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Genetic Variations of α-Methylacyl-CoA Racemase Are Associated with Sporadic Prostate Cancer Risk in Ethnically Homogenous Koreans
DC Field | Value | Language |
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dc.contributor.author | 박소희 | - |
dc.date.accessioned | 2014-12-18T09:58:07Z | - |
dc.date.available | 2014-12-18T09:58:07Z | - |
dc.date.issued | 2013 | - |
dc.identifier.issn | 2314-6133 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/89170 | - |
dc.description.abstract | Background. To assess if the variants of (R)-alpha-methyl-CoA racemase (AMACR) gene would be associated with the risk of sporadic prostate cancer in ethnically homogenous Koreans. Materials and Methods. We enrolled 194 patients with prostate cancer and 169 healthy controls. A total of 17 single nucleotide polymorphisms of the AMACR gene were selected. The distribution of each genotype and haplotype was analyzed and their association with the incidence of prostate cancer was evaluated. Further, we detected AMACR expression in tumor with immunohistochemistry and analyzed its association with genotype regarding prostate cancer risk. Results. AG or GG genotype of rs2278008 (E277K) tended to lower prostate cancer risk. The minor G allele was found to be a significant allele that decreased the risk of prostate cancer (adjusted OR, 0.57; 95% CI, 0.35–0.93, value = 0.025). In patients expression AMACR, AG or GG genotype was also significant genotype in terms of prostate cancer risk (adjusted OR, 0.47; 95% CI, 0.26–0.87, value = 0.017). Further, [GGCGG] haplotype consisted of five coding SNPs of rs2278008, rs34677, rs2287939, rs10941112, and rs3195676 which decreased the risk of prostate cancer ( value = 0.047). Conclusions. Genetic variations of AMACR are associated with the risk of sporadic prostate cancer that underwent radical prostatectomy in Koreans. | - |
dc.description.statementOfResponsibility | open | - |
dc.format | application/pdf | - |
dc.relation.isPartOf | BIOMED RESEARCH INTERNATIONAL | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Alleles | - |
dc.subject.MESH | Asian Continental Ancestry Group/genetics | - |
dc.subject.MESH | Gene Expression Regulation, Neoplastic | - |
dc.subject.MESH | Genetic Association Studies* | - |
dc.subject.MESH | Genetic Predisposition to Disease* | - |
dc.subject.MESH | Genotype | - |
dc.subject.MESH | Haplotypes | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Polymorphism, Single Nucleotide | - |
dc.subject.MESH | Prostatectomy | - |
dc.subject.MESH | Prostatic Neoplasms/genetics* | - |
dc.subject.MESH | Prostatic Neoplasms/pathology | - |
dc.subject.MESH | Prostatic Neoplasms/surgery | - |
dc.subject.MESH | Racemases and Epimerases/genetics* | - |
dc.subject.MESH | Risk Factors | - |
dc.title | Genetic Variations of α-Methylacyl-CoA Racemase Are Associated with Sporadic Prostate Cancer Risk in Ethnically Homogenous Koreans | - |
dc.type | Article | - |
dc.contributor.college | Graduate School of Public Health (보건대학원) | - |
dc.contributor.department | Graduate School of Public Health (보건대학원) | - |
dc.contributor.googleauthor | Sang-Jin Lee | - |
dc.contributor.googleauthor | Jae Young Joung | - |
dc.contributor.googleauthor | Hyekyoung Yoon | - |
dc.contributor.googleauthor | Jeong Eun Kim | - |
dc.contributor.googleauthor | Weon Seo Park | - |
dc.contributor.googleauthor | Ho Kyung Seo | - |
dc.contributor.googleauthor | Jinsoo Chung | - |
dc.contributor.googleauthor | Jung-Ah Hwang | - |
dc.contributor.googleauthor | Seung-Hyun Hong | - |
dc.contributor.googleauthor | Seungyoon Nam | - |
dc.contributor.googleauthor | Sohee Park | - |
dc.contributor.googleauthor | Jeongseon Kim | - |
dc.contributor.googleauthor | Kang Hyun Lee | - |
dc.contributor.googleauthor | Yeon-Su Lee | - |
dc.identifier.doi | 10.1155/2013/394285 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A01531 | - |
dc.relation.journalcode | J00315 | - |
dc.identifier.eissn | 2314-6141 | - |
dc.identifier.pmid | 24383053 | - |
dc.subject.keyword | Aged | - |
dc.subject.keyword | Alleles | - |
dc.subject.keyword | Asian Continental Ancestry Group/genetics | - |
dc.subject.keyword | Gene Expression Regulation, Neoplastic | - |
dc.subject.keyword | Genetic Association Studies* | - |
dc.subject.keyword | Genetic Predisposition to Disease* | - |
dc.subject.keyword | Genotype | - |
dc.subject.keyword | Haplotypes | - |
dc.subject.keyword | Humans | - |
dc.subject.keyword | Male | - |
dc.subject.keyword | Middle Aged | - |
dc.subject.keyword | Polymorphism, Single Nucleotide | - |
dc.subject.keyword | Prostatectomy | - |
dc.subject.keyword | Prostatic Neoplasms/genetics* | - |
dc.subject.keyword | Prostatic Neoplasms/pathology | - |
dc.subject.keyword | Prostatic Neoplasms/surgery | - |
dc.subject.keyword | Racemases and Epimerases/genetics* | - |
dc.subject.keyword | Risk Factors | - |
dc.contributor.alternativeName | Park, So Hee | - |
dc.contributor.affiliatedAuthor | Park, So Hee | - |
dc.rights.accessRights | free | - |
dc.citation.volume | 2013 | - |
dc.citation.startPage | 394285 | - |
dc.identifier.bibliographicCitation | BIOMED RESEARCH INTERNATIONAL, Vol.2013 : 394285, 2013 | - |
dc.identifier.rimsid | 34420 | - |
dc.type.rims | ART | - |
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