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[CTCF对人肝癌干细胞及细胞增殖的影响]

[Effects of CTCF on human liver cancer stem cells and cell proliferation].

作者信息

Liu Qiu-Ying, Xie Xiao-Yan, Wei Ling, Liu Jun, Shen Wen-Yan, Li Ran, Yu Xiao Qin, Qin Yang

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2014 Mar;45(2):196-201.

Abstract

OBJECTIVE

To explore the effects of CCCTC-binding factor (CTCF) on human liver cancer stem cells (HepG2) and cell proliferation of HepG2 and Nasopharyngeal carcinoma cell line (CNE1).

METHODS

The pEGFP-N1/CTCF, CTCF-shRNA and GFP-shRNA plasmids were constructed and transfected into HepG2 and CNE1 cells, and RT-PCR or Western blot were performed to detect the mRNA or protein levels of CTCF. The subpopulation of CD90+ cancer stem cells in HepG2 cells transfected with CTCF-shRNA plasmid or GFP-shRNA plasmid (as transfection control) were assayed by flow cytometry with the wild type HepG2 cells as control. Proliferation of cells transfected with CTCF-overexpression or CTCF-shRNA plasmid was evaluated by MTT assay.

RESULTS

The levels of both mRNA and protein of CTCF were increased in pEGFP-N1/CTCF transfected HepG2 and CNE1 cells compared to that in pEGFP-N1 transfected cells (P < 0.05), and decreased in CTCF-shRNA transfected cells compared to that in cells transfected with GFP-shRNA (P < 0.05). The results of flow cytometry demonstrated that, detection rate of CD90+ cells in cells transfected with CTCF-shRNA plasmid [(1.7330 +/- 0.4177)%] was obviously higher than that of wild-type HepG2 cells [(0.5750 +/- 0.0629)%] and cells transfected with GFP-shRNA plasmid [(0.3500 +/- 0.0866)%] (P < 0.05). The results of MTT analysis showed that, alteration of CTCF had no effect on cancer cell proliferation (P > 0.05).

CONCLUSION

CTCF inhibits human liver cancer stem cells but no effect on cell proliferation.

摘要

目的

探讨CCCTC结合因子(CTCF)对人肝癌干细胞(HepG2)以及HepG2和鼻咽癌细胞系(CNE1)细胞增殖的影响。

方法

构建pEGFP-N1/CTCF、CTCF-shRNA和GFP-shRNA质粒并转染至HepG2和CNE1细胞,进行RT-PCR或蛋白质免疫印迹法检测CTCF的mRNA或蛋白质水平。以野生型HepG2细胞为对照,采用流式细胞术检测转染CTCF-shRNA质粒或GFP-shRNA质粒(作为转染对照)的HepG2细胞中CD90+癌干细胞亚群。通过MTT法评估转染CTCF过表达或CTCF-shRNA质粒的细胞的增殖情况。

结果

与转染pEGFP-N1的细胞相比,转染pEGFP-N1/CTCF的HepG2和CNE1细胞中CTCF的mRNA和蛋白质水平均升高(P < 0.05),与转染GFP-shRNA的细胞相比,转染CTCF-shRNA的细胞中CTCF的mRNA和蛋白质水平均降低(P < 0.05)。流式细胞术结果表明,转染CTCF-shRNA质粒的细胞中CD90+细胞的检测率[(1.7330±0.4177)%]明显高于野生型HepG2细胞[(0.5750±0.0629)%]和转染GFP-shRNA质粒的细胞[(0.3500±0.0866)%](P < 0.05)。MTT分析结果表明,CTCF的改变对癌细胞增殖无影响(P > 0.05)。

结论

CTCF抑制人肝癌干细胞,但对细胞增殖无影响。

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