Model-dependent Nrf2 response in human liver cell lines
Cell-based study · Non-tumour THLE-2 and hepatoma-derived HepG2 human liver cell lines [1]
After 72 h, reported betanin treatment increased Nrf2–ARE binding and Nrf2 mRNA in THLE-2 cells. HepG2 cells showed no significant increase in ARE binding. This is a cellular pathway response, without evidence here of direct Nrf2 binding by betanin or clinical hepatoprotection.
| Endpoint | Reported result | Reference |
|---|---|---|
| Nrf2 binding to ARE-containing oligonucleotides | Direction and significance Increased in THLE-2 at 2, 10 and 20 µM (P < 0.05 vs control); no significant increase in HepG2. | [1] |
| Nrf2 transcript abundance in THLE-2 | Reported increase 21–30% increase at the tested 2, 10 and 20 µM concentrations; P < 0.05 vs control. | [1] |
Literature-Reported Treatment Conditions
- Treatment concentration
- 2, 10 and 20 µM
- Exposure duration
- 72 h
- Method
- Exposure in cell culture medium
- Vehicle
- 0.1% DMSO; matched DMSO-only control
- Reported limits
- Numerical reagent purity, isobetanin content and lot composition were not specified in the retrieved Chemicals section. These nominal doses do not establish purified-parent potency.
Methods and source locations
Compound reported in the paper: Betanin; Compound label in the paper: Sigma-Aldrich betanin (BET)
Attribute responses to the reported commercial betanin treatment in these cell lines. Do not infer Adooq lot validation, isolated-parent potency or universal Nrf2 activation.
Figures 2–3; Methods: Chemicals, Cell culture and treatment, Nrf2 binding assay, Quantitative PCR and statistics; Results: Nrf2 expression and activation
Nrf2 binding to ARE-containing oligonucleotides: Nrf2 Transcription Factor ELISA on nuclear extracts; positive control: Nrf2-transfected COS-7 nuclear extracts. Figure values are means from three separate experiments with standard errors. — Figure 3b and caption; Results: Effect of betanin on expression and activation of Nrf2; Methods: Nrf2 binding assay
Nrf2 transcript abundance in THLE-2: Quantitative PCR, normalization to TBP and PBGD; three separate experiments, standard errors. Range is reported in Results, not estimated from bars. — Figure 3a and caption; corresponding Results paragraph; Methods: Quantitative PCR