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前列腺特异性抗原(PSA)启动子多态性与PSA释放之间的关联。

Association between polymorphisms in the prostate-specific antigen (PSA) promoter and release of PSA.

作者信息

Sävblom C, Giwercman A, Malm J, Halldén C, Lundin K, Lilja H, Giwercman Y

机构信息

Department of Laboratory Medicine, Division of Clinical Chemistry, Lund University, Malmö University Hospital, Malmö, Sweden.

出版信息

Int J Androl. 2009 Oct;32(5):479-85. doi: 10.1111/j.1365-2605.2008.00882.x. Epub 2008 Mar 10.

Abstract

Variations in serum prostate-specific antigen (PSA) have been ascribed to A/G nucleotide polymorphisms located at -158 bp (rs266882) and -4643 bp (rs925013), relative to the transcription start site within the promoter of the PSA gene. PSA is also an androgen receptor target (AR) gene and polymorphisms in AR gene are known to affect AR function. Our objective was to compare the impact of these A/G polymorphisms separately or in combination with AR CAG micro satellite on regulation of PSA secretion into seminal plasma and blood in young men. Leukocyte DNA was extracted from 291 conscripts and genotyping performed with the Sequenom Mass Array System. PSA was measured with an immunofluorometric assay. Linear regression analysis was used to test the association of polymorphism frequencies with serum and seminal plasma levels of PSA. PSA gene polymorphisms at -158 bp or -4643 bp did not alone influence total PSA (tPSA) levels in seminal plasma or in blood. Homozygotes for the A-allele at -158 bp in combination with CAG > 22 had significantly higher serum levels of tPSA than subjects carrying the G-allele (p = 0.01). In conclusion, the PSA gene polymorphisms did not importantly influence the levels of tPSA in seminal plasma or in blood. tPSA in serum was influenced by interactions between PSA promoter variants and AR CAG polymorphism.

摘要

血清前列腺特异性抗原(PSA)的变化归因于PSA基因启动子内相对于转录起始位点位于-158bp(rs266882)和-4643bp(rs925013)处的A/G核苷酸多态性。PSA也是雄激素受体靶标(AR)基因,已知AR基因中的多态性会影响AR功能。我们的目的是比较这些A/G多态性单独或与AR CAG微卫星联合对年轻男性精浆和血液中PSA分泌调节的影响。从291名应征入伍者中提取白细胞DNA,并使用Sequenom Mass Array系统进行基因分型。用免疫荧光测定法测量PSA。采用线性回归分析来测试多态性频率与PSA血清和精浆水平之间的关联。-158bp或-4643bp处的PSA基因多态性单独并不影响精浆或血液中的总PSA(tPSA)水平。-158bp处A等位基因纯合子与CAG>22联合时,其血清tPSA水平显著高于携带G等位基因的受试者(p = 0.01)。总之,PSA基因多态性对精浆或血液中tPSA水平没有重要影响。血清中的tPSA受PSA启动子变体与AR CAG多态性之间相互作用的影响。

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