Cao Lideng, Li Zaiye, Song Jian, Xia Xin, Zhang Gaowei, Wang Hang, Zhao Hang
State Key Laboratory of Oral Diseases, National Center for Stomatology, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China.
Research Unit of Oral Carcinogenesis and Management, Chinese Academy of Medical Sciences, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China.
Proc Natl Acad Sci U S A. 2025 Jun 10;122(23):e2421061122. doi: 10.1073/pnas.2421061122. Epub 2025 Jun 5.
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.
富含基质的实体瘤致密细胞外基质(ECM)通过阻碍药物渗透,对有效的化疗构成重大障碍。在本研究中,成功开发了一种超分子水凝胶,可实现针对ECM设计的亲水性和疏水性药物的共递送和顺序释放。该水凝胶易于制备,具有自愈特性和出色的生物相容性。给药后,水凝胶首先释放吡非尼酮以抑制胶原蛋白生成,削弱ECM,随后释放紫杉醇,从而改善肿瘤渗透。这种顺序给药系统的有效性在口腔鳞状细胞癌和胰腺癌模型中得到了验证,这是富含ECM肿瘤的典型例子。体外实验显示出可控的顺序释放曲线,而使用细胞衍生和患者衍生异种移植模型的体内实验表明,与传统方法相比,该水凝胶在肿瘤抑制方面更有效。单次给药水凝胶可导致长期局部药物释放,在肿瘤组织中维持更高浓度的化疗药物,并有效减小肿瘤体积。本研究提供了一种在富含ECM的肿瘤中增强化疗的有前景策略,为局部、缓释癌症治疗提供了一种高效且微创的方法。