Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47691
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dc.contributor.authorNasirli F.-
dc.contributor.authorDaikh A.-
dc.contributor.authorDoğan N.M.-
dc.contributor.authorArslan Ş.-
dc.contributor.authorMutlu D.-
dc.contributor.authorSegueni N.-
dc.date.accessioned2023-01-09T21:29:38Z-
dc.date.available2023-01-09T21:29:38Z-
dc.date.issued2023-
dc.identifier.issn1573-4072-
dc.identifier.urihttps://doi.org/10.2174/1573407218666220510105639-
dc.identifier.urihttps://hdl.handle.net/11499/47691-
dc.description.abstractBackground: Breast cancer is a major cause of death in women worldwide. Propolis antitumor activity has become the subject of growing research related to breast cancer. Algerian propolis is being studied for its antitumor activity on several cell lines. However, little is known about its cytotoxic activity on the human breast adenocarcinoma cell line. Objective: The present study aimed to investigate the cytotoxic effect of Algerian propolis on human breast adenocarcinoma cells (MDA-MB-231) and explain its mechanism of action. Methods: Cytotoxic activity was evaluated using an MTT assay, and mechanisms involved in the cytotoxic activity were also investigated. In addition, the chemical profile was analyzed by the determination of TP and TF contents. Results: TP and TF of the tested propolis varied between 1.36±0.15 and 97.85±2.98 GAE ?g/mg for TP and 0.08±0.10 and 33.22±1,17QE ?g/mg for TF. Propolis treatment of MD-MB-231 cells for 24 hours was found to suppress the growth of the tested cell line in a dose-dependent manner. The tested propolis probably induced an intrinsic pathway of apoptosis through caspase cascade and activation of pro-apoptotic proteins, such as BAX, p53, and p21. In addition, cell proliferation was found to be inhibited by the diminution of CYCLIN2 and CDK4 activities associated with the increase in P21 acting as a protein inhibitor. Conclusion: Our results demonstrated that Algerian propolis could be used as a complementary treatment for breast cancer. Our propolis was found to suppress the growth of MDA-MB-231 cells by inducing apoptosis and inhibiting cell proliferation. © 2023 Bentham Science Publishers.en_US
dc.description.sponsorshipMinistère de l'Enseignement Supérieur et de la Recherche Scientifique, MESRS; Pamukkale Üniversitesi, PAÜ: 2019FEBE017en_US
dc.description.sponsorshipThis research was supported by Pamukkale University (2019FEBE017).en_US
dc.description.sponsorshipThe authors are grateful to Pamukkale University and the Ministry of Higher Education and Scientific Research, Algeria, for financial support.en_US
dc.language.isoenen_US
dc.publisherBentham Science Publishersen_US
dc.relation.ispartofCurrent Bioactive Compoundsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAlgerian propolisen_US
dc.subjectantitumor activityen_US
dc.subjectapoptosisen_US
dc.subjectcytotoxic activityen_US
dc.subjectgene expressionen_US
dc.subjectMDA-MB-231 cell lineen_US
dc.titleIn Vitro Evaluation of Cytotoxic Activity of Algerian propolis against Human Breast Adenocarcinoma (MDA-MB-231) Cells and Investigation of its Potential Mechanism of Actionen_US
dc.typeArticleen_US
dc.identifier.volume19en_US
dc.identifier.issue1en_US
dc.identifier.startpage28en_US
dc.identifier.endpage38en_US
dc.identifier.doi10.2174/1573407218666220510105639-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57223453976-
dc.authorscopusid57212510488-
dc.authorscopusid36117534100-
dc.authorscopusid8684142100-
dc.authorscopusid57212511655-
dc.authorscopusid6507513175-
dc.identifier.scopus2-s2.0-85144286397en_US
dc.identifier.scopusqualityQ3-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept17.02. Biology-
crisitem.author.dept17.02. Biology-
Appears in Collections:Fen Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
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