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孕烷X受体rs7643645多态性与前列腺癌患者前列腺特异性抗原水平升高的风险相关。

The PXR rs7643645 polymorphism is associated with the risk of higher prostate-specific antigen levels in prostate cancer patients.

作者信息

Reyes-Hernández Octavio D, Vega Libia, Jiménez-Ríos Miguel A, Martínez-Cervera Pedro F, Lugo-García Juan A, Hernández-Cadena Leticia, Ostrosky-Wegman Patricia, Orozco Lorena, Elizondo Guillermo

机构信息

Laboratorio de Genética y Diagnóstico Molecular, Hospital Juárez de México, México, D.F., México.

Departamento de Toxicología, Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional, México, D.F., México.

出版信息

PLoS One. 2014 Jun 12;9(6):e99974. doi: 10.1371/journal.pone.0099974. eCollection 2014.

Abstract

Levels of enzymes that determine testosterone catabolism such as CYP3A4 have been associated with prostate cancer (PCa) risk. Although some studies have related CYP3A41B allele, a gene polymorphism that modifies CYP3A4 expression level, with PCa risk, others have failed, suggesting that additional genetic variants may be involved. Expression of CYP3A4 is largely due to the activation of Pregnane X Receptor (PXR). Particularly, rs2472677 and rs7643645 PXR polymorphisms modify CYP3A4 expression levels. To evaluate whether PXR-HNF3β/T (rs2472677), PXR-HNF4/G (rs7643645), and CYP3A41B (rs2740574) polymorphisms are associated with PCa a case control-study was performed. The multiple testing analysis showed that the PXR-HNF4/G polymorphism was associated with higher levels of prostate-specific antigen (PSA) in patients with PCa (OR = 3.99, p = 0.03). This association was stronger in patients diagnosed at the age of 65 years or older (OR = 10.8, p = 0.006). Although the CYP3A4*1B/*1B genotype was overrepresented in PCa patients, no differences were observed in the frequency of this and PXR-HNF3β/T alleles between controls and cases. Moreover, no significant association was found between these polymorphisms and PSA, Gleason grade, or tumor lymph node metastasis.

摘要

决定睾酮分解代谢的酶(如CYP3A4)水平与前列腺癌(PCa)风险相关。尽管一些研究已将CYP3A41B等位基因(一种可改变CYP3A4表达水平的基因多态性)与PCa风险联系起来,但其他研究却未发现这种关联,这表明可能涉及其他基因变异。CYP3A4的表达很大程度上归因于孕烷X受体(PXR)的激活。特别是,PXR的rs2472677和rs7643645多态性会改变CYP3A4的表达水平。为了评估PXR-HNF3β/T(rs2472677)、PXR-HNF4/G(rs7643645)和CYP3A41B(rs2740574)多态性是否与PCa相关,我们进行了一项病例对照研究。多重检验分析表明,PXR-HNF4/G多态性与PCa患者中较高水平的前列腺特异性抗原(PSA)相关(比值比[OR]=3.99,p=0.03)。这种关联在65岁及以上诊断出的患者中更强(OR=10.8,p=0.006)。尽管CYP3A4*1B/*1B基因型在PCa患者中占比过高,但在对照组和病例组之间,该基因型及PXR-HNF3β/T等位基因的频率未观察到差异。此外,这些多态性与PSA、Gleason分级或肿瘤淋巴结转移之间未发现显著关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/4055777/1c4657fac6ec/pone.0099974.g001.jpg

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