Radiation Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, 9000 Rockville Pike, Building 10, CRC, Bethesda, MD 20892, USA.
Curr Oncol. 2023 Sep 7;30(9):8278-8293. doi: 10.3390/curroncol30090601.
Biomarkers for resistance in Glioblastoma multiforme (GBM) are lacking, and progress in the clinic has been slow to arrive. CD133 (prominin-1) is a membrane-bound glycoprotein on the surface of cancer stem cells (CSCs) that has been associated with poor prognosis, therapy resistance, and tumor recurrence in GBM. Due to its connection to CSCs, to which tumor resistance and recurrence have been partially attributed in GBM, there is a growing field of research revolving around the potential role of CD133 in each of these processes. However, despite encouraging results in vitro and in vivo, the biological interplay of CD133 with these components is still unclear, causing a lack of clinical application. In parallel, omic data from biospecimens that include CD133 are beginning to emerge, increasing the importance of understanding CD133 for the effective use of these highly dimensional data sets. Given the significant mechanistic overlap, prioritization of the most robust findings is necessary to optimize the transition of CD133 to clinical applications using patient-derived biospecimens. As a result, this review aims to compile and analyze the current research regarding CD133 as a functional unit in GBM, exploring its connections to prognosis, the tumor microenvironment, tumor resistance, and tumor recurrence.
胶质母细胞瘤(GBM)缺乏耐药的生物标志物,临床进展缓慢。CD133(prominin-1)是肿瘤干细胞(CSC)表面的一种膜结合糖蛋白,与 GBM 中的预后不良、耐药和肿瘤复发有关。由于它与 CSCs 的联系,部分归因于 GBM 中的肿瘤耐药和复发,因此围绕 CD133 在这些过程中的潜在作用的研究领域不断扩大。然而,尽管在体外和体内都有令人鼓舞的结果,但 CD133 与这些成分的生物学相互作用仍不清楚,导致缺乏临床应用。与此同时,包括 CD133 在内的生物标本的组学数据开始出现,这增加了理解 CD133 对于有效使用这些高维数据集的重要性。鉴于其显著的机制重叠,需要对最可靠的发现进行优先排序,以优化使用患者来源的生物标本将 CD133 转化为临床应用。因此,本综述旨在编译和分析目前关于 CD133 作为 GBM 中功能单位的研究,探讨其与预后、肿瘤微环境、肿瘤耐药和肿瘤复发的关系。