ArticleThe Journal of biological chemistry2026
Targeting the Golgi apparatus enhances PD-L1 blockade and synergizes with oxaliplatin to improve immunotherapy efficacy.
Article in The Journal of biological chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Targeting Golgi-STING Signaling to Reprogram Innate and Adaptive Immunity for the Treatment of Implant-Associated Infections.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Circadian control of immune homeostasis in cardiovascular health and disease.Frontiers in immunology · 2026Review
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Authors and funding
21 authors.
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Abstract
Immune checkpoint blockade targeting programmed death ligand-1 (PD-L1) has emerged as a cornerstone of cancer immunotherapy, yielding durable responses in subsets of patients across multiple malignancies. However, clinical outcomes remain limited because of incomplete blockade, low tumor immunogenicity, and poor targeting specificity. Here, we report the development of a chondroitin sulfate-modified liposomal formulation (OPCR-Lip) designed to achieve comprehensive PD-L1 blockade while reprogramming the tumor microenvironment to enhance immune activation. OPCR-Lip binds membrane-bound PD-L1, disrupts PD-L1 glycosylation, and inhibits exosomal PD-L1 secretion by damaging the Golgi apparatus, thereby mitigating immunosuppressive signaling. Codelivery of oxaliplatin further promotes immunogenic cell death, enhancing tumor immunogenicity and sustaining antitumor immunity in 4T1 breast tumor-bearing mice. The formulation's therapeutic precision was evaluated through circadian rhythm-based dosing, cross-species in vitro validation (canine and human breast cancer cells), and in vivo efficacy across melanoma and lung cancer models. Collectively, this study presents a promising therapeutic platform that augments PD-L1 blockade, broadens its clinical applicability, and improves treatment safety and effectiveness in solid tumors.
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