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一种新开发的 DNA 微阵列可用于评估细胞色素 p450 在食蟹猴中的诱导作用。

A newly developed DNA microarray is useful to assess induction of cytochromes p450 in the cynomolgus monkey.

机构信息

Drug Safety Research Laboratories, Shin Nippon Biomedical Laboratories, Ltd., Kagoshima, Japan.

出版信息

Drug Metab Pharmacokinet. 2011 Jun;26(3):228-35. doi: 10.2133/dmpk.DMPK-10-RG-099. Epub 2011 Jan 25.

DOI:10.2133/dmpk.DMPK-10-RG-099
PMID:21273731
Abstract

Cytochromes P450 (P450s or CYPs) are a gene family of highly homologous genes and include the CYP1-4 family, which is relevant to drug metabolism. In the cynomolgus monkey (which is frequently used in drug metabolism studies), numerous CYPs (mfCYPs) have been identified in the CYP1-4 family. DNA microarrays are useful for high-throughput screening assays; however, there is a potential problem with cross-hybridization of highly homologous genes in the gene family. This problem might be solved with the use of low-density DNA microarrays, with which specific validation can be performed for the genes on the microarray. We have developed a DNA microarray for the 20 mfCYPs and have evaluated and validated its specificity and usefulness. First, in both DNA microarray and quantitative polymerase chain reaction (qPCR) analyses, hepatic expression of each mfCYP correlated well, and similar tissue expression patterns were observed for five representative mfCYPs, confirming the specificity of the DNA microarray. Second, the usefulness of this DNA microarray was validated by induction analysis of mfCYPs in primary hepatocytes, which successfully detected known responders, but also novel responders (mfCYP2C43, mfCYP2C75, and mfCYP3A5 for rifampicin), as confirmed by qPCR analysis. This DNA microarray can thus be utilized for high-throughput assays during drug development.

摘要

细胞色素 P450(P450s 或 CYPs)是一个高度同源基因家族,包括与药物代谢相关的 CYP1-4 家族。在常用于药物代谢研究的食蟹猴中,已在 CYP1-4 家族中鉴定出许多 CYP(mfCYPs)。DNA 微阵列非常适用于高通量筛选测定;然而,基因家族中高度同源基因的交叉杂交存在潜在问题。使用低密度 DNA 微阵列可以解决此问题,该方法可以针对微阵列上的基因进行特定验证。我们已经开发了用于 20 种 mfCYP 的 DNA 微阵列,并对其特异性和有用性进行了评估和验证。首先,在 DNA 微阵列和定量聚合酶链反应(qPCR)分析中,每个 mfCYP 的肝表达相关性良好,并且五个代表性 mfCYP 的组织表达模式相似,证实了 DNA 微阵列的特异性。其次,通过对原代肝细胞中 mfCYP 的诱导分析验证了该 DNA 微阵列的有用性,该分析成功检测到了已知的应答者,还检测到了新的应答者(利福平的 mfCYP2C43、mfCYP2C75 和 mfCYP3A5),qPCR 分析也证实了这一点。因此,该 DNA 微阵列可用于药物开发过程中的高通量测定。

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引用本文的文献

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BMC Evol Biol. 2011 Oct 1;11:283. doi: 10.1186/1471-2148-11-283.
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Immunochemical detection of cytochrome P450 enzymes in liver microsomes of 27 cynomolgus monkeys.免疫化学检测 27 只食蟹猴肝微粒体中的细胞色素 P450 酶。
J Pharmacol Exp Ther. 2011 Nov;339(2):654-61. doi: 10.1124/jpet.111.185009. Epub 2011 Aug 17.