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MTX-PEG modified CG/DMMA polymeric micelles for targeted delivery of doxorubicin to induce synergistic autophagic death against triple negative breast cancer
Summary
Researchers developed methotrexate-polyethylene glycol (MTX-PEG) modified CG/DMMA polymeric micelles for targeted doxorubicin delivery to triple negative breast cancer (TNBC), aiming to reduce off-target toxicity and exploit synergistic autophagic cell death. The micelles effectively promoted autophagosome accumulation and disrupted autophagic flux in tumor cells, improving tumor-selective drug accumulation and anti-tumor efficacy in vitro.
<title>Abstract</title> The chemotherapy of triple negative breast cancer (TNBC) based on doxorubicin (DOX) regimens suffer from great challenges on toxicity and autophagy raised off-target. In this study, a conjugate methotrexate-polyethylene glycol (shorten as MTX-PEG) modified CG/DMMA polymeric micelles were prepared to endue DOX tumor selectivity and synergistic autophagic flux interference to reduce systematic toxicity and to improve anti-tumor capacity. The micelles could effectively promote the accumulation of autophagosomes in tumor cells and interfere with the degradation process of autophagic flux, collectively inducing autophagic death of tumor cells. In vivo and in vitro experiments showed that the micelles could exert improved anti-tumor effect and specificity, as well as reduced accumulation and damage of chemotherapeutic drugs in normal organs. The potential mechanism of synergistic autophagic death exerted by the synthesized micelles in MDA-MB-231 cells have been performed by autophagic flux-related pathway.
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