Department of Neurology and Cancer Center, West China Hospital, Sichuan University, Chengdu, 610041, China.
Front Med. 2019 Oct;13(5):531-539. doi: 10.1007/s11684-019-0700-1. Epub 2019 Jul 16.
Glioblastoma (GBM) is the most common and lethal primary neoplasm in the central nervous system. Despite intensive treatment, the prognosis for patients with GBM remains poor, with a median survival of 14-16 months. 90% of GBMs are primary GBMs that are full-blown at diagnosis without evidences of a pre-existing less-malignant precursor lesion. Therefore, identification of the cell(s) of origin for GBM-the normal cell or cell type that acquires the initial GBM-promoting genetic hit(s)-is the key to the understanding of the disease etiology and the development of novel therapies. Neural stem cells and oligodendrocyte precursor cells are the two major candidates for the cell(s) of origin for GBM. Latest data from human samples have reignited the longstanding debate over which cells are the clinically more relevant origin for GBMs. By critically analyzing evidences for or against the candidacy of each cell type, we highlight the most recent progress and debate in the field, explore the clinical implications, and propose future directions toward early diagnosis and preventive treatment of GBMs.
胶质母细胞瘤(GBM)是中枢神经系统中最常见和最致命的原发性肿瘤。尽管进行了强化治疗,GBM 患者的预后仍然很差,中位生存期为 14-16 个月。90%的 GBM 是原发性 GBM,在诊断时就已经完全发展,没有先前存在的低度恶性前体病变的证据。因此,确定 GBM 的起源细胞——发生初始 GBM 促进遗传变化的正常细胞或细胞类型——是了解疾病病因和开发新疗法的关键。神经干细胞和少突胶质前体细胞是 GBM 起源细胞的两个主要候选者。来自人类样本的最新数据重新引发了关于哪种细胞是 GBM 更具临床相关性起源的长期争论。通过批判性地分析每种细胞类型的候选证据,我们强调了该领域的最新进展和争议,探讨了其临床意义,并提出了早期诊断和预防性治疗 GBM 的未来方向。