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作 者:许新华[1] 苏进[1] 鲁明骞[2] 李道俊[1] 黄乔[2] 薛峰[1] 易芳[2]
机构地区:[1]三峡大学肿瘤研究所,湖北宜昌443003 [2]三峡大学第一临床医学院&宜昌市中心人民医院肿瘤科
出 处:《肿瘤防治研究》2011年第12期1346-1350,共5页Cancer Research on Prevention and Treatment
基 金:湖北省卫生厅科研资助项目(JX4B52);2011年宜昌市科技研究与开发项目(A11301-04);宜昌市中心人民医院2008年科研发展基金项目(KFJ2008005)
摘 要:目的从人鼻咽癌SUNE-1 5-8F细胞株中分离出CD44+细胞并探讨其生物学特性。方法常规培养SUNE-1 5-8F细胞,采用流式细胞学技术检测SUNE-1 5-8F细胞中CD44+的表达并用流式细胞仪分选CD44+细胞;采用四甲基偶氮唑蓝(MTT)法、克隆形成实验等检测并比较CD44+、CD44-细胞在体外增殖、分化等方面的差异;并用反转录聚合酶链反应(RT-PCR)检测干细胞基因Oct4、Bmi-1的表达。结果 CD44+细胞在鼻咽癌细胞中SUNE-1株所占的比率约为52.5%;新分选的CD44+细胞在无血清培养液和完全培养液中较CD44-及未分选细胞均显示出较强增殖能力;RT-PCR示Bmi-1和Oct4mRNA在CD44+细胞中的表达水平明显高于CD44-细胞。CD44+和CD44-细胞在接受2Gy放射处理后,其平均克隆生成效率分别为(23.44±1.90)%和(7.78±1.17)%(P<0.001);CD44+细胞较CD44-细胞在相同顺铂和多西他赛药物浓度下显示出更高的细胞存活率。结论 CD44+细胞具有类肿瘤干细胞特性,可能是鼻咽癌的重要肿瘤干细胞标志之一。Objective To separate,expansion,and explore the biological feature of CD44+ cells from the human nasopharyngeal carcinoma(NPC) SUNE-1 5-8F cell line.Methods Flow cytometry was used to detect the expression of CD44 in SUNE-1 5-8F.Fluorescence-activated Cell Sorting was applied to purify CD44+ cells.MTT assay or clone formation assay was used to detect the differences of CD44+ and CD44-cells in proliferation and differentiation ability.The expression of stem cell markers Oct4 and Bmi-1 was examined by reverse transcriptase polymerase chain reaction(RT-PCR).Results CD44 was positively expressed in about 52.5% of NPC SUNE-1 5-8F cell line.Regardless of serum-free medium and serum medium culture conditions,freshly sorted CD44+ cells showed stronger proliferative capacity than CD44-and unsorted CD44+ cells.The expression levels of Bmi-1 and Oct4 mRNA in CD44+ cells were significantly higher than that in CD44-cells.After 2Gy radiation,the average clone formation efficiency for CD44+ and CD44-cells was(23.44±1.90)% and(7.78±1.17)%(P0.001),respectively.After Cisplatin and Docetaxel treatment,CD44+ cells showed a higher survival rate in the same drug concentration compared with CD44-cells.Conclusion CD44+ cells have the biological characteristics of tumor stem cell and may be assumed as one of markers of NPC tumor stem cells.
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