نمایش مختصر رکورد

dc.date.accessioned1399-07-08T18:09:07Zfa_IR
dc.date.accessioned2020-09-29T18:09:07Z
dc.date.available1399-07-08T18:09:07Zfa_IR
dc.date.available2020-09-29T18:09:07Z
dc.date.issued2015-11-01en_US
dc.date.issued1394-08-10fa_IR
dc.identifier.citation(2015). Association between MTHFR C677T Polymorphism and Risk of Prostate Cancer: Evidence from 22 Studies with 10,832 Cases and 11,993 Controls. Asian Pacific Journal of Cancer Prevention, 16(11), 4525-4530.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_31119.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/37399
dc.description.abstract<b>Background:</b> The MTHFR C677T polymorphism is a genetic alteration affecting an enzyme involved infolate metabolism, but its relationship to host susceptibility to prostate cancer remains uncertain. The aim ofthis study was to investigate the association between MTHFR C677T polymorphism and prostate cancer byperforming a meta-analysis. Materials and <br/><b>Methods</b>: Pubmed and Web of Science databases were searched forcase-control studies investigating the association between MTHFR C677T polymorphism and prostate cancer.Odds ratios (OR) and 95% confidence intervals (95%CI) were used to assess any link. <br/><b>Results</b>: A total of 22independent studies were identified, including 10,832 cases and 11,993 controls. Meta-analysis showed thatthere was no obvious association between MTHFR C677T polymorphism and risk of prostate cancer underall five genetic models. There was also no obvious association between MTHFR C677T polymorphism andrisk of prostate cancer in the subgroup analyses of Caucasians. In contrast, MTHFR C677T polymorphismwas associated with increased risk for prostate cancer in Asians with the allele model (C vs G: OR=1.299, 95%CI =1.121-1.506, P=0.001, Pheterogeneity =0.120, I2=45%), additive genetic model (CC vs TT: OR =1.925, 95 %CI= 1.340-2.265, P=0.00, Pheterogeneity =0.587, I2=0.00%), recessive model (CC vs TT+TC: OR= 1.708, 95 % CI=1.233-2.367, P=0.001, Pheterogeneity =0.716, I2=0.00%), and heterozygote genetic model (CT vs TT: OR=2.193, 95% CI =1.510-3.186, P=0.000, Pheterogeneity =0.462, I2=0.00%). <br/><b>Conclusions</b>: These results suggest that the MTHFRC677T polymorphism does not contribute to the risk of prostate cancer from currently available evidence inpopulations overall and Caucasians. However, the meta analysis indicates that it may play a role in prostatecancer development in Asians.en_US
dc.format.extent1159
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.subjectMTHFR C677Ten_US
dc.subjectPolymorphismen_US
dc.subjectProstate Canceren_US
dc.subjectMeta Analysisen_US
dc.titleAssociation between MTHFR C677T Polymorphism and Risk of Prostate Cancer: Evidence from 22 Studies with 10,832 Cases and 11,993 Controlsen_US
dc.typeTexten_US
dc.citation.volume16
dc.citation.issue11
dc.citation.spage4525
dc.citation.epage4530


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