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. 2012 Oct 10;103(11):2027–2037. doi: 10.1111/j.1349-7006.2012.02412.x

Table 2.

mRNA changes between pRC3 versus WT8/HIF2aP531A

Unigene Symbol Description Fold change (pRC3/WT8) A Fold change (HIF2aP531A/mock) B Ratio A/B
Genes upregulated
Hs.303649 CCL2 Chemokine (C‐C motif) ligand 2 88.91 0.60 149.19
Hs.252820 PGF Placental growth factor 30.75 2.82 10.91
Hs.513617 MMP2 Matrix metallopeptidase 2 15.91 8.67 1.84
Hs.297413 MMP9 Matrix metallopeptidase 9 8.05 3.19 2.52
Hs.471200 NRP2 Neuropilin 2 7.60 1.12 6.76
Hs.149239 EFNB2 Ephrin‐B2 4.00 1.26 3.17
Hs.164226 THBS1 Thrombospondin 1 3.57 0.65 5.49
Hs.371147 THBS2 Thrombospondin 2 3.42 0.41 8.32
Hs.435215 VEGFC Vascular endothelial growth factor C 3.38 2.35 1.44
Hs.437008 EPHB4 EPH receptor B4 2.71 1.32 2.06
Hs.133379 TGFB2 Transforming growth factor, beta 2 2.69 0.55 4.89
Hs.76884 ID3 Inhibitor of DNA binding 3 2.64 1.23 2.14
Hs.517356 COL18A1 Collagen, type XVIII, alpha 1 2.24 0.68 3.28
Hs.73793 VEGFA Vascular endothelial growth factor A 2.12 2.05 1.03

The RT2 Profiler human angiogenesis PCR Arrays (SA Biosciences) were carried out according to the manufacturer's protocols. Expression levels of genes involved in angiogenesis were compared between WT8 and pRC3, WT8/HIF2a P531A, and WT8/mock cells. Five housekeeping genes were used as controls for each gene expression calculation, and the extent of change in expression of each gene was calculated using the DCt method. Only genes whose expression was upregulated or downregulated at least 2‐fold are shown in Table 2. When DCt was over 12, and therefore the expression was thought to be extremely low, the gene was omitted from the analysis.