NOD1: a metabolic modulator DOI Creative Commons

Ruobing Tang,

Chunguang Xie,

X.L. Zhang

и другие.

Frontiers in Endocrinology, Год журнала: 2025, Номер 15

Опубликована: Янв. 21, 2025

Nucleotide-binding oligomerization domain 1 (NOD1) is an intracellular pattern recognition receptor that detects injury signals and initiates inflammatory responses host defense. Furthermore, NOD1 serves as a metabolic mediator by influencing the metabolism of various tissues, including adipose tissue, liver, cardiovascular pancreatic β cells, adrenal glands, bones through diverse mechanisms. It has been discovered activated associated with pathological mechanisms certain diseases. This review presents comprehensive summary impact on tissue-specific metabolism.

Язык: Английский

Multi-omics joint analysis reveals that the Miao medicine Yindanxinnaotong formula attenuates non-alcoholic fatty liver disease DOI
Lei Huang, Qing Rao,

Chaoyan Wang

и другие.

Phytomedicine, Год журнала: 2024, Номер 135, С. 156026 - 156026

Опубликована: Сен. 21, 2024

Язык: Английский

Процитировано

5

Therapeutic Strategies for MASH: An Update on Drug Candidates Under Investigation in Late-Phase Clinical Trials DOI Creative Commons

Samuel Dinerman,

Yan Shu

International Journal of Translational Medicine, Год журнала: 2025, Номер 5(1), С. 7 - 7

Опубликована: Янв. 17, 2025

Metabolic dysfunction-associated steatohepatitis (MASH) is rapidly becoming a leading cause of hepatocellular carcinoma and end-stage liver transplantation. Characterized by hepatic steatosis, lobular inflammation, hepatocyte ballooning, there dire need to develop therapeutic strategies mitigate MASH alongside the subsequent fibrosis cirrhosis. For years, development for treatment had been considered graveyard, with various pharmacotherapies failing achieve clinical efficacy. However, recent Food Drug Administration (FDA) approval Madrigal Pharmaceuticals’ Resmetirom in United States provides positive step collective effort eradicate MASH. Granted, much about Resmetirom’s long-term efficacy safety still be determined multi-factorial nature pathogenesis, continuing evaluate alternative options remains best interest field. Currently, therapeutics previously approved other ailments, novel developed specifically MASH, are being evaluated late-phase trials. considering complex disease varying outcomes assess efficacy, achieving regulatory as continues rigorous endeavor. In this review, we summarize notable mechanistic backgrounds having achieved, or actively undergoing, trials offer our perspectives on anti-MASH development.

Язык: Английский

Процитировано

0

Targeting TCMR-associated cytokine genes for drug screening identifies PPARγ agonists as novel immunomodulatory agents in transplantation DOI Creative Commons
Lu Hu, Xiaolei Zhang, W. Zhang

и другие.

Frontiers in Immunology, Год журнала: 2025, Номер 16

Опубликована: Янв. 22, 2025

Objective T cell-mediated rejection (TCMR) remains a significant challenge in organ transplantation. This study aimed to define TCMR-associated cytokine gene set and identify drugs prevent TCMR through drug repurposing. Methods Gene expression profiles from kidney, heart, lung transplant biopsies were obtained the Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) between non-TCMR groups identified, their intersection with cytokine-related yielded an 11-gene (TCMR-Cs). To evaluate effectiveness of this set, diagnostic predictive model was constructed using Lasso regression multivariate logistic regression, validation independent datasets. Connectivity Map (CMap) analysis employed screen targeting TCMR-Cs. Experimental identified performed vitro cell activation Th1 differentiation assays, vivo mouse skin survival analysis. Results The TCMR-Cs exhibited outstanding performance for TCMR, achieving AUC 0.99 training cohorts maintaining strong test cohorts. CMap peroxisome proliferator-activated receptor gamma (PPARγ) agonists as potential therapeutic candidates. showed that PPARγ agonist rosiglitazone significantly suppressed reduced without cytotoxic effects. combination rapamycin prolonged graft survival. Conclusions defined novel effectively predicts agonists, which improve when combined rapamycin.

Язык: Английский

Процитировано

0

Lean MASLD and Cardiovascular Disease: A Review DOI

Nachum Lebovics,

Gabriel Heering,

William H. Frishman

и другие.

Cardiology in Review, Год журнала: 2025, Номер unknown

Опубликована: Март 21, 2025

Metabolic-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty disease, is prevalent worldwide and highly associated with cardiovascular (CVD). Lean MASLD defined by hepatic steatosis cardiometabolic risk factors in individuals a body mass index below 25 Western populations or 23 Asian populations. Paradoxically, some studies indicate that lean an elevated of (CV) CV mortality compared nonlean MASLD. patients exhibit distinctive metabolic, genetic, microbiome profiles contributing to increased visceral adiposity, sarcopenia, fibrosis, systemic inflammation, endothelial dysfunction. This review examines the epidemiology, pathophysiology, outcomes MASLD, addressing discrepancies literature. Furthermore, it highlights current clinical guidelines, emphasizes lifestyle modifications, discusses emerging pharmacotherapies potential treatment options.

Язык: Английский

Процитировано

0

NOD1: a metabolic modulator DOI Creative Commons

Ruobing Tang,

Chunguang Xie,

X.L. Zhang

и другие.

Frontiers in Endocrinology, Год журнала: 2025, Номер 15

Опубликована: Янв. 21, 2025

Nucleotide-binding oligomerization domain 1 (NOD1) is an intracellular pattern recognition receptor that detects injury signals and initiates inflammatory responses host defense. Furthermore, NOD1 serves as a metabolic mediator by influencing the metabolism of various tissues, including adipose tissue, liver, cardiovascular pancreatic β cells, adrenal glands, bones through diverse mechanisms. It has been discovered activated associated with pathological mechanisms certain diseases. This review presents comprehensive summary impact on tissue-specific metabolism.

Язык: Английский

Процитировано

0