Bioactive Sphingolipids in Docetaxel-Induced Apoptosis in Human Prostate Cancer Cells

dc.contributor.author Başsoy, Esen Yonca
dc.contributor.author Baran, Yusuf
dc.coverage.doi 10.1016/j.biopha.2011.10.003
dc.date.accessioned 2017-02-10T07:01:16Z
dc.date.available 2017-02-10T07:01:16Z
dc.date.issued 2012
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. © 2012 Elsevier Masson SAS. en_US
dc.description.sponsorship TUBITAK project number 109S215 and Turkish Academy of Sciences Outstanding Young Investigator Programme en_US
dc.identifier.citation Başsoy, E. Y., and Baran, Y. (2012). Bioactive sphingolipids in docetaxel-induced apoptosis in human prostate cancer cells. Biomedicine and Pharmacotherapy, 66(2), 103-110. doi:10.1016/j.biopha.2011.10.003 en_US
dc.identifier.doi 10.1016/j.biopha.2011.10.003 en_US
dc.identifier.doi 10.1016/j.biopha.2011.10.003
dc.identifier.issn 0753-3322
dc.identifier.scopus 2-s2.0-84858287935
dc.identifier.uri http://doi.org/10.1016/j.biopha.2011.10.003
dc.identifier.uri https://hdl.handle.net/11147/4826
dc.language.iso en en_US
dc.publisher Elsevier Ltd. en_US
dc.relation.ispartof Biomedicine and Pharmacotherapy en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Bioactive sphingolipids en_US
dc.subject Ceramides en_US
dc.subject Docetaxel en_US
dc.subject Glucosyle ceramide synthase en_US
dc.subject Prostate cancer en_US
dc.subject Sphingosine kinase 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.institutional Başsoy, Esen Yonca
gdc.author.institutional Baran, Yusuf
gdc.author.yokid 119193
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C5
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Molecular Biology and Genetics en_US
gdc.description.endpage 110 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.startpage 103 en_US
gdc.description.volume 66 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W2066313334
gdc.identifier.pmid 22326625
gdc.identifier.wos WOS:000302420800005
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype GOLD
gdc.oaire.diamondjournal false
gdc.oaire.impulse 5.0
gdc.oaire.influence 2.8412588E-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 Docetaxel
gdc.oaire.keywords Ceramides
gdc.oaire.keywords Glucosylceramides
gdc.oaire.keywords Sphingosine kinase
gdc.oaire.keywords Sphingosine
gdc.oaire.keywords Cell Line, Tumor
gdc.oaire.keywords Humans
gdc.oaire.keywords Prostate cancer
gdc.oaire.keywords Reverse Transcriptase Polymerase Chain Reaction
gdc.oaire.keywords Prostatic Neoplasms
gdc.oaire.keywords Drug Synergism
gdc.oaire.keywords Glucosyle ceramide synthase
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 Bioactive sphingolipids
gdc.oaire.keywords Taxoids
gdc.oaire.keywords Lysophospholipids
gdc.oaire.keywords Oxidoreductases
gdc.oaire.popularity 3.6016E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 03 medical and health sciences
gdc.oaire.sciencefields 0302 clinical medicine
gdc.openalex.collaboration National
gdc.openalex.fwci 0.70082472
gdc.openalex.normalizedpercentile 0.67
gdc.opencitations.count 9
gdc.plumx.crossrefcites 8
gdc.plumx.mendeley 17
gdc.plumx.pubmedcites 3
gdc.plumx.scopuscites 10
gdc.scopus.citedcount 10
gdc.wos.citedcount 8
relation.isAuthorOfPublication.latestForDiscovery 7bb863bb-9384-4a07-9fbb-b9c1ab7634a3
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4013-8abe-a4dfe192da5e

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