نمایش مختصر رکورد

dc.contributor.authorSoltaninejad, Vagihehen_US
dc.contributor.authorKazemipour, Nasrinen_US
dc.contributor.authorYaghoobi, Mohammad Mehdien_US
dc.contributor.authorPardakhty, Abbasen_US
dc.date.accessioned1399-07-09T03:49:56Zfa_IR
dc.date.accessioned2020-09-30T03:49:56Z
dc.date.available1399-07-09T03:49:56Zfa_IR
dc.date.available2020-09-30T03:49:56Z
dc.date.issued2020-03-01en_US
dc.date.issued1398-12-11fa_IR
dc.date.submitted2019-12-05en_US
dc.date.submitted1398-09-14fa_IR
dc.identifier.citationSoltaninejad, Vagiheh, Kazemipour, Nasrin, Yaghoobi, Mohammad Mehdi, Pardakhty, Abbas. (2020). Ethanolic Extract of Propolis from Kerman Area Triggers Apoptosis and Arrests Cell Cycle in Three Human Breast Cancer Cell Lines MDA-MB-231, SKBR and MCF-7. Journal of Kerman University of Medical Sciences, 27(2), 120-133. doi: 10.22062/jkmu.2020.90615en_US
dc.identifier.issn1023-9510
dc.identifier.issn2008-2843
dc.identifier.urihttps://dx.doi.org/10.22062/jkmu.2020.90615
dc.identifier.urihttp://jkmu.kmu.ac.ir/article_90615.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/248926
dc.description.abstract<strong>Background:</strong> Cancer is one of the major health problems worldwide and natural resources are being explored to develop anticancer drugs with fewer side effects. Iranian propolis contains components including flavonoids and polyphenols and has various medicinal properties. The aim of this study was to investigate the effect of Ethanolic Extract of Sirch Propolis (EESP) on three breast cancer cell lines. <strong>Methods:</strong> The MDA-MB-231, SKBR-3 and MCF-7 cells were treated for 24 and 48 h at the presence of 1% and 10% fetal bovine serum (FBS) concentration. MTT, BrdU and flow cytometry assays were used for measuring cytotoxicity, cell proliferation and apoptosis. <strong>Results:</strong> The highest cytotoxicity was seen on MDA-MB-231 cell at the presence of 1% and 10% FBS respectively following 48 h treatment. BrdU assay showed that treatment with 200 μg/ mL of EESP at the presence of 1% FBS for 48 h, reduced proliferation of MDA-MB-231 cell to 75% and that of MCF-7 and SKBR-3 cells to 70% and 60% respectively. Cell cycle analysis by flow cytometry showed that EESP at 200 μg/mL for 48h, induced G<sub>0</sub>/G<sub>1 </sub>phase arrest in MCF-7 and SKBR-3 cells and G<sub>2</sub>/M, S phase arrest in MDA-MB-231 cell. The cytotoxic effects of EESP were primarily found to be due to the induction of early stage apoptosis on SKBR-3 cell and early and late stage apoptosis on MCF-7 and MDA-MB-231 cells. <strong>Conclusion:</strong>The results demonstrated that EESP is a natural anticancer mixture capable of reducing breast cancer cells proliferation and inducing cell cycle arrest and apoptosis in them.en_US
dc.format.extent3831
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherKerman University of Medical Sciencesen_US
dc.relation.ispartofJournal of Kerman University of Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22062/jkmu.2020.90615
dc.subjectpropolisen_US
dc.subjectbreast canceren_US
dc.subjectCytotoxicityen_US
dc.subjectApoptosisen_US
dc.subjectCell cycleen_US
dc.titleEthanolic Extract of Propolis from Kerman Area Triggers Apoptosis and Arrests Cell Cycle in Three Human Breast Cancer Cell Lines MDA-MB-231, SKBR and MCF-7en_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentPh.D. student, Department of Pathobiology School of Veterinary Medicine, Shiraz University, Shiraz, Iranen_US
dc.contributor.departmentAssociate Professor, Department of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iranen_US
dc.contributor.departmentAssociate Professor, Department of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, Iranen_US
dc.contributor.departmentProfessor, Department of pharmaceutics, Faculty of pharmacy and pharmaceutical sciences, Kerman University of Medical Sciences, Kerman, Iranen_US
dc.citation.volume27
dc.citation.issue2
dc.citation.spage120
dc.citation.epage133


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