Please use this identifier to cite or link to this item: https://doi.org/10.1186/1476-4598-11-71
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dc.titleMicroRNA-146a inhibits G protein-coupled receptor-mediated activation of NF-?B by targeting CARD10 and COPS8 in gastric cancer
dc.contributor.authorCrone, S.G
dc.contributor.authorJacobsen, A
dc.contributor.authorFederspiel, B
dc.contributor.authorBardram, L
dc.contributor.authorKrogh, A
dc.contributor.authorLund, A.H
dc.contributor.authorFriis-Hansen, L
dc.date.accessioned2020-10-27T11:26:07Z
dc.date.available2020-10-27T11:26:07Z
dc.date.issued2012
dc.identifier.citationCrone, 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
dc.identifier.issn14764598
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181599
dc.description.abstractBackground: 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcaspase recruitment domain containing protein 10
dc.subjectCOP9 signalosome complex subunit 8
dc.subjectG protein coupled receptor
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectluciferase
dc.subjectlysophosphatidic acid
dc.subjectmicroRNA 146a
dc.subjecttranscription factor
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectarticle
dc.subjectcancer cell
dc.subjectenzyme activation
dc.subjectenzyme inhibition
dc.subjectgenetic transfection
dc.subjectin situ hybridization
dc.subjectmouse
dc.subjectnonhuman
dc.subjectpolymerase chain reaction
dc.subjectprotein analysis
dc.subjectprotein expression
dc.subjectprotein targeting
dc.subjectstomach cancer
dc.subjectupregulation
dc.subjectWestern blotting
dc.subjectAnimals
dc.subjectCARD Signaling Adaptor Proteins
dc.subjectCell Line, Tumor
dc.subjectCytokines
dc.subjectDisease Models, Animal
dc.subjectEnzyme Activation
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectMice
dc.subjectMice, Knockout
dc.subjectMicroRNAs
dc.subjectMonocytes
dc.subjectNF-kappa B
dc.subjectProteins
dc.subjectReceptors, G-Protein-Coupled
dc.subjectSignal Transduction
dc.subjectStomach Neoplasms
dc.subjectMus
dc.typeArticle
dc.contributor.departmentDEPARTMENT OF COMPUTER SCIENCE
dc.description.doi10.1186/1476-4598-11-71
dc.description.sourcetitleMolecular Cancer
dc.description.volume11
dc.description.page71
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