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dc.contributor.authorNejati-Koshki, K
dc.contributor.authorZarghami, N
dc.contributor.authorPourhassan-Moghaddam, M
dc.contributor.authorRahmati-Yamchi, M
dc.contributor.authorMollazade, M
dc.contributor.authorNasiri, M
dc.contributor.authorEsfahlan, RJ
dc.contributor.authorBarkhordari, A
dc.contributor.authorTayefi-Nasrabadi, H
dc.date.accessioned2018-08-26T08:04:17Z
dc.date.available2018-08-26T08:04:17Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49521
dc.description.abstractLeptin plays the role of mitogenic factor in the breast carcinogenesis. Therefore, it could be considered as a target for breast cancer therapy. Leptin gene expression could be modulated by activation of estrogen receptors. Silibinin is an herbal compound with anti-cancer activity on prostate and colorectal cancers. Based on the fact that targeting of leptin can be considered as a novel strategy for breast cancer therapy, the aim of this study was the investigation of potentiality of silibinin for inhibition of leptin gene expression and secretion, and its link with expression of estrogen receptors. Cytotoxic effect of silibinin on T47D breast cancer cells was investigated by MTT assay test after 24, 48 and 72 h treatments with different concentrations of silibinin. The levels of leptin, estrogen receptor alpha and estrogen receptor beta genes expression was measured by reverse-transcription real-time PCR. The amount of secreted leptin in the culture medium was determined by ELISA. Data were statistically analyzed by one-way ANOVA test. Silibinin inhibits growth of T47D cells in a time and dose dependent manner. There was significant difference between control and treated cells in the levels of leptin, estrogen receptor beta expression levels and the quantity of secreted leptin was decreased in the treated cells in comparison to control cells. In conclusion, silibinin inhibits the expression and the secretion of leptin and in the future it might probably be a drug candidate for breast cancer therapy through leptin targeting.
dc.language.isoEnglish
dc.relation.ispartofCYTOTECHNOLOGY
dc.subjectLeptin
dc.subjectSilibinin
dc.subjectBreast cancer
dc.subjectT47D cell line
dc.titleInhibition of leptin gene expression and secretion by silibinin: possible role of estrogen receptors
dc.typeArticle
dc.citation.volume64
dc.citation.issue6
dc.citation.spage719
dc.citation.epage726
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1007/s10616-012-9452-3


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