Gene interactions and pathways from curated databases and text-mining

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CTNNB1 — RELA

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Spiegelman et al., Oncogene 2002 : In the NIH3T3 cells, which express HOS, but not betaTrCP, Wnt/beta-catenin signaling leads to inhibition of HOS promoter activity and NF-kappaB-driven transcription as well as to stabilization of beta-catenin
Tselepis et al., Oncogene 2002 (Adenocarcinoma...) : This beta-catenin mediated transcription is independent of NF-kappaB activation
Deng et al., Cancer Cell 2002 (Breast Neoplasms...) : beta-catenin interacts with and inhibits NF-kappa B in human colon and breast cancer ... Importantly, activated beta-catenin was found to inhibit the expression of NF-kappa B target genes, including Fas and TRAF1 ... Furthermore, a strong inverse correlation was identified between the expression levels of beta-catenin and Fas in colon and breast tumor tissues, suggesting that beta-catenin regulates NF-kappa B and its targets in vivo
Deng et al., Mol Carcinog 2004 : beta-catenin has been recently found to interact with and inhibit nuclear factor kappa B (NF-kappaB)
Kuphal et al., Oncogene 2004 (Melanoma) : Furthermore, cytoplasmatic beta-catenin induced p38 and NFkappaB activation in malignant melanoma ... In summary, we conclude that loss of E-cadherin and cytoplasmatic beta-catenin induces p38 mediated NFkappaB activation, potentially revealing an important mechanism of tumorigenesis in malignant melanomas
Zuscik et al., Environ Health Perspect 2007 : Although Pb had no effect on basal CREB or Wnt/beta-catenin pathway activity, it induced NFkappaB signaling and inhibited AP-1 signaling
Cho et al., FEBS Lett 2008 (Neoplasms) : Downregulation of lzts2 increased the beta-catenin/Tcf promoter activity and inhibited NF-kappaB induced modulation of the nuclear translocation of beta-catenin
Zhang et al., Dev Cell 2009 : We find that Wnt/beta-catenin signaling is absolutely required for NF-kappaB activation, and that Edar is a direct Wnt target gene