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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 1

PC enhances T cell killing by downregulating PD-L1.

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PC enhances T cell killing by downregulating PD-L1.
(A) PC was identifie...
(A) PC was identified as a PD-L1 inhibitor from a screen of 209 natural molecules using Western blotting. (B) Total PD-L1 protein levels were determined by Western blotting analysis in RKO and H1975 cells following exposure to PC at concentrations of 0 μM, 10 μM, 20 μM, and 40 μM for 24 hours. (C) Quantification of B. (D) Western blotting analysis was performed to assess total PD-L1 protein expression in RKO and H1975 cells treated with 40 μM PC for various time intervals. (E) Quantification of D. (F–I) Membrane PD-L1 levels were measured by flow cytometry after treatment with varying PC concentrations (F) or durations (H), with quantifications in G and I. (J–M) Immunofluorescence detected membrane PD-L1 in RKO (J) and H1975 (L) cells after PC treatment (nuclei stained with DAPI; scale bar: 200 μm). Quantifications are in K and M. (N–Q) Pretreated RKO (9 hours) (N) and H1975 (24 hours) (O) cells were cocultured with PD-1–overexpressing Jurkat T cells for 24 hours at an effector-to-target ratio of 9:1. Prior to coculture, the Jurkat T cells were activated with phytohemagglutinin (PHA) (1 mg/mL) and PMA (50 ng/mL). The survival of target cells was quantified using crystal violet staining. Quantitative data from N and O are presented in P and Q, respectively. (R and S) Cytotoxicity of various PC concentrations on RKO and H1975 cells was assessed by EdU assay and the corresponding quantitation. (T) CCK-8 assay for cytotoxicity under the same conditions. The data shown are the mean ± SEM of triplicate experiments. Statistical differences were determined by 1-way ANOVA with Dunnett’s multiple-comparison 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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