慢性乙醇处理诱导的乙醇暴露滋养细胞的基因组改变

S. Clavé, X. Joya, A. Puiggros, Marta Bódalo, J. Salat-Batlle, M. Salido, B. Espinet, Ó. G. Algar, O. Vall
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引用次数: 3

摘要

背景:怀孕期间酒精的消耗会导致广泛的损害,但其机制的知识是缺乏的。目的:本研究的目的是确定反复乙醇处理后胎盘细胞系中乙醇引起的基因组改变,以描述细胞损伤的新基因组靶点。方法:采用标准剂量乙醇对体外人绒毛膜癌细胞JEG-3和BeWo的持续暴露模型。采用g带细胞遗传学和寡核苷酸单核苷酸多态性-阵列分析(CytoScan, Affymetrix)评估染色体异常和拷贝数改变(CNAs)。结果:在暴露的BeWo细胞中,除了存在衍生染色体4 [add(4)(p14)]外,尽管乙醇暴露,染色体异常并未发生变化。在SNP-Array分析中,共有21个CNAs是由乙醇暴露引起的,其中16个在JEG-3细胞系中,5个在BeWo细胞系中,而在对照组中没有发现。JEG-3和BeWo受乙醇影响的地区之间没有巧合。结论:反复暴露于乙醇的滋养细胞存在基因组不稳定性,导致CNAs。然而,在两个模型中,没有一个区域被同样地改变,认为它是乙醇暴露的目标区域。因此,需要进一步研究涉及不同模型和方法的靶基因调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic Alterations in Ethanol-Exposed Trophoblast Cell Lines Inducedby Chronic Ethanol Treatment
Background: Ethanol consumption during pregnancy results in a broad spectrum of damage, but the knowledge of its mechanism is lacking. Objective: The aim of this study is to determine ethanol-caused genomic alterations in placental cell lines after a repeated ethanol treatment in order to describe new genomic targets of cell damage. Methods: A model of sustained exposure to standard doses of ethanol on two in vitro human choriocarcinoma cell lines, JEG-3 and BeWo, was used. Chromosomic abnormalities and copy number alterations (CNAs) were assessed by G-Banding cytogenetics and oligonucleotide Single Nucleotide Polymorphism-Array analysis (CytoScan, Affymetrix). Results: Chromosomal abnormalities did not change despite ethanol exposure except for the presence of a derivative chromosome 4 [add(4)(p14)] in exposed BeWo cells. Regarding SNP-Array analysis, a total of 21 CNAs were found to be caused by ethanol exposure, 16 in JEG-3 cell line and 5 in BeWo cell line, which were not found in controls. There was no coincidence between JEG-3 and BeWo regions affected by ethanol. Conclusion: Trophoblast cell lines exposed repetitively to ethanol presented genomic instability resulting in CNAs. However, no region has been equally altered in both models to consider it an ethanol exposure target area. So, further studies involving different models and approaches that target gene regulation are required.
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