首页> 外文期刊>Journal of Pharmacy and Bioallied Sciences >Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism
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Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism

机译:参与胆固醇代谢的CYP7A1,CYP7B1和CYP27A1酶多态性患病率的种族差异

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It is well known that drug disposition and response are greatly determined by the activities of drug metabolizing enzymes, which are polymorphic. Some of these polymorphisms are clinically relevant and presented an ethnic-dependent pattern of distribution. The characterization of the genetic distribution of different populations allows the selection of therapeutic options in accordance with the genetic background, with the objective to avoid adverse reactions and inefficacy of the treatment. In this work, we studied selected genetic polymorphisms in drug metabolizing enzymes in three different ethnic groups – Portugal, Mozambique and Colombia. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) genotyping methods were developed for drug metabolizing enzymes, namely, cholesterol 7α-hydroxylase (CYP7A1) (–203A>C, –346C>T, –496C>T, N233S, G347S), sterol 27-hydroxylase (CYP27A1) (R164W, A169V, D273N, V400A) and oxysterol 7α-hydroxylase (CYP7B1) (–116C>G, R324H, 1774C>T) to characterize the allelic distribution of these polymorphisms among three different ethnic/geographic origins. A total of 12 CYP7A1, CYP27A1 and CYP7B1 genetic variants were genotyped in a sample of 92 Portuguese, 151 Mozambican and 91 Colombian subjects. The variants N233S in CYP7A1 and 1774C>T in CYP7B1 were not detected in any population studied. The promoter polymorphisms in CYP7A1 (–203A>C, –346C>T, –496C>T) had high frequency in the three ethnic groups. G347S (CYP7A1), R164W, A169V and V400A (CYP27A1) were present in a low frequency but with a similar distribution in the three ethnic groups. Significant differences were observed for D273N (CYP27A1), –346C>T (CYP7A1), –116C>G and R324H (CYP7B1)Our results demonstrate a high variability of drug metabolizing enzymes between the different populations analyzed, indicating that at least some of these polymorphisms are ethnic specific.Keywords: Cholesterol 7α-hydroxylase, drug metabolizing enzymes, oxysterol 7α-hydroxylase, sterol 27-hydroxylase
机译:众所周知,药物的处置和反应在很大程度上取决于多态性的药物代谢酶的活性。这些多态性中的某些与临床相关,并呈现出种族依赖性的分布模式。对不同人群的遗传分布进行表征可以根据遗传背景选择治疗选择,目的是避免不良反应和治疗无效。在这项工作中,我们研究了葡萄牙,莫桑比克和哥伦比亚这三个不同种族的药物代谢酶中选定的遗传多态性。开发了用于药物代谢酶的聚合酶链反应-限制性片段长度多态性(PCR-RFLP)基因分型方法,即胆固醇7α-羟化酶(CYP7A1)(–203A> C,–346C> T,–496C> T,N233S,G347S ),固醇27-羟化酶(CYP27A1)(R164W,A169V,D273N,V400A)和氧固醇7α-羟化酶(CYP7B1)(–116C> G,R324H,1774C> T)表征这些多态性在三个不同种族之间的等位基因分布/地理起源。在92位葡萄牙人,151位莫桑比克人和91位哥伦比亚受试者的样本中对总共12种CYP7A1,CYP27A1和CYP7B1基因变异进行了基因分型。在任何研究人群中均未检测到CYP7A1中的N233S变异体和CYP7B1中的1774C> T变异体。 CYP7A1(–203A> C,–346C> T,–496C> T)中的启动子多态性在三个族裔中均较高。 G347S(CYP7A1),R164W,A169V和V400A(CYP27A1)的出现频率较低,但在三个族裔中分布相似。对于D273N(CYP27A1),– 346C> T(CYP7A1),– 116C> G和R324H(CYP7B1)观察到显着差异。我们的结果表明,所分析的不同人群之间药物代谢酶的变异性很高,表明至少其中一些关键词:胆固醇7α-羟化酶,药物代谢酶,氧固醇7α-羟化酶,固醇27-羟化酶

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