<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Philipp J</submitter><funding>Federal Ministry of Education and Research of Germany (BMBF)</funding><pagination>30</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7709117</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(4)</volume><pubmed_abstract>Radiation-induced inflammation leading to the permeability of the endothelial barrier may increase the risk of cardiovascular disease. The aim of this study was to investigate potential mechanisms in vitro at the level of the proteome in human coronary artery endothelial cells (HCECest2) that were exposed to radiation doses of 0, 0.25, 0.5, 2.0 and 10 Gy (60Co-γ). Proteomics analysis was performed using mass spectrometry in a label-free data-independent acquisition mode. The data were validated using bioinformatics and immunoblotting. The low- and moderate-dose-irradiated samples (0.25 Gy, 0.5 Gy) showed only scarce proteome changes. In contrast, an activation of DNA-damage repair, inflammation, and oxidative stress pathways was seen after the high-dose treatments (2 and 10 Gy). The level </pubmed_abstract><journal>Proteomes</journal><pubmed_title>Radiation Response of Human Cardiac Endothelial Cells Reveals a Central Role of the cGAS-STING Pathway in the Development of Inflammation.</pubmed_title><pmcid>PMC7709117</pmcid><funding_grant_id>02NUK038B</funding_grant_id><pubmed_authors>Tapio S</pubmed_authors><pubmed_authors>Azimzadeh O</pubmed_authors><pubmed_authors>Le Gleut R</pubmed_authors><pubmed_authors>Toerne CV</pubmed_authors><pubmed_authors>Subedi P</pubmed_authors><pubmed_authors>Philipp J</pubmed_authors><pubmed_authors>Atkinson MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Radiation Response of Human Cardiac Endothelial Cells Reveals a Central Role of the cGAS-STING Pathway in the Development of Inflammation.</name><description>Radiation-induced inflammation leading to the permeability of the endothelial barrier may increase the risk of cardiovascular disease. The aim of this study was to investigate potential mechanisms in vitro at the level of the proteome in human coronary artery endothelial cells (HCECest2) that were exposed to radiation doses of 0, 0.25, 0.5, 2.0 and 10 Gy (60Co-γ). Proteomics analysis was performed using mass spectrometry in a label-free data-independent acquisition mode. The data were validated using bioinformatics and immunoblotting. The low- and moderate-dose-irradiated samples (0.25 Gy, 0.5 Gy) showed only scarce proteome changes. In contrast, an activation of DNA-damage repair, inflammation, and oxidative stress pathways was seen after the high-dose treatments (2 and 10 Gy). The level </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2026-04-07T22:21:57.527Z</modification><creation>2021-02-20T02:53:48Z</creation></dates><accession>S-EPMC7709117</accession><cross_references><pubmed>33114474</pubmed><doi>10.3390/proteomes8040030</doi></cross_references></HashMap>