Feng Wenyu, Lin Haiyingjie, Rothzerg Emel, Song Dezhi, Zhao Wenxiang, Ning Tingting, Wei Qingjun, Zhao Jinmin, Wood David, Liu Yun, Xu Jiake
Department of Orthopaedics, the Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
School of Biomedical Sciences, The University of Western Australia, Perth, WA, Australia.
Cancer Inform. 2023 Apr 18;22:11769351231161478. doi: 10.1177/11769351231161478. eCollection 2023.
Osteosarcoma (OS) is the most common primary cancer in the skeletal system, characterized by a high incidence of lung metastasis, local recurrence and death. Systemic treatment of this aggressive cancer has not improved significantly since the introduction of chemotherapy regimens, underscoring a critical need for new treatment strategies. TRAIL receptors have long been proposed to be therapeutic targets for cancer treatment, but their role in osteosarcoma remains unclear. In this study, we investigated the expression profile of four TRAIL receptors in human OS cells using total RNA-seq and single-cell RNA-seq (scRNA-seq). The results revealed that and but not and are differentially expressed in human OS cells as compared to normal cells. At the single cell level by scRNA-seq analyses, and are most abundantly expressed in endothelial cells of OS tissues among nine distinct cell clusters. Notably, in osteoblastic OS cells, is most abundantly expressed, followed by and Similarly, in an OS cell line U2-OS using RNA-seq, is most abundantly expressed, followed by and . According to the TARGET online database, poor patient outcomes were associated with low expression of . These results could provide a new perspective to design novel therapeutic targets of TRAIL receptors for the diagnosis, prognosis and treatment of OS and other cancers.
骨肉瘤(OS)是骨骼系统中最常见的原发性癌症,其特征是肺转移、局部复发和死亡的发生率很高。自从引入化疗方案以来,这种侵袭性癌症的全身治疗并没有显著改善,这突出表明迫切需要新的治疗策略。长期以来,肿瘤坏死因子相关凋亡诱导配体(TRAIL)受体一直被认为是癌症治疗的靶点,但其在骨肉瘤中的作用仍不清楚。在本研究中,我们使用全转录组测序(total RNA-seq)和单细胞RNA测序(scRNA-seq)研究了四种TRAIL受体在人骨肉瘤细胞中的表达谱。结果显示,与正常细胞相比,人骨肉瘤细胞中[具体受体名称1]和[具体受体名称2]有差异表达,而[具体受体名称3]和[具体受体名称4]没有。通过scRNA-seq分析在单细胞水平上,在九个不同的细胞簇中,[具体受体名称1]和[具体受体名称2]在骨肉瘤组织的内皮细胞中表达最为丰富。值得注意的是,在成骨细胞型骨肉瘤细胞中,[具体受体名称1]表达最为丰富,其次是[具体受体名称2]和[具体受体名称3]。同样,在使用RNA测序的骨肉瘤细胞系U2-OS中,[具体受体名称1]表达最为丰富,其次是[具体受体名称2]和[具体受体名称3]。根据TARGET在线数据库,患者预后不良与[具体受体名称1]的低表达有关。这些结果可为设计针对骨肉瘤及其他癌症的诊断、预后和治疗的TRAIL受体新型治疗靶点提供新的视角。