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. 2015 Sep 28;6(31):30453–30471. doi: 10.18632/oncotarget.5852

Table 7. WNT1/FGF3 Targets Increased in Human Breast Cancer Cells in Vivo: Ribosomes and Protein Synthesis.

Symbol Description Fold-Change P-value
Ribosome-related proteins (8)
SRPRB Signal recognition particle receptor subunit beta 4.68 9.97E-06
RPL15 60S ribosomal protein L15 4.60 1.28E-05
RPL13 60S ribosomal protein L19 4.48 1.98E-05
RPL13 60S ribosomal protein L13 4.48 1.98E-05
RPL14 60S ribosomal protein L14 4.45 2.15E-05
RPS5 40S ribosomal protein S5 4.41 2.45E-05
RPL4 60S ribosomal protein L4 3.05 1.79E-03
NPM1 NPM1 protein 2.42 9.50E-03
Translation initiation factors (3)
EIF2S1 Eukaryotic translation initiation factor 2, subunit 1 alpha, 35kDa 3.98 1.04E-04
EIF3D Eukaryotic translation initiation factor 3 subunit D 2.85 3.13E-03
EIF5B Eukaryotic translation initiation factor 5B 2.58 6.29E-03
Elongation factors (4)
EEF1B2 Elongation factor 1-beta 4.08 7.56E-05
EEF1G Elongation factor 1-gamma 3.71 2.44E-04
TUFM Elongation factor Tu, mitochondrial 3.38 6.74E-04
EEF1D Elongation factor 1-delta 2.50 7.67E-03
Enzymes for tRNA synthesis (4)
C22orf28 tRNA-splicing ligase RtcB homolog 4.59 1.37E-05
EPRS Bifunctional aminoacyl-tRNA synthetase (Glutamyl-Prolyl-tRNA Synthetase) 4.06 8.10E-05
DARS Aspartate--tRNA ligase, cytoplasmic 3.43 5.87E-04
WARS Tryptophan--tRNA ligase, cytoplasmic 2.48 8.17E-03
Protein folding chaperones (heat shock proteins) (11)
HSP90AB1 Heat shock protein HSP 90-beta 4.94 4.03E-06
PPIA Peptidyl-prolyl cis-trans isomerase A 4.29 3.74E-05
CANX Calnexin 3.99 9.88E-05
PDIA6 Protein disulfide-isomerase A6 3.62 3.22E-04
HSPD1 60 kDa heat shock protein, mitochondrial 3.42 5.93E-04
PPIB Peptidyl-prolyl cis-trans isomerase B 3.28 9.25E-04
HSPH1 Heat shock protein 105 kDa 3.18 1.22E-03
HSPA8 Heat shock cognate 71 kDa protein 3.11 1.49E-03
PDIA3 Protein disulfide-isomerase A3 2.53 7.22E-03
HSP90B1 Endoplasmin 2.43 9.33E-03
PDIA4 Protein disulfide-isomerase A4 2.13 1.89E-02

-Transcriptional profiling data derived from the analysis of N=28 breast cancer patients are shown, high-lighting the levels of fold-upregulation observed in the epithelial cancer cell compartment (relative to the tumor stroma), and corresponding p-values derived from the analysis of these clinical samples.