Effects of S100A6 gene silencing on proliferation and migration of human esophagus cancer cell line Eca109
10.3724/SP.J.1008.2014.00049
- Author:
Wen-Quan LU
1
Author Information
1. Department of Pharmacy, Changzheng Hospital, Second Military Medical University
- Publication Type:Journal Article
- Keywords:
Cell migration;
Cell proliferation;
Esophageal neoplasms;
Gene sliencing;
S100A6
- From:
Academic Journal of Second Military Medical University
2014;35(1):49-54
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the effects of S100A6 gene silencing on the proliferation and migration of Eca109 human esophagus cancer cells. Methods: The shRNA expression vectors were constructed using the shRNA sequences designed based on human S100A6's coding sequence, and were transfected into Eca109 cells via cationic liposome. The changes of S100A6 mRNA and protein in Eca109 cells transfected with the recombinant vectors were detected using real-time PCR and Western blotting analysis 48 hours after transfection, respectively; the proliferative curves of transfected cells were plotted using MTT assay; furthermore, the change in cellular migration ability was determined using wound healing assay. Results: The eukaryotic expression vector of shRNA targeting S100A6 was successfully constructed. Real-time PCR and Western blotting analysis results showed that S100A6 was effectively silenced by liposome-mediated transfection of the recombinant shRNA vectors in Eca109 cells. Compared with the untransfected cells, S100A6 mRNA and protein in transfected Eca109 cells were significantly decreased (P<0.05, P<0.01). Meanwhile, the proliferative activity of Eca109 cells was significantly inhibited by S100A6 silencing (P<0.01). It was found that the cellular migration was also suppressed by S100A6 gene interference. Conclusion: S100A6 gene can be effectively silenced by shRNA expression vectors, and the silence may lead to inhibition of the proliferation and migration of Eca109 cells.
