The effect and mechanism of erianin on the reversal of oxaliplatin resistance in human colon cancer cells

Multidrug resistance (MDR) is the main cause of chemotherapy failure in the treatment of colon cancer and the high expression of drug efflux protein P-gp is one of the main factors of MDR. P-gp expression is regulated by the signal transducer and activator of transcription 3 (STAT3) signaling pathway. In this study, human colon cancer oxaliplatin-resistant cells were treated with oxaliplatin combined with the natural product erianin. Then, we evaluated the impact of erianin on drug resistance, and explored the relationship between erianin-related oxaliplatin resistance and the Janus kinase 2/STAT3 signaling pathway in vitro. Our research showed that erianin could significantly inhibit the proliferation of human colon cancer oxaliplatin-resistant cells, and suppress the cell cycle of oxaliplatin-resistant cells in the G2/M phase, indicating that erianin could regulate the MDR phenotype of oxaliplatin-resistant cells, and its mechanism might be the inhibition of STAT3 signaling pathway and the significant reduction of P-gp expression. However, this study provides a theoretical basis for the clinical application of erianin in platinum-based chemotherapy for colon cancer.

Automated summary

Erianin significantly inhibits the proliferation of human colon cancer oxaliplatin-resistant cells and suppresses the cell cycle of these cells in the G2/M phase, indicating its potential to regulate MDR phenotype through the inhibition of STAT3 signaling pathway and reduction of P-gp expression. This study provides a theoretical basis for the clinical application of erianin in platinum-based chemotherapy for colon cancer.