 | Vol. 4.40 – 30 October, 2020 |
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| Researchers characterized two distinct mesothelial cell types as well as early hepatic stellate cells and revealed distinct spatiotemporal distributions for these populations. [Cell] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Scientists verified that Ether-Ã -go-go-1 (EAG1) promoted the proliferation of hepatocellular carcinoma both in vitro and in vivo. It promoted cell cycle progression by inhibiting the ubiquitination of SKP2. [Oncogene] |
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| Functional in vitro studies utilizing ATXN1LKO human cell lines revealed that loss of ATXN1L led to the accumulation of polyubiquitinated Capicua protein, promoting its degradation through the proteasome. [BMC Biology] |
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| MTT assays, flow cytometric analysis, Western blotting and immunohistochemistry identified that ZJQ-24 effectively suppressed hepatocellular carcinoma cell proliferation via G2/M phase arrest and caspase-dependent apoptosis but had no cytotoxic on normal cells. [Cell Death & Disease] |
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| In an acetaminophen-induced acute hepatic injury model, hepatocyte-specific miR-199a-3p knockout aggravated hepatic apoptosis. [Oncogenesis] |
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| Hepatic fibrosis is a disease characterized by excessive deposition of ECM in the liver. The authors investigated whether β-arrestin2 regulated oxidative stress in hepatic fibrosis. [Acta Pharmacologica Sinica] |
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| The 3D primary human hepatocytes spheroid model showed promise to be used in drug discovery projects to study drug metabolism, including unknown mechanisms, over an extended period of time. [Journal of Pharmaceutical Sciences] |
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| The authors summarize rapidly emerging clinical data on the promise and challenges of implementing immune checkpoint cascades in hepatocellular carcinoma and discuss the unmet need of biomarkers to predict response or resistance to therapy. [JAMA Oncology] |
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| Investigators summarize emerging aspects of antigen presentation, autoantibody production, and the application of novel therapeutic approaches in the characterization and treatment of autoimmune liver diseases. [Cellular & Molecular Immunology] |
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| Aligos Therapeutics, Inc. announced that it has dosed its first subject in a first-in-human Phase Ia/b clinical trial, ALG-000184-201. The study will evaluate ALG-000184, a small molecule class II capsid assembly modulator that targets hepatitis B virus capsid assembly as well as the establishment of covalently closed circular DNA. [Aligos Therapeutics, Inc.] |
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| The European Patent Office Technical Boards of Appeal has ruled in Sanofi and Regeneron’s favor, invalidating certain claims of Amgen’s European patent directed to PCSK9 antibodies relevant to Praluent®. Praluent will continue to be available in European countries where it is approved for use and for sale. [Sanofi] |
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| March 22 – March 24, 2021 Virtual |
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| Pfizer – Cambridge, Massachusetts |
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| Deep Genomics, Inc. – Toronto, Ontario, Canada |
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| Zhejiang University-University of Edinburgh Institute – Haining, Zhejiang, China |
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| Medical University of Vienna – Vienna, Austria |
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| University of Texas Southwestern Medical Center – Dallas, Texas, United States |
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