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hepatic cells

Hepatoprotective Effects of Sevoflurane against Hepatic Ischemia-Reperfusion Injury by Regulating microRNA-124-3p-Mediated TRAF3/CREB Axis

[Cell Death Discovery] Scientists defined the role of sevoflurane in hepatic ischemia-reperfusion injury as well as its underlying mechanism.

Ubiquitin Ligase E3 HUWE1/MULE Targets Transferrin Receptor for Degradation and Suppresses Ferroptosis in Acute Liver Injury

[Cell Death & Differentiation] The authors found that deficiency of Huwe1 in mice hepatocytes exacerbated ischemia-reperfusion injury and CCl4-induced liver injury with more ferroptosis occurrence, and that suppression of Huwe1 enhanced cellular sensitivity to ferroptosis in primary hepatocytes and mouse embryonic fibroblasts.

Hepcidin in Hepatocellular Carcinoma

[British Journal of Cancer] The authors explore hepcidin in HCC, presenting the levels of tissue and serum hepcidin and explaining the mechanisms that contribute to hepcidin reduction in HCC.

LncRNA MEG3 Up-Regulates SIRT6 by Ubiquitinating EZH2 and Alleviates Nonalcoholic Fatty Liver Disease

[Cell Death Discovery] Scientists presented the significant role of a novel signaling axis comprising long non-coding RNA maternally expressed gene 3 (MEG3), enhancer of zeste homolog 2 (EZH2), and sirtuin 6 (SIRT6) in controlling lipid accumulation, inflammation, and the progression of nonalcoholic fatty liver disease.

Mesenchymal Stem Cells Protect against Acetaminophen Hepatotoxicity by Secreting Regenerative Cytokine Hepatocyte Growth Factor

[Stem Cell Research & Therapy] MSCs were comparable to N-acetylcysteine against acetaminophen (APAP)-induced liver failure by secreting hepatocyte growth factor with less regenerative retardation concerns, thus facilitating the application of MSCs in clinical therapy for APAP liver failure.

Concurrent Disruption of the Ras/MAPK and NF-κB Pathways Induces Circadian Deregulation and Hepatocarcinogenesis

[Molecular Cancer Research] Scientists reported a gatekeeper function of the Ras/Erk and NF-κB pathways pathways by working in synergy to suppress liver tumorigenesis.

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