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Standardized genetic alteration score and predicted score for predicting recurrence status of gastric cancer

DC Field Value Language
dc.contributor.author정현철-
dc.date.accessioned2015-04-24T17:09:15Z-
dc.date.available2015-04-24T17:09:15Z-
dc.date.issued2009-
dc.identifier.issn0171-5216-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/104860-
dc.description.abstractPURPOSE: To build a standardized genetic alteration score (SGAS) based on genes that are related to a patient's recurrence status, and to obtain the predicted score (PS) for predicting a patient's recurrence status, which reflects the genetic information of the gastric cancer patient. METHODS: SGAS was constructed using linear combinations that best account for the variability in the data. This methodology was fit to and validated using cDNA microarray-based CGH data obtained from the Cancer Metastasis Research Center at Yonsei University. RESULTS: When classifying cancer patients, the accuracy was 92.59% in the leave-one-out validation method. CONCLUSIONS: SGAS provided PS for the risk of recurrence, which was capable of discriminating a patient's recurrence status. A total of 59 genes were found to have a high frequency of alteration in either the recurrence or non-recurrence status. SGAS was found to be a significant risk factor on recurrence and explained 31% variability of the 59 genes.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1501~1512-
dc.relation.isPartOfJOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHFemale-
dc.subject.MESHGene Dosage*-
dc.subject.MESHHumans-
dc.subject.MESHLogistic Models-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Recurrence, Local/epidemiology*-
dc.subject.MESHProbability-
dc.subject.MESHStomach Neoplasms/genetics*-
dc.titleStandardized genetic alteration score and predicted score for predicting recurrence status of gastric cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorMijung Kim-
dc.contributor.googleauthorHyun Cheol Chung-
dc.identifier.doi10.1007/s00432-009-0597-1-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03773-
dc.relation.journalcodeJ01283-
dc.identifier.eissn1432-1335-
dc.identifier.pmid19449028-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs00432-009-0597-1-
dc.subject.keywordcDNA microarray-based CGH-
dc.subject.keywordGene copy number change-
dc.subject.keywordCorrect classification rate-
dc.subject.keywordFactor analysis-
dc.subject.keywordLogistic regression model-
dc.contributor.alternativeNameChung, Hyun Cheol-
dc.contributor.affiliatedAuthorChung, Hyun Cheol-
dc.citation.volume135-
dc.citation.number11-
dc.citation.startPage1501-
dc.citation.endPage1512-
dc.identifier.bibliographicCitationJOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, Vol.135(11) : 1501-1512, 2009-
dc.identifier.rimsid42528-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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