Suppr超能文献

SULT2A1等位基因变异与非裔美国男性血浆肾上腺雄激素及前列腺癌的关联

Association of SULT2A1 allelic variants with plasma adrenal androgens and prostate cancer in African American men.

作者信息

Wilborn Teresa W, Lang Nicholas P, Smith Michelle, Meleth Sreelatha, Falany Charles N

机构信息

Department of Pharmaceutical Sciences, Samford University, Birmingham, AL 35229, USA.

出版信息

J Steroid Biochem Mol Biol. 2006 Jun;99(4-5):209-14. doi: 10.1016/j.jsbmb.2006.01.006. Epub 2006 Apr 17.

Abstract

Dehydroepiandrosterone (DHEA) sulfate which is present at micromolar levels in the plasma, can be desulfated to supply free DHEA for metabolism to androgens or estrogens in peripheral tissues. Human cytosolic sulfotransferase (SULT) 2A1 catalyzes DHEA sulfation in the adrenal cortex. Three SULT2A1 nonsynonymous coding single nucleotide polymorphisms (SNPs), identified only in African Americans (AA), are associated with decreased levels of activity and expression as compared to wild-type cDNA when expressed in COS cells. To test whether the SNPs are associated with decreased plasma androgens, 124 normal AA men were genotyped and plasma DHEA, DHEA-sulfate and testosterone levels determined. The two SNPs identified in these participants occurred at allelic frequencies of 0.044 (G187C) and 0.101 (G781A). The G187C SNP was highly linked to the G781A SNP. Although no differences in hormone levels were associated with the individual SNPs, a significant increase in the DHEA:DHEA-sulfate ratio was observed in participants with a heterozygous G187C/G781A genotype. Increased free DHEA levels may result in increased testosterone synthesis and stimulation in the prostate, therefore a group of AA prostate cancer (PC) patients and controls were genotyped. No significant association of the presence of the different SULT2A1 alleles with the occurrence of PC was detected.

摘要

硫酸脱氢表雄酮(DHEA)在血浆中的浓度为微摩尔水平,可被去硫酸化以提供游离DHEA,供外周组织代谢为雄激素或雌激素。人胞质硫酸转移酶(SULT)2A1催化肾上腺皮质中的DHEA硫酸化。仅在非裔美国人(AA)中鉴定出的三种SULT2A1非同义编码单核苷酸多态性(SNP),与在COS细胞中表达时相比野生型cDNA的活性和表达水平降低有关。为了测试这些SNP是否与血浆雄激素水平降低有关,对124名正常AA男性进行了基因分型,并测定了血浆DHEA、硫酸脱氢表雄酮和睾酮水平。在这些参与者中鉴定出的两个SNP的等位基因频率分别为0.044(G187C)和0.101(G781A)。G187C SNP与G781A SNP高度连锁。虽然激素水平的差异与单个SNP无关,但在具有杂合G187C/G781A基因型的参与者中观察到DHEA:硫酸脱氢表雄酮比值显著增加。游离DHEA水平升高可能导致睾酮合成增加并刺激前列腺,因此对一组AA前列腺癌(PC)患者和对照组进行了基因分型。未检测到不同SULT2A1等位基因的存在与PC发生之间的显著关联。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验