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http://hdl.handle.net/11452/30340
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DC Field | Value | Language |
---|---|---|
dc.date.accessioned | 2023-01-09T11:59:51Z | - |
dc.date.available | 2023-01-09T11:59:51Z | - |
dc.date.issued | 2017-04-10 | - |
dc.identifier.citation | Tezcan, G. vd. (2017). ''Olea europaea leaf extract and bevacizumab synergistically exhibit beneficial efficacy upon human glioblastoma cancer stem cells through reducing angiogenesis and invasion in vitro''. Biomedicine and Pharmacotherapy, 90, 713-723. | en_US |
dc.identifier.issn | 0753-3322 | - |
dc.identifier.uri | https://doi.org/10.1016/j.biopha.2017.04.022 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0753332217307813 | - |
dc.identifier.uri | 1950-6007 | - |
dc.identifier.uri | http://hdl.handle.net/11452/30340 | - |
dc.description.abstract | Patients with glioblastoma multiforme (GBM) that are cancer stem-cell-positive (GSC [+]) essentially cannot benefit from anti-angiogenic or anti-invasive therapy. In the present study, the potential anti-angiogenic and anti-invasive effects of Olea europaea (olive) leaf extract (OLE) were tested using GSC (+) tumours. OLE (2 mg/mL) caused a significant reduction in tumour weight, vascularisation, invasiveness and migration (p = 0.0001, p < 0.001, p = 0.004; respectively) that was associated with reducing the expression of VEGFA, MMP-2 and MMP-9. This effect was synergistically increased in combination with bevacizumab. Therefore, our current findings may contribute to research on drugs that inhibit the invasiveness of GBM. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Research & experimental medicine | en_US |
dc.subject | Pharmacology & pharmacy | en_US |
dc.subject | Angiogenesis | en_US |
dc.subject | Glioblastoma cancer stem cell | en_US |
dc.subject | Invasion | en_US |
dc.subject | MMP2 | en_US |
dc.subject | MMP9 | en_US |
dc.subject | Olea europaea leaf extract | en_US |
dc.subject | VEGFA | en_US |
dc.subject | Antiangiogenic therapies | en_US |
dc.subject | Mesenchymal transition | en_US |
dc.subject | Antioxidant activity | en_US |
dc.subject | Olive oil | en_US |
dc.subject | Oleuropein | en_US |
dc.subject | Expression | en_US |
dc.subject | Polyphenols | en_US |
dc.subject | Gata6 | en_US |
dc.subject | Proliferation | en_US |
dc.subject | Microrna-153 | en_US |
dc.subject.mesh | Angiogenesis inhibitors | en_US |
dc.subject.mesh | Bevacizumab | en_US |
dc.subject.mesh | Cell line | en_US |
dc.subject.mesh | Tumor | en_US |
dc.subject.mesh | Cell movement | en_US |
dc.subject.mesh | Drug synergism | en_US |
dc.subject.mesh | Glioblastoma | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Matrix metalloproteinase 2 | tr_TR |
dc.subject.mesh | Matrix metalloproteinase 9 | en_US |
dc.subject.mesh | Neoplasm invasiveness | en_US |
dc.subject.mesh | Neoplastic stem cells | en_US |
dc.subject.mesh | Neovascularization, pathologic | en_US |
dc.subject.mesh | Olea | en_US |
dc.subject.mesh | Plant extracts | en_US |
dc.subject.mesh | Plant leaves | en_US |
dc.subject.mesh | Vascular endothelial growth factor A | en_US |
dc.title | Olea europaea leaf extract and bevacizumab synergistically exhibit beneficial efficacy upon human glioblastoma cancer stem cells through reducing angiogenesis and invasion in vitro | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000402471000087 | tr_TR |
dc.identifier.scopus | 2-s2.0-85017569324 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Nöroşirürji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı. | tr_TR |
dc.relation.bap | OUAP(T) 2013/22, 2013 | en_US |
dc.relation.bap | HDP(T)-2016/14, 2016 | tr_TR |
dc.contributor.orcid | 0000-0001-5472-9065 | tr_TR |
dc.contributor.orcid | 0000-0002-1619-6680 | tr_TR |
