Que Yukang, Ding Tianming, Wang Huming, Xu Shenglin, He Peng, Shen Qiling, Cao Kun, Luo Yang, Hu Yong
Department of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Department of Orthopedics, Yangzhou East Hospital, Yangzhou, Jiangsu, China.
J Cell Mol Med. 2025 Mar;29(5):e70424. doi: 10.1111/jcmm.70424.
Osteosarcoma (OS) is the most frequent primary solid malignancy of bone, whose course is usually dismal without efficient treatments. The aim of the study was to discover novel risk models to more accurately predict and improve the prognosis of patients with osteosarcoma. The single-cell RNA sequencing (scRNA-seq) data was obtained from the GEO database. Bulk RNA-seq data and microarray data of OS were obtained from the TARGET and GEO databases respectively. A clustering tree was plotted to classify all cells into different clusters. The "cellchat" R package was used to establish and visualise cell-cell interaction networks. Then Univariate COX regression analysis was used to determine the prognostic CAF-related genes, followed by the Lasso-Cox regression analysis to build a risk on the prognostic CAF-related genes. Finally, from multiple perspectives, the signature was validated as an accurate and dependable tool in predicting the prognosis and guiding treatment therapies in OS patients. From the single-cell dataset, six OS patients and 46,544 cells were enrolled. All cells were classified into 22 clusters, and the clusters were annotated to 14 types of cells. Subsequently, CAFs were observed as a vital TME components. In cell-cell interaction networks in OS cells, CAFs had a profound impact as four roles. Via the Univariate COX regression analysis, 14 CAF-related genes were screened out. By the Lasso-Cox regression analyses, 11 key CAF-related genes were obtained, based on which an 11-gene signature that could predict the prognosis of osteosarcoma patients was constructed. According to the median of risk scores, all patients were grouped in to the high- and low-risk group, and their overall survival, activated pathways, immune cell infiltrations, and drug sensitivity were significantly differential, which may have important implications for the clinical treatment of patients with osteosarcoma. Our study, a systematic analysis of gene and regulatory genes, has proven that CAF-related genes had excellent diagnostic and prognostic capabilities in OS, and it may reshape the TME in OS. The novel CAF-related risk signature can effectively predict the prognosis of OS and provide new strategies for cancer treatment.
骨肉瘤(OS)是最常见的原发性骨实体恶性肿瘤,若没有有效的治疗方法,其病程通常很不乐观。本研究的目的是发现新的风险模型,以更准确地预测和改善骨肉瘤患者的预后。单细胞RNA测序(scRNA-seq)数据来自GEO数据库。骨肉瘤的批量RNA-seq数据和微阵列数据分别来自TARGET和GEO数据库。绘制聚类树将所有细胞分类到不同的簇中。使用“cellchat”R包建立并可视化细胞-细胞相互作用网络。然后采用单变量COX回归分析确定预后的CAF相关基因,接着进行Lasso-Cox回归分析以建立基于预后CAF相关基因的风险模型。最后,从多个角度验证该特征作为预测骨肉瘤患者预后和指导治疗方案的准确可靠工具。从单细胞数据集中,纳入了6例骨肉瘤患者和46544个细胞。所有细胞被分为22个簇,并将这些簇注释为14种细胞类型。随后,观察到癌相关成纤维细胞(CAFs)是肿瘤微环境(TME)的重要组成部分。在骨肉瘤细胞的细胞-细胞相互作用网络中,CAFs作为四种角色具有深远影响。通过单变量COX回归分析,筛选出14个CAF相关基因。通过Lasso-Cox回归分析,获得了11个关键的CAF相关基因,并基于此构建了一个可预测骨肉瘤患者预后的11基因特征。根据风险评分的中位数,将所有患者分为高风险组和低风险组,他们的总生存期、激活通路、免疫细胞浸润和药物敏感性存在显著差异,这可能对骨肉瘤患者的临床治疗具有重要意义。我们的研究,即对基因和调控基因的系统分析,已证明CAF相关基因在骨肉瘤中具有出色的诊断和预后能力,并且可能重塑骨肉瘤中的肿瘤微环境。新的CAF相关风险特征可以有效地预测骨肉瘤的预后,并为癌症治疗提供新策略。