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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 2

PC attenuates MC38 tumor growth in C57BL/6 mice.

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PC attenuates MC38 tumor growth in C57BL/6 mice.
C57BL/6 mice or nude mi...
C57BL/6 mice or nude mice were subcutaneously implanted with 1 × 107 MC38 colon cancer cells. Upon reaching a tumor volume of approximately 50 mm3, different doses of PC were administered via oral gavage. n = 5 mice per group. Tissues were harvested approximately 2 weeks after the initiation of treatment. (A) Experimental flowchart and tumor schematic in C57BL/6 mice. (B–E) Tumor growth curves in C57BL/6 mice treated with different doses of PC, specifically showing 0 (C), 25 (D), and 50 (E) mg/kg. (F) Statistical analysis of subcutaneous tumor weights in C57BL/6 mice. (G) C57BL/6 mice body weight changes. (H–K) In nude mice bearing MC38 subcutaneous tumors (H), 50 mg/kg PC showed no effect on tumor growth (I), tumor weight (J), or body weight (K) versus the 0 mg/kg control. Further analyses were conducted on C57BL/6 mouse tumors: (L) Western blot detection of PD-L1 protein expression; (M–T) flow cytometry analysis of tumor-infiltrating lymphocytes identified the following populations: Tregs (M, CD4+CD25+Foxp3+), MDSCs (N, CD11b+Gr-1+ in CD45+), cytotoxic T cells (O, CD8+GzmB+), NK cells (P, NK1.1+), B cells (Q, B220+), M1 macrophages (R and S; CD86+ and CD80+), and M2 macrophages (T, CD206+). (U and V) Immunohistochemical analysis of MC38 tumors from PC-treated C57BL/6 mice quantified multiple markers — including CD8, cleaved caspase-3, Ki-67, Foxp3, TUNEL, PD-L1, CD86, CD206, CD11c, and NK1.1 — across 3 representative tumor regions. (V) Positive staining was quantified using ImageJ (NIH) and statistically analyzed with GraphPad Prism. The data shown are the mean ± SEM. Statistical differences were determined by 1-way ANOVA with Dunnett’s multiple-comparison test for all panels except B and G (analyzed by 2-way ANOVA) and I–K (analyzed by unpaired 2-tailed Student’s t test). *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001.

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