Department of Neurosurgery, The 2nd Hospital of Dalian Medical University, Dalian, PR China.
Liaoning Provincial Center for Clinical Research on Neurological Diseases, The 1st Hospital of Dalian Medical University, Dalian, PR China; Liaoning Provincial Key Laboratory for Research on Pathogenic Mechanisms of Neurological Diseases, The 1st Hospital of Dalian Medical University, Dalian, PR China.
Brain Res Bull. 2019 Nov;153:334-340. doi: 10.1016/j.brainresbull.2019.09.012. Epub 2019 Sep 30.
Glioblastoma (GBM) is one of the most malignant and aggressive primary brain tumor, with a mean life expectancy of less than 15 months. The malignant nature of GBM prompts the need for further research on its tumorigenesis and novel treatments to improve its outcome. One of the promising research targets is autophagy, a fundamental metabolic process of degrading and recycling cellular components. Interventions to activate or inhibit autophagy have both been proposed as GBM therapies, suggesting a controversial, context-dependent role of autophagy in GBM tumorigenesis. In this review, we highlight the molecular links between GBM and autophagy with the focus on the effects of autophagy on the stemness maintenance, metabolism and proteostasis in GBM tumorigenesis. Understanding the molecular pathways involved in autophagy target is critical for GBM therapy.
胶质母细胞瘤(GBM)是最恶性和侵袭性的原发性脑肿瘤之一,平均预期寿命不到 15 个月。GBM 的恶性本质促使人们需要进一步研究其肿瘤发生机制和新的治疗方法,以改善其预后。自噬是细胞成分降解和回收的基本代谢过程,是有前途的研究靶点之一。激活或抑制自噬都被提议作为 GBM 的治疗方法,这表明自噬在 GBM 肿瘤发生中的作用存在争议,依赖于具体的背景。在这篇综述中,我们强调了 GBM 与自噬之间的分子联系,重点关注自噬对 GBM 肿瘤发生中干细胞维持、代谢和蛋白质平衡的影响。了解自噬靶点所涉及的分子途径对于 GBM 治疗至关重要。