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MBD2和MBD3在胃癌发生过程中mRNA表达水平降低。

Reduced mRNA expression levels of MBD2 and MBD3 in gastric carcinogenesis.

作者信息

Pontes Thaís Brilhante, Chen Elizabeth Suchi, Gigek Carolina Oliveira, Calcagno Danielle Queiroz, Wisnieski Fernanda, Leal Mariana Ferreira, Demachki Samia, Assumpção Paulo Pimentel, Artigiani Ricardo, Lourenço Laércio Gomes, Burbano Rommel Rodriguez, Arruda Cardoso Smith Marília

机构信息

Disciplina de Genética, Departamento de Morfologia e Genética, Universidade Federal de São Paulo, Rua Botucatu, 740 - Ed. Leitão da Cunha - 1ºandar, São Paulo, 04023-900, SP, Brazil.

出版信息

Tumour Biol. 2014 Apr;35(4):3447-53. doi: 10.1007/s13277-013-1455-y. Epub 2013 Dec 13.

Abstract

Aberrant methylation has been reported in several neoplasias, including gastric cancer. The methyl-CpG-binding domain (MBD) family proteins have been implicated in the chromatin remodeling process, leading to the modulation of gene expression. To evaluate the role of MBD2 and MBD3 in gastric carcinogenesis and the possible association with clinicopathological characteristics, we assessed the mRNA levels and promoter methylation patterns in gastric tissues. In this study, MBD2 and MBD3 mRNA levels were determined by RT-qPCR in 28 neoplastic and adjacent nonneoplastic and 27 gastritis and non-gastritis samples. The promoter methylation status was determined by bisulfite sequencing, and we found reduced MBD2 and MBD3 levels in the neoplastic samples compared with the other groups. Moreover, a strong correlation between the MBD2 and MBD3 expression levels was observed in each set of paired samples. Our data also showed that the neoplastic tissues exhibited higher MBD2 promoter methylation than the other groups. Interestingly, the non-gastritis group was the only one with positive methylation in the MBD3 promoter region. Furthermore, a weak correlation between gene expression and methylation was observed. Therefore, our data suggest that DNA methylation plays a minor role in the regulation of MBD2 and MBD3 expression, and the presence of methylation at CpGs that interact with transcription factor complexes might also be involved in the modulation of these genes. Moreover, reduced mRNA expression of MBD2 and MBD3 is implicated in gastric carcinogenesis, and thus, further investigations about these genes should be conducted for a better understanding of the role of abnormal methylation involved in this neoplasia.

摘要

在包括胃癌在内的多种肿瘤中均有异常甲基化的报道。甲基化CpG结合域(MBD)家族蛋白与染色质重塑过程有关,进而导致基因表达的调控。为了评估MBD2和MBD3在胃癌发生中的作用以及与临床病理特征的可能关联,我们检测了胃组织中的mRNA水平和启动子甲基化模式。在本研究中,通过RT-qPCR测定了28例肿瘤组织及相邻非肿瘤组织以及27例胃炎和非胃炎样本中MBD2和MBD3的mRNA水平。通过亚硫酸氢盐测序确定启动子甲基化状态,我们发现与其他组相比,肿瘤样本中MBD2和MBD3水平降低。此外,在每组配对样本中均观察到MBD2和MBD3表达水平之间存在强相关性。我们的数据还显示,肿瘤组织的MBD2启动子甲基化水平高于其他组。有趣的是,非胃炎组是MBD3启动子区域唯一存在阳性甲基化的组。此外,观察到基因表达与甲基化之间存在弱相关性。因此,我们的数据表明DNA甲基化在MBD2和MBD3表达的调控中起次要作用,与转录因子复合物相互作用的CpG位点处的甲基化存在也可能参与这些基因的调控。此外,MBD2和MBD3的mRNA表达降低与胃癌发生有关,因此,应对这些基因进行进一步研究,以更好地了解异常甲基化在这种肿瘤形成中的作用。

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