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miRNAs and NFKB1 and TRAF6 target genes: The initial functional study in CD14+ monocytes in rheumatoid arthritis patients.
Silva, Isaura Isabelle Fonseca Gomes da; Nascimento, Denise de Queiroga; Barbosa, Alexandre Domingues; Souto, Fabricio Oliveira; Maia, Maria de Mascena Diniz; Crovella, Sergio; Souza, Paulo Roberto Eleuterio de; Sandrin-Garcia, Paula.
Afiliação
  • Silva IIFGD; Universidade Federal de Pernambuco, Programa de Pós-Graduação em Genética e Biologia Molecular, Recife, PE, Brazil.
  • Nascimento DQ; Instituto Keizo Asami, Recife, PE, Brazil.
  • Barbosa AD; Universidade Federal de Pernambuco, Programa de Pós-Graduação em Genética e Biologia Molecular, Recife, PE, Brazil.
  • Souto FO; Instituto Keizo Asami, Recife, PE, Brazil.
  • Maia MMD; Policlínica Jamacy de Medeiros, Cabo de Santo Agostinho, PE, Brazil.
  • Crovella S; Universidade Federal de Pernambuco, Hospital das Clínicas, Recife, PE, Brazil.
  • Souza PRE; Instituto Keizo Asami, Recife, PE, Brazil.
  • Sandrin-Garcia P; Universidade Federal de Pernambuco, Centro Acadêmico do Agreste, Caruaru, PE, Brazil.
Genet Mol Biol ; 47(2): e20230235, 2024.
Article em En | MEDLINE | ID: mdl-39058384
ABSTRACT
We predicted miRNAs with regulatory impact on NFKB1 and TRAF6 gene expression and selected the miR-194-5p, miR-124-3p, miR-9-5p, and miR-340-5p and their target genes for expression analyses on CD14+ monocytes from rheumatoid arthritis (RA) patients and healthy controls. Additionally, we evaluated the influence of genes and miRNA expression on RA patients' cytokine levels. No difference was observed in genes or miRNAs expression when compared to healthy controls and RA patients or clinical parameters. However, we found a significant difference between miR-194-5p and miR-9-5p levels (FC=-2.31; p=0.031; FC=-3.05;p=0.031, respectively) and non-prednisone users as compared to prednisone using patients. We conducted correlation analyses to identify the strength of the relationship between expression data and cytokine plasma levels. We observed a moderate positive correlation between miR-124-3p expression and IL-6 plasma levels (r=0.46; p=0.033). In addition, overexpression of miRNAs was concomitant to TRAF6 and NFKB1 genes as indicated by correlation analyses TRAF6 and miR-194-5p (r=0.60;p<0.001) and miR-9-5p (r=0.63;p<0.001) and NFKB1 and miR-194-5p (r=0.72;p<0.001), miR-9-5p (r=0.72;p<0.001) and miR-340-5p (r=0.61;p<0.001). NFKB1 and TRAF6 genes and miRNAs monocyte expression do not appear to be related to RA but showed a significant difference in different groups of RA therapy. In addition, increased levels of miRNAs can be linked to concomitant overexpression of TRAF6 and NFKB1 in monocytes and act as its regulators.