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Presentation transcript:

Supplementary Information 1 47.5 32.5 25 wt DCRD D1 empty sFRP1 Blot: anti-Myc B sFRP1 empty wt DCRD D1 47.5 32.5 25 Blot: anti-Myc 47.5 32.5 25 wt DCRD D1 empty sFRP1 Blot: anti-Myc C Western blot analysis of extracts from cells transfected using the same conditions as the corresponding reporter assays in Figure 2. (A) 22Rv1 cells, (B) LNCaP cells, (C) LNCaP-r cells. Due to the low transfection efficiency of LNCaP cells, these cells were cultured in the presence of G418 after transfection and G418-resistant cells were then pooled for further analysis. sFRP1 derivatives are expressed at comparable levels in all cell lines tested here.

Supplementary Information 2 sFRP1 - - + + Wnt3A - + - + Blot: anti-Myc (for sFRP1) B sFRP1 - - + + b-catenin WT SA WT SA Blot: anti-Myc (for sFRP1) IP: anti-HA Blot: anti-b-catenin C - - sFRP1 + + - - Wnt5A + + Blot: anti-Myc (for sFRP1) Blot: Wnt5A Western blot analysis of extracts from 22Rv1 cells transfected using the same conditions as the aforementioned reporter assays. (A) Transfections corresponding to Figure 3 (Wnt3a antibodies were not sensitive enough to detect the low level of transfected Wnt3a in these experiments), (B) Transfections corresponding to Figure 4, (C) Transfections corresponding to Figure 6D. Regarding (B), detection of HA-tagged beta-catenin in cell extracts was not possible. Therefore, anti-HA ips were probed for HA-tagged beta-catenin.