Polymorphism in the Promoter Region of NFE2L2 Gene Is a Genetic Marker of Susceptibility to Cirrhosis Associated with Alcohol Abuse.
Kemper Nunes Dos SantosRodrigo M FlorentinoAndressa FrançaAntônio Carlos Melo Lima FilhoMarcone Loiola Dos SantosDabny MissiaggiaMatheus de Castro FonsecaIgor Brasil CostaPaula Vieira Teixeira VidigalMichael H NathansonFernanda de Oliveira LemosM Fatima LeitePublished in: International journal of molecular sciences (2019)
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.
Keyphrases
- oxidative stress
- genome wide
- nuclear factor
- dna methylation
- copy number
- poor prognosis
- transcription factor
- toll like receptor
- dna damage
- diabetic rats
- gene expression
- long non coding rna
- newly diagnosed
- early onset
- ejection fraction
- binding protein
- genetic diversity
- genome wide identification
- dna binding
- peritoneal dialysis