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dc.contributor.authorHsieh, Yao-Yuanen_US
dc.contributor.authorChang, Chi-Chenen_US
dc.contributor.authorWang, Yu-Kuoen_US
dc.contributor.authorHsu, Kung-Haoen_US
dc.contributor.authorChen, Chih-Pingen_US
dc.contributor.authorHsu, Chin-Muen_US
dc.contributor.authorTsai, Fuu-Jenen_US
dc.date.accessioned2014-12-08T15:06:48Z-
dc.date.available2014-12-08T15:06:48Z-
dc.date.issued2010-06-01en_US
dc.identifier.issn0250-7005en_US
dc.identifier.urihttp://hdl.handle.net/11536/5337-
dc.description.abstractObjectives: To investigate the roles of insulin-like growth factor II (IGF2), myeloperoxidase (MPO), E-cadherin (CDH1), urokinase and xeroderma pigmentosum group A and D (XPA, XPD) polymorphisms upon leiomyoma susceptibility. Study Design: Women were divided into: group I, leiomyoma (n=158); group 2, non-leiomyoma (n=156). Polymorphisms (IGF2 exon 9*A/G, MPO-463*A/G, CDH1-Pml I, urokinase-ApaL, XPA*A-23G, XPD*Lys751Gln) were amplified by polymerase chain reaction and detected by electrophoresis after restriction enzyme digestion. Genotype and allelic frequencies were compared between both groups. Results: Associations between leiomyoma with IGF2 and CDH1 polymorphism exist. Proportions of IGF2 exon 9*AA/AG/GG in and CDH1* CC/CT/TT in the groups were: group I, 38/39.2/22.8% and 27.8/66.5/5.7%; group 2, 22.4/53.9/23.7% and 21.2/64.1/14.7. MPO, urokinase, XPA and XPD in both groups were non-significantly different. Proportions of MPO*AA/AG/GG, urokinase*CC/CT/TT, XPA*AA/AG/GG and XPD*AA/AC/CC were: group 1: 1.9/23.4/74.7%, 0.6/7/92.4%, 20.9/55.1/24%, 85.4/14.6/0%; group 2: 3.8/24.4/71.8%, 1.3/4.5/94.2%, 22.4/53.9/23.7%, 84.6/15.4/0%. Conclusion: IGF2*A allele and CDH1*C allele were correlated with leiomyoma susceptibility, which may be associated with leiomyoma development. MPO, urokinase, XPA and XPD polymorphisms are not related to leiomyoma susceptibilities.en_US
dc.language.isoen_USen_US
dc.subjectCadherinen_US
dc.subjectinsulin-like growth factoren_US
dc.subjectleiomyomaen_US
dc.subjectmyeloperoxidaseen_US
dc.subjectpolymorphismen_US
dc.subjecturokinaseen_US
dc.subjectxeroderma pigmentosumen_US
dc.titleInsulin-like Growth Factors II exon 9 and E-cadherin-Pml I but not Myeloperoxidase Promoter-463, Urokinase-ApaL I nor Xeroderma Pigmentosum Polymorphisms Are Associated with Higher Susceptibility to Leiomyomaen_US
dc.typeArticleen_US
dc.identifier.journalANTICANCER RESEARCHen_US
dc.citation.volume30en_US
dc.citation.issue6en_US
dc.citation.spage2203en_US
dc.citation.epage2208en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000280230300042-
dc.citation.woscount2-
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