Bmi-1对干性相关分子转录调控的初步研究-第三军医大学学报.DOC

Bmi-1对干性相关分子转录调控的初步研究-第三军医大学学报.DOC

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Bmi-1对干性相关分子转录调控的初步研究-第三军医大学学报

Bmi-1调节干性(Stemness)相关分子转录的初步分析 阮 艳1,蹇 锐1,程小星2,牛翰婕2,周恒宇3,郑宏庭3,胡福泉3)第三军医大学1基础医学部微生物学教研室,重庆400038;3新桥医院内分泌科,重庆 4000372解放军总医院309临床部,北京 100091 摘 要:目的Bmi-1对转录的。方法构建Bmi-1过表达载体pCI-GFP-bmi1和pCI-GFP-hbmi1;瞬时转染ES细胞CCE和人神经胶质瘤细胞U87;半定量RT-PCR检测、、c-yc、lf4和ox2及肿瘤细胞中CD133、Nestin等干性分子的表达结果Bmi-1过表达的表达,、ox2和lf4的表达无明显变化结论Bmi-1参与了对肿瘤及胚胎干细胞中干性相关分子的转录调节。 关键词:Bmi-1;;;转录调控 中图法分类号:Q2; Q7; R394 文献标识码:A Transcriptional Regulatory Effects of Bmi-1 on Stemness Associated Genes Ruan Yan1, Jian Rui1, Cheng Xiao-Xing 2, Zhou Heng-Yu 3, Zheng Hong-Ting3 (1Department of Microbiology, Third Military Medical University, Chongqing 400038, China; 2PLA General Hospital, 309th Clinical Division, Beijing 100091, China; 3Department of Endocrinology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China) Abstract: Objective To investigate the transcriptional regulatory effects of Bmi-1 on stemness-associated genes in cancer and embryonic stem cells. Methods: Eukaryotic expression vector pCI-GFP-mbmi and pCI-GFP-hbmi was constructed and transiently transfected into CCE and U87 cells respectively. Semi-quantitative RT-PCR was used to detect mRNA expression of stemness factors in ES cells and tumor cells. Clone formation essay was used to elucidate the potential to form self-renewal clones of CCE. Results Overexpression of Bmi-1 in CCE up-regulated the expression of Nanog. The expression of other stemness factors such as Oct-4, Sox2 and Klf4 had no significant change. U87 cells transiently transfected with Bmi-1 promoted the expression of Oct-4 and Nestin. The expression level of c-Myc was reduced in the two cell lines. Overexpression of Bmi-1 promoted the formation of self-renewal clones in CCE cells. Conclusion Bmi-1 was involved in the transcriptional regulation of stemness-associated genes in cancer and embryonic stem cells . Key words: Bmi-1; Stem cells; Stemness associated genes; Transcriptional regulation 肿瘤干细胞(Cancer Stem Cells, CSCs)是肿瘤组织

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