dc.contributor.orcid | 0000-0002-3820-424X | tr_TR |
dc.contributor.orcid | 0000-0002-5956-8755 | tr_TR |
dc.contributor.orcid | 0000-0001-7904-883X | tr_TR |
dc.identifier.startpage | 713 | tr_TR |
dc.identifier.endpage | 723 | tr_TR |
dc.identifier.volume | 90 | tr_TR |
dc.relation.journal | Biomedicine and Pharmacotherapy | en_US |
dc.contributor.buuauthor | Tezcan, Gülçin | - |
dc.contributor.buuauthor | Taşkapılıoğlu, Mevlut Özgür | - |
dc.contributor.buuauthor | Tunca, Berrin | - |
dc.contributor.buuauthor | Bekar, Ahmet | - |
dc.contributor.buuauthor | Demirci, Hilal | - |
dc.contributor.buuauthor | Kocaeli, Hasan | - |
dc.contributor.buuauthor | Aksoy, Seçil Ak | - |
dc.contributor.buuauthor | Egeli, Ünal | - |
dc.contributor.buuauthor | Cecener, Gülşah | - |
dc.contributor.buuauthor | Tolunay, Şahsine | - |
dc.contributor.researcherid | AAI-1612-2021 | tr_TR |
dc.contributor.researcherid | AAH-1420-2021 | tr_TR |
dc.contributor.researcherid | ABB-8161-2020 | tr_TR |
dc.contributor.researcherid | AAH-3843-2020 | tr_TR |
dc.contributor.researcherid | AAW-5254-2020 | tr_TR |
dc.contributor.researcherid | ABI-6078-2020 | tr_TR |
dc.contributor.researcherid | AAP-9988-2020 | tr_TR |
dc.identifier.pubmed | 28419967 | tr_TR |
dc.subject.wos | Medicine, research & experimental | en_US |
dc.subject.wos | Pharmacology & pharmacy | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q2 | en_US |
dc.contributor.scopusid | 25650627600 | tr_TR |
dc.contributor.scopusid | 25936798300 | tr_TR |
dc.contributor.scopusid | 6602965754 | tr_TR |
dc.contributor.scopusid | 6603677218 | tr_TR |
dc.contributor.scopusid | 57193932262 | tr_TR |
dc.contributor.scopusid | 6603500567 | tr_TR |
dc.contributor.scopusid | 57193933334 | tr_TR |
dc.contributor.scopusid | 55665145000 | tr_TR |
dc.contributor.scopusid | 6508156530 | tr_TR |
dc.contributor.scopusid | 6602604390 | tr_TR |
dc.subject.scopus | Cancer Stem Cell; Insurance Markets; Operational Risk | en_US |
dc.subject.emtree | Angiogenesis inhibitor | en_US |
dc.subject.emtree | Bevacizumab | en_US |
dc.subject.emtree | Gelatinase A | en_US |
dc.subject.emtree | Gelatinase B | en_US |
dc.subject.emtree | Olea europaea extract | en_US |
dc.subject.emtree | Plant extract | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Vasculotropin A | en_US |
dc.subject.emtree | Angiogenesis inhibitor | en_US |
dc.subject.emtree | Bevacizumab | en_US |
dc.subject.emtree | Gelatinase A | en_US |
dc.subject.emtree | Gelatinase B | en_US |
dc.subject.emtree | Plant extract | en_US |
dc.subject.emtree | Vasculotropin A | en_US |
dc.subject.emtree | Antiangiogenic activity | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Cancer inhibition | en_US |
dc.subject.emtree | Cancer stem cell | en_US |
dc.subject.emtree | Cell invasion | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Drug potentiation | en_US |
dc.subject.emtree | Glioblastoma | en_US |
dc.subject.emtree | Glioblastoma cell line | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Human cell | en_US |
dc.subject.emtree | In vitro study | en_US |
dc.subject.emtree | Migration inhibition | en_US |
dc.subject.emtree | Olive tree | en_US |
dc.subject.emtree | Plant leaf | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Cancer stem cell | en_US |
dc.subject.emtree | Cell motion | en_US |
dc.subject.emtree | Chemistry | en_US |
dc.subject.emtree | Drug effects | en_US |
dc.subject.emtree | Drug potentiation | en_US |
dc.subject.emtree | Glioblastoma | en_US |
dc.subject.emtree | Metabolism | en_US |
dc.subject.emtree | Neovascularization (pathology) | en_US |
dc.subject.emtree | Olive tree | en_US |
dc.subject.emtree | Pathology | en_US |
dc.subject.emtree | Plant leaf | en_US |
dc.subject.emtree | Tumor cell line | en_US |
dc.subject.emtree | Tumor invasion | en_US |
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