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dc.contributor.authorTurna, Özge
dc.contributor.authorBaykal, Aslıhan
dc.contributor.authorKüçükkara, Elif Sözen
dc.contributor.authorÖzten, Özge
dc.contributor.authorÖzkan, Asuman Deveci
dc.contributor.authorEskiler, Gamze Güney
dc.contributor.authorLim, Hyun Soo
dc.date.accessioned2022-02-09T12:29:26Z
dc.date.available2022-02-09T12:29:26Z
dc.date.issued2021
dc.identifier.issn0268-8921
dc.identifier.issn1435-604X
dc.identifier.urihttps://doi.org/10.1007/s10103-021-03324-y
dc.identifier.urihttps://hdl.handle.net/20.500.14002/256
dc.description.abstractCanine mammary gland tumors (CMGTs) are heterogeneous disease and subclassified [sarcomas (S), carcinomas (C), and carcinosarcomas (CS)] according to histopathological differentiation. Photodynamic therapy (PDT) is a promising treatment strategy based on the use of a photosensitizer (PS) activated by light. However, the therapeutic potential of PDT in the treatment of CMGTs has not been investigated, yet. Therefore, the aim of this study was to determine the in vitro protocol of 5-ALA-based-PDT for the treatment of three subtypes of CMGTs, for the first time. The intracellular PpIX florescence intensity was measured for 5-ALA (0.5 and 1 mM). After irradiation with different light doses (6, 9, 12, 18, and 24 J/cm(2)) for two different modes [continuous wave (CW) and pulse radiation (PR)], the cytotoxic effects of 5-ALA (0.5 and 1 mM) on the subtypes (C, S, and CS) of CMGTs were analyzed by WST-1. Finally, the optimal PDT treatment protocol was validated through Annexin V and AO/EtBr staining. Our results showed that 1 mM 5-ALA for 4-h incubation was the best treatment condition in all subtypes of CMGTs due to higher intracellular PpIX level. After irradiation with different light doses, PR mode was more effective in S primary cells at 9 J/cm(2). However, a significant decrease in the viability of C and CS cells was detected at 12 /cm(2) in CW mode (p < 0.05). Additionally, 1 mM 5-ALA induced apoptotic cell death in each subtype of CMGTs. Our preliminary findings suggest that (i) each subtype of CMGTs differentially responds to PDT and (ii) the light dose and mode could play an important role in the effective PDT treatment. However, further studies are needed to investigate the role of the different light sources and PDT-based apoptotic cell death in CMGTs cells.en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey, TUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [1001, 119O383]en_US
dc.description.sponsorshipThis work was supported by the Scientific and Technological Research Council of Turkey, TUBITAK 1001 (no. 119O383).en_US
dc.language.isoengen_US
dc.publisherSpringer London Ltden_US
dc.relation.ispartofLasers in Medical Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPhotodynamic therapyen_US
dc.subject5-Aminolevulinic aciden_US
dc.subjectCanine mammary gland tumoren_US
dc.subjectApoptosisen_US
dc.titleEfficacy of 5-aminolevulinic acid-based photodynamic therapy in different subtypes of canine mammary gland cancer cellsen_US
dc.typearticleen_US
dc.authoridUcmak, Melih / 0000-0002-8688-127X
dc.authoridKaleli, Suleyman / 0000-0002-6043-2521
dc.authoridYILDIZ, Salih Zeki / 0000-0001-5086-8770
dc.authoridBilir, Cemil / 0000-0002-1372-4791
dc.authoridguney eskiler, gamze / 0000-0002-2088-9914
dc.authoridBAYKAL, ASLIHAN / 0000-0002-2107-1874
dc.authoridSozen Kucukkara, Elif / 0000-0002-4246-7333
dc.departmentEnstitüler, Lisansüstü Eğitim Enstitüsü, Biyomedikal Mühendisliği Ana Bilim Dalıen_US
dc.identifier.doi10.1007/s10103-021-03324-y
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidLim, Hyun Soo/ABD-3910-2021
dc.authorwosidUcmak, Melih/D-3017-2019
dc.authorwosidBilir, Cemil/A-2491-2017
dc.authorwosidKaleli, Suleyman/F-2072-2018
dc.authorscopusid57223189229
dc.authorscopusid57223181378
dc.authorscopusid57217151702
dc.authorscopusid57223180626
dc.authorscopusid57210072482
dc.authorscopusid57190947987
dc.authorscopusid57211748339
dc.identifier.wosWOS:000646098700001en_US
dc.identifier.scopus2-s2.0-85105156515en_US
dc.identifier.pmid33937952en_US


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