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Single-nucleotide polymorphisms in the promoter of the CDK5 gene and lung cancer risk in a Korean population

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dc.contributor.authorChoi, Hyo Seon-
dc.contributor.authorLee, Youngin-
dc.contributor.authorPark, Kyong Hwa-
dc.contributor.authorSung, Jae Sook-
dc.contributor.authorLee, Jong-Eun-
dc.contributor.authorShin, Eun-Soon-
dc.contributor.authorRyu, Jeong-Seon-
dc.contributor.authorKim, Yeul Hong-
dc.date.accessioned2021-09-08T17:26:42Z-
dc.date.available2021-09-08T17:26:42Z-
dc.date.issued2009-05-
dc.identifier.issn1434-5161-
dc.identifier.issn1435-232X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120089-
dc.description.abstractCyclin-dependent kinase 5 (CDK5), a proline-directed serine/threonine kinase, which was originally known for its regulatory role in neuronal activities, has recently been suggested to play a role in extraneuronal activities. For example, a recent study detected overexpression of the CDK5 gene in non-small-cell lung cancer. Therefore, in order to explore the association of the CDK5 gene with lung cancer risk in a Korean population, the genotypes of the CDK5 promoter region were determined in 407 lung cancer patients and 402 normal participants. The result showed that the -904 G>A genotype affected susceptibility to lung cancer risk (odd ratios (OR)=1.53, 95% confidence interval (CI)=1.02-2.32). Furthermore, subsequent haplotype analysis of three single-nucleotide polymorphism (SNP) regions suggested that the A-G-C haplotype was associated with a higher overall risk of lung cancer (OR=1.59, 95% CI=1.16-2.18). These results suggest that CDK5 promoter polymorphisms contribute to the genetic susceptibility to lung cancer in the Korean population. Journal of Human Genetics (2009) 54, 298-303; doi:10.1038/jhg.2009.29; published online 3 April 2009-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleSingle-nucleotide polymorphisms in the promoter of the CDK5 gene and lung cancer risk in a Korean population-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1038/jhg.2009.29-
dc.identifier.scopusid2-s2.0-67649566961-
dc.identifier.wosid000266538400008-
dc.identifier.bibliographicCitationJOURNAL OF HUMAN GENETICS, v.54, no.5, pp 298 - 303-
dc.citation.titleJOURNAL OF HUMAN GENETICS-
dc.citation.volume54-
dc.citation.number5-
dc.citation.startPage298-
dc.citation.endPage303-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusCYCLIN-DEPENDENT KINASE-5-
dc.subject.keywordPlusDIRECTED PROTEIN-KINASE-
dc.subject.keywordPlusCELL-DIFFERENTIATION-
dc.subject.keywordPlusACTIVATOR P35NCK5A-
dc.subject.keywordPlusMONOCYTIC CELLS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusHAPLOTYPE-
dc.subject.keywordPlusSNPS-
dc.subject.keywordAuthorcyclin-dependent kinase 5 (CDK5)-
dc.subject.keywordAuthorlung cancer-
dc.subject.keywordAuthorsingle-nucleotide polymorphism-
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