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Resveratrol suppresses growth of human ovarian cancer cells in culture and in a murine xenograft model: Eukaryotic elongation factor 1A2 as a potential target

DC Field Value Language
dc.contributor.authorLee, Mee-Hyun-
dc.contributor.authorChoi, Bu Young-
dc.contributor.authorKundu, Joydeb Kumar-
dc.contributor.authorShin, Young Kee-
dc.contributor.authorNa, Hye-Kyung-
dc.contributor.authorSurh, Young-Joon-
dc.date.accessioned2013-01-22T02:27:11Z-
dc.date.available2013-01-22T02:27:11Z-
dc.date.created2017-11-15-
dc.date.issued2009-10-
dc.identifier.citationCancer Research, Vol.69 No.18, pp.7449-7458-
dc.identifier.issn0008-5472-
dc.identifier.other2805-
dc.identifier.urihttps://hdl.handle.net/10371/80932-
dc.description.abstractThe eukaryotic elongation factor 1A2 (eEF1A2) is known to retain oncogenic potential and is recognized as a novel target for cancer prevention and therapy. Resveratrol (trans-3,4',5-trihydroxystilbene), a phytoalexin present in grapes, has been reported to possess chemopreventive and chemotherapeutic activities. In the present study, we examined the growth-inhibitory effects of resveratrol in human ovarian cancer PA-1 cells, considering eEF1A2 as a potential molecular target. Pretreatment with resveratrol attenuated proliferation of serum-starved PA-1. cells stimulated with insulin or serum. Resveratrol also activated caspase-9, -7, and -3 and induced apoptosis in PA-1 cells in the presence of insulin or serum. Insulin or serum stimulation of PA-1 cells resulted in the marked induction of eEF1A2, which was suppressed by pretreatment with resveratrol. Moreover, resveratrol inhibited insulin- or serum-induced soft-agar colony formation in eEF1A2-transfected NIH3T3 cells. An antibody array directed to assess the phosphorylation of protein kinases revealed that treatment with insulin or serum induced the phosphorylation of Akt in PA-1 cells. Pharmacologic inhibition of Akt with LY294002 abrogated insulin- or serum-induced eEF1A2 expression and increased the caspase-3 activity. In another experiment, i.p. administration of resveratrol retarded the growth of PA-1 cell xenograft and the expression of eEF1A2 in athymic nude mice in association with decreased bromodeoxyuridine positivity, reduced expression of proliferating cell nuclear antigen, increased the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling and caspase-3 staining, and diminished CD31 positivity. Taken together, eEF1A2 may he considered as a potential molecular target for the antiproliferative effects of resveratrol in PA-1 ovarian cancer cells. [Cancer Res 2009;69(18):7449-58]-
dc.language영어-
dc.language.isoenko_KR
dc.publisherAmerican Association for Cancer Research-
dc.titleResveratrol suppresses growth of human ovarian cancer cells in culture and in a murine xenograft model: Eukaryotic elongation factor 1A2 as a potential target-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.identifier.doi10.1158/0008-5472.CAN-09-1266-
dc.citation.journaltitleCancer Research-
dc.description.tc21-
dc.identifier.wosid000269954000040-
dc.identifier.scopusid2-s2.0-70349736107-
dc.citation.endpage7458-
dc.citation.number18-
dc.citation.startpage7449-
dc.citation.volume69-
dc.identifier.sci000269954000040-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorShin, Young Kee-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusFACTOR EEF1A2-
dc.subject.keywordPlusCOLON-CANCER-
dc.subject.keywordPlusKAPPA-B-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusINSULIN-
dc.subject.keywordPlusLINES-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusCHEMOPREVENTION-
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  • College of Pharmacy
  • Department of Pharmacy
Research Area Agricultural Sciences

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