| Vol. 9.42 – 29 October, 2020 |
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| As SARS-CoV-2 primarily infects the respiratory tract, investigators developed a lung organoid model using human pluripotent stem cells (hPSCs), and generated complementary hPSC-derived colonic organoids to explore the response of colonic cells to SARS-CoV-2 infection. [Nature] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| The authors demonstrated that respiratory viral infection induces distinct fibroblast activation states, which they term extracellular matrix-synthesizing, damage-responsive and interferon-responsive states. They provide evidence that excess activity of damage-responsive lung fibroblasts drives lethal immunopathology during severe influenza virus infection. [Nature] |
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| Researchers investigated the occurrence of epithelial–mesenchymal transition (EMT) in airways native tissue, primary cells and cell lines expressing mutant cystic fibrosis transmembrane conductance regulator through the expression of epithelial and mesenchymal markers as well as EMT-associated transcription factors. [Cell Death & Disease] |
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| Scientists incorporated protein information to analyze the expression of ACE2, the SARS-CoV-2 receptor, together with co-factors, TMPRSS2 and Furin, at single cell level in situ, which they called protein-proofed single-cell RNA (pscRNA) profiling. [iScience] |
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| In vivo, Fostamatinib reduced Mucin-1 (MUC1) abundance in lung epithelial cells in a mouse model of acute lung injury. In vitro, SYK inhibition by the active metabolite R406 promoted MUC1 removal from the cell surface. [Cell Reports Medicine] |
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| Differential lncRNAs were screened by microarray assay, then the expression was detected in LUAD tumor tissues and cell lines by qPCR. The influence on radiation response was assessed via in vitro and in vivo assays, and autophagy levels were evaluated by western blot and transmission electron microscopy. [Cell Death & Disease] |
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| Scientists showed that low SAM and SH3 domain-containing protein 1 (SASH1) mRNA expression was associated with poor survival in adenocarcinoma. Supporting this, modulation of SASH1 levels in a panel of lung cancer cell lines mediated changes in cellular proliferation and sensitivity to cisplatin. [Scientific Reports] |
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| Researchers compared effects of plasma-activated medium with effects of conventional clinical thermal therapy on both lung cancer cells and benign cells for management of malignant pleural effusion. [Scientific Reports] |
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| Investigators uncovered that ERK3, a ubiquitously expressed atypical MAPK, was required for KRAS-mediated NSCLC tumors. ERK3 is highly expressed in lung cancers, and oncogenic KRAS led to the activation and stabilization of the ERK3 protein. [Cancer Gene Therapy] |
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| The authors revealed a distinct ossification-related tuberculosis (TB) lung signature, which may be associated with the activation of the BMP/SMAD/RUNX2 pathway in Mycobacterium tuberculosis-infected macrophages that can restrain mycobacterial survival and promote osteogenic differentiation of mesenchymal stem cells. [Communications Biology] |
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| Investigators explore topics of pulmonary neuroendocrine cell (PNEC) development; PNEC interaction with other lung structural cells, immune cells, and lung-innervating neurons; PNEC activation; and emerging knowledge on their physiological and pathological roles. [Developmental Cell] |
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| Arcus Biosciences, Inc. announced a collaboration with AstraZeneca to evaluate domvanalimab, Arcus’s investigational anti-TIGIT antibody, in combination with Imfinzi in a registrational Phase III clinical trial in patients with unresectable Stage III non-small cell lung cancer (NSCLC). [Arcus Biosciences, Inc.] |
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| aTyr Pharma, Inc. announced that it has entered into a research collaboration with the Medical University of South Carolina. [aTyr Pharma, Inc.] |
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| Boehringer Ingelheim announced the initiation of a Phase II clinical trial of BI 764198, an inhibitor of TRPC6, a receptor-operated cation channel. This potent and selective inhibitor of TRPC6 may alleviate the damage to the lung and decrease the risk or severity of acute respiratory complications in patients hospitalized for COVID-19. [Boehringer Ingelheim International GmbH] |
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| March 17 – March 19, 2021 Virtual |
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| Fred Hutchinson Cancer Research Center – Seattle, Washington, United States |
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| Justus-Liebig-Universität Gießen – Giessen, Germany |
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| University of Saskatchewan – Saskatoon, Saskatchewan, Canada |
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| University of California, San Diego – La Jolla, California, United States |
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| Old Dominion University – Norfolk, Virginia, United States |
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