Department of Neurobiology, Center for Glial Biology in Medicine, University of Alabama at Birmingham, 1719 6th Avenue South, CIRC 425, Birmingham, Alabama 35294, USA.
Nat Rev Neurosci. 2014 Jul;15(7):455-65. doi: 10.1038/nrn3765.
Malignant gliomas are devastating tumours that frequently kill patients within 1 year of diagnosis. The major obstacle to a cure is diffuse invasion, which enables tumours to escape complete surgical resection and chemo- and radiation therapy. Gliomas use the same tortuous extracellular routes of migration that are travelled by immature neurons and stem cells, frequently using blood vessels as guides. They repurpose ion channels to dynamically adjust their cell volume to accommodate to narrow spaces and breach the blood-brain barrier through disruption of astrocytic endfeet, which envelop blood vessels. The unique biology of glioma invasion provides hitherto unexplored brain-specific therapeutic targets for this devastating disease.
恶性胶质瘤是一种破坏性肿瘤,患者在确诊后 1 年内常因该病死亡。目前治愈的主要障碍是肿瘤弥漫性浸润,导致肿瘤无法完全通过手术切除、化疗和放疗来治疗。胶质瘤通过不成熟神经元和干细胞所走的同样曲折的细胞外迁移途径进行迁移,通常利用血管作为向导。它们重新利用离子通道来动态调整细胞体积,以适应狭窄的空间,并通过破坏包围血管的星形细胞终足来突破血脑屏障。胶质瘤浸润的独特生物学为这种毁灭性疾病提供了迄今为止尚未开发的大脑特异性治疗靶点。