Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/27965
Full metadata record
DC FieldValueLanguage
dc.contributor.authorManjegowda, Mohan C-
dc.contributor.authorDeb, Gauri-
dc.contributor.authorLimaye, Anil M-
dc.date.accessioned2014-04-11T13:13:29Z-
dc.date.available2014-04-11T13:13:29Z-
dc.date.issued2014-04-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/27965-
dc.description312-316en_US
dc.description.abstractInvestigations using in vitro and in vivo models of breast carcinogenesis have demonstrated anti-neoplastic activity of the green tea polyphenol, epigallocatechin gallate (EGCG). Although a number of molecular targets of EGCG have been identified, its impact on the expression of estrogen target genes is not completely understood. Here, we examined the mRNA expression levels of two estrogen target genes, namely Trefoil Factor 1 (pS2) and Progesterone Receptor (PR) in MCF-7 cells treated with EGCG. We observed that treatment with 40 µM EGCG, which caused only 20% decrease in cell viability, resulted in increased steady state expression levels of pS2 and PR mRNA. This suggests that EGCG may exert its biological activities, at least in part, by influencing the expression of estrogen target genes.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.52(04) [April 2014]en_US
dc.subjectBreast canceren_US
dc.subjectCarcinogenesisen_US
dc.subjectEpigallocatechin gallateen_US
dc.subjectEstrogen responsive markersen_US
dc.subjectMCF-7en_US
dc.subjectProgesterone receptoren_US
dc.subjectTrefoil Factor 1 (pS2)en_US
dc.titleEpigallocatechin gallate induces the steady state mRNA levels of pS2 and PR genes in MCF-7 breast cancer cellsen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.52(04) [April 2014]

Files in This Item:
File Description SizeFormat 
IJEB 52(4) 312-316.pdf394.53 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.