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

机译:NFE2L2基因启动子区域中的多态性是与酒精滥用相关的肝硬化易感性的遗传标记。

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摘要

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.
机译:酒精性肝病(ALD)是由酒精过度消费引起的高度普遍的病理频谱。与ALD相关的发病率和死亡率在全球范围内呈上升趋势,因此需要早期诊断和检测ALD易感性的策略。作为ALD易感性标志物的潜在候选者是转录因子核因子红系相关因子2(Nrf2),由核因子红系2相关因子2基因(NFE2L2)编码。 Nrf2调节蛋白质的表达,从而防止因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。对来自被诊断为由ALD引起的肝硬化的患者的标本进行了基因分型,以分析其三个NFE2L2单核苷酸多态性(SNP)(SNP:rs35652124,rs4893819和rs6721961)。分别用苏木精和曙红和免疫组化法测定炎症评分和Nrf2表达。 SNP rs4893819和rs6721961与ALD没有特别的联系,但是对SNP rs35652124的分析表明,这种多态性是ALD的诱因。此外,SNP rs35652124与较低水平的Nrf2表达相关。此外,来自具有这种多态性的ALD患者的肝脏样品显示出更严重的炎症活性。在一起,这些发现提供了证据,即编码Nrf2的基因NFE2L2中的SNP rs35652124变异是对ALD易感性的潜在遗传标记。

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