| Vol. 8.05 – 9 February, 2024 |
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| Investigators found that HIV and HIV gp120 activated AKT and ERK signaling and subsequently upregulated hypoxia-inducible factor-1α (HIF-1α) to increase HBV-induced transforming growth factor beta 1 (TGF-β1) and profibrogenic gene expression in hepatocytes and hepatic stellate cells. [Journal Of Hepatology] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Researchers uncovered decreased Cdkn2a/b and persistent Cdk4/6 activation as the mechanism driving uhrf1 mutant hepatocytes into S-phase. This induced replication stress, DNA damage and Atr activation. [Nucleic Acids Research] |
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| The essential role of Par-3 Family Cell Polarity Regulator (PARD3) in mediating hepatic tumorigenesis was assessed in diet-induced spontaneous liver tumour and syngeneic tumour models. The mechanism of PARD3 was delineated by bulk and single-cell RNA sequencing. [Journal Of Experimental & Clinical Cancer Research] |
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| qRT-PCR, Western blot, and immunohistochemistry assays were used to detect the related molecule levels. HE, Masson’s trichrome, and Sirius Red staining were used to assess the pathological changes in mice’s liver tissues. [American Journal Of Gastroenterology] |
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| Scientists found that the proportion of liver progenitor cells double positive for the ligand of glucocorticoid-induced tumor necrosis factor receptor and SRY-related HMG box transcription 9 among nonparenchymal cells increased time-dependently upon diet supplemented with ethionine injury and reduced after recovery. [Cell Death & Disease] |
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| Oral administration of Arbidol significantly ameliorated bile duct ligated-induced liver injury/fibrosis as reflected by decreased serum levels of alanine aminotransferase, aspartate aminotransferase, reduced collagen deposition, and diminished mRNA expression of fibrosis markers. [European Journal Of Pharmacology] |
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| In an iron overload-induced liver fibrosis model in mice and in ferric ammonium citrate-stimulated primary hepatocytes, treatment with rifaximin showed significant therapeutic effects. [Toxicology And Applied Pharmacology] |
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| Researchers engineered nanoliposomes containing phosphatase and tensin homolog deleted on chromosome ten (PTEN) plasmids, plumbagin, and antioxidant cerium oxide nanoparticles to restore the PTEN expression and inhibit the AKT/PI3K pathway. [Biomedical Materials] |
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| Investigators employed 3D printing techniques to automate the fabrication process of tissue spheroids on a chip. This allowed the simultaneous high-throughput printing of human liver spheroids and their surrounding polymeric flow chamber “chips” containing inner channels in a single step. [Tissue Engineering Part A] |
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| The pathological features of liver fibrosis and the current anti-fibrosis drugs in clinical trials are briefly introduced, followed by a detailed introduction of the therapeutic nanoagents for the precise delivery of anti-fibrosis drugs. [Journal Of Materials Chemistry B] |
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| The FDA has granted fast track designation to the investigational T cell therapy BST02 as a treatment for patients with liver cancer, according to a press release from Biosyngen. [Cancer Network] |
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| Eli Lilly on February 6, 2024 said its highly popular drug used for weight loss and diabetes showed promise as a treatment for fatty liver disease in a midstage trial. [CNBC] |
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| March 24 – 29, 2024 Galveston, Texas, United States |
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| University of Texas MD Anderson Cancer Center – Houston, Texas, United States |
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| University College London – London, England, United Kingdom |
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| University of Antwerp – Antwerp, Belgium |
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| National University of Singapore – Singapore, Singapore |
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| National University of Singapore – Singapore, Singapore |
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