Integrating single-cell and bulk transcriptomes to reveal prognostic and immunological features of ecDNA-related genes in osteosarcoma.

IF 5.1
Jinyan Feng, Jianchao Liu, Houzhi Yang, Yiqin Li, Yao Xu, Xiuxin Han, Chao Zhang, Guowen Wang
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Abstract

Background: The role of extrachromosomal DNA (ecDNA)-related genes in osteosarcoma remains largely unexplored. The aim of this study is to investigate the association between ecDNA-related genes and prognosis and tumor microenvironment (TME) in osteosarcoma.

Methods: Differential gene expression analysis of GEO datasets was conducted to identify ecDNA-related genes in osteosarcoma. Based on bulk RNA-seq data, a novel ecDNA-related Gene Prognostic Score Model (EGPSM) was developed using an integrated framework of 101 machine learning algorithms, which was validated in training, testing, and external cohorts. The associations between risk scores, prognosis, and TME characteristics were comprehensively evaluated. Single-cell RNA sequencing (scRNA-seq) data were further analyzed to elucidate the relationship between EGPSM, pro-tumor behaviors, and immune modulation in osteosarcoma, as well as to identify key prognostic genes involved in tumor progression. Lastly, we conducted in vitro and in vivo assays to characterize the biological roles of MTDH and to elucidate its regulatory effects on CD8⁺ T cell function.

Results: A robust EGPSM was constructed, demonstrating superior predictive accuracy with a maximum C-index of 0.803. High-risk patients exhibited poorer survival, higher metastatic potential, and an "immune-cold" TME characterized by diminished CD8⁺ T/NK cell infiltration and impaired effector functions. Single-cell analysis confirmed the enrichment of malignant cells and depletion of T/NK populations with lower effector scores in the high-risk group. MTDH was identified as a key driver; functional assays showed it promotes proliferation and invasion while inhibiting apoptosis. Notably, MTDH knockdown potentiated CD8⁺ T-cell cytotoxicity by increasing the levels of granzyme B, IFN-γ, and perforin.

Conclusion: The newly developed EGPSM represents an effective tool for prognostic assessment and therapeutic stratification in osteosarcoma. MTDH may serve as a promising prognostic biomarker and therapeutic target.

整合单细胞和整体转录组揭示骨肉瘤中ecdna相关基因的预后和免疫学特征。
背景:染色体外DNA (ecDNA)相关基因在骨肉瘤中的作用仍未被充分研究。本研究旨在探讨ecdna相关基因与骨肉瘤预后及肿瘤微环境(tumor microenvironment, TME)的关系。方法:对GEO数据集进行差异基因表达分析,鉴定骨肉瘤中ecdna相关基因。基于大量RNA-seq数据,使用101个机器学习算法的集成框架开发了一种新的ecdna相关基因预后评分模型(EGPSM),并在训练、测试和外部队列中进行了验证。综合评估风险评分、预后和TME特征之间的关系。我们进一步分析单细胞RNA测序(scRNA-seq)数据,以阐明EGPSM、促瘤行为和骨肉瘤免疫调节之间的关系,并确定参与肿瘤进展的关键预后基因。最后,我们通过体外和体内实验来表征MTDH的生物学作用,并阐明其对CD8 + T细胞功能的调控作用。结果:构建了稳健的EGPSM模型,预测准确率最高,c指数为0.803。高危患者表现出较差的生存率,较高的转移潜力,并且以CD8 + T/NK细胞浸润减少和效应功能受损为特征的“免疫冷”TME。单细胞分析证实了高危组中恶性细胞的富集和效应评分较低的T/NK群体的耗竭。MTDH被确定为关键驱动因素;功能实验表明,它能促进细胞增殖和侵袭,抑制细胞凋亡。值得注意的是,MTDH敲除通过增加颗粒酶B、IFN-γ和穿孔素的水平增强了CD8⁺的t细胞毒性。结论:新开发的EGPSM是骨肉瘤预后评估和治疗分层的有效工具。MTDH可能是一种有前景的预后生物标志物和治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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