A high level of reduced glutathione is a major factor contributing to the radioresistance observed in solid tumors. To address this radioresistance associated with glutathione, we fabricated a cinnamaldehyde (CA) polymer prodrug, referred to as PDPCA. This prodrug was created by synthesizing a pendent CA prodrug with acetal linkages in a hydrophobic block, forming a self-assembled into a core-shell nanoparticle in aqueous media. Additionally, it encapsulated all-trans retinoic acid (ATRA) for synchronous delivery, resulting in PDPCA@ATRA. The PDPCA@ATRA nanoparticles accumulated reactive oxygen species through both endogenous and exogenous pathways, enhancing ferroptosis by depleting glutathione. This approach has demonstrated efficacy in overcoming tumor radioresistance in vivo and in vitro and promoting the ferroptosis and enhancing the cytotoxic T lymphocyte (CTL) response for lung tumors to anti-PD-1 (αPD-1) immunotherapy. Furthermore, this study revealed that PDPCA@ATRA nanoparticles promoted ferroptosis through the NRF2-GPX4 signaling pathway, suggeating the potential for further investigation into the combination of radiotherapy and αPD-1 immune checkpoint inhibitors in cancer treatment. This article is protected by copyright. All rights reserved.This article is protected by copyright. All rights reserved.
