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解读自噬在黑色素瘤中的预后价值及免疫治疗策略:整合单细胞测序与机器学习

Deciphering the prognostic value and immunotherapeutic strategy of aggrephagy in melanoma: Integrating single-cell sequencing and machine learning.

作者信息

Li Zihao, Xie Jiaheng, Li Liqun, He Yucang, Chen Wanying, Dai Hao, Zhao Songyun

机构信息

Department of Plastic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Department of Plastic Surgery, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Semin Oncol. 2025 Jul 21;52(5):152371. doi: 10.1016/j.seminoncol.2025.152371.

Abstract

This study aimed to investigate the role of aggrephagy in cutaneous melanoma (CM) and explore its potential as a biomarker for prognosis and therapeutic targeting. We utilized single-cell sequencing technology and machine learning algorithms to analyze melanoma transcriptome data from the TCGA database and validated our findings using 3 independent datasets from the GEO database. By employing enrichment scoring in single-cell sequencing, we identified characteristic expression patterns of different cell types involved in aggrephagy and constructed an aggrephagy-related signature (ARS). We further evaluated the association of ARS with clinical features, immune cell infiltration, tumor mutational load (TMB), and immune checkpoint gene expression. Additionally, we conducted in vivo experiments by knocking down TPX2, the most critical oncogene in ARS, using shRNA and assessed its effects on tumor proliferation and T-cell growth via subcutaneous tumor formation assays and flow cytometry in mice. The ARS demonstrated robust prognostic predictive power across multiple datasets, with higher ARS scores associated with poorer overall survival (OS) and lower levels of immune cell infiltration. Patients with low ARS scores were more likely to benefit from immune checkpoint inhibitor therapies, while those with high scores exhibited increased sensitivity to 2 common chemotherapeutic agents. Compared to published melanoma prognostic models, our ARS showed higher accuracy and stability. The construction of an ARS-related nomogram further facilitated more accurate clinical decision-making. In vivo experiments confirmed that TPX2 knockdown inhibited tumor proliferation and enhanced T-cell growth, highlighting its critical role in CM progression. Our study highlights the complex functions of the aggrephagy-related signature in cutaneous melanoma, underscoring its potential as a therapeutic target and a valuable tool for prognostic assessment.

摘要

本研究旨在探讨聚集体自噬在皮肤黑色素瘤(CM)中的作用,并探索其作为预后和治疗靶点生物标志物的潜力。我们利用单细胞测序技术和机器学习算法分析了来自TCGA数据库的黑色素瘤转录组数据,并使用来自GEO数据库的3个独立数据集验证了我们的发现。通过在单细胞测序中采用富集评分,我们确定了参与聚集体自噬的不同细胞类型的特征性表达模式,并构建了一个聚集体自噬相关特征(ARS)。我们进一步评估了ARS与临床特征、免疫细胞浸润、肿瘤突变负荷(TMB)和免疫检查点基因表达的关联。此外,我们通过使用shRNA敲低ARS中最关键的癌基因TPX2进行体内实验,并通过小鼠皮下肿瘤形成试验和流式细胞术评估其对肿瘤增殖和T细胞生长的影响。ARS在多个数据集中显示出强大的预后预测能力,ARS评分越高,总生存期(OS)越差,免疫细胞浸润水平越低。ARS评分低的患者更有可能从免疫检查点抑制剂治疗中获益,而评分高的患者对2种常用化疗药物的敏感性增加。与已发表的黑色素瘤预后模型相比,我们的ARS显示出更高的准确性和稳定性。构建与ARS相关的列线图进一步促进了更准确的临床决策。体内实验证实,TPX2敲低抑制了肿瘤增殖并增强了T细胞生长,突出了其在CM进展中的关键作用。我们的研究强调了聚集体自噬相关特征在皮肤黑色素瘤中的复杂功能,强调了其作为治疗靶点和预后评估有价值工具的潜力。

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