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[1]許揚(yáng)梅 龔福生 劉沁穎 劉施佳 黃麗潔 鄭秋紅.MiR-194過表達(dá)和抑制表達(dá)對肝癌細(xì)胞株Hep-3b中側(cè)群細(xì)胞增殖的影響[J].福建醫(yī)藥雜志,2019,41(06):141-144.
 XU Yangmei,GONG Fusheng,LIU Qinying,et al.Influence of miR-194 up and down-expression on liver cancer stem cells[J].FUJIAN MEDICAL JOURNAL,2019,41(06):141-144.
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MiR-194過表達(dá)和抑制表達(dá)對肝癌細(xì)胞株Hep-3b中側(cè)群細(xì)胞增殖的影響()
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《福建醫(yī)藥雜志》[ISSN:1002-2600/CN:35-1071/R]

卷:
41
期數(shù):
2019年06期
頁碼:
141-144
欄目:
基礎(chǔ)研究
出版日期:
2019-12-25

文章信息/Info

Title:
Influence of miR-194 up and down-expression on liver cancer stem cells
文章編號:
1002-2600(2019)06-0141-05
作者:
許揚(yáng)梅 龔福生 劉沁穎 劉施佳 黃麗潔 鄭秋紅1
福建醫(yī)科大學(xué)附屬腫瘤醫(yī)院 福建省腫瘤醫(yī)院 福建省腫瘤生物治療重點(diǎn)實(shí)驗(yàn)室(福州 350014)
Author(s):
XU Yangmei GONG Fusheng LIU Qinying LIU Shijia HUANG Lijie ZHENG Qiuhong.
Fujian Provincial Key Laboratory of Tumor Biotherapy,Fujian Medical University Cancer Hospital& Fujian Cancer Hospital,Fuzhou, Fujian 350014, China
關(guān)鍵詞:
微小RNA 慢病毒載體 肝癌 干細(xì)胞
Keywords:
MicroRNA lentivirus vector liver cancer stem cell
分類號:
R735.7
文獻(xiàn)標(biāo)志碼:
B
摘要:
目的 研究MicroRNA-194(miR-194)過表達(dá)和抑制表達(dá)對細(xì)胞株Hep-3b中側(cè)群細(xì)胞增殖功能影響。方法 構(gòu)建miR-194過表達(dá)和抑制表達(dá)慢病毒并感染Hep-3b細(xì)胞。流式細(xì)胞儀鑒定各感染組SP側(cè)群比例,QPCR檢測各組細(xì)胞miR-194-5p表達(dá),CCK- 8法檢測各組細(xì)胞增殖能力,軟瓊脂克隆形成實(shí)驗(yàn)檢測細(xì)胞克隆形成能力。結(jié)果 流式細(xì)胞儀鑒定發(fā)現(xiàn)miR-194過表達(dá)Hep-3b組SP細(xì)胞含量與miR-194抑制表達(dá)Hep-3b組差異具有統(tǒng)計(jì)學(xué)意義(LSD-t=3.550,P=0.012)。QPCR檢測顯示miR-194過表達(dá)Hep-3b組miR-194-5p水平高于miR-194抑制表達(dá)Hep-3b組(LSD-t=4.680,P=0.007)。CCK- 8實(shí)驗(yàn)表明miR-194過表達(dá)Hep-3b組和miR-194抑制表達(dá)Hep-3b組細(xì)胞增殖能力差異有統(tǒng)計(jì)學(xué)意義(LSD-t=5.621,P=0.002)。軟瓊脂克隆形成實(shí)驗(yàn)顯示miR-194過表達(dá)Hep-3b組比miR-194抑制表達(dá)Hep-3b組形成細(xì)胞克隆少(LSD-t=5.849,P=0.001)。結(jié)論 成功構(gòu)建了miR-194過表達(dá)和抑制細(xì)胞株,miR-194抑制組顯示明顯的干細(xì)胞特征,其含有更多SP細(xì)胞,具有更強(qiáng)的細(xì)胞增殖能力和自我更新能力。
Abstract:
Objective To study the influence of miR-194 up and down-expression Hep-3b cell lines on the proliferation ability of SP cells.Methods Hep-3b was used to construct miR-194 up and down-expression cell lines via lentivirus infection.Flow cytometry was applied to identify SP cells.QPCR assay was adopted to test the expression of miR-194-5p in those cell lines.CCK-8 assay was conducted to study the proliferation ability of cells and soft agar colony formation assay was conducted to test colony-forming ability.Results Each infected cell line maintained good growth.Flow cytometry analysis showed that the SP percentage were significantly different between miR-194 up and down-regulation Hep-3b groups(LSD-t=3.550,P=0.012).QPCR assay of miR-194-5p showed statistic difference between miR-194 up and down-regulation Hep-3b groups(LSD-t=4.680,P=0.007).CCK-8 assay showed different growth ability between miR-194 up and down-regulation Hep-3b groups(LSD-t=5.621,P=0.002).Soft agar colony formation assay results less colonies formed in miR-194 up-regulation Hep-3b group than miR-194 down-regulation Hep-3b group(LSD-t=5.849,P=0.001).Conclusion miR-194 up-regulation Hep-3b group than miR-194 down-regulation Hep-3b group were successfully constructed.miR-194 down-regulation Hep-3b group contains more SP cells, possess stronger growth ability and self-renewal ability, showing stronger proliferation and self-renewal ability.

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更新日期/Last Update: 2019-12-25