Department of Orthopaedics, First Affiliated Hospital of Dalian Medical University, Dalian, PR China.
Key Laboratory of Molecular Mechanism for Repair and Remodeling of Orthopaedic Diseases, Liaoning province, 116011, Dalian, Liaoning, PR China.
BMC Genomics. 2024 Apr 17;25(1):379. doi: 10.1186/s12864-024-10283-5.
Tumor cells exhibit a heightened susceptibility to lysosomal-dependent cell death (LCD) compared to normal cells. However, the role of LCD-related genes (LCD-RGs) in Osteosarcoma (OS) remains unelucidated. This study aimed to elucidate the role of LCD-RGs and their mechanisms in OS using several existing OS related datasets, including TCGA-OS, GSE16088, GSE14359, GSE21257 and GSE162454.
Analysis identified a total of 8,629 DEGs1, 2,777 DEGs2 and 21 intersection genes. Importantly, two biomarkers (ATP6V0D1 and HDAC6) linked to OS prognosis were identified to establish the prognostic model. Significant differences in risk scores for OS survival were observed between high and low-risk cohorts. Additionally, scores of dendritic cells (DC), immature DCs and γδT cells differed significantly between the two risk cohorts. Cell annotations from GSE162454 encompassed eight types (myeloid cells, osteoblastic OS cells and plasma cells). ATP6V0D1 was found to be significantly over-expressed in myeloid cells and osteoclasts, while HDAC6 was under-expressed across all cell types. Moreover, single-cell trajectory mapping revealed that myeloid cells and osteoclasts differentiated first, underscoring their pivotal role in patients with OS. Furthermore, ATP6V0D1 expression progressively decreased with time.
A new prognostic model for OS, associated with LCD-RGs, was developed and validated, offering a fresh perspective for exploring the association between LCD and OS.
与正常细胞相比,肿瘤细胞对溶酶体依赖性细胞死亡(LCD)更为敏感。然而,LCD 相关基因(LCD-RGs)在骨肉瘤(OS)中的作用仍不清楚。本研究旨在使用几个现有的 OS 相关数据集,包括 TCGA-OS、GSE16088、GSE14359、GSE21257 和 GSE162454,阐明 LCD-RGs 在 OS 中的作用及其机制。
分析共鉴定出 8629 个差异表达基因 1、2777 个差异表达基因 2 和 21 个交集基因。重要的是,鉴定出两个与 OS 预后相关的生物标志物(ATP6V0D1 和 HDAC6)来建立预后模型。高低风险队列之间 OS 生存的风险评分存在显著差异。此外,两个风险队列之间树突状细胞(DC)、未成熟 DC 和 γδT 细胞的评分差异显著。GSE162454 的细胞注释包括八种类型(髓样细胞、成骨 OS 细胞和浆细胞)。发现 ATP6V0D1 在髓样细胞和破骨细胞中显著过表达,而 HDAC6 在所有细胞类型中均表达下调。此外,单细胞轨迹映射显示髓样细胞和破骨细胞首先分化,这突出了它们在 OS 患者中的关键作用。此外,ATP6V0D1 的表达随时间逐渐降低。
开发并验证了一个与 LCD-RGs 相关的 OS 新预后模型,为探索 LCD 与 OS 之间的关联提供了新的视角。