De Fazio Emerson, Pittarello Matilde, Gans Alessandro, Ghosh Bikona, Slika Hasan, Alimonti Paolo, Tyler Betty
Department of Medicine, Vita-Salute San Raffaele University School of Medicine, 20132 Milan, Italy.
Department of Medicine, Humanitas University School of Medicine, 20089 Rozzano, Italy.
Int J Mol Sci. 2024 Feb 22;25(5):2563. doi: 10.3390/ijms25052563.
Gliomas are diffusely infiltrating brain tumors whose prognosis is strongly influenced by their extent of invasion into the surrounding brain tissue. While lower-grade gliomas present more circumscribed borders, high-grade gliomas are aggressive tumors with widespread brain infiltration and dissemination. Glioblastoma (GBM) is known for its high invasiveness and association with poor prognosis. Its low survival rate is due to the certainty of its recurrence, caused by microscopic brain infiltration which makes surgical eradication unattainable. New insights into GBM biology at the single-cell level have enabled the identification of mechanisms exploited by glioma cells for brain invasion. In this review, we explore the current understanding of several molecular pathways and mechanisms used by tumor cells to invade normal brain tissue. We address the intrinsic biological drivers of tumor cell invasion, by tackling how tumor cells interact with each other and with the tumor microenvironment (TME). We focus on the recently discovered neuronal niche in the TME, including local as well as distant neurons, contributing to glioma growth and invasion. We then address the mechanisms of invasion promoted by astrocytes and immune cells. Finally, we review the current literature on the therapeutic targeting of the molecular mechanisms of invasion.
胶质瘤是弥漫性浸润性脑肿瘤,其预后受到肿瘤侵入周围脑组织程度的强烈影响。低级别胶质瘤边界更清晰,而高级别胶质瘤是具有广泛脑浸润和播散的侵袭性肿瘤。胶质母细胞瘤(GBM)以其高侵袭性和预后不良而闻名。其低生存率归因于其复发的必然性,这是由微观脑浸润导致的,使得手术根除难以实现。对GBM生物学在单细胞水平的新见解,使得识别胶质瘤细胞用于脑侵袭的机制成为可能。在这篇综述中,我们探讨了目前对肿瘤细胞用于侵入正常脑组织的几种分子途径和机制的理解。我们通过探讨肿瘤细胞如何相互作用以及与肿瘤微环境(TME)相互作用,来研究肿瘤细胞侵袭的内在生物学驱动因素。我们关注TME中最近发现的神经元生态位,包括局部和远处的神经元,它们促进胶质瘤的生长和侵袭。然后我们阐述星形胶质细胞和免疫细胞促进侵袭的机制。最后,我们综述了目前关于侵袭分子机制的治疗靶点的文献。