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Bioactive sphingolipids in docetaxel-induced apoptosis in human prostate cancer cells

dc.contributor.author Bassoy, Esen Yonca
dc.contributor.author Baran, Yusuf
dc.date.accessioned 2023-11-18T10:06:36Z
dc.date.available 2023-11-18T10:06:36Z
dc.date.issued 2012
dc.description Bassoy, Esen Yonca/0000-0001-8870-7040; Baran, Yusuf/0000-0002-1056-4673 en_US
dc.description.abstract In this study, we examined the possible roles of ceramide/sphingosine-1-phosphate and ceramide/glucosyleceramide signaling in docetaxel-induced apoptosis by examining expression levels of the glucosyleceramide synthase and sphingosine kinase-1 and ceramide synthase gene family. As confirmed by isobologram analysis, docetaxel in combination with agents that increase intracellular ceramide levels increased the cytotoxic and apoptotic effects of docetaxel synergistically. More importantly, RT-PCR results revealed that expression levels of glucosyleceramide synthase and sphingosine kinase-1 were downregulated and ceramide synthase genes were upregulated in response to docetaxel. This study identifies mechanisms underlying the involvement of ceramide metabolizing genes in docetaxel-induced apoptosis in prostate cancer cells. (c) 2012 Elsevier Masson SAS. All rights reserved. en_US
dc.description.sponsorship TUBITAK [109S215]; Turkish Academy of Sciences Outstanding Young Investigator Programme en_US
dc.description.sponsorship They thank Prof Dr Anne Frary for critically reviewing the manuscript. This study was supported by TUBITAK project number 109S215 to Y.B and by the Turkish Academy of Sciences Outstanding Young Investigator Programme to Y.B. en_US
dc.identifier.citation 9
dc.identifier.doi 10.1016/j.biopha.2011.10.003
dc.identifier.issn 0753-3322
dc.identifier.issn 1950-6007
dc.identifier.uri https://doi.org/10.1016/j.biopha.2011.10.003
dc.identifier.uri http://standard-demo.gcris.com/handle/123456789/7012
dc.language.iso en en_US
dc.publisher Elsevier France-editions Scientifiques Medicales Elsevier en_US
dc.relation.ispartof Biomedicine & Pharmacotherapy
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Prostate cancer en_US
dc.subject Bioactive sphingolipids en_US
dc.subject Ceramides en_US
dc.subject Sphingosine kinase en_US
dc.subject Glucosyle ceramide synthase en_US
dc.subject Docetaxel en_US
dc.title Bioactive sphingolipids in docetaxel-induced apoptosis in human prostate cancer cells en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Bassoy, Esen Yonca/0000-0001-8870-7040
gdc.author.id Baran, Yusuf/0000-0002-1056-4673
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
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gdc.description.department Izmir Institute of Technology İYTE en_US
gdc.description.departmenttemp [Bassoy, Esen Yonca; Baran, Yusuf] Izmir Inst Technol, Dept Mol Biol & Genet, Canc Genet & Mol Hematol Lab, TR-35430 Izmir, Turkey en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 66 en_US
gdc.description.wosquality Q1
gdc.identifier.pmid 22326625
gdc.identifier.wos WOS:000302420800005
gdc.oaire.accepatencedate 2012-03-01
gdc.oaire.accesstype Gold
gdc.oaire.diamondjournal false
gdc.oaire.downloads 89
gdc.oaire.impulse 5
gdc.oaire.influence 3.2087133E-9
gdc.oaire.influencealt 9
gdc.oaire.isgreen true
gdc.oaire.keywords Male
gdc.oaire.keywords Down-Regulation
gdc.oaire.keywords Antineoplastic Agents
gdc.oaire.keywords Apoptosis
gdc.oaire.keywords Glucosylceramides
gdc.oaire.keywords Sphingosine
gdc.oaire.keywords Cell Line, Tumor
gdc.oaire.keywords Humans
gdc.oaire.keywords Reverse Transcriptase Polymerase Chain Reaction
gdc.oaire.keywords Prostatic Neoplasms
gdc.oaire.keywords Drug Synergism
gdc.oaire.keywords Up-Regulation
gdc.oaire.keywords Gene Expression Regulation, Neoplastic
gdc.oaire.keywords Phosphotransferases (Alcohol Group Acceptor)
gdc.oaire.keywords Glucosyltransferases
gdc.oaire.keywords Taxoids
gdc.oaire.keywords Lysophospholipids
gdc.oaire.keywords Oxidoreductases
gdc.oaire.magid 2066313334
gdc.oaire.popularity 4.744025E-9
gdc.oaire.popularityalt 2.2789195
gdc.oaire.publicfunded false
gdc.oaire.relevantdates created:2012-01-30
gdc.oaire.relevantdates published-print:2012-03-01
gdc.oaire.relevantdates issued:2012-01-01
gdc.oaire.relevantdates published-online:2012-01-25
gdc.oaire.sciencefields 03022001 Oncology/Infectious causes of cancer
gdc.oaire.sciencefields 03 medical and health sciences
gdc.oaire.sciencefields 0302 clinical medicine
gdc.oaire.sciencefields 030220 oncology & carcinogenesis
gdc.oaire.views 72
gdc.opencitations.count 9
gdc.plumx.crossrefcites 5
gdc.plumx.mendeley 16
gdc.plumx.pubmedcites 3
gdc.plumx.scopuscites 10
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