2008
Farnesoid X receptor (FXR) is a member of the nuclear receptor superfamily of ligand-activated transcription factors. As a metabolic regulator, FXR plays key roles in bile acid, cholesterol, lipid, and glucose metabolism. Therefore, FXR is a potential drug target for a number of metabolic disorders, especially those related to the metabolic syndrome ...
Yan-Dong Wang   +2 more
exaly   +3 more sources

Dysregulation of Farnesoid X Receptor on Neutrophil Homeostasis Exacerbates Intestinal Inflammation via the mTORC1‐Glycolysis Signaling Pathway [PDF]

open access: yesMedComm
Neutrophils significantly accumulate within the inflamed intestinal mucosa of patients with inflammatory bowel disease (IBD), where the farnesoid X receptor (FXR) is typically downregulated.
Dengfeng Kang   +15 more
doaj   +2 more sources

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