Effects of stably silencing FOXM1 by shRNA on cell growth of hepatocellular carcinoma in vitro
10.3760/cma.j.issn.1007-631X.2011.05.013
- VernacularTitle:短发卡RNA稳定沉默FOXM1对肝癌细胞体外生长的影响
- Author:
Hongcheng SUN
;
Min LI
;
Jilin LU
;
Dong JIN
;
Dongwang YAN
;
Chongzhi ZHOU
;
Junwei FAN
;
Huamei TANG
;
Zhihai PENG
- Publication Type:Journal Article
- Keywords:
liver neoplasms;
RNA interference;
F0XM1 protein;
Gene silencing
- From:
Chinese Journal of General Surgery
2011;26(5):398-401
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the effect of sustained silencing Forkhead box Ml (F0XM1) gene by short-hairpin RNA (shRNA) expression vector on cell growth of hepatocelluar carcinoma (HCC) in vitro.Methods Four shRNA expression vectors targeting different sequences of human F0XM1 mRNA were constructed.The expression vector with the best interfering effect and the negative control plasmid were used to transfect HCC cell line QGY-7703, stably transfected cell clones were selected by neomycin (G418).Cell growth was evaluated by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay and colony formation was assessed by clonogenic assay.Cell apoptosis was detected by double staining with APC conjugated Annexin V and PI.Results F0XM1 protein was detected with different levels in all these studied human cell lines.The expression vector shRNA-1026 exhibited excellent interference effect after transient transfection, which showed 38.5% and 53.2% reduction of FOXM1 mRNA and protein level respectively.The growth of QGY-7703 cells was inhibited after stable inhibition of FOXM1 expression by shRNA-1026, which was indicated by decreased absorbance value of the test group after culture for 48, 72 and 96 h compared to control group (t = 10.830,3.578 and 5.734 respectively, P ＜ 0.05).Stable inhibition of F0XM1 also led to reduced colony formation ( t = 5.336, P ＜ 0.05 ) and increased apoptosis of QGY-7703 cells in comparison to control cells (t = 6.827, P ＜ 0.05 ).Conclusions Stable silencing F0XM1 gene by shRNA suppresses the growth of HCC cells in vitro.
