Identification of Beilschmiedia tsangii Root Extract as a Liver Cancer Cell-Normal Keratinocyte Dual-Selective NRF2 Regulator
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Published on: January 26, 2024
Yi-Siao Chen1,2,3,4, Hsun-Shuo Chang3,4,5,6, Hui-Hua Hsiao7,8,9,10
1Ph.D. Program in Environmental and Occupational Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Abstract:
Transcription factor nuclear factor erythroid 2-related factor 2 (NRF2) plays a crucial role in regulating the expression of genes participating in cellular defense mechanisms against oxidative or xenobiotic insults. However, there is increasing evidence showing that hyperactivation of NRF2 is associated with chemoresistance in several cancers, including hepatocellular carcinoma (HCC), thus making NRF2 an attractive target for cancer therapy. Another important issue in cancer medication is the adverse effects of these substances on normal cells. Here, we attempted to identify a dual-selective NRF2 regulator that exerts opposite effects on NRF2-hyperactivated HCC cells and normal keratinocytes. An antioxidant response element driven luciferase reporter assay was established in Huh7 and HaCaT cells as high-throughput screening platforms. Screening of 3,000 crude extracts from the Taiwanese Indigenous Plant Extract Library resulted in the identification of Beilschmiedia tsangii (BT) root extract as a dual-selective NRF2 regulator. Multiple compounds were found to contribute to the dual-selective effects of BT extract on NRF2 signaling in two cell lines. BT extract reduced NRF2 protein level and target gene expression levels in Huh7 cells but increased them in HaCaT cells. Furthermore, notable combinatory cytotoxic effects of BT extract and sorafenib on Huh7 cells were observed. On the contrary, sorafenib-induced inflammatory reactions in HaCaT cells were reduced by BT extract. In conclusion, our results suggest that the combination of a selective NRF2 activator and inhibitor could be a practical strategy for fine-tuning NRF2 activity for better cancer treatment and that plant extracts or partially purified fractions could be a promising source for the discovery of dual-selective NRF2 regulators.
Insights
Researchers identified a Taiwanese plant extract, Beilschmiedia tsangii, as a dual-selective regulator of nuclear factor erythroid 2-related factor 2 (NRF2). This extract targets cancer cells while protecting normal cells, offering a novel strategy for cancer therapy.
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Nuclear factor erythroid 2-related factor 2 (NRF2) regulates cellular defense but its hyperactivation promotes chemoresistance in cancers like hepatocellular carcinoma (HCC).
- Targeting NRF2 is a promising cancer therapy strategy, yet minimizing adverse effects on normal cells remains a challenge.
Purpose of the Study:
- To identify a dual-selective NRF2 regulator with opposing effects on NRF2-hyperactivated HCC cells and normal keratinocytes.
- To explore novel therapeutic strategies for hepatocellular carcinoma with reduced side effects.
Main Methods:
- High-throughput screening using antioxidant response element-driven luciferase reporter assays in Huh7 (HCC) and HaCaT (keratinocyte) cells.
- Screening of 3,000 Taiwanese Indigenous Plant Extract Library samples.
- Evaluation of Beilschmiedia tsangii (BT) root extract's effects on NRF2 signaling and its combination with sorafenib.
Main Results:
- Beilschmiedia tsangii (BT) root extract identified as a dual-selective NRF2 regulator.
- BT extract decreased NRF2 levels in Huh7 cells but increased them in HaCaT cells.
- BT extract enhanced sorafenib's cytotoxicity in Huh7 cells and reduced sorafenib-induced inflammation in HaCaT cells.
Conclusions:
- Dual-selective NRF2 regulators, like BT extract, offer a promising approach for fine-tuning NRF2 activity in cancer therapy.
- Plant extracts are a valuable source for discovering novel dual-selective NRF2 regulators to improve cancer treatment efficacy and safety.
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