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Isolation, cultivation and identification of human lung adenocarcinoma stem cells

机译:人肺腺癌干细胞的分离培养及鉴定

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摘要

Recently, an increasing number of studies have demonstrated that lung cancer is a stem cell disease. However, ideal cell surface markers for isolating stem cells in lung cancer are yet to be identified. In the present study, a cell population with a cluster of differentiation (CD)133(+) phenotype was successfully isolated from a single cell suspension of lung adenocarcinoma tissue using magnetic-activated cell sorting (MACS) and enriched in a serum-free culture. In comparison to CD133(-) cells, the CD133(+) cells exhibited an enhanced capacity for self-renewal and differentiation, and a greater potential for in vivo tumor formation, in non-obese diabetic/severe combined immunodeficient (NOD/SCID) mice. Tumors could be induced in NOD/SCID mice by the transplantation of 10(2) stem-like cells per mouse. The results of the present study demonstrated that CD133 may serve as a specific cell surface marker for lung adenocarcinoma stem cells, and that MACS combined with serum-free culture is an effective method for isolating and enriching lung cancer stem cells.
机译:最近,越来越多的研究表明肺癌是一种干细胞疾病。然而,尚未确定用于分离肺癌干细胞的理想细胞表面标记。在本研究中,使用磁激活细胞分选法(MACS)从肺腺癌组织的单细胞悬液中成功分离出具有分化(CD)133(+)表型簇的细胞群,并富集了无血清培养物。与CD133(-)细胞相比,CD133(+)细胞在非肥胖/严重合并免疫缺陷(NOD / SCID)中表现出增强的自我更新和分化能力,并具有更大的体内肿瘤形成潜力。老鼠。通过在每只小鼠中移植10(2)个干细胞样细胞,可以在NOD / SCID小鼠中诱发肿瘤。本研究结果表明,CD133可以作为肺腺癌干细胞的特异性细胞表面标志物,而MACS与无血清培养相结合是分离和富集肺癌干细胞的有效方法。

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