Kampers Linde F C, Metselaar Dennis S, Vinci Maria, Scirocchi Fabio, Veldhuijzen van Zanten Sophie, Eyrich Matthias, Biassoni Veronica, Hulleman Esther, Karremann Michael, Stücker Wilfried, Van Gool Stefaan W
Immun-Onkologisches Zentrum Köln, 50674 Köln, Germany.
Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Cancers (Basel). 2025 Mar 4;17(5):879. doi: 10.3390/cancers17050879.
Malignant glioma is a highly aggressive, therapeutically non-responsive, and deadly disease with a unique tumor microenvironment (TME). Of the 14 currently recognized and described cancer hallmarks, five are especially implicated in malignant glioma and targetable with repurposed drugs: cancer stem-like cells, in general, and glioma stem-like cells in particular (GSCs), vascularization and hypoxia, metabolic reprogramming, tumor-promoting inflammation and sustained proliferative signaling. Each hallmark drives malignant glioma development, both individually and through interactions with other hallmarks, in which the TME plays a critical role. To combat the aggressive malignant glioma spatio-temporal heterogeneity driven by TME interactions, and to overcome its therapeutic challenges, a combined treatment strategy including anticancer therapies, repurposed drugs and multimodal immunotherapy should be the aim for future treatment approaches.
恶性胶质瘤是一种具有高度侵袭性、对治疗无反应且致命的疾病,具有独特的肿瘤微环境(TME)。在目前公认和描述的14个癌症标志中,有5个尤其与恶性胶质瘤相关,并且可以用重新利用的药物进行靶向治疗:一般的癌症干细胞,特别是胶质瘤干细胞(GSCs)、血管生成和缺氧、代谢重编程、肿瘤促进炎症和持续的增殖信号。每个标志都单独或通过与其他标志的相互作用驱动恶性胶质瘤的发展,其中TME起着关键作用。为了对抗由TME相互作用驱动的侵袭性恶性胶质瘤时空异质性,并克服其治疗挑战,包括抗癌疗法、重新利用的药物和多模式免疫疗法的联合治疗策略应成为未来治疗方法的目标。