胶质母细胞瘤是由神经干细胞转化为肿瘤干细胞引起的吗

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL University of Toronto Medical Journal Pub Date : 2010-06-13 DOI:10.5015/UTMJ.V87I3.1247
S. Jeimy
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引用次数: 0

摘要

胶质母细胞瘤是最常见和侵袭性的成人脑恶性肿瘤,其特征是存在形态多样的神经细胞类型,其形成和维持肿瘤的能力不同。这种癌症对常规治疗的明显耐药性引发了确定治疗靶向细胞群的尝试。在其他恶性肿瘤,如白血病中已经发现了肿瘤启动细胞的定义池。与正常干细胞一样,这些€œcancer干细胞 (CSCs)具有广泛的自我更新能力和多能性;然而,CSC的起源仍然难以捉摸。最近,在成人大脑的海马体、亚脑室区(SVZ)和嗅球中发现了一小部分静止的、未分化的、被称为神经干细胞(NSCs)的多能细胞。自发现以来,人们一直假设NSCs可能作为大脑中可能转化为CSCs的组织特异性干细胞的仓库。本文的目的是根据现有实验模型的优点和缺陷,对文献进行批判性回顾,以证明NSCs中的致癌突变使其成为胶质母细胞瘤中的CSCs。对大脑中CSC形成机制的深入了解可能有助于优化当前的治疗方法,因为NSC- >CSC形成的途径将为特异性靶向这种臭名昭著的抗治疗恶性肿瘤提供机会。
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Does Glioblastoma arise from Oncogenic Transformation of Neural Stem Cells into Cancer Stem Cells
Glioblastoma, the most common and aggressive adult brain malignancy, is characterized by the presence of morphologically diverse neural cell types that differ in their ability to form and maintain tumours. The marked resistance of this cancer to conventional treatments has sparked attempts to identify therapeutically targetable cellular populations. Defined pools of tumour initiating cells have already been identified in other malignancies, i.e., leukemia. Like normal stem cells, these “cancer stem cells” (CSCs) have extensive self renewal capacity and multipotency; however, the origin of the CSC remains elusive. Recently, a small percentage of quiescent, undifferentiated, multipotent cells termed neural stem cells (NSCs) were found in the hippocampus, sub‐ventricular zone (SVZ), and olfactory bulb of the adult human brain. Since their discovery, it has been hypothesized that NSCs may act as a depot of tissue‐specific stem cells in the brain that may be transformed into CSCs. The purpose of this essay is to critically review the literature to demonstrate that oncogenic mutations in NSCs allow them to become CSCs in glioblastomas, in light of the advantages and flaws of existing experimental models. Insights into the mechanism of CSC formation in the brain may allow for the optimization of current therapeutic approaches, as pathways in NSC-->CSC formation will provide opportunities to specifically target this notoriously treatment‐resistant malignancy.
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University of Toronto Medical Journal
University of Toronto Medical Journal MEDICINE, GENERAL & INTERNAL-
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