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Plasticity in Glioma Stem Cell Phenotype and Its Therapeutic Implication

机译:胶质瘤干细胞表型的可塑性及其治疗意义

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摘要

The marked heterogeneity in glioblastoma (GBM) may be induced through dynamic differentiation and dedifferentiation process of glioma cells. The hypothesis that environmental stimuli induce these phenotypic changes, including dedifferentiation into the stem cell phenotype which contributes to the high invasiveness and resultant poor outcome in GBM patients, is recently being proven. In the process of cancer invasion and metastasis, the phenotypic change has also been described as epithelial-mesenchymal transition (EMT). This biological process is mainly dependent on hypoxic stimuli and also on transforming growth factor-β (TGF-β) released from glioma stem cells, mesenchymal stem cells, and myeloid cells recruited by hypoxia. The tumor microenvironment, especially hypoxia, inducing such dynamic phenotypic changes can be a good therapeutic target in the treatment of GBM.
机译:胶质母细胞瘤(GBM)的明显异质性可以通过胶质瘤细胞的动态分化和去分化过程来诱导。最近已经证实了环境刺激引起这些表型改变的假说,包括去分化成干细胞表型,这导致了GBM患者的高侵袭性和不良预后。在癌症侵袭和转移的过程中,表型改变也被描述为上皮-间质转化(EMT)。该生物学过程主要依赖于低氧刺激,还依赖于由低氧募集的胶质瘤干细胞,间充质干细胞和髓样细胞释放的转化生长因子-β(TGF-β)。诱导这种动态表型改变的肿瘤微环境,尤其是缺氧,可以作为GBM治疗的良好治疗靶标。

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