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布地奈德、苯乙基异硫氰酸酯和香烟烟雾对小鼠肝脏和肺部 microRNA 表达的调控。

Modulation of microRNA expression by budesonide, phenethyl isothiocyanate and cigarette smoke in mouse liver and lung.

机构信息

Department of Health Sciences, University of Genoa, Via A. Pastore 1, I-16132 Genoa, Italy.

出版信息

Carcinogenesis. 2010 May;31(5):894-901. doi: 10.1093/carcin/bgq037. Epub 2010 Feb 9.

Abstract

Although microRNAs (miRNA) have extensively been investigated in cancer research, less attention has been paid to their regulation by carcinogens and/or protective factors in early stages of the carcinogenesis process. The present study was designed to evaluate the modulation of mRNA expression as related to exposure of neonatal mice to environmental cigarette smoke (ECS) and to treatment with chemopreventive agents. Exposure to ECS started immediately after birth and for 2 weeks after weaning. Thereafter, groups of mice received daily either budesonide (BUD) or phenethyl isothiocyanate (PEITC) with the diet. The expression of 576 miRNAs was evaluated by miRNA microarray in liver and lung. In sham-exposed mice, the expression of miRNAs tended to be higher in liver than in lung. ECS downregulated the expression of a number of miRNAs in lung, whereas mixed alterations were observed in liver. PEITC and BUD did not substantially affect the physiological situation in lung, whereas both agents caused intense variations in liver, reflecting the occurrence of damage mechanisms, such as inflammation, DNA and protein damage, cellular stress, proliferation and apoptosis. PEITC and BUD protected the lung from ECS-induced alterations of miRNA expression but exhibited some adverse effects in liver.

摘要

虽然 microRNAs(miRNA)在癌症研究中已经得到广泛研究,但对于它们在致癌作用过程的早期阶段被致癌物质和/或保护因素调节的关注较少。本研究旨在评估与新生小鼠接触环境香烟烟雾(ECS)和化学预防剂治疗相关的 mRNA 表达的调节。暴露于 ECS 始于出生后并持续 2 周断奶后。此后,用饮食每日给予小鼠组布地奈德(BUD)或苯乙基异硫氰酸酯(PEITC)。通过 miRNA 微阵列评估肝脏和肺中 576 种 miRNA 的表达。在假暴露的小鼠中,miRNA 的表达在肝脏中高于肺。ECS 下调了肺中许多 miRNA 的表达,而在肝脏中观察到混合改变。PEITC 和 BUD 没有实质性地影响肺的生理状况,而两种药物都在肝脏中引起强烈的变化,反映出发生了炎症、DNA 和蛋白质损伤、细胞应激、增殖和凋亡等损伤机制。PEITC 和 BUD 保护肺免受 ECS 诱导的 miRNA 表达改变,但在肝脏中表现出一些不良反应。

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