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SSEA-1 is an enrichment marker for tumor-initiating cells in human glioblastoma.

机译:SSEA-1是人类胶质母细胞瘤中肿瘤起始细胞的富集标记。

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摘要

CD133+ populations of human glioblastoma multiforme (GBM) cells are reportedly enriched for tumor stem cells (TSCs) or tumor-initiating cells (TICs). Approximately 40% of freshly isolated GBM specimens, however, do not contain CD133+ tumor cells, raising the possibility that CD133 may not be a universal enrichment marker for GBM TSCs/TICs. Here we demonstrate that stage-specific embryonic antigen 1(SSEA-1/LeX)+ GBM cells fulfill the functional criteria for TSC/TIC, since (1) SSEA-1+ cells are highly tumorigenic in vivo, unlike SSEA-1- cells; (2) SSEA-1+ cells can give rise to both SSEA-1+ and SSEA-1- cells, thereby establishing a cellular hierarchy; and (3) SSEA-1+ cells have self-renewal and multilineage differentiation potentials. A distinct subpopulation of SSEA-1+ cells was present in all but one of the primary GBMs examined (n = 24), and most CD133+ tumor cells were also SSEA-1+, suggesting that SSEA-1 may be a general TSC/TIC enrichment marker in human GBMs.
机译:据报道,人类多形胶质母细胞瘤(GBM)细胞的CD133 +群体富含肿瘤干细胞(TSC)或肿瘤引发细胞(TIC)。然而,大约40%的新鲜分离的GBM标本不包含CD133 +肿瘤细胞,这增加了CD133可能不是GBM TSC / TICs的通用富集标记的可能性。在这里,我们证明阶段特异性胚胎抗原1(SSEA-1 / LeX)+ GBM细胞满足TSC / TIC的功能标准,因为(1)SSEA-1 +细胞在体内具有高度致瘤性,这与SSEA-1-细胞不同; (2)SSEA-1 +细胞可以同时产生SSEA-1 +和SSEA-1-细胞,从而建立细胞层次。 (3)SSEA-1 +细胞具有自我更新和多系分化的潜能。除了一个受检查的主要GBM(n = 24)之外,所有其他细菌均存在SSEA-1 +细胞的独特亚群,并且大多数CD133 +肿瘤细胞也是SSEA-1 +,这表明SSEA-1可能是一般的TSC / TIC人类GBMs中的富集标记。

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