Effects of the juçara fruit (Euterpe edulis Martius) pulp and lyophilized extract on NRF2, KEAP1, SOD1, and GPX2 expression in human colorectal cancer cell lines.
L A MilholliJuliana DalbóC V M S CoutoM M OliveiraJ G Dos SantosGabriela Tonini PeterleAnderson Barros ArchanjoPollyanna Ibrahim SilvaJankerle N BoeloniFabio Daumas NunesA M Á da SilvaLeonardo Oliveira TrivilinPublished in: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas (2023)
We investigated the effects of the juçara fruit (Euterpe edulis Martius) pulp and lyophilized extract on the expression of cytoprotective genes nuclear factor erythroid 2 (NF-E2)-related factor 2 (NRF2), kelch-like ECH-associated protein 1 (KEAP1), superoxide dismutase (SOD1), and glutathione peroxidase (GPX2) in human colorectal cancer cell lines (HT-29 and Caco-2). Cells were cultured for 24 h in Dulbecco's Modified Eagle's Medium containing juçara fruit pulp (5, 10, or 50 mg/mL) or lyophilized extract (0.05, 0.1, or 0.5 mg/mL), and gene expression was quantified using real-time quantitative reverse transcription polymerase chain reaction. All studied genes showed significant variation in gene expression among different concentrations of pulp or lyophilized extract. Overall, the expression of the selected genes decreased in both cell lines following exposure to the pulp or lyophilized extract in a dose-dependent manner for most of the concentrations studied. In summary, our study showed that the compounds in juçara fruit inhibited the expression of cytoprotective genes associated with the antioxidant response and that, although not cytotoxic at the concentrations studied, they could potentially block the activation of the NRF2/KEAP1 pathway.
Keyphrases
- oxidative stress
- gene expression
- poor prognosis
- nuclear factor
- endothelial cells
- induced apoptosis
- anti inflammatory
- genome wide
- toll like receptor
- dna methylation
- binding protein
- signaling pathway
- long non coding rna
- hydrogen peroxide
- protein protein
- high resolution
- small molecule
- induced pluripotent stem cells
- genome wide identification
- transcription factor
- inflammatory response
- pi k akt
- lps induced