Evaluation of changes in expression pattern of oxidative stress genes under the influence of adalimumab.
Beniamin Oskar GrabarekDominika Wcisło-DziadeckaAdrianna SanakiewiczCelina Kruszniewska-RajsJoanna Magdalena GolaPublished in: Dermatologic therapy (2019)
The psoriasis therapy consists of the inhibition of cytokines involved in inducing and development of this disease. The aim of the study was to evaluate the changes in the expression of genes related to the oxidative stress phenomenon in the culture of normal human dermal fibroblasts of Normal Human Dermal Fibroblasts (NHDF) exposed to adalimumab. NHDF culture was exposed to adalimumab for 2-, 8-, and 24-hr periods. The control consisted of the same cells not exposed to adalimumab. The oligonucleotide microarrays HG-U133A 2.0 were used to analyze the changes in gene expression in NHDF culture. Analysis showed that there are 3,881 ID mRNA involved in the induction and development of oxidative stress, the expression of which changes significantly due to the exposure of NHDF cells to adalimumab (p < .05) among 1,369 ID mRNA of them. These include genes associated with apoptosis, the p38 MAPK pathway and the PDGF pathway, and above all with pathways not yet classified. Studies have shown that two genes: NR4A2 and IL1RN, whose expression has changed the most, expressed as Fold Change (FC) seem to be the most promising molecular markers to monitor therapy and loss of cell sensitivity to treatment.
Keyphrases
- oxidative stress
- induced apoptosis
- poor prognosis
- rheumatoid arthritis
- cell cycle arrest
- gene expression
- juvenile idiopathic arthritis
- binding protein
- endothelial cells
- endoplasmic reticulum stress
- genome wide
- dna damage
- cell death
- ulcerative colitis
- ischemia reperfusion injury
- dna methylation
- long non coding rna
- induced pluripotent stem cells
- genome wide identification
- bone marrow
- stem cells
- cell therapy
- disease activity
- cell proliferation
- pi k akt
- heat shock
- mesenchymal stem cells
- living cells
- data analysis