人肝脏药物代谢和转运基因表达的性别差异。

Journal of drug metabolism & toxicology Pub Date : 2012-01-01 Epub Date: 2012-07-10 DOI:10.4172/2157-7609.1000119
Lun Yang, Yan Li, Huixiao Hong, Ching-Wei Chang, Li-Wu Guo, Beverly Lyn-Cook, Leming Shi, Baitang Ning
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引用次数: 92

摘要

人类药物代谢酶和转运体(DMETs)基因表达的性别差异导致药物吸收、分布、代谢和排泄的差异,可能影响药物疗效和不良反应。然而,现有的旨在鉴定DMET基因二态表达差异的研究受到样本量和基因谱数量的限制。以374个DMET基因为重点,我们分析了先前发表的由人类男性(n=234)和女性(n=193)肝脏样本组成的基因表达数据集,并确定了77个因性别而表现出差异表达的基因。为了描述DMET基因差异表达的生物学功能和调控机制,我们进行了共表达网络分析。此外,还讨论了人类肝脏dmet表达性别差异的临床意义。本研究可能有助于更好地了解男性和女性在药物/异种药物反应和人类疾病易感性方面的个体间差异,从而实现个性化医疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sex Differences in the Expression of Drug-Metabolizing and Transporter Genes in Human Liver.

Sex Differences in the Expression of Drug-Metabolizing and Transporter Genes in Human Liver.

Sex Differences in the Expression of Drug-Metabolizing and Transporter Genes in Human Liver.

Sex Differences in the Expression of Drug-Metabolizing and Transporter Genes in Human Liver.

Human sex differences in the gene expression of drug metabolizing enzymes and transporters (DMETs) introduce differences in drug absorption, distribution, metabolism and excretion, possibly affecting drug efficacy and adverse reactions. However, existing studies aimed at identifying dimorphic expression differences of DMET genes are limited by sample size and the number of genes profiled. Focusing on a list of 374 DMET genes, we analyzed a previously published gene expression data set consisting of human male (n=234) and female (n=193) liver samples, and identified 77 genes showing differential expression due to sex. To delineate the biological functionalities and regulatory mechanisms for the differentially expressed DMET genes, we conducted a co-expression network analysis. Moreover, clinical implications of sex differences in the expression of human hepatic DMETs are discussed. This study may contribute to the realization of personalized medicine by better understanding the inter-individual differences between males and females in drug/xenobiotic responses and human disease susceptibilities.

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