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. 2007 Sep 25;7:182. doi: 10.1186/1471-2407-7-182

Table 2.

Top 20 pathways in the 500 signatures of ER-positive and ER-negative tumors evaluated by Global Test

Pathways GO_ID P Frequency
ER-positive tumors
 Apoptosis 6915 3.06E-7 250
 Regulation of cell cycle 74 2.46E-5 203
 Protein amino acid phosphorylation 6468 2.48E-5 114
 Cytokinesis 910 6.13E-5 165
 Cell motility 6928 0.00015 93
 Cell cycle 7049 0.00028 138
 Cell surface receptor-linked signal transd. 7166 0.00033 172
 Mitosis 7067 0.00036 256
 Intracellular protein transport 6886 0.00054 141
 Mitotic chromosome segregation 70 0.00057 98
 Ubiquitin-dependent protein catabolism 6511 0.00074 158
 DNA repair 6281 0.00079 156
 Induction of apoptosis 6917 0.00083 115
 Immune response 6955 0.00094 167
 Protein biosynthesis 6412 0.0010 145
 DNA replication 6260 0.0015 92
 Oncogenesis 7048 0.0020 228
 Metabolism 8152 0.0021 83
 Cellular defense response 6968 0.0025 131
 Chemotaxis 6935 0.0027 89
ER-negative tumors
 Regulation of cell growth 1558 0.00012 136
 Regul. of G-coupled receptor signaling 8277 0.00013 153
 Skeletal development 1501 0.00024 160
 Protein amino acid phosphorylation 6468 0.0051 151
 Cell adhesion 7155 0.0065 110
 Carbohydrate metabolism 5975 0.0066 86
 Nuclear mRNA splicing, via spliceosome 398 0.0067 203
 Signal transduction 7165 0.0078 160
 Cation transport 6812 0.0098 160
 Calciumion transport 6816 0.010 93
 Protein modification 6464 0.011 132
 Intracellular signaling cascade 7242 0.012 135
 mRNA processing 6397 0.012 81
 RNA splicing 8380 0.014 192
 Endocytosis 6897 0.026 166
 Regul. of transcription from PolII promoter 6357 0.031 109
 Regulation of cell cycle 74 0.043 88
 Protein complex assembly 6461 0.048 183
 Protein biosynthesis 6412 0.063 99
 Cell cycle 7049 0.084 72

Each of the top 20 over-represented pathways that have the highest frequencies in the 500 signatures of ER-positive and ER-negative tumors were subjected to Global Test program [12, 14]. The Global Test examines the association of a group of genes as a whole to a specific clinical parameter, in this case DMFS, and generates an asymptotic theory p value for the pathway. The pathways are ranked by their p value in the respective ER-subgroup of tumors.