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dc.contributor.authorErsoz, M.
dc.contributor.authorCoskun, Z. M.
dc.contributor.authorAcikgoz, B.
dc.contributor.authorKaralti, I.
dc.contributor.authorCobanoglu, G.
dc.contributor.authorSesal, C.
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T15:56:39Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T15:56:39Z
dc.date.issued2017
dc.identifier.issn0145-5680
dc.identifier.issn1165-158X
dc.identifier.urihttps://dx.doi.org/10.14715/cmb/2017.63.7.12
dc.identifier.urihttp://hdl.handle.net/11446/2352
dc.descriptionWOS: 000418143900012en_US
dc.descriptionPubMed ID: 28838343en_US
dc.description.abstractThe aim of this study was to investigate the anti-proliferative, apoptotic, cytotoxic, and anti-oxidant effects of extracts from the lichen Cladonia pocillumon human breast cancer cells (MCF-7), and to characterize the anti-microbial features. MCF-7 cells were treated with methanolic C. pocillum extract for 24h. The cytotoxicity of the extract was tested with MTT. Moreover, its anti-proliferative effects were examined with immunocytochemical method. Apoptosis and biochemical parameters were detected in MCF-7. The methanol and chloroform extracts of the lichen were tested for anti-microbial activity against Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa, and Candida albicans using the disc diffusion method and calculation of minimal inhibitory concentrations. Although BrdU incorporation was not observed in MCF-7 cells treated with methanol extract at a concentration above 0.2 mg/ mL, a significant decrease was observed int he percentage of PCNA immunoreactive cells in groups treated with 0.2, 0.4, 06, and 0.8 mg/mL methanol extracts of C. pocillum (49 +/- 6.3, 44 +/- 5.2, 23 +/- 2.5, 0, respectively) compared to that of control (85 +/- 4.5). The percentage of apoptotic cells significantly increased in groups treated with 0.2, 0.4, 0.6, and 0.8 mg/mL extracts of the C. pocillum (54 +/- 3.5, 76 +/- 2.6, 77 +/- 1.8, 82 +/- 4.2, respectively) compared with that of control group (3.9 +/- 1.5). The half-maximal inhibitory concentration of the methanol extract against MCF-7 cells was 0.802 mg/mL. Although the chloroform extract showed more effective anti-microbial activity overall, the methanol extract showed higher anti-fungal activity. Collectively, the results of our study indicate that C. pocillum extracts have strong anti-microbial and apoptotic effects. This lichen therefore shows potential for development as a natural anti-microbial, anti-oxidant, and apoptotic agent.en_US
dc.description.sponsorshipMarmara University [FEN-A-200611-0208]en_US
dc.description.sponsorshipWe thank Prof. Dr. Engin Ozhatay (The Manager of Marmara University Research Center for Natural Herbs and Water Products) for providing us accommodation and transportation during collection of lichen material. The strains were provided by the Medical Microbiology Department of the Medicine Faculty of Yeditepe University, Istanbul, Turkey. This study was supported by The Research Fund of Marmara University with the project number FEN-A-200611-0208.en_US
dc.language.isoengen_US
dc.publisherC M B ASSOCen_US
dc.identifier.doi10.14715/cmb/2017.63.7.12en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCell proliferationen_US
dc.subjectLichenen_US
dc.subjectMicrobial activityen_US
dc.subjectMCF-7en_US
dc.subjectTUNELen_US
dc.titleIn vitro evaluation of cytotoxic, anti-proliferative, anti-oxidant, apoptotic, and anti-microbial activities of Cladonia pocillumen_US
dc.typearticleen_US
dc.relation.journalCELLULAR AND MOLECULAR BIOLOGYen_US
dc.departmentDBÜen_US
dc.identifier.issue7en_US
dc.identifier.volume63en_US
dc.identifier.startpage69en_US
dc.identifier.endpage75en_US
dc.contributor.authorID0000-0002-3549-2872en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Ersoz, M. -- Coskun, Z. M.] Istanbul Bilim Univ, Fac Arts & Sci, Dept Mol Biol & Genet, Istanbul, Turkey -- [Acikgoz, B. -- Cobanoglu, G. -- Sesal, C.] Marmara Univ, Sci & Art Fac, Dept Biol, Istanbul, Turkey -- [Karalti, I.] Yeditepe Univ, Med Fac, Clin Microbiol Lab, Istanbul, Turkeyen_US


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