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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 102 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。但是,尚未确定用于分离肺癌干细胞的理想细胞表面标志物。在本研究中,通过磁激活细胞分选(MACS)成功地从肺腺癌组织的单细胞悬液中分离出具有分化(CD)133 + 表型簇的细胞群,并在无血清培养。与CD133 -细胞相比,CD133 + 细胞在非肥胖状态下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能。糖尿病/严重联合免疫缺陷(NOD / SCID)小鼠。每只小鼠移植10 2 干样细胞可在NOD / SCID小鼠中诱导肿瘤。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,MACS结合无血清培养是分离和富集肺癌干细胞的有效方法。

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