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Sunitinib synergizes the antitumor effect of cisplatin via modulation of ERCC1 expression in models of gastric cancer

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dc.contributor.authorYoon, Young-Kwang-
dc.contributor.authorIm, Seock-Ah-
dc.contributor.authorMin, Ahrum-
dc.contributor.authorKim, Hwang-Phill-
dc.contributor.authorHur, Hyung-Seok-
dc.contributor.authorLee, Kyung-Hun-
dc.contributor.authorHan, Sae-Won-
dc.contributor.authorSong, Sang-Hyun-
dc.contributor.authorOh, Do Youn-
dc.contributor.authorKim, Tae-You-
dc.contributor.authorKim, Woo Ho-
dc.contributor.authorBang, Yung-Jue-
dc.date.accessioned2021-01-31T11:02:12Z-
dc.date.available2021-01-31T11:02:12Z-
dc.date.created2020-12-23-
dc.date.created2020-12-23-
dc.date.created2020-12-23-
dc.date.created2020-12-23-
dc.date.created2020-12-23-
dc.date.issued2012-08-28-
dc.identifier.citationCancer Letters, Vol.321 No.2, pp.128-136-
dc.identifier.issn0304-3835-
dc.identifier.other119646-
dc.identifier.urihttps://hdl.handle.net/10371/172981-
dc.description.abstractWe evaluated the effects of sunitinib monotherapy and in combination with cisplatin in human gastric cancer cell lines. Sunitinib showed antiproliferative effect in gastric cancer cells line with high PDGFRA expression. Knockdown of PDGFRA showed that sunitinib sensitivity was correlated with the basal expression of PDGFRA. Synergistic growth inhibitory activity in combination with cisplatin was identified. We further explored how sunitinib potentiated the activity of cisplatin. We found that sunitinib treatment resulted in the down-regulation of ERCC1 expression via the modulation of PDGFRA expression in gastric cancer cells. The effect was verified via SNU484 xenograft model. Our data support the rationale of clinical trial using sunitinib in combination of cisplatin in gastric cancer. (c) 2012 Elsevier Ireland Ltd. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleSunitinib synergizes the antitumor effect of cisplatin via modulation of ERCC1 expression in models of gastric cancer-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1016/j.canlet.2012.01.019-
dc.citation.journaltitleCancer Letters-
dc.identifier.wosid000304899600004-
dc.identifier.scopusid2-s2.0-84862809405-
dc.citation.endpage136-
dc.citation.number2-
dc.citation.startpage128-
dc.citation.volume321-
dc.identifier.sci000304899600004-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorIm, Seock-Ah-
dc.contributor.affiliatedAuthorOh, Do Youn-
dc.contributor.affiliatedAuthorKim, Tae-You-
dc.contributor.affiliatedAuthorKim, Woo Ho-
dc.contributor.affiliatedAuthorBang, Yung-Jue-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusENDOTHELIAL GROWTH-FACTOR-
dc.subject.keywordPlusTYROSINE KINASE INHIBITOR-
dc.subject.keywordPlusPHASE-III-
dc.subject.keywordPlusFACTOR RECEPTOR-
dc.subject.keywordPlusCELL CARCINOMA-
dc.subject.keywordPlusTUMOR-GROWTH-
dc.subject.keywordPlusMITOMYCIN-C-
dc.subject.keywordPlusDNA-REPAIR-
dc.subject.keywordPlusSU11248-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordAuthorSunitinib-
dc.subject.keywordAuthorPDGFRA overexpression-
dc.subject.keywordAuthorChemosensitizer-
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