|
CCND2 |
−3.0 |
0.0004 |
β-catenin target gene; facilitates cell cycle progression from G1 to S phases |
|
WNT2B |
−4.6 |
0.0004 |
Induces nephrogenesis; promotes epithelial differentiation |
|
FZD4 |
−1.9 |
0.0039 |
Promotes ureteric bud branching morphogenesis |
|
DAAM1 |
−1.4 |
0.0075 |
Maintains cytoskeleton architecture; knockdown reduces pronephric epithelial markers |
|
FRZB |
−2.7 |
0.0089 |
sFRP3; candidate tumor suppressor |
|
WNT11 |
−1.4 |
0.0093 |
Secreted from UB tips; regulates UB epithelial branching; non-canonical pathway; redundant function with WNT5B |
|
SLC9A3R1 |
−1.6 |
0.0117 |
Scaffold protein; may enhance Wnt signaling |
|
PITX2 |
−1.6 |
0.0152 |
Morphogen |
CITED1 |
KREMEN1 |
+1.6 |
0.0278 |
DKK1 receptor; Wnt antagonist |
|
NLK |
−1.2 |
0.0295 |
Serine/threonine kinase; negative regulator of Wnt/β-catenin nuclear effects (analogous to CTNNBIP1) |
|
WNT5B |
−1.7 |
0.0341 |
Non-canonical; detected in minority of Wilms tumor; redundant function with WNT11 |
|
TCF7L1 |
−1.3 |
0.0372 |
Mediates Wnt/β-catenin signaling; necessary for terminal differentiation |
|
DKK1 |
+4.6 |
0.0379 |
Wnt inhibitor; represses nephrogenesis; promotes stemness |
|
SENP2 |
−1.2 |
0.0428 |
Sumoylation activity |
|
CTNNBIP1 |
−1.7 |
0.0440 |
Wnt antagonist; promotes ureteric bud branching morphogenesis; down-regulated in 1p-deleted WT |
|
CSNK2A1 |
−1.4 |
0.0458 |
Serine/threonine kinase |
|
FBXW2 |
−1.5 |
0.0488 |
Ubiquitin ligase |
|
WNT16 |
−1.5 |
0.0494 |
Developmentally regulated activity |
|
BTRC |
−1.4 |
0.0065 |
Ubiquitin ligase; ubiquitinates β-catenin |
|
NLK |
−1.2 |
0.0295 |
Serine/threonine kinase; negative regulator of Wnt/β-catenin nuclear effects (analogous to CTNNBIP1) |
ΔNES |
CTNNBIP1 |
−1.7 |
0.0296 |
Wnt antagonist; promotes ureteric bud branching morphogenesis; down-regulated in 1p-deleted WT |
|
DVL1 |
+1.2 |
0.0339 |
Signal transducer of Wnt pathway; pro-proliferative; increases β-catenin tumorigenicity in neuroblastoma |
|
CCND2 |
−1.6 |
0.0409 |
β-catenin target gene; facilitates cell cycle progression from G1 to S phases |
TARGETS |
Gene |
Fold change |
p-value |
Biological Function |
CITED1 |
IGF2 |
+1.5 |
0.017 |
Loss of imprinting of IGF2 is the most common genetic or epigenetic alteration found in Wilms tumor (~50%) |
|
PTGS2 |
+2.2 |
0.026 |
Synthesizes prostaglandins (PGE2); important to normal nephrogensis; regulator of tumorigenesis and disease progression |
|
CTSD |
−2.1 |
0.037 |
Stimulates apoptosis |
|
PTGS2 |
+2.1 |
0.043 |
Synthesizes prostaglandins (PGE2); important to normal nephrogensis; regulator of tumorigenesis and disease progression |
ΔNES |
HDAC11 |
−1.7 |
0.044 |
Transcriptional co-repressor; binding partner of HDAC6; expressed specifically in kidney |
|
PIK3C2A |
−1.6 |
0.046 |
Receptor-linked serine/threonine kinase; AKT pathway |
|
AKT1 |
−1.8 |
0.048 |
Cytosolic serine/threonine kinase |