SOX2
CD44细胞
内斯汀
癌症干细胞
细胞培养
干细胞标记物
生物
干细胞
细胞
癌细胞
神经球
分子生物学
细胞分化
癌症研究
细胞生物学
癌症
成体干细胞
神经干细胞
生物化学
转录因子
基因
遗传学
作者
Xin Hong,Khalil Chedid,Steven N. Kalkanis
出处
期刊:International Journal of Oncology
[Spandidos Publications]
日期:2012-08-21
卷期号:41 (5): 1693-1700
被引量:101
标识
DOI:10.3892/ijo.2012.1592
摘要
In addition to the primary culturing of cancer stem cells (CSCs) from tumor tissues, CSCs are found in established tumor cell lines. However, it is unclear how culture conditions affect CSC enrichment. Additionally, the differentiation potential of cell line-derived CSCs has not been well studied. In our study, the glioblastoma cell lines LN229, T98G, U251n and U87, were cultured as spheres in serum-containing medium (serum spheres) or serum-free medium (serum-free spheres). We found that LN229 and U251n cells expressed multiple stem cell markers such as Nestin, Sox2, Musashi-1 and CD44, and their serum spheres expressed even higher levels of Nestin, Sox2 and Musashi-1 compared to monolayer cells and serum‑free spheres. LN229 and U251n cells showed higher migration and colony formation potential compared to T98G and U87 cells, which did not express Nestin, Sox2 and Musashi-1. Serum spheres of LN229 and U251n cells also exhibited higher resistance to temozolomide compared to serum-free spheres. All tumor cell lines showed neuronal differentiation (Tuj-1 positive). Only U251n serum spheres exhibited both astrocytic (GFAP‑positive) and neuronal differentiation. We conclude that sphere culture in serum-containing medium provides the most efficient enrichment of cancer stem cells. U251n cells are distinguished from other tumor cells due to their potential for multilineage differentiation.
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