Sforna Luigi, Cenciarini Marta, Belia Silvia, D'Adamo Maria Cristina, Pessia Mauro, Franciolini Fabio, Catacuzzeno Luigi
Department of Chemistry, Biology and Biotechnology, University of Perugia Perugia, Italy.
Faculty of Medicine, Section of Physiology and Biochemistry, Department of Experimental Medicine, University of Perugia Perugia, Italy.
Front Cell Neurosci. 2015 Jan 15;8:467. doi: 10.3389/fncel.2014.00467. eCollection 2014.
The malignancy of glioblastoma multiform (GBM), the most common and aggressive form of human brain tumors, strongly correlates with the presence of hypoxic areas, but the mechanisms controlling the hypoxia-induced aggressiveness are still unclear. GBM cells express a number of ion channels whose activity supports cell volume changes and increases in the cytosolic Ca(2+) concentration, ultimately leading to cell proliferation, migration or death. In several cell types it has previously been shown that low oxygen levels regulate the expression and activity of these channels, and more recent data indicate that this also occurs in GBM cells. Based on these findings, it may be hypothesized that the modulation of ion channel activity or expression by the hypoxic environment may participate in the acquisition of the aggressive phenotype observed in GBM cells residing in a hypoxic environment. If this hypothesis will be confirmed, the use of available ion channels modulators may be considered for implementing novel therapeutic strategies against these tumors.
多形性胶质母细胞瘤(GBM)是人类脑肿瘤中最常见且侵袭性最强的类型,其恶性程度与缺氧区域的存在密切相关,但控制缺氧诱导的侵袭性的机制仍不清楚。GBM细胞表达多种离子通道,这些通道的活性支持细胞体积变化并增加胞质Ca(2+)浓度,最终导致细胞增殖、迁移或死亡。此前在几种细胞类型中已表明,低氧水平会调节这些通道的表达和活性,最近的数据表明GBM细胞中也会发生这种情况。基于这些发现,可以推测缺氧环境对离子通道活性或表达的调节可能参与了在缺氧环境中GBM细胞所观察到的侵袭性表型的获得。如果这一假设得到证实,则可以考虑使用现有的离子通道调节剂来实施针对这些肿瘤的新型治疗策略。