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Determination of genes related to gastrointestinal tract origin cancer cells using a cDNA microarray

DC FieldValueLanguage
dc.contributor.author김상철-
dc.contributor.author김태문-
dc.contributor.author라선영-
dc.contributor.author박찬희-
dc.contributor.author서민영-
dc.contributor.author정하진-
dc.contributor.author정현철-
dc.contributor.author조가비-
dc.date.accessioned2017-10-26T06:19:22Z-
dc.date.available2017-10-26T06:19:22Z-
dc.date.issued2005-
dc.identifier.issn1078-0432-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/150791-
dc.description.abstractPURPOSE: We evaluated the genome-wide gene expression profiles of various cancer cell lines to identify the gastrointestinal tract cancer cell-related genes. EXPERIMENTAL DESIGN: Gene expression profilings of 27 cancer cell lines and 9 tissues using 7.5K human cDNA microarrays in indirect design with Yonsei reference RNA composed of 11 cancer cell line RNAs were done. The significant genes were selected using significant analysis of microarray in various sets of data. The selected genes were validated using real-time PCR analysis. RESULTS: After intensity-dependent, within-print-tip normalization by loess method, we observed that expression patterns of cell lines and tissues were substantially different, divided in two discrete clusters. Next, we selected 115 genes that discriminate gastrointestinal cancer cell lines from others using significant analysis of microarray. Among the expression profiles of five gastric cancer cell lines, 66 genes were identified as differentially expressed genes related to metastatic phenotype. YCC-16, which was established from the peripheral blood of one advanced gastric cancer patient, produced a unique gene expression pattern resembling the profiles of lymphoid cell lines. Quantitative real-time reverse transcription-PCR results of selected genes, including PXN, KRT8, and ITGB5, were correlated to microarray data and successfully discriminate the gastrointestinal tract cancer cell lines from hematologic malignant cell lines. CONCLUSIONS: A gene expression database could serve as a useful source for the further investigation of cancer biology using the cell lines.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Association for Cancer Research-
dc.relation.isPartOfClinical Cancer Research-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleDetermination of genes related to gastrointestinal tract origin cancer cells using a cDNA microarray-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.googleauthorTae Moon Kim-
dc.contributor.googleauthorHa Jin Jeong-
dc.contributor.googleauthorMin Young Seo-
dc.contributor.googleauthorSang Chul Kim-
dc.contributor.googleauthorGabee Cho-
dc.contributor.googleauthorChan Hee Park-
dc.contributor.googleauthorTae Soo Kim-
dc.contributor.googleauthorKyu Hyun Park-
dc.contributor.googleauthorHyun Cheol Chung-
dc.contributor.googleauthorSun Young Rha-
dc.contributor.localIdA00530-
dc.contributor.localIdA01069-
dc.contributor.localIdA01316-
dc.contributor.localIdA01712-
dc.contributor.localIdA01880-
dc.contributor.localIdA03757-
dc.contributor.localIdA03773-
dc.contributor.localIdA03800-
dc.relation.journalcodeJ00564-
dc.contributor.alternativeNameKim, Sang Chul-
dc.contributor.alternativeNameKim, Tae Moon-
dc.contributor.alternativeNameRha, Sun Young-
dc.contributor.alternativeNamePark, Chan Hee-
dc.contributor.alternativeNameSeo, Min Young-
dc.contributor.alternativeNameJeong, Ha Jin-
dc.contributor.alternativeNameChung, Hyun Cheol-
dc.contributor.alternativeNameCho, Gabee-
dc.citation.volume11-
dc.citation.number1-
dc.citation.startPage79-
dc.citation.endPage86-
dc.identifier.bibliographicCitationClinical Cancer Research, Vol.11(1) : 79-86, 2005-
dc.date.modified2017-05-04-
Appears in Collections:
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
5. Research Institutes (연구소) > Cancer Metastasis Research Center (암전이연구센터) > 1. Journal Papers

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