Publication | Closed Access
Wnt/β-catenin up-regulates Midkine expression in glioma cells.
10
Citations
10
References
2015
Year
Cancer ResearchSignaling PathwayGliomaMultiple Tumor GrowthGlioma CellsMidkine ExpressionMedicineCancer Cell BiologyMolecular OncologyMidkine GeneRadiation OncologyCancer BiologyCell BiologyCell SignalingCell DevelopmentTumor BiologyCancer GrowthMolecular Signaling
Midkine, also known as neurite growth-promoting factor 2 (NEGF2), plays an important role in cell proliferation, apoptosis and differentiation. Recent studies have shown that Midkine is up-regulated in several types of human cancers. However, the molecular mechanism for its up-regulation remains poorly understood. Activation of Wnt/β-catenin signaling is viewed as crucial for multiple tumor growth and metastasis, including glioma. In the present study, we found that Wnt3a administration or transfection of a constitutively activated β-catenin promoted Midkine expression in glioma cells. We further identified a TCF/LEF binding site, with which beta-catenin interacts, on the proximal promoter region of Midkine gene, by luciferase reporter and chromatin immunoprecipitation assays. Thus, our results suggest a previously unknown Wnt/β-catenin/Midkine molecular network controlling glioma development.
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