Zou Tiannan, Liu Weibing, Wang Zeyu, Chen Jiayu, Lu Sheng, Huang Kun, Li Weichao
Department of Orthopedic Surgery, The First People's Hospital of Yunnan Province, Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.
Faculty of Medical Science, Kunming University of Science and Technology, Kunming, China.
Front Med (Lausanne). 2021 Mar 5;8:642615. doi: 10.3389/fmed.2021.642615. eCollection 2021.
Targeting cancer-specific messenger RNAs (mRNAs) may offer novel insights into therapeutic strategies in osteosarcoma. This study aimed to discover possible osteosarcoma-specific mRNA and probe its biological functions. Based on mRNA-seq data from the TARGET database, stromal and immune scores were estimated for each osteosarcoma sample via the ESTIMATE algorithm. Stromal and immune mRNAs were obtained via integration of differentially expressed mRNAs between high and low stromal / immune score groups. Among hub and prognostic mRNAs, C3AR1 mRNA was focused and its prognostic value was assessed. The associations between C3AR1 mRNA and immune cells were analyzed via the CIBERSORT algorithm. Its expression was verified in osteosarcoma tissues and cells by RT-qPCR and western blot. The functions of C3AR1 were investigated by a series of experiments. Low stromal and immune scores were both indicative of unfavorable outcomes for osteosarcoma patients. Eighty-eight up-regulated and seven down-regulated stromal and immune mRNAs were identified. Among 30 hub mRNAs, low expression of C3AR1 mRNA indicated worse outcomes than its high expression. There was a lower mRNA expression of C3AR1 in metastatic than non-metastatic osteosarcoma. C3AR1 mRNA was closely correlated to various immune cells such as macrophages. C3AR1 was verified to be down-regulated in osteosarcoma tissues and cells. Its overexpression suppressed proliferation, migration and invasion and induced apoptosis in osteosarcoma cells. C3AR1 mRNA could be a promising therapeutic target for osteosarcoma, linked with prognosis and tumor microenvironment.
靶向癌症特异性信使核糖核酸(mRNA)可能为骨肉瘤的治疗策略提供新的见解。本研究旨在发现可能的骨肉瘤特异性mRNA并探究其生物学功能。基于来自TARGET数据库的mRNA测序数据,通过ESTIMATE算法估算每个骨肉瘤样本的基质和免疫评分。通过整合高、低基质/免疫评分组之间差异表达的mRNA获得基质和免疫mRNA。在中心和预后mRNA中,聚焦于C3AR1 mRNA并评估其预后价值。通过CIBERSORT算法分析C3AR1 mRNA与免疫细胞之间的关联。通过RT-qPCR和蛋白质印迹在骨肉瘤组织和细胞中验证其表达。通过一系列实验研究C3AR1的功能。低基质和免疫评分均表明骨肉瘤患者预后不良。鉴定出88个上调和7个下调的基质和免疫mRNA。在30个中心mRNA中,C3AR1 mRNA低表达表明预后比高表达更差。转移性骨肉瘤中C3AR1的mRNA表达低于非转移性骨肉瘤。C3AR1 mRNA与多种免疫细胞如巨噬细胞密切相关。证实C3AR1在骨肉瘤组织和细胞中下调。其过表达抑制骨肉瘤细胞的增殖、迁移和侵袭并诱导其凋亡。C3AR1 mRNA可能是骨肉瘤有前景的治疗靶点,与预后和肿瘤微环境相关。