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Sequential drug release system: Targeting the tumor ECM for enhanced chemotherapy efficacy.

Proceedings of the National Academy of Sciences of the United States of America 2025 Vol.122(23) p. e2421061122

Cao L, Li Z, Song J, Xia X, Zhang G, Wang H, Zhao H

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The dense extracellular matrix (ECM) of stroma-rich solid tumors acts as a significant barrier to effective chemotherapy by hindering drug penetration.

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APA Cao L, Li Z, et al. (2025). Sequential drug release system: Targeting the tumor ECM for enhanced chemotherapy efficacy.. Proceedings of the National Academy of Sciences of the United States of America, 122(23), e2421061122. https://doi.org/10.1073/pnas.2421061122
MLA Cao L, et al.. "Sequential drug release system: Targeting the tumor ECM for enhanced chemotherapy efficacy.." Proceedings of the National Academy of Sciences of the United States of America, vol. 122, no. 23, 2025, pp. e2421061122.
PMID 40472035

Abstract

The dense extracellular matrix (ECM) of stroma-rich solid tumors acts as a significant barrier to effective chemotherapy by hindering drug penetration. In this study, a supramolecular hydrogel was successfully developed, enabling the codelivery and sequential release of hydrophilic and lipophilic drugs designed to target the ECM. The hydrogel is easy to prepare, has self-healing properties and excellent biocompatibility. Upon administration, the hydrogel first releases pirfenidone to inhibit collagen production, weakening the ECM, followed by the release of paclitaxel, which improves tumor penetration. The effectiveness of this sequential drug delivery system was validated in both oral squamous cell carcinoma and pancreatic cancer models, a classic example of a tumor with abundant ECM. In vitro experiments showed controlled sequential release profiles, whereas in vivo experiments using cell-derived and patient-derived xenograft models revealed that the hydrogel was more effective at tumor suppression compared to traditional methods. Single administration of the hydrogel led to long-term localized drug release, maintaining higher concentrations of chemotherapeutic agents in the tumor tissue and effectively reducing the tumor volume. This study provided a promising strategy to enhance chemotherapy in ECM-dense tumors, offering an efficient and minimally invasive method for localized, sustained-release cancer therapy.

MeSH Terms

Extracellular Matrix; Humans; Animals; Hydrogels; Mice; Drug Delivery Systems; Paclitaxel; Xenograft Model Antitumor Assays; Cell Line, Tumor; Drug Liberation; Antineoplastic Agents; Pancreatic Neoplasms; Mice, Nude

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