CpG-oligodeoxynucleotides suppress the proliferation of A549 lung adenocarcinoma cells via toll-like receptor 9 signaling and upregulation of Runt-related transcription factor 3 expression

The aim of the present study was to investigate the effect of CpG-oligodeoxynucelotides (CpG-ODN) on the proliferation of the A549 human lung adenocarcinoma cell line and the expression of Runt-related transcription factor 3 (Runx3) and investigate the association between the toll-like receptor 9 (T...

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Veröffentlicht in:Biomedical reports 2014-05, Vol.2 (3), p.374-377
Hauptverfasser: BARNIE, PRINCE AMOAH, ZHANG, PAN, LU, PING, CHEN, XIAOBO, SU, ZHAOLIANG, WANG, SHENGJUN, XU, HUAXI
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container_issue 3
container_start_page 374
container_title Biomedical reports
container_volume 2
creator BARNIE, PRINCE AMOAH
ZHANG, PAN
LU, PING
CHEN, XIAOBO
SU, ZHAOLIANG
WANG, SHENGJUN
XU, HUAXI
description The aim of the present study was to investigate the effect of CpG-oligodeoxynucelotides (CpG-ODN) on the proliferation of the A549 human lung adenocarcinoma cell line and the expression of Runt-related transcription factor 3 (Runx3) and investigate the association between the toll-like receptor 9 (TLR9) signaling pathway and Runx3 expression during A549 cell proliferation. Different concentrations of CpG-ODN were used in this study to stimulate A549 cells and the expression of Runx3 at the mRNA or protein level was detected by reverse transcription-polymerase chain reaction or western blot analysis. Moreover, Runx3 siRNA was synthesized and transiently transfected into the A549 cells and the MTT assay was used to detect the effects of CpG-ODN on transfected cell growth. Our data demonstrated that CpG-ODN significantly inhibited the proliferation of A549 cells. The expression of Runx3 in the mRNA and protein level was increased in A549 cells stimulated by CpG-ODN. The CpG-ODN-stimulated cell proliferation was significantly inhibited in Runx3 siRNA-transfected A549 cells. In conclusion, CpG-ODN may bind to TLR9, inhibit the proliferation of A549 cells and upregulate the expression of Runx3.
doi_str_mv 10.3892/br.2014.257
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Different concentrations of CpG-ODN were used in this study to stimulate A549 cells and the expression of Runx3 at the mRNA or protein level was detected by reverse transcription-polymerase chain reaction or western blot analysis. Moreover, Runx3 siRNA was synthesized and transiently transfected into the A549 cells and the MTT assay was used to detect the effects of CpG-ODN on transfected cell growth. Our data demonstrated that CpG-ODN significantly inhibited the proliferation of A549 cells. The expression of Runx3 in the mRNA and protein level was increased in A549 cells stimulated by CpG-ODN. The CpG-ODN-stimulated cell proliferation was significantly inhibited in Runx3 siRNA-transfected A549 cells. 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source Spandidos Publications Journals; PubMed Central; EZB Electronic Journals Library
subjects A549 cancer cells
Adenocarcinoma
Apoptosis
Cell growth
Cell proliferation
Chemical synthesis
CpG islands
CpG-oligodeoxynucleotides
Deoxyribonucleic acid
Development and progression
DNA
Gastric cancer
Gene expression
Genetic aspects
Health aspects
Immune system
Investigations
Lung cancer
Metastasis
Oligodeoxynucleotides
Oligonucleotides
Polymerase chain reaction
proliferation
Proteins
Reverse transcription
Runt-related transcription factor 3
Runx3 protein
Signal transduction
siRNA
TLR9 protein
toll-like receptor 9
Toll-like receptors
Transcription factors
Tumorigenesis
title CpG-oligodeoxynucleotides suppress the proliferation of A549 lung adenocarcinoma cells via toll-like receptor 9 signaling and upregulation of Runt-related transcription factor 3 expression
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