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NASH

Updates on Novel Pharmacotherapeutics for the Treatment of Nonalcoholic Steatohepatitis

[Acta Pharmacologica Sinica] The authors summarize the latest data of new medications which have completed phase II or III trials for the treatment of nonalcoholic steatohepatitis, and discuss the rationale and preliminary results of several combinatory options.

Inhibition of Carnitine Palmitoyl-Transferase 1A in Hepatic Stellate Cells Protects against Fibrosis

[Journal of Hepatology] The authors showed that carnitine palmitoyltransferase 1A expression was elevated in hepatic stellate cells of patients with non-alcoholic steatohepatitis, showing a positive correlation with the fibrosis score.

Growth Hormone and Insulin-Like Growth Factor I Regulation of Nonalcoholic Fatty Liver Disease

[Journal of Clinical Endocrinology & Metabolism] Investigators focus on the potential role of growth hormone and insulin-like growth factor I in the regulation of hepatic steatosis, inflammation, and fibrosis.

Axcella Therapeutics Announces FDA Fast Track Designation for AXA1125 in NASH

[Axcella Therapeutics] Axcella Therapeutics announced that the US FDA has granted a Fast Track Designation to AXA1125 for the treatment of non-alcoholic steatohepatitis (NASH) with liver fibrosis.

A Robust Gene Expression Signature for NASH in Liver Expression Data

[Scientific Reports] Researchers identified 130 genes significantly differentially expressed in non-alcoholic steatohepatitis (NASH) versus a mixed group of non-alcoholic fatty liver disease and healthy controls.

Dicer Deletion in Hepatocytes Promotes Macrophages M1 Polarization through Dysregulated miR-192-3p/IGF2 in Non-Alcoholic Steatohepatitis and Hepatocellular Carcinoma

[Cancer Gene Therapy] In hepatic cells, Dicer deletion delivered distinct lipid profile and increased lipid oxidation. Mechanically, Dicer deletion caused declined miR-192-3p and increased IGF2 in hepatocytes.

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