Methylation of the ESR1 promoters in visceral adipose tissue and its relationship with obesity.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Filiz Güçlü-Geyik, Turgay Erginel, Çağrı Güleç, Pınar Köseoğlu-Büyükkaya, Nihan Erginel-Ünaltuna
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Abstract

Background: Obesity is associated with decreased ESR1 expression level in visceral adipose tissue. However, it is unclear exactly what mechanisms are responsible for this decline. The aim of this study was to investigate the impact of aberrant methylation of the ESR1 alternative promoters on decreased ESR1 expression and its connection to obesity.

Methods: Visceral adipose tissues and peripheral blood cells were obtained from 21 patients (non-obese and obese) undergoing inguinal hernia or gallbladder removal. Alternative promoter regions, C, E2 and F of the ESR1 gene, were analyzed by Methylation-Specific PCR (MSP) and mRNA levels were measured by quantitative real-time PCR (qPCR) in both visceral adipose tissue and peripheral blood cells. All statistical analyses were performed by SPSS (23.0).

Results: The methylation percentage in the three promoter regions of ESR1 was not different in obese individuals compared to non-obese individuals. We observed that promoter C had the highest methylation frequency in obese patients, although it was not statistically significant. Additionally, we observed that the hypermethylation of ESR1's promoter C was significantly associated with lower mRNA expression level in obesity (p = 0.020).

Conclusion: This study suggests that methylation of ESR1 promoter C may be a factor in the development of obesity or a consequence of obesity. Further studies with advanced methods and larger study groups are needed to clarify this issue.

内脏脂肪组织中 ESR1 启动子的甲基化及其与肥胖的关系。
背景:肥胖与内脏脂肪组织中 ESR1 表达水平下降有关。然而,目前尚不清楚造成这种下降的确切机制。本研究旨在探讨 ESR1 替代启动子异常甲基化对 ESR1 表达下降的影响及其与肥胖的关系:方法:从 21 名接受腹股沟疝或胆囊切除术的患者(非肥胖和肥胖)中获取内脏脂肪组织和外周血细胞。通过甲基化特异性 PCR(MSP)分析了 ESR1 基因的 C、E2 和 F 等替代启动子区域,并通过实时定量 PCR(qPCR)测定了内脏脂肪组织和外周血细胞中的 mRNA 水平。所有统计分析均采用 SPSS(23.0)进行:肥胖者与非肥胖者相比,ESR1三个启动子区域的甲基化百分比没有差异。我们观察到启动子 C 在肥胖患者中的甲基化频率最高,但没有统计学意义。此外,我们还观察到,ESR1启动子C的高甲基化与肥胖症患者较低的mRNA表达水平显著相关(p = 0.020):本研究表明,ESR1启动子C的甲基化可能是肥胖症发病的一个因素,也可能是肥胖症的一个后果。要弄清这一问题,还需要采用先进的方法和更大的研究群体进行进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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