Department of Neurosurgery, Harvey Cushing Neuro-oncology Laboratories, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Cancer Program, BROAD Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Stem Cell Reports. 2017 Jun 6;8(6):1497-1505. doi: 10.1016/j.stemcr.2017.04.024. Epub 2017 May 18.
Despite the importance of molecular subtype classification of glioblastoma (GBM), the extent of extracellular vesicle (EV)-driven molecular and phenotypic reprogramming remains poorly understood. To reveal complex subpopulation dynamics within the heterogeneous intratumoral ecosystem, we characterized microRNA expression and secretion in phenotypically diverse subpopulations of patient-derived GBM stem-like cells (GSCs). As EVs and microRNAs convey information that rearranges the molecular landscape in a cell type-specific manner, we argue that intratumoral exchange of microRNA augments the heterogeneity of GSC that is reflected in highly heterogeneous profile of microRNA expression in GBM subtypes.
尽管胶质母细胞瘤(GBM)的分子亚型分类很重要,但对于细胞外囊泡(EV)驱动的分子和表型重编程的程度仍了解甚少。为了揭示异质性肿瘤内生态系统中的复杂亚群动态,我们对患者来源的 GBM 干细胞样细胞(GSCs)的表型多样的亚群中的 microRNA 表达和分泌进行了表征。由于 EV 和 microRNA 传递的信息以细胞类型特异性的方式重新排列分子景观,我们认为肿瘤内 microRNA 的交换增加了 GSC 的异质性,这反映在 GBM 亚型中 microRNA 表达的高度异质谱上。