نمایش مختصر رکورد

dc.date.accessioned1399-07-08T18:07:20Zfa_IR
dc.date.accessioned2020-09-29T18:07:20Z
dc.date.available1399-07-08T18:07:20Zfa_IR
dc.date.available2020-09-29T18:07:20Z
dc.date.issued2015-09-01en_US
dc.date.issued1394-06-10fa_IR
dc.identifier.citation(2015). Effect of Sesamin on Apoptosis and Cell Cycle Arrest in Human Breast Cancer MCF-7 Cells. Asian Pacific Journal of Cancer Prevention, 16(9), 3779-3783.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_30988.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/36705
dc.description.abstractDietary prevention has been known to reduce breast cancer risk. Sesamin is one of the major components insesame seeds and has been widely studied and proven to have anti-proliferation and anti-angiogenic effects oncancer cells. In this study, the influence of sesamin was tested in the human breast cancer MCF-7 cell line forcell viability (MTT assay) and cell cycling (flow cytometry). Results showed that sesamin dose-dependently (1,10 and 50 μM) reduced the cell viability and increased LDH release and apoptosis (TUNEL assay). In addition,there was a significant increase of sub-G1 phase arrest in the cell cycle after sesamin treatment. Furthermore,sesamin increased the expression of apoptotic markers of Bax, caspase-3, and cell cycle control proteins, p53 andcheckpoint kinase 2. Taken together, these results suggested that sesamin might be used as a dietary supplementf or prevention of breast cancer by modulating apoptotic signal pathways and inhibiting tumor cell growth.en_US
dc.format.extent647
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.subjectSesaminen_US
dc.subjectbreast canceren_US
dc.subjectApoptosisen_US
dc.subjectCell cycleen_US
dc.titleEffect of Sesamin on Apoptosis and Cell Cycle Arrest in Human Breast Cancer MCF-7 Cellsen_US
dc.typeTexten_US
dc.citation.volume16
dc.citation.issue9
dc.citation.spage3779
dc.citation.epage3783


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