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Cited 144 time in webofscience Cited 158 time in scopus
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dc.contributor.authorNoh, DY-
dc.contributor.authorAhn, SJ-
dc.contributor.authorLee, RA-
dc.contributor.authorPark, IA-
dc.contributor.authorKim, JH-
dc.contributor.authorSuh, PG-
dc.contributor.authorRyu, SH-
dc.contributor.authorLee, KH-
dc.contributor.authorHan, JS-
dc.date.accessioned2016-03-31T13:19:20Z-
dc.date.available2016-03-31T13:19:20Z-
dc.date.created2009-08-12-
dc.date.issued2000-12-20-
dc.identifier.issn0304-3835-
dc.identifier.other2001-OAK-0000001961-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19565-
dc.description.abstractPhospholipase D (PLD) catalyzes the hydrolysis of phosphatidylcholine (PC) to produce phosphatidic acid (PA) and choline. PLD is a major enzyme implicated in important cellular processes. such as cell proliferation. We designed this study to investigate the expression of PLD in human breast carcinomas and non-malignant tissues using RT-PCR, Western blot analysis, immunohistochemistry and an Arf-dependent PLD activity assay. We examined about 550 bp of PCR product and 120 kDa of PLD protein, Our results showed that PLD protein and mRNA levels were overexpressed in 14 of 17 breast cancer tissues, We also observed increased expression by immunohistochemistry and Arf-dependent PLD activity in microsomes of human breast tumors, which correlated well with PLD expression. PLD expression was elevated in human breast tumors compared with normal breast tissues. These results implicate a possible role of PLD in human breast tumorigenesis and suggest that PLD may be useful as a marker for malignant disease in the breast. (C) 2000 Elsevier Science Ireland Ltd, All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCI IRELAND LTD-
dc.relation.isPartOfCANCER LETTERS-
dc.subjectphospholipase D-
dc.subjectbreast cancer tissues-
dc.subjecttumorigenesis-
dc.subjectPROTEIN-KINASE-C-
dc.subjectADP-RIBOSYLATION FACTOR-
dc.subjectCANINE KIDNEY-CELLS-
dc.subjectPHOSPHATIDIC-ACID-
dc.subjectPLASMA-MEMBRANES-
dc.subjectPHOSPHATIDYLCHOLINE HYDROLYSIS-
dc.subjectSIGNAL-TRANSDUCTION-
dc.subjectENDOTHELIAL-CELLS-
dc.subjectRAT HEPATOCYTES-
dc.subjectGROWTH-FACTOR-
dc.titleOverexpression of phospholipase D1 in human breast cancer tissues-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/S0304-3835(00)00612-1-
dc.author.googleNoh, DY-
dc.author.googleAhn, SJ-
dc.author.googleLee, RA-
dc.author.googlePark, IA-
dc.author.googleKim, JH-
dc.author.googleSuh, PG-
dc.author.googleRyu, SH-
dc.author.googleLee, KH-
dc.author.googleHan, JS-
dc.relation.volume161-
dc.relation.issue2-
dc.relation.startpage207-
dc.relation.lastpage214-
dc.contributor.id10052640-
dc.relation.journalCANCER LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationCANCER LETTERS, v.161, no.2, pp.207 - 214-
dc.identifier.wosid000168440000011-
dc.date.tcdate2019-01-01-
dc.citation.endPage214-
dc.citation.number2-
dc.citation.startPage207-
dc.citation.titleCANCER LETTERS-
dc.citation.volume161-
dc.contributor.affiliatedAuthorSuh, PG-
dc.contributor.affiliatedAuthorRyu, SH-
dc.identifier.scopusid2-s2.0-0034695165-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc126-
dc.type.docTypeArticle-
dc.subject.keywordPlusPROTEIN-KINASE-C-
dc.subject.keywordPlusADP-RIBOSYLATION FACTOR-
dc.subject.keywordPlusCANINE KIDNEY-CELLS-
dc.subject.keywordPlusPHOSPHATIDIC-ACID-
dc.subject.keywordPlusPLASMA-MEMBRANES-
dc.subject.keywordPlusPHOSPHATIDYLCHOLINE HYDROLYSIS-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusRAT HEPATOCYTES-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordAuthorphospholipase D-
dc.subject.keywordAuthorbreast cancer tissues-
dc.subject.keywordAuthortumorigenesis-
dc.relation.journalWebOfScienceCategoryOncology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-

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Dept of Life Sciences
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