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多形性成胶质细胞瘤的肿瘤基因组学及其信号通路 被引量:3

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摘要 多形性成胶质细胞瘤(Glioblastoma Multiforme,GBM)是成年人中最常见的原发性脑瘤,包括原发性和继发性GBM。GBM的遗传学的变异主要包括杂合性的丧失(Loss of heterozygosity,LOH)以及众多的基因突变和表达异常。其产生的机理与DNA修复的错误以及许多生长因子和癌基因信号通路有关。具有无限自我更新能力的胶质细胞瘤的干细胞(Gloima stem cells)可能来自停止发育的神经祖细胞或来自去分化的星形胶质细胞,是GBM复发的主要原因,有可能成为GBM治疗的新的靶点。
作者 吴南 冯华
出处 《国际神经病学神经外科学杂志》 2010年第3期246-250,共5页 Journal of International Neurology and Neurosurgery
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参考文献26

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同被引文献65

  • 1陈飞兰,张华蓉,卞修武,陈剑鸿,蒋雪峰,王清良.诺帝对大鼠C6脑胶质瘤的诱导分化治疗作用及对信号转导分子STAT3和p-STAT3蛋白表达的影响[J].中华神经外科杂志,2005,21(6):359-362. 被引量:10
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  • 3张煜,崔尧元,吴伟忠,孙瑞霞,刘银坤.STAT3信号通路影响人胶质瘤细胞株存活和凋亡的研究[J].中华神经外科杂志,2007,23(2):99-102. 被引量:10
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