Hong Jinjiong, Wang Xiaofeng, Yu Liang, Li Jie, Hu Haoliang, Mao Weisheng
Department of Hand Surgery, Department of Plastic Reconstructive Surgery, Ningbo No. 6 Hospital, Ningbo 315040, China.
Department of Spine Surgery, Ningbo No. 6 Hospital, Ningbo 315040, China.
J Oncol. 2022 Oct 12;2022:5040458. doi: 10.1155/2022/5040458. eCollection 2022.
In childhood and adolescence, the prevailing bone tumor is osteosarcoma associated with frequent recurrence and lung metastasis. This research focused on predicting the survival and immune landscape of osteosarcoma by developing a prognostic signature and establishing aging-related genes (ARGs) subtypes.
The training group comprised of the transcriptomic and associated clinical data of 84 patients with osteosarcoma accessed at the TARGET database and the validation group consisted of 53 patients from GSE21257. The aging-related subtypes were identified using unsupervised consensus clustering analysis. The ARG signature was developed utilizing multivariate Cox analysis and LASSO regression. The prognostic value was assessed using the univariate and multivariate Cox analyses, Kaplan-Meier plotter, time-dependent ROC curve, and nomogram. The functional enrichment analyses were performed by GSEA, GO, and KEGG analysis, while the ssGSEA, ESTIMATE, and CIBERSORT analyses were conducted to reveal the immune landscape in osteosarcoma.
The two clusters of osteosarcoma patients formed based on 543 ARGs, depicted a considerable difference in the tumor microenvironment, and the overall survival and immune cell infiltration rate varied as well. Among these, the selected 23 ARGs were utilized for the construction of an efficient predictive prognostic signature for the overall survival prediction. The testing in the validation group of osteosarcoma patients confirmed the status of the high-risk score as an independent indicator for poor prognosis, which was already identified as such using the univariate and multivariate Cox analyses. Furthermore, the ARG signature could distinguish different immune-related functions, infiltration status of immune cells, and tumor microenvironment, as well as predict the immunotherapy response of osteosarcoma patients.
The aging-related subtypes were identified and a prognostic signature was developed in this research, which determined different prognoses and allowed for treatment of osteosarcoma patients to be tailored. Additionally, the immunotherapeutic response of individuals with osteosarcoma could also be predicted by the ARG signature.
在儿童和青少年时期,最常见的骨肿瘤是骨肉瘤,其复发频繁且易发生肺转移。本研究旨在通过开发一种预后特征并建立衰老相关基因(ARG)亚型来预测骨肉瘤的生存情况和免疫格局。
训练组由TARGET数据库中84例骨肉瘤患者的转录组及相关临床数据组成,验证组由来自GSE21257的53例患者组成。使用无监督一致性聚类分析确定衰老相关亚型。利用多变量Cox分析和LASSO回归开发ARG特征。使用单变量和多变量Cox分析、Kaplan-Meier绘图仪、时间依赖性ROC曲线和列线图评估预后价值。通过GSEA、GO和KEGG分析进行功能富集分析,同时进行ssGSEA、ESTIMATE和CIBERSORT分析以揭示骨肉瘤中的免疫格局。
基于543个ARG形成的两组骨肉瘤患者在肿瘤微环境方面存在显著差异,总体生存率和免疫细胞浸润率也有所不同。其中,选择的23个ARG用于构建高效的总体生存预测预后特征。在骨肉瘤患者验证组中的测试证实了高风险评分作为预后不良的独立指标的地位,这已经通过单变量和多变量Cox分析得到确认。此外,ARG特征可以区分不同的免疫相关功能、免疫细胞浸润状态和肿瘤微环境,还可以预测骨肉瘤患者的免疫治疗反应。
本研究确定了衰老相关亚型并开发了一种预后特征,该特征决定了不同的预后情况,并允许对骨肉瘤患者进行个性化治疗。此外,ARG特征还可以预测骨肉瘤患者的免疫治疗反应。