An RNA aptamer that specifically binds pancreatic adenocarcinoma up-regulated factor inhibits migration and growth of pancreatic cancer cells

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dc.contributor.authorY H Kim-
dc.contributor.authorH J Sung-
dc.contributor.authorS Kim-
dc.contributor.authorE O Kim-
dc.contributor.authorJ W Lee-
dc.contributor.authorJ Y Moon-
dc.contributor.authorK Choi-
dc.contributor.authorJ E Jung-
dc.contributor.authorY Lee-
dc.contributor.authorSang Seok Koh-
dc.contributor.authorS G Rhee-
dc.contributor.authorK Heo-
dc.contributor.authorI H Kim-
dc.date.accessioned2017-04-19T09:25:45Z-
dc.date.available2017-04-19T09:25:45Z-
dc.date.issued2011-
dc.identifier.issn0304-3835-
dc.identifier.uri10.1016/j.canlet.2011.08.027ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10379-
dc.description.abstractPreviously, we reported that a novel secretory protein, pancreatic adenocarcinoma up-regulated factor (PAUF), which is highly expressed in pancreatic cancer and mediates the growth and metastasis of pancreatic cancer cells. In this study, we generated and characterized a 2'-fluoropyrimidine modified RNA aptamer (P12FR2) directed against human PAUF. P12FR2 binds specifically to human PAUF with an estimated apparent K D of 77. nM. P12FR2 aptamer inhibits PAUF-induced migration of PANC-1, human pancreatic cancer cells, in a wound healing assay. Moreover, intraperitoneal injection of P12FR2 decreased tumor growth by about 60% in an in vivo xenograft model with CFPAC-1 pancreatic cancer cells, without causing a loss of weight in the treated mice. Taken together, we propose here that PAUF-specific RNA aptamer, P12FR2, has the potential to be effective in the therapy of human pancreatic cancer.-
dc.publisherElsevier-
dc.titleAn RNA aptamer that specifically binds pancreatic adenocarcinoma up-regulated factor inhibits migration and growth of pancreatic cancer cells-
dc.title.alternativeAn RNA aptamer that specifically binds pancreatic adenocarcinoma up-regulated factor inhibits migration and growth of pancreatic cancer cells-
dc.typeArticle-
dc.citation.titleCancer Letters-
dc.citation.number1-
dc.citation.endPage83-
dc.citation.startPage76-
dc.citation.volume313-
dc.contributor.affiliatedAuthorSang Seok Koh-
dc.contributor.alternativeName김윤희-
dc.contributor.alternativeName성호진-
dc.contributor.alternativeName김수경-
dc.contributor.alternativeName김은옥-
dc.contributor.alternativeName이지원-
dc.contributor.alternativeName문주영-
dc.contributor.alternativeName최경호-
dc.contributor.alternativeName정지은-
dc.contributor.alternativeName이양순-
dc.contributor.alternativeName고상석-
dc.contributor.alternativeName이서구-
dc.contributor.alternativeName허균-
dc.contributor.alternativeName김인후-
dc.identifier.bibliographicCitationCancer Letters, vol. 313, no. 1, pp. 76-83-
dc.identifier.doi10.1016/j.canlet.2011.08.027-
dc.subject.keywordAnticancer drug-
dc.subject.keywordAptamer-
dc.subject.keywordPancreatic cancer-
dc.subject.keywordPAUF-
dc.subject.keywordSELEX-
dc.subject.localAnticancer drug-
dc.subject.localanti-cancer drug-
dc.subject.localanticancer drug-
dc.subject.localAnti-cancer drugs-
dc.subject.localAnticancer drugs-
dc.subject.localAnti-Cancer Drugs-
dc.subject.localAnti-cancer drug-
dc.subject.localAnticancer Drug-
dc.subject.localaptamer-
dc.subject.localAptamers-
dc.subject.localAptamer-
dc.subject.localpancreatic cancer-
dc.subject.localPancreatic cancer-
dc.subject.localPAUF-
dc.subject.localSELEX-
dc.description.journalClassY-
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