microRNA-146a inhibits G protein-coupled receptor-mediated activation of NF-κB by targeting CARD10 and COPS8 in gastric cancer

被引:82
作者
Crone, Stephanie Geisler
Jacobsen, Anders [2 ,3 ]
Federspiel, Birgitte [1 ]
Bardram, Linda [4 ]
Krogh, Anders [2 ]
Lund, Anders H. [5 ,6 ]
Friis-Hansen, Lennart [1 ]
机构
[1] Univ Copenhagen, Rigshosp, Dept Pathol, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, Inst Mol Biol, Bioinformat Ctr, DK-2100 Copenhagen, Denmark
[3] Mem Sloan Kettering Canc Ctr, Computat Biol Ctr, New York, NY 10021 USA
[4] Univ Copenhagen, Rigshosp, Dept Surg Gastroenterol, DK-2100 Copenhagen, Denmark
[5] Univ Copenhagen, Ctr Epigenet, DK-2100 Copenhagen, Denmark
[6] Univ Copenhagen, BRIC Biotech Res & Innovat Ctr, DK-2100 Copenhagen, Denmark
关键词
Stomach cancer; Non-coding RNA; Cytokines; EXPRESSION; CELLS; INVASION; PATHWAYS; GENES; INFLAMMATION; MACROPHAGES; PROGRESSION; METASTASIS; CARCINOMA;
D O I
10.1186/1476-4598-11-71
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
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页数:14
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