Please use this identifier to cite or link to this item: https://doi.org/10.1186/1476-4598-11-71
Title: MicroRNA-146a inhibits G protein-coupled receptor-mediated activation of NF-?B by targeting CARD10 and COPS8 in gastric cancer
Authors: Crone, S.G
Jacobsen, A 
Federspiel, B
Bardram, L
Krogh, A
Lund, A.H
Friis-Hansen, L
Keywords: caspase recruitment domain containing protein 10
COP9 signalosome complex subunit 8
G protein coupled receptor
immunoglobulin enhancer binding protein
luciferase
lysophosphatidic acid
microRNA 146a
transcription factor
unclassified drug
animal experiment
animal model
article
cancer cell
enzyme activation
enzyme inhibition
genetic transfection
in situ hybridization
mouse
nonhuman
polymerase chain reaction
protein analysis
protein expression
protein targeting
stomach cancer
upregulation
Western blotting
Animals
CARD Signaling Adaptor Proteins
Cell Line, Tumor
Cytokines
Disease Models, Animal
Enzyme Activation
Gene Expression Regulation, Neoplastic
Humans
Mice
Mice, Knockout
MicroRNAs
Monocytes
NF-kappa B
Proteins
Receptors, G-Protein-Coupled
Signal Transduction
Stomach Neoplasms
Mus
Issue Date: 2012
Citation: Crone, S.G, Jacobsen, A, Federspiel, B, Bardram, L, Krogh, A, Lund, A.H, Friis-Hansen, L (2012). MicroRNA-146a inhibits G protein-coupled receptor-mediated activation of NF-?B by targeting CARD10 and COPS8 in gastric cancer. Molecular Cancer 11 : 71. ScholarBank@NUS Repository. https://doi.org/10.1186/1476-4598-11-71
Rights: Attribution 4.0 International
Abstract: Background: Gastric cancer is the second most common cause of cancer-related death in the world. Inflammatory signals originating from gastric cancer cells are important for recruiting inflammatory cells and regulation of metastasis of gastric cancer. Several microRNAs (miRNA) have been shown to be involved in development and progression of gastric cancer. miRNA-146a (miR-146a) is a modulator of inflammatory signals, but little is known about its importance in gastric cancer. We therefore wanted to identify targets of miR-146a in gastric cancer and examine its biological roles.Results: The expression of miR-146a was evaluated by quantitative PCR (qPCR) and found up-regulated in the gastrin knockout mice, a mouse model of gastric cancer, and in 73% of investigated human gastric adenocarcinomas. Expression of miR-146a by gastric cancer cells was confirmed by in situ hybridization. Global analysis of changes in mRNA levels after miR-146a transfection identified two transcripts, caspase recruitment domain-containing protein 10 (CARD10) and COP9 signalosome complex subunit 8 (COPS8), as new miR-146a targets. qPCR, Western blotting and luciferase assays confirmed these transcripts as direct miR-146a targets. CARD10 and COPS8 were shown to be part of the G protein-coupled receptor (GPCR) pathway of nuclear factor-kappaB (NF-kappaB) activation. Lysophosphatidic acid (LPA) induces NF-kappaB activation via this pathway and over-expression of miR-146a inhibited LPA-induced NF-kappaB activation, reduced LPA-induced expression of tumor-promoting cytokines and growth factors and inhibited monocyte attraction.Conclusions: miR-146a expression is up-regulated in a majority of gastric cancers where it targets CARD10 and COPS8, inhibiting GPCR-mediated activation of NF-kappaB, thus reducing expression of NF-kappaB-regulated tumor-promoting cytokines and growth factors. By targeting components of several NF-kappaB-activating pathways, miR-146a is a key component in the regulation of NF-kappaB activity. © 2012 Crone et al.; licensee BioMed Central Ltd.
Source Title: Molecular Cancer
URI: https://scholarbank.nus.edu.sg/handle/10635/181599
ISSN: 14764598
DOI: 10.1186/1476-4598-11-71
Rights: Attribution 4.0 International
Appears in Collections:Elements
Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1186_1476-4598-11-71.pdf2.31 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons