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Differential gene expression profiles of metastases in paired primary and metastatic colorectal carcinomas

DC Field Value Language
dc.contributor.author김호근-
dc.contributor.author민병소-
dc.contributor.author유권태-
dc.contributor.author이한나-
dc.contributor.author이환석-
dc.contributor.author강현주-
dc.contributor.author김남규-
dc.date.accessioned2015-05-19T17:06:46Z-
dc.date.available2015-05-19T17:06:46Z-
dc.date.issued2008-
dc.identifier.issn0030-2414-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/107526-
dc.description.abstractBACKGROUND AND METHODS: Despite the overwhelming clinical significance of metastases, the cellular and molecular mechanisms involved are largely unknown. In order to define significant differences between primary colon carcinomas and their metastases, we analyzed gene expression profiles of 12 sets of triple-paired tissues using 19 K human oligonucleotide microarrays. A total of 36 microarray experiments were analyzed by unsupervised two-way hierarchical clustering and multi-dimensional scaling (MDS). RESULTS: Both methods completely distinguished normal mucosa from carcinoma, but failed to demonstrate a complete classification of primary and metastatic carcinomas. We found a separable tendency to be classified into the primary and metastatic colon carcinomas by MDS. In supervised hierarchical clustering, we identified 80 genes that were differentially expressed between paired primary and metastatic colon carcinomas. The 80 identified genes also successfully distinguished three validation sets of primary and lung-metastatic colon carcinomas. A specific set of genes was identified that distinguished the metastasis from the corresponding primary tumor in nearly half of the metastases analyzed. CONCLUSIONS: We suggest that a more accurate model of the metastatic potential is based on a global tumor expression pattern along with the appearance of distinct metastatic variants. This molecular profiling may be useful for the future study of colon cancer metastasis.-
dc.description.statementOfResponsibilityopen-
dc.format.extent92~101-
dc.relation.isPartOfONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHColorectal Neoplasms/genetics*-
dc.subject.MESHColorectal Neoplasms/pathology-
dc.subject.MESHColorectal Neoplasms/therapy-
dc.subject.MESHFemale-
dc.subject.MESHGene Expression Profiling*-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms/genetics*-
dc.subject.MESHLiver Neoplasms/secondary-
dc.subject.MESHLiver Neoplasms/therapy-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHOligonucleotide Array Sequence Analysis-
dc.titleDifferential gene expression profiles of metastases in paired primary and metastatic colorectal carcinomas-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Surgery (외과학)-
dc.contributor.googleauthorKwi Hye Koh-
dc.contributor.googleauthorHwanseok Rhee-
dc.contributor.googleauthorHyun Ju Kang-
dc.contributor.googleauthorEungi Yang-
dc.contributor.googleauthorKwon Tae You-
dc.contributor.googleauthorHanna Lee-
dc.contributor.googleauthorByung Soh Min-
dc.contributor.googleauthorNam Kyu Kim-
dc.contributor.googleauthorSuk Woo Nam-
dc.contributor.googleauthorHoguen Kim-
dc.identifier.doi10.1159/000155211-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01183-
dc.contributor.localIdA01402-
dc.contributor.localIdA02454-
dc.contributor.localIdA03334-
dc.contributor.localIdA00353-
dc.contributor.localIdA03275-
dc.contributor.localIdA00092-
dc.relation.journalcodeJ02416-
dc.identifier.eissn1423-0232-
dc.identifier.pmid18784436-
dc.identifier.urlhttp://www.karger.com/Article/FullText/155211-
dc.subject.keywordColon carcinomas-
dc.subject.keywordGene expression-
dc.subject.keywordMetastasis-
dc.subject.keywordMicroarray-
dc.contributor.alternativeNameKim, Ho Keun-
dc.contributor.alternativeNameMin, Byung Soh-
dc.contributor.alternativeNameYou, Kwon Tae-
dc.contributor.alternativeNameLee, Han Na-
dc.contributor.alternativeNameRhee, Hwan Seok-
dc.contributor.alternativeNameKang, Hyun Ju-
dc.contributor.alternativeNameKim, Nam Kyu-
dc.contributor.affiliatedAuthorKim, Ho Keun-
dc.contributor.affiliatedAuthorMin, Byung Soh-
dc.contributor.affiliatedAuthorYou, Kwon Tae-
dc.contributor.affiliatedAuthorRhee, Hwan Seok-
dc.contributor.affiliatedAuthorKim, Nam Kyu-
dc.contributor.affiliatedAuthorLee, Hanna-
dc.contributor.affiliatedAuthorKang, Hyun Ju-
dc.rights.accessRightsnot free-
dc.citation.volume75-
dc.citation.number1-2-
dc.citation.startPage92-
dc.citation.endPage101-
dc.identifier.bibliographicCitationONCOLOGY, Vol.75(1-2) : 92-101, 2008-
dc.identifier.rimsid57266-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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