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Proanthocyanidins enhance antitumor immunity by promoting ubiquitin-proteasomal PD-L1 degradation via stabilization of LKB1 and SYVN1
Mengting Xu, Xuwen Lin, Hanchi Xu, Hongmei Hu, Xinying Xue, Qing Zhang, Dianping Yu, Saisai Tian, Mei Xie, Linyang Li, Xiaoyu Tao, Xinru Li, Simeng Li, Shize Xie, Yating Tian, Xia Liu, Hanchen Xu, Qun Wang, Weidong Zhang, Sanhong Liu
Mengting Xu, Xuwen Lin, Hanchi Xu, Hongmei Hu, Xinying Xue, Qing Zhang, Dianping Yu, Saisai Tian, Mei Xie, Linyang Li, Xiaoyu Tao, Xinru Li, Simeng Li, Shize Xie, Yating Tian, Xia Liu, Hanchen Xu, Qun Wang, Weidong Zhang, Sanhong Liu
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Research Article Immunology Oncology

Proanthocyanidins enhance antitumor immunity by promoting ubiquitin-proteasomal PD-L1 degradation via stabilization of LKB1 and SYVN1

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Abstract

Programmed cell death 1 ligand 1–targeted (PD-L1–targeted) immune checkpoint inhibitors are revolutionizing cancer therapy. However, strategies to induce endogenous PD-L1 degradation represent an emerging therapeutic paradigm. Here, we identified proanthocyanidins (PC) as a potent inducer of PD-L1 degradation through an endoplasmic reticulum–associated degradation (ERAD) mechanism. Mechanistically, PC exerted dual effects: First, it targeted and stabilized LKB1 to activate AMPK in tumor cells, subsequently inducing the phosphorylation of PD-L1 at Ser195 — a disruption that in turn impaired glycosylation of PD-L1 and promoted its retention in the ER. Second, PC directly bound to the E3 ubiquitin ligase SYVN1 to increase its protein stability, which strengthened PD-L1–SYVN1 binding, thereby accelerating K48-linked ubiquitination and proteasomal degradation of ER-retained PD-L1. This cascade culminated in the activation of CD8+ T cell–dominated antitumor immune responses, accompanied by suppression of myeloid-derived suppressor cells and regulatory T cells. In preclinical models of lung and colorectal cancer, PC exhibited synergistic antitumor efficacy when combined with anti–cytotoxic T lymphocyte antigen 4 (anti–CTLA-4) antibodies. Notably, PC also potently inhibited the progression of azoxymethane/dextran sodium sulfate–induced orthotopic colorectal cancer in mice. Collectively, our findings unveil an antitumor mechanism of PC, establishing this small-molecule compound as an ERAD pathway–exploiting immune checkpoint modulator with promising translational potential for cancer therapy.

Authors

Mengting Xu, Xuwen Lin, Hanchi Xu, Hongmei Hu, Xinying Xue, Qing Zhang, Dianping Yu, Saisai Tian, Mei Xie, Linyang Li, Xiaoyu Tao, Xinru Li, Simeng Li, Shize Xie, Yating Tian, Xia Liu, Hanchen Xu, Qun Wang, Weidong Zhang, Sanhong Liu

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Figure 3

PC demonstrates a significant preventative effect against AOM/DSS-induced colon cancer.

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PC demonstrates a significant preventative effect against AOM/DSS-induce...
(A) Flowchart of the AOM/DSS model in male C57BL/6 mice. n = 5 mice per group. ig, itragastric. (B) Representation of colonic morphology in control, PC (50 mg/kg), AOM/DSS, and AOM/DSS+PC (50 mg/kg) groups. (C) Statistical analysis of colon length in control, PC, AOM/DSS, and AOM/DSS+PC groups. 1-way ANOVA with Dunnett multiple comparisons test. (D) Body weight changes in mice from control, PC, AOM/DSS, and AOM/DSS+PC groups. 2-way ANOVA with Tukey’s multiple comparison test. (E) Statistical analysis of tumor size (< 2 mm3, 2–4 mm3, > 4 mm3) in the colons of mice from AOM/DSS and AOM/DSS+PC groups. 2-way ANOVA with Šídák multiple comparisons test. (F) Total number of colonic tumors in AOM/DSS and AOM/DSS+PC groups. (G) H&E staining of colon tissues from control, PC, AOM/DSS, and AOM/DSS+PC groups was performed to observe histological changes. (H) H&E staining of liver, spleen, and kidney tissues from control, PC, AOM/DSS, and AOM/DSS+PC groups. (I) Immunohistochemical analysis of tumor-associated markers (CD8, C-caspase-3, Ki-67, Foxp3, TUNEL, PD-L1, F4/80, CD86, CD206, CD11c, and NK1.1) in colon tissues from AOM/DSS and AOM/DSS+PC groups. For each tumor sample, 3 representative regions of interest (ROIs) were analyzed. The ROIs were selected to focus on viable tumor areas while systematically avoiding obvious necrotic regions, large blood vessels, and tissue folds to ensure an accurate assessment of staining within the tumor parenchyma. Positive markers were then quantified using ImageJ software. (J) Quantitative analysis of immunohistochemical markers from I. The data shown are the mean ± SEM. (F and J) Unpaired 2-tailed Student’s t test. *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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