Effect and mechanism of xCT on invasion and migration of nasopharyngeal carcinoma cells in vitro
10.3760/cma.j.issn.1008-1372.2014.09.008
- VernacularTitle:xCT在鼻咽癌细胞体外迁移侵袭中的作用及机制
- Author:
Yafei LI
;
Chengkun WANG
;
Bo PENG
;
Yixue GU
;
Zhimin HE
- Publication Type:Journal Article
- Keywords:
Gene expression;
Nasopharyngeal neoplasms/pathology;
Nasopharyngeal neoplasms/genetics;
Cell proliferation;
Neoplasm invasiveness;
Polymerase chain reaction;
Matrix metalloproteinase 1
- From:
Journal of Chinese Physician
2014;16(9):1181-1185
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the role of xCT in the metastasis and drug resistance of nasopharyngeal carcinoma (NPC),to provide new evidences for the mechanism of NPC metastasis and drug resistance,and to enhance effects of chemotherapy.Methods Fluorescence quantitative polymerase chain reaction (PCR) and Western blot were used to detect the xCT expression of 5-8F and 6-10B.The xCT eukaryotic expression vector was constructed to transient transfect 6-10B cell lines.The 5-8F cell lines were treated with xCT antisense oligodeoxynucleotide (ASO).Scratching assay and transwell method were used to detect the cell metastasis and invasion abilities.The expressions of matrix metalloproteinase 1 (MMP1) of all the cell lines were surveyed by Western blot.Results The results of fluorescence quantitative PCR and Western blot showed that the expression of xCT in 5-8F was higher than 6-10B in the levels of mRNA and protein.Exogenous overexpression of xCT enhanced metastasis and invasion abilities of 6-10B cells.Silencing and inhibition of xCT could decrease metastasis and invasion abilities of 5-8F cells.The expressions of MMP1 protein in 5-8F were higher than 6-10B,and they were positively correlated with the expression of xCT.Conclusions xCT is closely related to the metastasis and invasion abilities of nasopharyngeal carcinoma.xCT could enhance the metastasis and invasion abilities of NPC cells.xCT might mediate proliferation and matastasis/invasion of NPC cells through MMP1.
