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Dieudonné et al., Cancer Res 2010
(Bone Neoplasms...) :
High
Wnt signaling
represses the proapoptotic proteoglycan
syndecan-2 in osteosarcoma cells ... Wnt3a stimulation, beta-catenin activation, and TCF overexpression resulted in syndecan-2 repression, whereas
Wnt inhibition using sFRP-1
increased syndecan-2 expression in U2OS cells ... These results indicate that
Wnt/beta-catenin and Wnt/RhoA signaling
contribute to
syndecan-2 repression ... The high activity of the canonical Wnt pathway in the different osteosarcoma cells
induces a constitutive repression of
syndecan-2 transcription, whereas
Wnt/RhoA signaling blocks the amplification loop of syndecan-2 expression
Dieudonné et al., J Bone Miner Res 2012
(Bone Neoplasms...) :
We previously showed that
Wnt/ß-catenin/T-cell factor ( TCF ) activation are
responsible for the repression of
syndecan-2 , a key modulator of apoptosis and chemosensitivity in osteosarcoma cells, suggesting a role of Wnt signaling in chemoresistance