4.8 Article

Nanoprodrug ratiometrically integrating autophagy inhibitor and genotoxic agent for treatment of triple-negative breast cancer

Journal

BIOMATERIALS
Volume 283, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2022.121458

Keywords

Autophagy; Combination; Co-assembled nanoprodrug; DNA repair; Triple-negative breast cancer

Funding

  1. National Natural Science Foundation of China [21975218, 32101128, 51773176]
  2. National Key Research and Development Program of China [2019YFA0802202]
  3. 111 Project [B13026]

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Effective combination therapies are urgently needed for the treatment of triple-negative breast cancer (TNBC). In this study, researchers found that the autophagy inhibitor hydroxychloroquine (HCQ) and the topoisomerase I inhibitor 7-ethyl-10-hydroxycamptothecin (SN38) exhibit synergistic effects when combined at a specific molar ratio. They further developed a glutathione-responsive self-assembled combination nanoparticle (Combo NP) that integrates the two drugs at the optimized ratio. In TNBC cells, the Combo NP significantly enhanced the cytotoxic effects of SN38 by blocking autophagy, leading to improved therapeutic benefit in metastatic TNBC models.
Effective combination therapies are urgently needed to treat triple-negative breast cancer (TNBC), which is insensitive to the existing treatment regimens. However, the synergistic potency of traditional small-molecule combinations is limited in TNBC mainly due to mismatched molar ratios, inconsistent pharmacokinetics, and intratumoral accumulation of individual drugs. Here, we find that the autophagy inhibitor hydroxychloroquine (HCQ) and the topoisomerase I inhibitor 7-ethyl-10-hydroxycamptothecin (SN38) exhibit synergistic effects when the molar ratio reaches 5:1. We further develop a glutathione-responsive self-assembled combination nanoparticle (Combo NP) to integrate individual HCQ and SN38 polymeric prodrugs at the optimized ratio. In TNBC cells treated with Combo NP, HCQ-mediated autophagy blockage significantly enhances the DNA damage and apoptotic effect of SN38, manifesting synergistically cytotoxic effects of Combo NP. In vivo evaluations show that Combo NP maintains the molar ratio of HCQ to SN38 within the synergistic range in mouse blood circulation and intratumoral tissues. More importantly, Combo NP elicits superior therapeutic benefit in metastatic TNBC models, compared to free drug combination as well as single drug nanoparticles. Taken together, our engineered nanosystem highlights a nanoprodrug-based chemosensitizing approach for improving the therapeutic response to TNBC, addressing the major challenges of the current combination therapy.

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