Effect of semaphorin 4D on the proliferation, migration and angiogenic of human pancreatic carcinoma cells
10.7683/xxyxyxb.2017.12.005
- VernacularTitle:轴突诱导因子4D对人胰腺癌细胞增殖、迁移及血管生成的影响
- Author:
jiang Ru JIA
1
;
yan Li HOU
;
chen Qing YIN
;
fang Li LI
;
wu Geng YANG
Author Information
1. 邯郸市中心医院普外一科
- Keywords:
RNA interference;
semaphorin 4D;
pancreatic carcinoma cells;
proliferation and migration ability;
angiogenesis
- From:
Journal of Xinxiang Medical College
2017;34(12):1063-1067
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effects of semaphorin 4D(Sema4D) on the proliferation,migration and angiogenic of human pancreatic carcinoma cells.Methods Sema4D-siRNA was designed and synthesized and transfected into human pancreatic carcinoma cells.After 48 hours of transient infection,the changes of expression of Sema4D mRNA before and after transfection were detected by reverse transcription-polymeruse chain reaction method.And after 72 hours of transient infection,the changes of expression of Sema4D protein before and after transfection were detected by Western blot method.The changes of growth of the transfected cells were observed by methyl thiazolyl terazolium assay.Using transwell migration test and scratch repair test to detect the changes of migration ability of human pancreatic carcinoma cells after transfection.Using tubule formation assay to observe the effect of supernatant of pancreatic carcinoma cell cultures on angiogenesis after transfection.Results Compared with the negative control group and blank control group,the expression of Sema4D mRNA and Sema4D protein and the growth rate of pancreatic carcinoma cells decreased significantly (P ＜ 0.05).In transwell migration test and scratch repair test,it was observed that Pancreatic cancer cells penetrating cell number and scratch repair rate were significantly lower than that in negative control group and blank control group (P ＜ 0.05).Tubule formation assay showed that there were significant differences in angiogenesis numbers among siRNA transfection group(0.5 ± 0.02),negative control group(1.45 ± 0.60) and blank control group (1.37 ± 0.52) (P ＜ 0.05).Conclusion Sema4D-siRNA can induce RNA interference in pancreatic carcinoma cells and down-regulate the expression of Sema4D gene,which can inhibit the proliferation of pancreatic carcinoma cells,significantly reduce the migration ability of pancreatic carcinoma ceils and inhibit angiogenesis.
