Demonstrates enhanced chemotherapy outcomes in triple-negative breast cancer, suggesting a novel therapeutic approach.
BACKGROUND: Triple-negative breast cancer is in urgent need of precise and effective therapeutic regimens due to drug resistance, which was mainly caused by increased drug efflux based on P-glycoprotein. Therefore, there is an urgent need for precisely regulated therapeutic strategies to reverse tumor drug resistance. RESULTS: This study developed an ultrasound-responsive bacterial-nanocomplex △E@PtkDOX-Fe NMs which was able to achieve ideal chemotherapy/chemodynamic therapeutic effect. The experiments showed that △E@PtkDOX-Fe NMs could be ultrasonically modulated to promote reactive oxygen species production, which in turn inhibited the expression of P-glycoprotein in 4T1/ADR cells (P<0.05) and increased the intracellular accumulation of DOX (P<0.05), thereby reducing the activity of drug-resistant tumor cells by 63.19% (P<0.001) and inhibiting the growth of drug-resistant tumors in vivo (P<0.01). CONCLUSION: In this study, we successfully constructed an ultrasound-responsive bacterial-nanocomplex that can increase the local reactive oxygen species level in tumors and thus reverse tumor drug resistance, which provides a method for accurate and controllable reversal of tumor drug resistance, and establishes a mode of accurate and efficient reversal of tumor drug-resistant sensitizing chemotherapy/chemodynamic therapy. STATEMENT OF SIGNIFICANCE: to boost ROS generation. These effects trigger DOX release and suppress P-gp expression, sensitizing tumor cells to chemotherapy and improving chemodynamic therapy (CDT) outcomes. This work establishes a spatiotemporally controllable, cascade-amplified combined treatment modality for drug-resistant tumors.
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Feng et al. (2026) studied this question.
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