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作 者:刘佳[1] 纪新强[1] 武加利[1] 张文卿[2]
机构地区:[1]青岛大学医学院附属医院妇科,山东青岛266003 [2]青岛大学医学院病原生物学教研室,山东青岛266071
出 处:《中华肿瘤防治杂志》2011年第6期424-427,共4页Chinese Journal of Cancer Prevention and Treatment
基 金:山东省自然科学基金(Y2008c33)
摘 要:目的:从人卵巢癌细胞系A2780中分离培养卵巢癌干细胞,并对其特性进行鉴定。方法:将A2780细胞消化,离心制成单细胞悬液,悬浮于含有生长因子的无血清培养基(SFM)中获得肿瘤细胞微球体,流式细胞仪检测细胞表面分子标志CD44和CD133的表达;Transwell小室侵袭实验检测肿瘤微球体的体外侵袭能力;CCK-8检测微球体细胞的增殖能力,比较两种细胞的倍增时间;将肿瘤微球体置于含有血清的培养基使其诱导分化,并观察其形态学变化。结果:A2780可在SFM中形成可悬浮生长、稳定传代的肿瘤细胞微球体。与贴壁的肿瘤细胞相比,微球体高表达干细胞标志CD44和CD133(P<0.05),具有更强的体外侵袭力(t=9.354,P<0.05)和增殖能力(t=13.682,P<0.05),及更短的倍增时间(t=3.773,P<0.05),在血清环境下可分化为普通的肿瘤细胞。结论:用含有生长因子的SFM悬浮卵巢癌细胞系A2780可获得卵巢癌肿瘤细胞微球体,此细胞球体中富集有肿瘤干细胞。OBJECTIVE: To isolate and cultivate ovarian tumor stem ceils from human ovarian tumor cell line A2780, and identify their biological properties. METHODS: Cells A2780 were dissociated into single tumor cells, suspended in specific serum-free medium (SFM) to acquire ovarian tumor stem cell spheres. The expression of cell surface markers CD44 and CD133 was detected with flow-cytometry. Transwell inva- sive method was utilized to analyze the invasive ability in vitro and CCK-8 assays were performed to detect their proliferating potentiality. To compare their doubling time, and observe the inducing differentiation and cytologic and morphologie characteristics of the stem cell spheres. RESULTS: Nonadherent and serial-propagating tumor stem cells could be obtained from cell line A2780, which highly expressed stem cell markers CD44 and CD133 (P〈0. 05) ,with stronger invasive ability in vitro (t= 9. 354, P〈0.05) ,stronger propagating capability (t=13. 682, P〈0.05)and shorter doubling time (t=3. 773,P〈0.05). They could differentiate normal tumor cells in serum supplemented medium condition. CONCLUSION: Ovarian tumor stem cell spheres can be obtained by serum-free suspended culture, which is enriched with this kind of stem cells.
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