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L-甲硫氨酸通过抑制NR1I2/PCSK9信号通路促进CD8 T细胞杀伤肝细胞癌。

L-methionine promotes CD8 T cells killing hepatocellular carcinoma by inhibiting NR1I2/PCSK9 signaling.

作者信息

Yuan Chengsha, Hu Changpeng, Zhou Huyue, Liu Wuyi, Lai Wenjing, Liu Yafeng, Yin Yue, Li Guobing, Zhang Rong

机构信息

Department of Pharmacy, The Second Affiliated Hospital of Army Medical University, Chongqing, China.

Department of Pharmacy, The Second Affiliated Hospital of Army Medical University, Chongqing, China.

出版信息

Neoplasia. 2025 Jun;64:101160. doi: 10.1016/j.neo.2025.101160. Epub 2025 Mar 29.

Abstract

BACKGROUND

Liver cancer has consistently high incidence and mortality rates among malignant tumors. PCSK9, a target for hypercholesterolemia therapy, has recently been identified as an inhibitor of anti-tumor immunity, and targeting PCSK9 effectively inhibits tumor progression. However, small molecule inhibitors are lacking due to its flat protein structure.

METHODS

PCSK9 transcription inhibitor screening was conducted using a PCSK9 promoter-driven td-Tomato plasmid. Quantitative real-time PCR and immunoblotting were employed to assess the effect of L-methionine on PCSK9 expression in HCC cell lines. Co-culture experiments were performed to evaluate the impact of L-methionine on CD8 T cell-mediated killing of liver cancer cells. RNA sequencing, CUT&Tag, gene editing, and luciferase reporter assays were utilized to identify the transcription factor regulating PCSK9. Additionally, liver cancer xenograft and spontaneous liver cancer mouse models were used to evaluate the anti-cancer efficacy of L-methionine.

RESULTS

Our study identified L-methionine, an essential amino acid, as a transcriptional inhibitor of PCSK9. The optimal dose of L-methionine to inhibit PCSK9 expression and enhance CD8 T cell-mediated killing of liver cancer cells in vitro is 50 μM. Furthermore, intraperitoneal injection of 5 mg/kg/day of L-methionine significantly inhibited tumor growth in both liver cancer xenograft and spontaneous liver cancer mouse models. Mechanistically, we identified NR1I2 as a key transcription factor for PCSK9 and their crucial binding site was TGCACCCTGACAC. L-methionine inhibits PCSK9 transcription by downregulating NR1I2.

CONCLUSIONS

This work demonstrates that L-methionine promotes CD8 T cell-mediated killing of hepatocellular carcinoma by inhibiting NR1I2/PCSK9 signaling. Our study introduces a novel and convenient approach to inhibit PCSK9 and provides a theoretical basis for the rational supplementation of L-methionine in liver cancer patients.

摘要

背景

肝癌在恶性肿瘤中一直具有较高的发病率和死亡率。前蛋白转化酶枯草溶菌素9(PCSK9)是高胆固醇血症治疗的靶点,最近被确定为抗肿瘤免疫的抑制剂,靶向PCSK9可有效抑制肿瘤进展。然而,由于其扁平的蛋白质结构,小分子抑制剂较为缺乏。

方法

使用PCSK9启动子驱动的td-番茄质粒进行PCSK9转录抑制剂筛选。采用定量实时聚合酶链反应(qRT-PCR)和免疫印迹法评估L-蛋氨酸对肝癌细胞系中PCSK9表达的影响。进行共培养实验以评估L-蛋氨酸对CD8 T细胞介导的肝癌细胞杀伤作用的影响。利用RNA测序、CUT&Tag、基因编辑和荧光素酶报告基因检测来鉴定调节PCSK9的转录因子。此外,使用肝癌异种移植和自发性肝癌小鼠模型来评估L-蛋氨酸的抗癌疗效。

结果

我们的研究确定必需氨基酸L-蛋氨酸是PCSK9的转录抑制剂。在体外抑制PCSK9表达并增强CD8 T细胞介导的肝癌细胞杀伤作用的L-蛋氨酸最佳剂量为50μM。此外,腹腔注射5mg/kg/天的L-蛋氨酸在肝癌异种移植和自发性肝癌小鼠模型中均显著抑制肿瘤生长。机制上,我们确定核受体亚家族1I组成员2(NR1I2)是PCSK9的关键转录因子,其关键结合位点为TGCACCCTGACAC。L-蛋氨酸通过下调NR1I2抑制PCSK9转录。

结论

这项工作表明L-蛋氨酸通过抑制NR1I2/PCSK9信号促进CD8 T细胞介导的肝细胞癌杀伤作用。我们的研究引入了一种新颖且便捷的抑制PCSK9的方法,并为肝癌患者合理补充L-蛋氨酸提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d70/11997342/0beaa5b57ff9/gr1.jpg

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