Nowacka Agnieszka, Śniegocki Maciej, Smuczyński Wojciech, Bożiłow Dominika, Ziółkowska Ewa
Department of Neurosurgery, Nicolas Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, ul. Curie Skłodowskiej 9, 85-094 Bydgoszcz, Poland.
Department of Physiotherapy, Nicolas Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, ul. Techników 3, 85-801 Bydgoszcz, Poland.
Cells. 2025 Mar 11;14(6):407. doi: 10.3390/cells14060407.
Glioblastoma, the most common primary malignant brain tumor in adults, carries a poor prognosis, with a median survival of just 15 months, significantly impacting patients' quality of life. The aggressive growth of these highly vascularized tumors relies heavily on angiogenesis, driven primarily by vascular endothelial growth factor-A. Therefore, VEGF signaling pathway has become a prime therapeutic target in GBM treatment over the past decade. While anti-angiogenic treatment showed promise, agents like bevacizumab have ultimately failed to improve overall survival. This highlights the presence of compensatory angiogenic mechanisms that bypass VEGF inhibition, necessitating further investigation into resistance mechanisms and the development of more effective therapeutic strategies. This review examined the current landscape of anti-angiogenic agents for GBM, analyzed the mechanisms driving resistance to these therapies, and explored potential strategies for enhancing their effectiveness.
胶质母细胞瘤是成人中最常见的原发性恶性脑肿瘤,预后较差,中位生存期仅为15个月,严重影响患者的生活质量。这些高度血管化肿瘤的侵袭性生长严重依赖血管生成,主要由血管内皮生长因子-A驱动。因此,在过去十年中,VEGF信号通路已成为胶质母细胞瘤治疗的主要治疗靶点。虽然抗血管生成治疗显示出前景,但贝伐单抗等药物最终未能提高总生存期。这突出了存在绕过VEGF抑制的代偿性血管生成机制,需要进一步研究耐药机制并开发更有效的治疗策略。本综述研究了胶质母细胞瘤抗血管生成药物的现状,分析了对这些疗法产生耐药性的机制,并探索了提高其有效性的潜在策略。