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. 2016 Oct 12;31(1):238–255. doi: 10.1096/fj.201600675R

TABLE 3.

Signaling pathways activated/inhibited significantly in response to Alk4 down-regulation using the OncoFinder method

Name State P
GSK3 pathway (gene expression via CTNNB1) Activated 9.34E–07
GSK3 pathway (b-CTNN degradation) Activated 1.02E–05
JAK mStat Pathway (JAK degradation) Inhibited 1.02E–05
Ubiquitin proteasome–dependent proteolysis pathway Activated 4.00E–05
WNT pathway (cell fate proliferation, differentiation, adhesion and survival) Unclear 4.77E–05
CD40 pathway Activated 2.17E–04
TNF main pathway Activated 2.51E–04
p38 pathway (translation) Unclear 3.27E–04
IL-2 pathway (IL-2 gene expression) Activated 5.14E–04
SMAD signaling network pathway Unclear 7.27E–04
GSK3 pathway (glycogen synthesis) Inhibited 1.04E–03
mTOR main pathway Activated 1.42E–03
WNT main pathway Unclear 1.47E–03
PTEN pathway (apoptosis) Inhibited 2.00E–03
GSK3 pathway (protein synthesis) Inhibited 2.41E–03
TNF pathway (gene expression and cell survival) Activated 2.41E–03
AKT main pathway Activated 2.48E–03
IL-2 main pathway Activated 2.88E–03
IGF1R pathway (glycogen synthesis) Inhibited 3.91E–03

GSK3, glycogen synthase kinase 3; IGF1R, insulin growth factor- 1 receptor; mTOR, mammalian target of rapamycin; PTEN, phosphatase and tensin homolog; SMAD, mothers against decapentaplegic homolog 3 Wnt, wingless-type MMTV integration site family.