Effect of calreticulin gene silencing on proliferation and invaison in human hepatocellular carcinoma cells
10.3760/cma.j.issn.1007-8118.2015.06.012
- VernacularTitle:钙网蛋白基因沉默对人肝癌细胞的增殖及侵袭能力的影响
- Author:
Jianwen YE
;
Chuang ZHOU
;
Bing YAN
;
Jia YANG
;
Zhe FU
;
Wenchao TANG
;
Wenlong ZHAI
- Publication Type:Journal Article
- Keywords:
Calreticulin;
Hepatocellular carcinoma cells;
Small interfering RNA;
p-Akt protein
- From:
Chinese Journal of Hepatobiliary Surgery
2015;21(6):405-409
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effect of calreticulin (CRT) on cell proliferation and invasion of human hepatocellular carcinoma cell line SMMC-7721 and HepG2.Methods SMMC-7721 and HepG2 cells were transfected with small interfering RNA (siRNA).The transfection rate was detected by immunoflurescence and western blot.The cell proliferation,invasion and apoptosis of SMMC-7721 and HepG2 cells were determined by using cell counting kit-8 (CCK-8) assays,transwell assays and flow cytometry,respectively.The p-Akt and Akt levels were detected by western blot.Results The growth inhibition rate in the siRNA experimental group of SMMC-7721 and HepG2 cells for 24,36 and 48 h were (41.0 ±2.2) %,(46.5 ±1.6)%,(59.7 ±2.2)% and (36.8 ±2.7)%,(47.3 ± 1.8)%,(61.5 ±3.2)%,respectively.The apoptosis rate after down-regulating the expression of CRT in SMMC-7721 and HepG2 cells for 36h were (45.2 ± 9.1) % and (48.9 ± 8.0) %,respectively.Compared with the blank group and the negative control group,the growth inhibition rate in the siRNA experimental group was lower (P <0.05),but the apoptosis rate was significantly higher (P < 0.05).Transwell experiments confirmed that the numbers of invaded SMMC-7721 and HepG2 cells in the blank group and the negative control group and siRNA experimental group were (96.8±7.3),(95.6±5.4),(34.0±4.2) and (124.0 ±9.9),(121.6 ±7.0),(70.4±9.5),respectively,indicating that cell invasion in the siRNA experimental group was significantly suppressed (P < 0.05).The expression of p-Akt was decreased (P < 0.05) after down-regulating the expression of CRT for 36h.Conclusion CRT gene silencing by siRNA can inhibit the SMMC-7721 and HepG2 cell proliferation and invasion,but increase the cell apoptosis by regulating PI3K/Akt signal pathway.