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Association of Foxp3 promoter polymorphisms with susceptibility to endometrial cancer in the Chinese Han women.


ABSTRACT: To evaluate the association between Foxp3 gene polymorphisms (rs3761548 and rs5902434) and susceptibility to endometrial cancer (EC), we report a hospital case-control study involving 602 women, consisting of 269 patients with EC and 333 healthy controls. Genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism. Our results suggest that the frequency of the A allele in rs3761548 in patients with EC was significantly lower than that in healthy controls (20.3% vs 26.4%, odds ratio [OR] 0.71, 95% confidence interval [CI]: 0.54-0.93, P?=?.012), while the heterozygous AC genotype showed a significant protective effect on EC in codominant, dominant, and overdominant models (adjusted OR 0.64, 95% CI: 0.45-0.91, P?=?.039; OR 0.65, 95% CI: 0.47-0.91, P?=?.011; OR 0.67, 95% CI: 0.47-0.94, P?=?.02, respectively), and AA genotype was more frequent in patients with cervical invasion (recessive model: OR 3.55, 95% CI: 1.10-11.44, P?=?.046). Moreover, ATT/ATT genotype (rs5902434) was conferred a lower risk of EC in the recessive model (adjusted OR 0.58, 95% CI: 0.35-0.96, P?=?.031). From the data generated, we conclude that Foxp3 promoter polymorphisms are associated with susceptibility to EC in Chinese Han women.

SUBMITTER: You D 

PROVIDER: S-EPMC6392658 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Association of Foxp3 promoter polymorphisms with susceptibility to endometrial cancer in the Chinese Han women.

You Di D   Wang Yanyun Y   Zhang Yan Y   Li Qin Q   Yu Xiuzhang X   Yuan Mingwei M   Lan Zhu Z   Zeng Xi X   Zhou Bin B   Song Yaping Y   Su Min M   Zhang Lin L   Xi Mingrong M  

Medicine 20180501 18


To evaluate the association between Foxp3 gene polymorphisms (rs3761548 and rs5902434) and susceptibility to endometrial cancer (EC), we report a hospital case-control study involving 602 women, consisting of 269 patients with EC and 333 healthy controls. Genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism. Our results suggest that the frequency of the A allele in rs3761548 in patients with EC was significantly lower than that in healthy controls (20.3%  ...[more]

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