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Determination of genes related to gastrointestinal tract origin cancer cells using a cDNA microarray
DC Field | Value | Language |
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dc.contributor.author | 김상철 | - |
dc.contributor.author | 김태문 | - |
dc.contributor.author | 라선영 | - |
dc.contributor.author | 박찬희 | - |
dc.contributor.author | 서민영 | - |
dc.contributor.author | 정하진 | - |
dc.contributor.author | 정현철 | - |
dc.contributor.author | 조가비 | - |
dc.date.accessioned | 2017-10-26T06:19:22Z | - |
dc.date.available | 2017-10-26T06:19:22Z | - |
dc.date.issued | 2005 | - |
dc.identifier.issn | 1078-0432 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/150791 | - |
dc.description.abstract | PURPOSE: 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.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | American Association for Cancer Research | - |
dc.relation.isPartOf | CLINICAL CANCER RESEARCH | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Determination of genes related to gastrointestinal tract origin cancer cells using a cDNA microarray | - |
dc.type | Article | - |
dc.publisher.location | United States | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Yonsei Biomedical Research Center (연세의생명연구원) | - |
dc.contributor.department | Yonsei Biomedical Research Center (연세의생명연구원) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.department | Yonsei Biomedical Research Center (연세의생명연구원) | - |
dc.contributor.department | Yonsei Biomedical Research Center (연세의생명연구원) | - |
dc.contributor.department | Yonsei Biomedical Research Center (연세의생명연구원) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.department | Yonsei Biomedical Research Center (연세의생명연구원) | - |
dc.contributor.googleauthor | Tae Moon Kim | - |
dc.contributor.googleauthor | Ha Jin Jeong | - |
dc.contributor.googleauthor | Min Young Seo | - |
dc.contributor.googleauthor | Sang Chul Kim | - |
dc.contributor.googleauthor | Gabee Cho | - |
dc.contributor.googleauthor | Chan Hee Park | - |
dc.contributor.googleauthor | Tae Soo Kim | - |
dc.contributor.googleauthor | Kyu Hyun Park | - |
dc.contributor.googleauthor | Hyun Cheol Chung | - |
dc.contributor.googleauthor | Sun Young Rha | - |
dc.identifier.doi | OAK-2005-04728 | - |
dc.contributor.localId | A00530 | - |
dc.contributor.localId | A01069 | - |
dc.contributor.localId | A01316 | - |
dc.contributor.localId | A01712 | - |
dc.contributor.localId | A01880 | - |
dc.contributor.localId | A03757 | - |
dc.contributor.localId | A03773 | - |
dc.contributor.localId | A03800 | - |
dc.relation.journalcode | J00564 | - |
dc.contributor.alternativeName | Kim, Sang Chul | - |
dc.contributor.alternativeName | Kim, Tae Moon | - |
dc.contributor.alternativeName | Rha, Sun Young | - |
dc.contributor.alternativeName | Park, Chan Hee | - |
dc.contributor.alternativeName | Seo, Min Young | - |
dc.contributor.alternativeName | Jeong, Ha Jin | - |
dc.contributor.alternativeName | Chung, Hyun Cheol | - |
dc.contributor.alternativeName | Cho, Gabee | - |
dc.citation.volume | 11 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 79 | - |
dc.citation.endPage | 86 | - |
dc.identifier.bibliographicCitation | CLINICAL CANCER RESEARCH, Vol.11(1) : 79-86, 2005 | - |
dc.date.modified | 2017-05-04 | - |
dc.identifier.rimsid | 44751 | - |
dc.type.rims | ART | - |
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