Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Division of Head and Neck Surgery, Department of Otorhinolaryngology, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Cancer Res. 2018 Dec 1;78(23):6632-6642. doi: 10.1158/0008-5472.CAN-18-0650. Epub 2018 Oct 15.
: Circulating tumor cells (CTC) are known to be present in the blood of patients with glioblastoma (GBM). Here we report that GBM-derived CTC possess a cancer stem cell (CSC)-like phenotype and contribute to local tumorigenesis and recurrence by the process of self-seeding. Genetic probes showed that mouse GBM-derived CTC exhibited Sox2/ETn transcriptional activation and expressed glioma CSC markers, consistent with robust expression of stemness-associated genes including SOX2, OCT4, and NANOG in human GBM patient-derived samples containing CTC. A transgenic mouse model demonstrated that CTC returned to the primary tumor and generated new tumors with enhanced tumorigenic capacity. These CTCs were resistant to radiotherapy and chemotherapy and to circulation stress-induced cell apoptosis. Single-cell RNA-seq analysis revealed that Wnt activation induced stemness and chemoresistance in CTC. Collectively, these findings identify GBM-derived CTC as CSC-like cells and suggest that targeting Wnt may offer therapeutic opportunities for eliminating these treatment-refractory cells in GBM. SIGNIFICANCE: These findings identify CTCs as an alternative source for tumor invasion and recurrence through local micrometastasis, warranting eradication of systemic "out-of-tumor" CTCs as a promising new therapeutic opportunity for GBM.
循环肿瘤细胞(CTC)已知存在于胶质母细胞瘤(GBM)患者的血液中。在这里,我们报告说,GBM 衍生的 CTC 具有癌症干细胞(CSC)样表型,并通过自我播种过程促进局部肿瘤发生和复发。遗传探针表明,源自小鼠的 GBM 的 CTC 表现出 Sox2/ETn 转录激活,并表达神经胶质瘤 CSC 标志物,与包含 CTC 的人类 GBM 患者衍生样本中强大的干性相关基因表达一致,包括 SOX2、OCT4 和 NANOG。转基因小鼠模型表明,CTC 回到原发性肿瘤并产生具有增强致瘤能力的新肿瘤。这些 CTC 对放射治疗和化学疗法以及循环应激诱导的细胞凋亡具有抗性。单细胞 RNA-seq 分析显示,Wnt 激活诱导 CTC 中的干性和化学抗性。总之,这些发现将 GBM 衍生的 CTC 鉴定为 CSC 样细胞,并表明靶向 Wnt 可能为消除 GBM 中这些治疗耐药细胞提供治疗机会。意义:这些发现将 CTC 鉴定为通过局部微转移进行肿瘤侵袭和复发的另一种来源,需要消除系统中的“肿瘤外”CTC,这是治疗 GBM 的一种有前途的新治疗机会。