Luo Yuanguo, Lv Bo, He Shaokang, Zou Kai, Hu Kezhi
Department of Orthopedics, The 923rd Hospital of the Joint Logistics Support Force of the People's Liberation Army, Nanning, People's Republic of China.
Department of Orthopedics, People's Hospital of Guilin, Guilin, Guangxi, 541001, People's Republic of China.
Int J Gen Med. 2021 May 7;14:1773-1783. doi: 10.2147/IJGM.S312277. eCollection 2021.
Osteosarcoma is the most common malignant bone cancer affecting adolescents and young adults. This study aimed to screen potential diagnostic and therapeutic markers for osteosarcoma.
Differential expression analysis between osteosarcoma and control was performed in GSE99671, the differentially expressed genes (DEGs) were subjected to co-expression analysis. Enrichment analysis was employed to identify the biological functions and KEGG signaling pathways of module genes. In addition, a differential analysis was also performed between recurrent and non-recurrent osteosarcoma samples in GSE39055, and enrichment analysis was performed for DEGs. Further, Kaplan-Meier curve analysis was performed on the module genes, and receiver operating characteristic (ROC) curve was drawn. Comparison of the module with the highest correlation to osteosarcoma identified key genes. Cox regression model was utilized to identify the predictive ability of key genes for the prognosis of osteosarcoma.
A total of 13 co-expression modules were identified from 4871 DEGs of GSE99671, module 1 had the highest positive correlation with osteosarcoma. Module genes were mainly enriched in autophagy and macrophage migration functions. A total of 1126 DEGs were obtained from GSE39055, significantly involved in neutrophil mediated immunity. Screening of genes with area under the ROC curve (AUC) values greater than 0.73 in both GSE99671 and GSE39055 identified 5 key genes when compared with genes from module 1. The nomogram results showed that ATF5, CHCHD8, ENOPH1, and LOC286367 might predict 5-year or 8-year survival time of osteosarcoma patients. The Cox model results confirmed that the signals of ATF5, CHCHD8, and LOC286367 were robust, and it may be used in the diagnosis, treatment, and prognosis of osteosarcoma.
We found that ATF5, CHCHD8, and LOC286367 can effectively identify osteosarcoma tumorigenesis and even recurrence status. This is helpful for early diagnosis and treatment, improving the clinical treatment of patients with osteosarcoma.
骨肉瘤是影响青少年和年轻成年人的最常见恶性骨癌。本研究旨在筛选骨肉瘤潜在的诊断和治疗标志物。
在GSE99671中进行骨肉瘤与对照之间的差异表达分析,对差异表达基因(DEGs)进行共表达分析。采用富集分析来确定模块基因的生物学功能和KEGG信号通路。此外,在GSE39055中对复发性和非复发性骨肉瘤样本也进行了差异分析,并对DEGs进行了富集分析。进一步地,对模块基因进行Kaplan-Meier曲线分析,并绘制受试者工作特征(ROC)曲线。将与骨肉瘤相关性最高的模块进行比较,确定关键基因。利用Cox回归模型确定关键基因对骨肉瘤预后的预测能力。
从GSE99671的4871个DEGs中总共鉴定出13个共表达模块,模块1与骨肉瘤的正相关性最高。模块基因主要富集于自噬和巨噬细胞迁移功能。从GSE39055中获得了1126个DEGs,显著参与中性粒细胞介导的免疫。与模块1中的基因相比,在GSE99671和GSE39055中筛选出ROC曲线下面积(AUC)值大于0.73的基因,确定了5个关键基因。列线图结果显示,ATF5、CHCHD8、ENOPH1和LOC286367可能预测骨肉瘤患者的5年或8年生存时间。Cox模型结果证实,ATF5、CHCHD8和LOC286367的信号很强,可用于骨肉瘤的诊断、治疗和预后判断。
我们发现ATF5、CHCHD8和LOC286367能够有效识别骨肉瘤的肿瘤发生甚至复发状态。这有助于早期诊断和治疗,改善骨肉瘤患者的临床治疗效果。