https://scholars.lib.ntu.edu.tw/handle/123456789/569627
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Chang M.-C. | en_US |
dc.contributor.author | YI-JANE CHEN | en_US |
dc.contributor.author | Liou E.J. | en_US |
dc.contributor.author | WAN-YU TSENG | en_US |
dc.contributor.author | Chan C.-P. | en_US |
dc.contributor.author | Lin H.-J. | en_US |
dc.contributor.author | Liao W.-C. | en_US |
dc.contributor.author | Chang Y.-C. | en_US |
dc.contributor.author | Jeng P.-Y. | en_US |
dc.contributor.author | JIIANG-HUEI JENG | en_US |
dc.creator | Chang M.-C.;Chen Y.-J.;Liou E.J.;Wan-Yu Tseng;Chan C.-P.;Lin H.-J.;Liao W.-C.;Chang Y.-C.;Jeng P.-Y.;Jeng J.-H. | - |
dc.date.accessioned | 2021-07-06T03:43:49Z | - |
dc.date.available | 2021-07-06T03:43:49Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 1949-2553 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996629626&doi=10.18632%2foncotarget.12578&partnerID=40&md5=29857e10f1cbf600ff9067882cce7d27 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/569627 | - |
dc.description.abstract | Cardiovascular diseases (atherosclerosis, stroke, myocardiac infarction etc.) are the major systemic diseases of elder peoples in the world. This is possibly due to increased levels of oxidized low-density lipoproteins (oxLDLs) such as 7-ketocholesterol (7-KC) and lysophosphatidylcholine (LPC) that damage vascular endothelial cells, induce inflammatory responses, to elevate the risk of cardiovascular diseases, Alzheimer's disease, and age-related macular degeneration. However the toxic effects of 7-KC on endothelial cells are not known. In this study, 7-KC showed cytotoxicity to endothelial cells at concentrations higher than 10 μg/ml. 7-KC stimulated ATM/Chk2, ATR-Chk1 and p53 signaling pathways in endothelial cells. 7-KC also induced G0/G1 cell cycle arrest and apoptosis with an inhibition of Cyclin dependent kinase 1 (Cdk1) and cyclin B1 expression. Secretion and expression of IL-8 in endothelial cells were stimulated by 7-KC. 7-KC further induced intracellular ROS production as shown by increase in DCF fluorescence and Akt phosphorylation. LY294002 attenuated the 7-KC-induced apoptosis and IL-8 mRNA expression of endothelial cells. These results indicate that oxLDLs such as 7-KC may contribute to the pathogenesis of atherosclerosis, thrombosis and cardiovascular diseases by induction of endothelial damage, apoptosis and inflammatory responses. These events are associated with ROS production, activation of ATM/Chk2, ATR/Chk1, p53 and PI3K/Akt signaling pathways. | - |
dc.publisher | Impact Journals LLC | - |
dc.relation.ispartof | Oncotarget | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | 7 oxocholesterol; ATM protein; checkpoint kinase 1; checkpoint kinase 2; cyclin B1; interleukin 8; phosphatidylinositol 3 kinase; protein kinase B; protein p53; 7-ketocholesterol; ATM protein; biological marker; checkpoint kinase 1; checkpoint kinase 2; cholesterol derivative; cytokine; interleukin 8; phosphatidylinositol 3 kinase; protein kinase B; apoptosis; Article; atherosclerosis; cardiovascular disease; cell cycle arrest; controlled study; cytokine production; cytokine release; cytotoxicity; disease association; endothelium cell; enzyme activation; enzyme inhibition; enzyme phosphorylation; fluorescence analysis; G0 phase cell cycle arrest; G1 phase cell cycle checkpoint; gene; IL 8 gene; immune response; intracellular membrane; molecular pathology; protein expression; signal transduction; thrombosis; biosynthesis; cell cycle; cell survival; drug effects; endothelium cell; flow cytometry; gene expression; genetics; human; metabolism; signal transduction; Apoptosis; Ataxia Telangiectasia Mutated Proteins; Biomarkers; Cell Cycle; Cell Survival; Checkpoint Kinase 1; Checkpoint Kinase 2; Cytokines; Endothelial Cells; Flow Cytometry; Gene Expression; Humans; Interleukin-8; Ketocholesterols; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; Signal Transduction | - |
dc.title | 7-Ketocholesterol induces ATM/ATR, Chk1/Chk2, PI3K/Akt signalings, cytotoxicity and IL-8 production in endothelial cells | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.18632/oncotarget.12578 | - |
dc.identifier.pmid | 27740938 | - |
dc.identifier.scopus | 2-s2.0-84996629626 | - |
dc.relation.pages | 74473-74483 | - |
dc.relation.journalvolume | 7 | - |
dc.relation.journalissue | 46 | - |
item.openairetype | journal article | - |
item.fulltext | no fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.grantfulltext | none | - |
crisitem.author.dept | Dentistry | - |
crisitem.author.dept | School of Dentistry | - |
crisitem.author.dept | Dentistry-NTUH | - |
crisitem.author.dept | Dentistry | - |
crisitem.author.dept | School of Dentistry | - |
crisitem.author.dept | Dentistry-NTUH | - |
crisitem.author.dept | Clinical Dentistry | - |
crisitem.author.dept | Dentistry-NTUH | - |
crisitem.author.dept | School of Dentistry | - |
crisitem.author.orcid | 0000-0002-9178-8379 | - |
crisitem.author.orcid | 0000-0002-9012-3703 | - |
crisitem.author.orcid | 0000-0002-2068-5380 | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
顯示於: | 臨床牙醫學研究所 |
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