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Novel biomarker candidates for colorectal cancer metastasis: A meta-analysis of in vitro studies

DC Field Value Language
dc.contributor.authorNguyen Phuoc Long-
dc.contributor.authorLee, Wun Jun-
dc.contributor.authorNguyen Truong Huy-
dc.contributor.authorLee, Seul Ji-
dc.contributor.authorPark, Jeong Hill-
dc.contributor.authorKwon, Sung Won-
dc.creator박정일-
dc.date.accessioned2018-01-24T05:59:31Z-
dc.date.available2020-04-05T05:59:31Z-
dc.date.created2017-11-15-
dc.date.issued2016-09-
dc.identifier.citationCancer Informatics, Vol.15, pp.11-17-
dc.identifier.issn1176-9351-
dc.identifier.urihttps://hdl.handle.net/10371/138962-
dc.description.abstractColorectal cancer (CRC) is one of the most common and lethal cancers. Although numerous studies have evaluated potential biomarkers for early diagnosis, current biomarkers have failed to reach an acceptable level of accuracy for distant metastasis. In this paper, we performed a gene set meta-analysis of in vitro microarray studies and combined the results from this study with previously published proteomic data to validate and suggest prognostic candidates for CRC metastasis. Two microarray data sets included found 21 significant genes. Of these significant genes, ALDOA, IL8 (CXCL8), and PARP4 had strong potential as prognostic candidates. LAMB2, MCM7, CXCL23A, SERPINA3, ABCA3, ALDH3A2, and POLR2I also have potential. Other candidates were more controversial, possibly because of the biologic heterogeneity of tumor cells, which is a major obstacle to predicting metastasis. In conclusion, we demonstrated a meta-analysis approach and successfully suggested ten biomarker candidates for future investigation.-
dc.language영어-
dc.language.isoenen
dc.publisherLibertas Academica-
dc.titleNovel biomarker candidates for colorectal cancer metastasis: A meta-analysis of in vitro studies-
dc.typeArticle-
dc.identifier.doi10.4137/CIN.S40301-
dc.citation.journaltitleCancer Informatics-
dc.identifier.scopusid2-s2.0-84994037011-
dc.description.srndOAIID:RECH_ACHV_DSTSH_NO:T201631248-
dc.description.srndRECH_ACHV_FG:RR00200001-
dc.description.srndADJUST_YN:-
dc.description.srndEMP_ID:A001923-
dc.description.srndCITE_RATE:0-
dc.description.srndDEPT_NM:약학과-
dc.description.srndEMAIL:hillpark@snu.ac.kr-
dc.description.srndSCOPUS_YN:Y-
dc.citation.endpage17-
dc.citation.startpage11-
dc.citation.volume15-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorPark, Jeong Hill-
dc.contributor.affiliatedAuthorKwon, Sung Won-
dc.identifier.srndT201631248-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusNUCLEOTIDE EXCISION-REPAIR-
dc.subject.keywordPlusEPITHELIAL-MESENCHYMAL TRANSITION-
dc.subject.keywordPlusEXPRESSION PROFILES-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusCARCINOMA CELLS-
dc.subject.keywordPlusCOLON-CANCER-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusFUTURE-
dc.subject.keywordPlusROLES-
dc.subject.keywordAuthorcolorectal cancer-
dc.subject.keywordAuthorbiomarker candidate-
dc.subject.keywordAuthormicroarray analysis-
dc.subject.keywordAuthorproteomics-
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