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长链非编码RNA LINC02499调节人肝细胞中CYP3A5的表达。

Long non-coding RNA LINC02499 regulates the expression of CYP3A5 in human liver cells.

作者信息

Li Chengcheng, Li Langzhang, Zhang Siqi, Zhang Yawen, Yang Tianxing, Li Liang

机构信息

Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Shatai Road 1023, Guangzhou, 510515, Guangdong, China.

出版信息

Arch Toxicol. 2025 Jul 2. doi: 10.1007/s00204-025-04120-1.

Abstract

Cytochrome P450 3A5 (CYP3A5) is a critical drug-metabolizing enzyme in human hepatocytes, playing a key role in the metabolism of various clinically relevant drugs, with considerable variability in gene expression across individuals. Long non-coding RNAs (lncRNAs) are likely to be important regulators within the CYP3A5 regulatory network in the liver. In this study, we employed a computational approach to estimate Sobol's sensitivity indices (SSI) under generalized linear models, applied to liver RNA expression microarray data (GTEx v8). The SSI-based analysis revealed that the long non-coding RNA LINC02499 exhibits the highest SSI value in relation to CYP3A5 expression in the liver. Furthermore, we conducted a comprehensive evaluation of LINC02499's biological characteristics and confirmed its regulatory role in CYP3A5 expression through real-time quantitative PCR and Western blotting experiments at the cellular level. We also demonstrated the direct interaction between miR-329-5p and both LINC02499 and CYP3A5 mRNA using dual-luciferase reporter assays and electrophoretic mobility shift assays (EMSA). In conclusion, our findings outline a regulatory network in which LINC02499 functions as a molecular sponge, mitigating the post-transcriptional inhibitory effect of miR-329-5p on CYP3A5 expression.

摘要

细胞色素P450 3A5(CYP3A5)是人类肝细胞中一种关键的药物代谢酶,在多种临床相关药物的代谢中起关键作用,个体间基因表达存在显著差异。长链非编码RNA(lncRNA)可能是肝脏中CYP3A5调控网络内的重要调节因子。在本研究中,我们采用一种计算方法来估计广义线性模型下的索伯尔敏感性指数(SSI),并将其应用于肝脏RNA表达微阵列数据(GTEx v8)。基于SSI的分析表明,长链非编码RNA LINC02499在肝脏中与CYP3A5表达相关的SSI值最高。此外,我们对LINC02499的生物学特性进行了全面评估,并通过细胞水平的实时定量PCR和蛋白质免疫印迹实验证实了其对CYP3A5表达的调控作用。我们还使用双荧光素酶报告基因检测和电泳迁移率变动分析(EMSA)证明了miR-329-5p与LINC02499和CYP3A5 mRNA之间的直接相互作用。总之,我们的研究结果勾勒出一个调控网络,其中LINC02499作为分子海绵发挥作用,减轻miR-329-5p对CYP3A5表达的转录后抑制作用。

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