Zimmer Niklas, Trzeciak Emily R, Müller Andreas, Licht Philipp, Sprang Bettina, Leukel Petra, Mailänder Volker, Sommer Clemens, Ringel Florian, Tuettenberg Jochen, Kim Ella, Tuettenberg Andrea
Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
Department of Neurosurgery, University Medical Center Mainz, 55131 Mainz, Germany.
Cancers (Basel). 2023 Dec 5;15(24):5711. doi: 10.3390/cancers15245711.
Glioblastoma (GB) is notoriously resistant to therapy. GB genesis and progression are driven by glioblastoma stem-like cells (GSCs). One goal for improving treatment efficacy and patient outcomes is targeting GSCs. Currently, there are no universal markers for GSCs. Glycoprotein A repetitions predominant (GARP), an anti-inflammatory protein expressed by activated regulatory T cells, was identified as a possible marker for GSCs. This study evaluated GARP for the detection of human GSCs utilizing a multidimensional experimental design that replicated several features of GB: (1) intratumoral heterogeneity, (2) cellular hierarchy (GSCs with varied degrees of self-renewal and differentiation), and (3) longitudinal GSC evolution during GB recurrence (GSCs from patient-matched newly diagnosed and recurrent GB). Our results indicate that GARP is expressed by GSCs across various cellular states and disease stages. GSCs with an increased GARP expression had reduced self-renewal but no alterations in proliferative capacity or differentiation commitment. Rather, GARP correlated inversely with the expression of GFAP and PDGFR-α, markers of astrocyte or oligodendrocyte differentiation. GARP had an abnormal nuclear localization (GARP) in GSCs and was negatively associated with patient survival. The uniformity of GARP/GARP expression across different types of GSCs suggests a potential use of GARP as a marker to identify GSCs.
胶质母细胞瘤(GB)对治疗具有众所周知的抗性。GB的发生和进展由胶质母细胞瘤干细胞(GSCs)驱动。提高治疗效果和患者预后的一个目标是靶向GSCs。目前,尚无GSCs的通用标志物。糖蛋白A重复序列占主导(GARP),一种由活化调节性T细胞表达的抗炎蛋白,被确定为GSCs的一种可能标志物。本研究利用多维实验设计评估GARP用于检测人类GSCs,该设计复制了GB的几个特征:(1)肿瘤内异质性,(2)细胞层次结构(具有不同程度自我更新和分化能力的GSCs),以及(3)GB复发期间GSCs的纵向演变(来自患者匹配的新诊断和复发性GB的GSCs)。我们的结果表明,GARP在各种细胞状态和疾病阶段的GSCs中均有表达。GARP表达增加的GSCs自我更新能力降低,但增殖能力或分化倾向无改变。相反,GARP与星形胶质细胞或少突胶质细胞分化标志物GFAP和PDGFR-α的表达呈负相关。GARP在GSCs中具有异常的核定位(GARP),并且与患者生存率呈负相关。不同类型GSCs中GARP/GARP表达的一致性表明GARP有可能用作识别GSCs的标志物。