Glioblastoma Tumor Microenvironment and Purinergic Signaling: Implications for Novel Therapies

被引:0
|
作者
Bedeschi, Martina [1 ]
Cavassi, Elena [1 ]
Romeo, Antonino [2 ]
Tesei, Anna [1 ]
机构
[1] IRCCS Ist Romagnolo Studio Tumori IRST Dino Amador, Biosci Lab, I-47014 Meldola, Italy
[2] IRCCS Ist Romagnolo Studio Tumori IRST Dino Amador, Radiat Oncol Unit, I-47014 Meldola, Italy
关键词
purinergic receptors; glioblastoma; tumor microenvironment; purinergic antagonists; P2X7; RECEPTOR; BRAIN-TUMORS; GLIOMA; LANDSCAPE; MICROGLIA; CELLS; TEMOZOLOMIDE; MACROPHAGES; NUCLEOTIDE; SUBTYPES;
D O I
10.3390/ph18030385
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glial-origin brain tumors, particularly glioblastomas (GBMs), are known for their devastating prognosis and are characterized by rapid progression and fatal outcomes. Despite advances in surgical resection, complete removal of the tumor remains unattainable, with residual cells driving recurrence that is resistant to conventional therapies. The GBM tumor microenviroment (TME) significantly impacts tumor progression and treatment response. In this review, we explore the emerging role of purinergic signaling, especially the P2X7 receptor (P2X7R). Due to its unique characteristics, it plays a key role in tumor progression and offers a potential therapeutic strategy for GBM through TME modulation. We discuss also the emerging role of the P2X4 receptor (P2X4R) as a promising therapeutic target. Overall, targeting purinergic signaling offers a potential approach to overcoming current GBM treatment limitations.
引用
收藏
页数:18
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