CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration

被引:27
|
作者
Zheng, Jiajia [1 ]
Zhu, Xi [2 ]
Zhang, Jie [1 ]
机构
[1] Peking Univ, Hosp 3, Dept Lab Med, Beijing 100191, Peoples R China
[2] Capital Med Univ, Beijing Friendship Hosp, Dept Urol, Beijing, Peoples R China
关键词
CXCL5; Bladder cancer; T24; cells; Cells proliferation and migration; MESENCHYMAL TRANSITION; GENE-EXPRESSION; PROSTATE-CANCER; E-CADHERIN; POOR-PROGNOSIS; PEPTIDE ENA-78; OVEREXPRESSION; ANGIOGENESIS; PROGRESSION; CHEMOKINE;
D O I
10.1016/j.bbrc.2014.01.172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CXCL5 (epithelial neutrophil activating peptide-78) which acts as a potent chemoattractant and activator of neutrophil function was reported to play a multifaceted role in tumorigenesis. To investigate the role of CXCL5 in bladder cancer progression, we examined the CXCL5 expression in bladder cancer tissues by real-time PCR and Western blot, additionally, we used shRNA-mediated silencing to generate stable CXCL5 silenced bladder cancer 124 cells and defined its biological functions. Our results demonstrated that mRNA and protein of CXCL5 is increased in human bladder tumor tissues and cell lines, downregulation of CXCL5 in T24 cells resulted in significantly decreased cell proliferation, migration and increased cell apoptosis in vitro through Snail, PI3K-AKT and ERK1/2 signaling pathways. These data suggest that CXCL5 is critical for bladder tumor growth and progression, it may represent a potential application in cancer diagnosis and therapy. (c) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:18 / 24
页数:7
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