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

Abstract

Highlights: • We first demonstrated CXCL5 is highly expressed in human bladder tumor tissues and cells. • CXCL5 knockdown inhibits proliferation, migration and promotes apoptosis in T24 cells. • CXCL5 knockdown inhibits Snail, PI3K-AKT and ERK1/2 signaling pathways in T24 cells. • CXCL5 is critical for bladder tumor growth and progression. - Abstract: 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 T24 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, down-regulation 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.

Authors:
 [1];  [2];  [1]
  1. Department of Laboratory Medicine, Peking University Third Hospital, Beijing (China)
  2. Department of Urology, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing (China)
Publication Date:
OSTI Identifier:
22416320
Resource Type:
Journal Article
Journal Name:
Biochemical and Biophysical Research Communications
Additional Journal Information:
Journal Volume: 446; Journal Issue: 1; Other Information: Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); Journal ID: ISSN 0006-291X
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; ANIMAL TISSUES; APOPTOSIS; BIOLOGICAL FUNCTIONS; BLADDER; CELL PROLIFERATION; DIAGNOSIS; HUMAN POPULATIONS; IN VITRO; MESSENGER-RNA; NEOPLASMS; NEUTROPHILS; PEPTIDES; POLYMERASE CHAIN REACTION; SNAILS; THERAPY

Citation Formats

Zheng, Jiajia, Zhu, Xi, and Zhang, Jie. CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration. United States: N. p., 2014. Web. doi:10.1016/J.BBRC.2014.01.172.
Zheng, Jiajia, Zhu, Xi, & Zhang, Jie. CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration. United States. https://doi.org/10.1016/J.BBRC.2014.01.172
Zheng, Jiajia, Zhu, Xi, and Zhang, Jie. 2014. "CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration". United States. https://doi.org/10.1016/J.BBRC.2014.01.172.
@article{osti_22416320,
title = {CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration},
author = {Zheng, Jiajia and Zhu, Xi and Zhang, Jie},
abstractNote = {Highlights: • We first demonstrated CXCL5 is highly expressed in human bladder tumor tissues and cells. • CXCL5 knockdown inhibits proliferation, migration and promotes apoptosis in T24 cells. • CXCL5 knockdown inhibits Snail, PI3K-AKT and ERK1/2 signaling pathways in T24 cells. • CXCL5 is critical for bladder tumor growth and progression. - Abstract: 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 T24 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, down-regulation 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.},
doi = {10.1016/J.BBRC.2014.01.172},
url = {https://www.osti.gov/biblio/22416320}, journal = {Biochemical and Biophysical Research Communications},
issn = {0006-291X},
number = 1,
volume = 446,
place = {United States},
year = {Fri Mar 28 00:00:00 EDT 2014},
month = {Fri Mar 28 00:00:00 EDT 2014}
}