Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid

Kitz, K; Windischhofer, W; Leis, HJ; Huber, E; Kollroser, M; Malle, E.
15-Deoxy-Δ12,14-prostaglandin J2 induces Cox-2 expression in human osteosarcoma cells through MAPK and EGFR activation involving reactive oxygen species.
Free Radic Biol Med. 2011; 50(7):854-865
Web of Science PubMed FullText FullText_MUG

 

Autor/innen der Med Uni Graz:
Huber Evelyn
Kitz Kerstin
Kollroser Manfred
Leis Hans-Jörg
Malle Ernst
Windischhofer Werner
Altmetrics:

Dimensions Citations:

Plum Analytics:
Abstract:
Prostaglandins (PGs), important modulators in bone biology, may also contribute to tumor formation and progression in human osteosarcoma. 15-Deoxy-Δ(12,14)-PGJ(2) (15d-PGJ(2)), a metabolite of PGD(2) and PPARγ-ligand, exerts a panel of biological activities via receptor-dependent and -independent mechanisms. As inducible cyclooxygenase-2 (Cox-2) is a candidate inflammatory marker in human osteosarcoma and a rate-limiting enzyme in PG biosynthesis, this study aimed at investigating intracellular redox status and signaling cascades leading to Cox-2 induction in human MG-63 osteosarcoma cells. 15d-PGJ(2) induced the accumulation of reactive oxygen species (ROS) that in turn may lead to upregulation of Cox-2 via two different routes in a PPARγ-independent manner. First, phosphorylation of p38 MAPK directly enhances Cox-2 expression by promoting mRNA stability. Second, 15d-PGJ(2) induces activation of epidermal growth factor receptors and downstream activation of Cox-2 via phosphorylation of p42/44 MAPK. Glutathione precursor molecules reversed enhanced ROS levels and Cox-2 expression. Functional activity of Cox-2 expression was tested by measurement of PGE(2) and PGF(2α). The synthetic compound 9,10-dihydro-15d-PGJ(2) lacking the α,β-unsaturated carbonyl group in the cyclopentenone ring did not exhibit the cellular responses observed with 15d-PGJ(2). We conclude that the electrophilic carbon atom of 15d-PGJ(2) is responsible for alterations in intracellular redox status and Cox-2 expression.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Cell Line, Tumor -
Cyclooxygenase 2 - genetics
Dinoprost - analysis
Dinoprostone - analysis
Gene Expression - drug effects
Glutathione - metabolism
Humans -
Mice -
Mitogen-Activated Protein Kinase 1 - genetics
Mitogen-Activated Protein Kinase 3 - genetics
Neoplasms -
Osteosarcoma - genetics
Oxidation-Reduction - drug effects
Phosphorylation - drug effects
Prostaglandin D2 - analogs & derivatives
RNA Stability - genetics
Reactive Oxygen Species - metabolism
Receptor, Epidermal Growth Factor - genetics
Signal Transduction - drug effects
Up-Regulation -
p38 Mitogen-Activated Protein Kinases - genetics

Find related publications in this database (Keywords)
ROS 15-Deoxy-Delta(12,14)-PGJ(2)
Cyclooxygenase Epidermal growth factor receptor
Mitogen-activated protein kinase
Prostaglandins
Eicosanoids Peroxisome proliferator-activated receptor
NF-kappa B
Free radicals
© Meduni Graz Impressum