| Vol. 9.31 – 13 August, 2020 |
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| Investigators observed that hederagenin induced the increased autophagosomes in lung cancer cells concomitantly with the upregulation of LC3-II and p62, which indicated the impairment of autophagic flux. [Cell Death & Disease] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Formation of neutrophil extracellular traps (NETs) and neutrophil swarming was seen in a mouse model of neutrophilic asthma. Additionally, NETs were found to stimulate airway cells to express CXCL1, CXCL2, and CXCL8 via the TLR4/NF-κB pathway, which recruited neutrophils to the inflammation site. [Aging] |
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| Scientists investigated the effect of prenatal smoke exposure on lung epithelial cell differentiation and linked this with Amphiregulin-epidermal growth factor receptor signaling in one-day old mouse offspring. [American Journal of Physiology-Lung Cellular and Molecular Physiology] |
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| Deleted in malignant brain tumors 1 (DMBT1) expression was up‐regulated in human lung tissue after fetal/peri‐/postnatal hypoxia. Additionally, in vitro experiments showed increased DMBT1 RNA expression in A549 cells after hypoxia. [Pediatric Pulmonology] |
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| Researchers demonstrated that Mex3a knockdown significantly inhibited lung adenocarcinoma cell migration and invasion in vitro and metastasis in nude mice. [Cell Death & Disease] |
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| Scientists developed a lactate‐dependent cell proliferation assay and found that dynamin‐related protein (DRP1), which was highly expressed in KRAS‐mutant non‐small cell lung cancer (NSCLC), was required for tumor cells to proliferate and used lactate as fuel, demonstrating the critical role of DRP1 in the metabolic reprogramming of NSCLC. [Cancer Science] |
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| Expression patterns of circRACGAP1 and miR-144-5p in non-small cell lung cancer tissues and cell lines were quantified by qRT-PCR analysis. Then, the function of circRACGAP1 on cell proliferation and tumorigenesis were confirmed in vitro and in vivo using CCK-8 assay, colony formation, EdU incorporation, and xenograft technique. [Cancer Gene Therapy] |
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| Scientists investigated the role of fibrinogen-like protein 1 (FGL1) in regulating gefitinib resistance of PC9/GR non-small cell lung cancer. [Respiratory Research] |
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| Researchers sought to investigate the potential effects of luteolin as a tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) sensitizer in non-small cell lung cancer cells. [Archives of Biochemistry and Biophysics] |
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| Elevated never in mitosis gene A-related kinase 2 level promoted the rapid cell cycle progression and favored the rapid proliferation of epidermal growth factor receptor-mutant non-small cell lung cancer cells. [Molecular and Cellular Biochemistry] |
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| Investigators determined the fundamental mechanism of microRNA-608 in the development of lung cancer. [Bosnian Journal of Basic Medical Sciences] |
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| The authors comprehensively summarize the emerging upstream regulators, downstream substrates, mouse models, clinical relevance, and candidate inhibitors for SIKs, and shed light on SIKs as the potential therapeutic targets for cancer therapies. [Signal Transduction and Targeted Therapy] |
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| Daiichi Sankyo Company, Limited announced that it has entered into a clinical trial collaboration with AstraZeneca to evaluate the combination of patritumab deruxtecan, a HER3 directed DXd antibody drug conjugate, and TAGRISSO, an epidermal growth factor receptor tyrosine kinase inhibitor, in patients with EGFR-mutated advanced or metastatic non-small cell lung cancer. [Daiichi Sankyo Company, Limited] |
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| Boehringer Ingelheim announced that the first patient has enrolled in InPedILD™, a global Phase III trial assessing the dosing and safety profile of nintedanib in children and adolescents between six and 17 years old with clinically significant fibrosing interstitial lung disease. [Boehringer Ingelheim International GmbH] |
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| Arrowhead Pharmaceuticals Inc. announced that it has dosed the first subjects in AROENaC1001, a Phase I/II clinical study of ARO-ENaC, the company’s investigational RNA interference therapeutic being developed as a treatment for patients with cystic fibrosis, which is a rare disease caused by genetic mutations that lead to progressive deterioration in lung function due to poor clearance of mucus and associated recurrent infections. [Arrowhead Pharmaceuticals Inc.] |
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| November 2 – November 3 Virtual |
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| Institut Mondor de Recherche Biomédicale – Creteil, France |
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| University of British Columbia – Vancouver, British Columbia, Canada |
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| Institute for Computational Medicine – Baltimore, Maryland, United States |
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| Columbia University Medical Center – New York, New York, United States |
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| Fred Hutchinson Cancer Research Center – Seattle, Washington, United States |
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