<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>144</volume><submitter>Khan I</submitter><pubmed_abstract>The outbreak of Novel Coronavirus 2019 (COVID-19) represents a global threat to the public healthcare. The viral spike (S) glycoprotein is the key molecule for viral entry through interaction with angiotensin converting enzyme 2 (ACE2) receptor molecules present on the cell membranes. Moreover, it has been established that COVID-19 interacts and infects brain cells in humans via ACE2. Therefore in the light of these known facts we hypothesized that viral S protein molecule may bind to the other overexpressed receptor molecules in glioma cells and may play some role in glioma tumorogenesis. Thus we leverage docking analysis (HEX and Z-DOCK) between viral S protein and epidermal growth factor receptors (EGFR), vascular endothelial growth factor receptors (VEGFR) and hepatocyte growth factor </pubmed_abstract><journal>Medical hypotheses</journal><pagination>110009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7303027</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Can COVID-19 induce glioma tumorogenesis through binding cell receptors?</pubmed_title><pmcid>PMC7303027</pmcid><pubmed_authors>Khan I</pubmed_authors><pubmed_authors>Hatiboglu MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Can COVID-19 induce glioma tumorogenesis through binding cell receptors?</name><description>The outbreak of Novel Coronavirus 2019 (COVID-19) represents a global threat to the public healthcare. The viral spike (S) glycoprotein is the key molecule for viral entry through interaction with angiotensin converting enzyme 2 (ACE2) receptor molecules present on the cell membranes. Moreover, it has been established that COVID-19 interacts and infects brain cells in humans via ACE2. Therefore in the light of these known facts we hypothesized that viral S protein molecule may bind to the other overexpressed receptor molecules in glioma cells and may play some role in glioma tumorogenesis. Thus we leverage docking analysis (HEX and Z-DOCK) between viral S protein and epidermal growth factor receptors (EGFR), vascular endothelial growth factor receptors (VEGFR) and hepatocyte growth factor </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2026-04-07T23:48:58.047Z</modification><creation>2020-08-14T07:01:19Z</creation></dates><accession>S-EPMC7303027</accession><cross_references><pubmed>32758869</pubmed><doi>10.1016/j.mehy.2020.110009</doi></cross_references></HashMap>