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dc.contributor.authorHanikoğlu, Ayşegül
dc.contributor.authorKüçüksayan, Ertan
dc.contributor.authorHanikoğlu, Ferhat
dc.contributor.authorÖzben, Tomris
dc.contributor.authorMenounou, Georgia
dc.contributor.authorSansone, Anna
dc.contributor.authorFerreri, Carla
dc.date.accessioned2021-02-19T21:16:27Z
dc.date.available2021-02-19T21:16:27Z
dc.date.issued2020
dc.identifier.issn0008-4212
dc.identifier.issn1205-7541
dc.identifier.urihttps://doi.org/10.1139/cjpp-2019-0352
dc.identifier.urihttps://hdl.handle.net/20.500.12868/432
dc.descriptionKucuksayan, Ertan/0000-0002-1611-0875en_US
dc.descriptionWOS: 000518813900002en_US
dc.descriptionPubMed: 31545905en_US
dc.description.abstractBreast cancer is a worldwide commonly found malignancy in women and effective treatment is regarded as a huge clinical challenge even in the presence of several treatment options. Extensive literature is available demonstrating polyphenols as phytopharmaceutical anticancer agents. Among the polyphenols, quercetin and curcumin have been reported to have a strong potential against breast cancer. However, so far, no comprehensive study has been performed to demonstrate the anticarcinogenic effects of curcumin, quercetin, and their combinations with somatostatin on the fatty acid profile of breast cancer cell membranes. We used MCF-7 and MDA-MB231 breast cancer cells incubated with curcumin and quercetin for 24 h, in the absence and presence of somatostatin, at their EC50 concentrations to evaluate membrane fatty acid based functional lipidomics together with the followup of EGFR and MAPK signaling pathways. The two cell lines gave different membrane free fatty acid reorganization. In MCF-7 cells, the following changes were observed: an increase of omega 6 linoleic acid in the cells incubated with somatostatin + quercetin and quercetin and a decrease of omega 3 acids in the cells incubated with somatostatin + curcumin compared to somatostatin and significant increases of monounsaturated fatty acid (MUFA), mono-trans arachidonic acid levels and docosapentaenoic acid for the cells incubated with somatostatin + quercetin compared to the control cells. In MDA-MB231 cells, incubations with curcumin, quercetin, and somatostatin + quercetin induced the most significant membrane remodeling with the increase of stearic acid, diminution of omega 6 linoleic, arachidonic acids, and omega 3 (docosapentaenoic and docosahexaenoic acids). Distinct signaling pathway changes were found for these cell lines. In MCF-7 cells, separate or combined incubations with somatostatin and quercetin, significantly decreased EGFR and incubation with curcumin decreased MAPK signaling. In MDA-MB231 cells, incubation with curcumin decreased AKT1 and p-AKT1 (Thr308) levels. Incubation with curcumin and quercetin decreased the EGFR levels. Our results showed that cytostatic and antioxidant treatments can be combined to induce membrane fatty acid changes, including lipid isomerization as specific free radical driven process, and to influence signaling pathways. This study aimed to contribute to the literature on these antioxidants in the treatment of breast cancer to clarify the effects and mechanisms in combination with somatostatin.en_US
dc.description.sponsorshipCOST ActionEuropean Cooperation in Science and Technology (COST) [CM1201]; STSM grant of the COST Action [CM1201]; COST (European Cooperation in Science and Technology)European Cooperation in Science and Technology (COST) [NutRedOx-CA16112]; TUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [217S253]; Akdeniz University Research FundsAkdeniz University [TDK-2017-2096]; Marie Sklodowska-Curie Innovative Training Network (ITN) ClickGene [H2020-MSCA-ITN-2014-642023]en_US
dc.description.sponsorshipThe authors thank the scientific environment and the meeting opportunity created by the COST Action CM1201 "Biomimetic Radical Chemistry." A.H. thanks the support of an STSM grant of the COST Action CM1201 for carrying out part of this work. The authors also acknowledge the networking opportunity created by the COST Action NutRedOx-CA16112 supported by COST (European Cooperation in Science and Technology) to continue their collaboration. This study was supported and funded by TUBITAK (project No. 217S253) and Akdeniz University Research Funds (TDK-2017-2096). C.F., G.M., and C.C. acknowledge funding from the Marie Sklodowska-Curie Innovative Training Network (ITN) ClickGene (H2020-MSCA-ITN-2014-642023).en_US
dc.language.isoengen_US
dc.publisherCanadian Science Publishingen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectsomatostatinen_US
dc.subjectcurcuminen_US
dc.subjectquercetinen_US
dc.subjectbreast canceren_US
dc.subjectcell signalingen_US
dc.subjectmembrane fatty acid profileen_US
dc.titleEffects of somatostatin, curcumin, and quercetin on the fatty acid profile of breast cancer cell membranesen_US
dc.typearticleen_US
dc.contributor.departmentALKÜen_US
dc.contributor.institutionauthor0-belirlenecek
dc.identifier.doi10.1139/cjpp-2019-0352
dc.identifier.volume98en_US
dc.identifier.issue3en_US
dc.identifier.startpage131en_US
dc.identifier.endpage138en_US
dc.relation.journalCanadian Journal of Physiology And Pharmacologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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