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10.1016/j.jtho.2021.07.002

http://scihub22266oqcxt.onion/10.1016/j.jtho.2021.07.002
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suck abstract from ncbi


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pmid34274504      J+Thorac+Oncol 2021 ; 16 (11): 1821-1839
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  • Lung Cancer Models Reveal Severe Acute Respiratory Syndrome Coronavirus 2-Induced Epithelial-to-Mesenchymal Transition Contributes to Coronavirus Disease 2019 Pathophysiology #MMPMID34274504
  • Stewart CA; Gay CM; Ramkumar K; Cargill KR; Cardnell RJ; Nilsson MB; Heeke S; Park EM; Kundu ST; Diao L; Wang Q; Shen L; Xi Y; Zhang B; Della Corte CM; Fan Y; Kundu K; Gao B; Avila K; Pickering CR; Johnson FM; Zhang J; Kadara H; Minna JD; Gibbons DL; Wang J; Heymach JV; Byers LA
  • J Thorac Oncol 2021[Nov]; 16 (11): 1821-1839 PMID34274504show ga
  • INTRODUCTION: Coronavirus disease 2019 is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which enters host cells through the cell surface proteins ACE2 and TMPRSS2. METHODS: Using a variety of normal and malignant models and tissues from the aerodigestive and respiratory tracts, we investigated the expression and regulation of ACE2 and TMPRSS2. RESULTS: We find that ACE2 expression is restricted to a select population of epithelial cells. Notably, infection with SARS-CoV-2 in cancer cell lines, bronchial organoids, and patient nasal epithelium induces metabolic and transcriptional changes consistent with epithelial-to-mesenchymal transition (EMT), including up-regulation of ZEB1 and AXL, resulting in an increased EMT score. In addition, a transcriptional loss of genes associated with tight junction function occurs with SARS-CoV-2 infection. The SARS-CoV-2 receptor, ACE2, is repressed by EMT through the transforming growth factor-beta, ZEB1 overexpression, and onset of EGFR tyrosine kinase inhibitor resistance. This suggests a novel model of SARS-CoV-2 pathogenesis in which infected cells shift toward an increasingly mesenchymal state, associated with a loss of tight junction components with acute respiratory distress syndrome-protective effects. AXL inhibition and ZEB1 reduction, as with bemcentinib, offer a potential strategy to reverse this effect. CONCLUSIONS: These observations highlight the use of aerodigestive and, especially, lung cancer model systems in exploring the pathogenesis of SARS-CoV-2 and other respiratory viruses and offer important insights into the potential mechanisms underlying the morbidity and mortality of coronavirus disease 2019 in healthy patients and patients with cancer alike.
  • |*COVID-19[MESH]
  • |*Lung Neoplasms[MESH]
  • |Bronchi[MESH]
  • |Humans[MESH]
  • |Lung[MESH]
  • |Peptidyl-Dipeptidase A[MESH]


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