Pan Yuan, Monje Michelle
Department of Symptom Research, University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.
Department of Neurology, Stanford University, CA, 94305, USA.
Adv Biol (Weinh). 2022 Sep;6(9):e2200122. doi: 10.1002/adbi.202200122. Epub 2022 Aug 11.
Brain tumors are devastating diseases of the central nervous system. Brain tumor pathogenesis depends on both tumor-intrinsic oncogenic programs and extrinsic microenvironmental factors, including neurons and glial cells. Glial cells (oligodendrocytes, astrocytes, and microglia) make up half of the cells in the brain, and interact with neurons to modulate neurodevelopment and plasticity. Many brain tumor cells exhibit transcriptomic profiles similar to macroglial cells (oligodendrocytes and astrocytes) and their progenitors, making them likely to subvert existing neuron-glial interactions to support tumor pathogenesis. For example, oligodendrocyte precursor cells, a putative glioma cell of origin, can form bona fide synapses with neurons. Such synapses are recently identified in gliomas and drive glioma pathophysiology, underscoring how brain tumor cells can take advantage of neuron-glial interactions to support cancer progression. In this review, it is briefly summarized how neurons and their activity normally interact with glial cells and glial progenitors, and it is discussed how brain tumor cells utilize neuron-glial interactions to support tumor initiation and progression. Unresolved questions on these topics and potential avenues to therapeutically target neuron-glia-cancer interactions in the brain are also pointed out.
脑肿瘤是中枢神经系统的毁灭性疾病。脑肿瘤的发病机制取决于肿瘤内在的致癌程序和外在的微环境因素,包括神经元和神经胶质细胞。神经胶质细胞(少突胶质细胞、星形胶质细胞和小胶质细胞)占大脑细胞的一半,并与神经元相互作用以调节神经发育和可塑性。许多脑肿瘤细胞表现出与大胶质细胞(少突胶质细胞和星形胶质细胞)及其祖细胞相似的转录组特征,这使得它们有可能颠覆现有的神经元 - 神经胶质相互作用以支持肿瘤发病机制。例如,少突胶质前体细胞,一种假定的胶质瘤起源细胞,可以与神经元形成真正的突触。这种突触最近在胶质瘤中被发现,并驱动胶质瘤的病理生理学,突出了脑肿瘤细胞如何利用神经元 - 神经胶质相互作用来支持癌症进展。在这篇综述中,简要总结了神经元及其活动通常如何与神经胶质细胞和神经胶质祖细胞相互作用,并讨论了脑肿瘤细胞如何利用神经元 - 神经胶质相互作用来支持肿瘤的起始和进展。还指出了关于这些主题的未解决问题以及在大脑中治疗性靶向神经元 - 神经胶质 - 癌症相互作用的潜在途径。