Mazzoleni Stefania, Galli Rossella
Neural Stem Cell Biology Unit, Division of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, Milan, Italy.
Front Biosci (Elite Ed). 2012 Jan 1;4(1):205-13. doi: 10.2741/e370.
Glioblastoma multiforme (GBM) represents the most aggressive and deadliest brain tumor of adults. To date, cell heterogeneity within GBM has been explained by the "hierarchical" model of tumorigenesis, aka the "cancer stem cell" hypothesis. In agreement with this model, only rare tumor cells, namely the cancer stem cells (CSCs), are responsible for GBM initiation and, as such, are considered the favored target of therapy. However, multiple evidence has recently indicated that tumor-initiating cells (TICs) may not represent a restricted and infrequent GBM component; rather, they might constitute most of the cells within the tumor bulk. Here we review several studies that recently shed new light on the process of gliomagenesis. We critically analyze the methodological inconsistencies and drawbacks that are causing protracted controversy in the field. Finally, we discuss the clinical implications and the novel therapeutic scenarios that have been put forward by the presence of functionally and molecularly distinct subpopulations of GBM-initiating cells within the same tumor.
多形性胶质母细胞瘤(GBM)是成人中最具侵袭性和致命性的脑肿瘤。迄今为止,GBM内的细胞异质性已通过肿瘤发生的“分层”模型(即“癌症干细胞”假说)来解释。与该模型一致,只有罕见的肿瘤细胞,即癌症干细胞(CSCs),才是GBM起始的原因,因此被认为是治疗的首选靶点。然而,最近有多项证据表明,肿瘤起始细胞(TICs)可能并不代表GBM中一个受限且罕见的组成部分;相反,它们可能构成肿瘤主体中的大部分细胞。在此,我们回顾了最近为胶质瘤发生过程带来新见解的几项研究。我们批判性地分析了导致该领域长期存在争议的方法学不一致和缺陷。最后,我们讨论了同一肿瘤内功能和分子上不同的GBM起始细胞亚群的存在所提出的临床意义和新的治疗方案。