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Article: IκBα polymorphisms were associated with increased risk of gastric cancer in a southern Chinese population: A case-control study

TitleIκBα polymorphisms were associated with increased risk of gastric cancer in a southern Chinese population: A case-control study
Authors
KeywordsGene polymorphism
Gastric cancer
IκBα
Risk factor
Issue Date2011
Citation
Life Sciences, 2011, v. 88, n. 17-18, p. 792-797 How to Cite?
AbstractAim: Nuclear factor-kappa B inhibitor alpha (IκBα) polymorphisms were found to be associated with inflammatory diseases. However, the association between IκBα polymorphisms with gastric cancer is still unknown. We aim to investigate the association between IκBα polymorphisms and gastric cancer risk in a large population-based case-control study among southern Chinese. Main methods: A population-based case-control study was conducted between 1999 and 2006 in Guangdong Province, China. A total of 1010 gastric cancer patients and 1500 healthy controls were enrolled in this study. IκBα polymorphisms were identified by sequencing of IκBα gene ranging from the 2 kb promoter region to the 3.5 kb genomic region. Polymorphisms in IκBα were analyzed by TaqMan SNP genotyping assay. Key findings: rs17103265 deletion homozygote (-/-) had significantly increased gastric cancer risk (OR = 2.11, 95% CI = 1.17-3.83, P = 0.01), compared with rs17103265 T homozygote (TT). rs17103265 (-/-) genotype was significantly associated with increased risk of intestinal-type gastric cancer with (OR = 2.21, 95% CI = 1.19-4.08, P = 0.01), but not with the diffuse or mix type of gastric cancer. rs17103265 (-/-) was associated with poorly differentiated gastric cancer (OR = 2.05, 95% CI = 1.07-3.94, P = 0.03), but not with moderately or well differentiated gastric cancer. A significant decrease in luciferase activity was observed in rs17103265 deletion allele as compared with the vector containing the rs17103265 T allele (P < 0.0001). rs17103265 polymorphism was not associated with the prognosis of gastric cancer patients. Significance: IκBα rs17103265 deletion homozygote is a novel genetic risk factor for gastric carcinogenesis, especially for the development of certain subtypes of gastric cancer in southern Chinese population. © 2011 Elsevier Inc.
Persistent Identifierhttp://hdl.handle.net/10722/207023
ISSN
2015 Impact Factor: 2.685
2015 SCImago Journal Rankings: 1.056

 

DC FieldValueLanguage
dc.contributor.authorWang, Shiyan-
dc.contributor.authorZhang, Mingdong-
dc.contributor.authorZeng, Zhirong-
dc.contributor.authorTian, Linwei-
dc.contributor.authorWu, Kaichun-
dc.contributor.authorChu, JianHong-
dc.contributor.authorFan, Daiming-
dc.contributor.authorHu, Pinjin-
dc.contributor.authorSung, Joseph-
dc.contributor.authorYu, Jun-
dc.date.accessioned2014-12-09T04:31:15Z-
dc.date.available2014-12-09T04:31:15Z-
dc.date.issued2011-
dc.identifier.citationLife Sciences, 2011, v. 88, n. 17-18, p. 792-797-
dc.identifier.issn0024-3205-
dc.identifier.urihttp://hdl.handle.net/10722/207023-
dc.description.abstractAim: Nuclear factor-kappa B inhibitor alpha (IκBα) polymorphisms were found to be associated with inflammatory diseases. However, the association between IκBα polymorphisms with gastric cancer is still unknown. We aim to investigate the association between IκBα polymorphisms and gastric cancer risk in a large population-based case-control study among southern Chinese. Main methods: A population-based case-control study was conducted between 1999 and 2006 in Guangdong Province, China. A total of 1010 gastric cancer patients and 1500 healthy controls were enrolled in this study. IκBα polymorphisms were identified by sequencing of IκBα gene ranging from the 2 kb promoter region to the 3.5 kb genomic region. Polymorphisms in IκBα were analyzed by TaqMan SNP genotyping assay. Key findings: rs17103265 deletion homozygote (-/-) had significantly increased gastric cancer risk (OR = 2.11, 95% CI = 1.17-3.83, P = 0.01), compared with rs17103265 T homozygote (TT). rs17103265 (-/-) genotype was significantly associated with increased risk of intestinal-type gastric cancer with (OR = 2.21, 95% CI = 1.19-4.08, P = 0.01), but not with the diffuse or mix type of gastric cancer. rs17103265 (-/-) was associated with poorly differentiated gastric cancer (OR = 2.05, 95% CI = 1.07-3.94, P = 0.03), but not with moderately or well differentiated gastric cancer. A significant decrease in luciferase activity was observed in rs17103265 deletion allele as compared with the vector containing the rs17103265 T allele (P < 0.0001). rs17103265 polymorphism was not associated with the prognosis of gastric cancer patients. Significance: IκBα rs17103265 deletion homozygote is a novel genetic risk factor for gastric carcinogenesis, especially for the development of certain subtypes of gastric cancer in southern Chinese population. © 2011 Elsevier Inc.-
dc.languageeng-
dc.relation.ispartofLife Sciences-
dc.subjectGene polymorphism-
dc.subjectGastric cancer-
dc.subjectIκBα-
dc.subjectRisk factor-
dc.titleIκBα polymorphisms were associated with increased risk of gastric cancer in a southern Chinese population: A case-control study-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.lfs.2011.02.016-
dc.identifier.pmid21376060-
dc.identifier.scopuseid_2-s2.0-79954622970-
dc.identifier.volume88-
dc.identifier.issue17-18-
dc.identifier.spage792-
dc.identifier.epage797-

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