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NFE2L2 基因启动子区域多态性是与酒精滥用相关的肝硬化易感性的遗传标志物。

Polymorphism in the Promoter Region of NFE2L2 Gene Is a Genetic Marker of Susceptibility to Cirrhosis Associated with Alcohol Abuse.

机构信息

Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.

Laboratório Nacional de Biociências (LNBio), Centro de Pesquisa em Energia e Materiais (CNPEM), Campinas, SP 13083-970, Brazil.

出版信息

Int J Mol Sci. 2019 Jul 23;20(14):3589. doi: 10.3390/ijms20143589.

Abstract

Alcoholic liver disease (ALD) is a highly prevalent spectrum of pathologies caused by alcohol overconsumption. Morbidity and mortality related to ALD are increasing worldwide, thereby demanding strategies for early diagnosis and detection of ALD predisposition. A potential candidate as a marker for ALD susceptibility is the transcription factor nuclear factor erythroid-related factor 2 (Nrf2), codified by the nuclear factor erythroid 2-related factor 2 gene (NFE2L2). Nrf2 regulates expression of proteins that protect against oxidative stress and inflammation caused by alcohol overconsumption. Here, we assessed genetic variants of NFE2L2 for association with ALD. Specimens from patients diagnosed with cirrhosis caused by ALD were genotyped for three NFE2L2 single nucleotide polymorphisms (SNP) (SNPs: rs35652124, rs4893819, and rs6721961). Hematoxylin & eosin and immunohistochemistry were performed to determine the inflammatory score and Nrf2 expression, respectively. SNPs rs4893819 and rs6721961 were not specifically associated with ALD, but analysis of SNP rs35652124 suggested that this polymorphism predisposes to ALD. Furthermore, SNP rs35652124 was associated with a lower level of Nrf2 expression. Moreover, liver samples from ALD patients with this polymorphism displayed more severe inflammatory activity. Together, these findings provide evidence that the SNP rs35652124 variation in the Nrf2-encoding gene NFE2L2 is a potential genetic marker for susceptibility to ALD.

摘要

酒精性肝病 (ALD) 是一种由过度饮酒引起的高度普遍的病理学谱。与 ALD 相关的发病率和死亡率在全球范围内正在增加,因此需要制定早期诊断和检测 ALD 易感性的策略。转录因子核因子红细胞相关因子 2 (Nrf2) 是一种潜在的候选标志物,其由核因子红细胞 2 相关因子 2 基因 (NFE2L2) 编码。Nrf2 调节蛋白质的表达,这些蛋白质可防止由过度饮酒引起的氧化应激和炎症。在这里,我们评估了 NFE2L2 的遗传变异与 ALD 的关联。对诊断为 ALD 引起的肝硬化的患者的样本进行了三个 NFE2L2 单核苷酸多态性 (SNP) (SNP:rs35652124、rs4893819 和 rs6721961) 的基因分型。进行苏木精和伊红染色和免疫组织化学染色,分别确定炎症评分和 Nrf2 表达。SNP rs4893819 和 rs6721961 与 ALD 没有特异性关联,但对 SNP rs35652124 的分析表明,这种多态性易患 ALD。此外,SNP rs35652124 与 Nrf2 表达水平降低相关。此外,具有这种多态性的 ALD 患者的肝组织样本显示出更严重的炎症活动。总之,这些发现提供了证据表明,Nrf2 编码基因 NFE2L2 中的 SNP rs35652124 变异是 ALD 易感性的潜在遗传标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7d/6678089/d03d5a538e93/ijms-20-03589-g001.jpg

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