This pipeline maps genes, with mutation or copy number alteration AND this alteration is highly correlated with mRNA expression, to pathways curated in the KEGG and BIOCARTA databases. It identifies pathways significantly enriched with these genes. The pipeline also identifies pathways significantly enriched with marker genes of each expression subtype of cancer.
genes with mutation: identified by the Mutation_Significance pipeline
genes with copy number alteration: identified by the CopyNumber_Gistic2 pipeline
correlation between copy number and mRNA expression: identified by the Correlate_CopyNumber_vs_mRNA pipeline
marker genes and expression subtypes: identified by the mRNAConsensusClustering pipeline
There are 81 genes with significant mutation (Q value <= 0.1) and 256 genes with significant copy number alteration (Q value <= 0.25). The identified marker genes (Q value <= 0.01 or within top 2000) are 1163 for subtype 1, 1163 for subtype 2, 1163 for subtype 3. Pathways significantly enriched with these genes (Q value <= 0.01) are identified :
1 pathways significantly enriched with genes with copy number alteration or mutation.
3 pathways significantly enriched with marker genes of gene expression subtype 1
4 pathways significantly enriched with marker genes of gene expression subtype 2
6 pathways significantly enriched with marker genes of gene expression subtype 3
Pathway | Nof Genes | Nof CNV_Mut | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_UBIQUITIN_MEDIATED_PROTEOLYSIS | 137 | 12 | 2.5 | 0 | 0.0005 |
KEGG_OLFACTORY_TRANSDUCTION | 389 | 18 | 1.5 | 0.0001 | 0.01 |
BIOCARTA_PROTEASOME_PATHWAY | 19 | 4 | 3.7 | 0.0002 | 0.023 |
KEGG_GLIOMA | 65 | 6 | 2.5 | 0.0006 | 0.04 |
KEGG_BLADDER_CANCER | 42 | 5 | 2.9 | 0.0005 | 0.04 |
SAE1,CUL5,CUL1,SKP2,UBE2L3,UBE2F,MDM2,UBE2S,UBE3A,PARK2,BIRC2,CUL4A
OR2T2,OR2T8,OR2AK2,OR51B2,OR2T33,OR5AC2,OR8H1,OR4D5,OR2A5,OR10A4,OR6F1,OR2G6,OR4M2,OR4M1,OR5M9,OR14A16,OR6K3,OR10G8
UBE3A,PSMB5,PSMB4,PSMB1
HRAS,PTEN,CDKN2A,RB1,MAPK1,MDM2
HRAS,CDKN2A,RB1,MAPK1,MDM2
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_GLUTATHIONE_METABOLISM | 50 | 12 | 2.2 | 0 | 0.0017 |
KEGG_DRUG_METABOLISM_CYTOCHROME_P450 | 72 | 14 | 1.9 | 0 | 0.0022 |
KEGG_METABOLISM_OF_XENOBIOTICS_BY_CYTOCHROME_P450 | 70 | 13 | 1.8 | 0 | 0.005 |
KEGG_AXON_GUIDANCE | 129 | 15 | 1.2 | 0.0023 | 0.15 |
KEGG_DILATED_CARDIOMYOPATHY | 92 | 12 | 1.4 | 0.0022 | 0.15 |
GSTM5,GSTM1,GPX2,GSTM2,GSR,GSTM3,GCLC,GSTO1,GSTA3,GSTA4,GSTA5,GGT7
CYP2C19,GSTM5,GSTM1,GSTM2,GSTM3,ALDH3B2,ALDH3B1,ADH5,ALDH3A1,FMO3,GSTO1,GSTA3,GSTA4,GSTA5
CYP2C19,GSTM5,GSTM1,GSTM2,GSTM3,ALDH3B2,ALDH3B1,ADH5,ALDH3A1,GSTO1,GSTA3,GSTA4,GSTA5
PLXNA1,PLXNB1,EFNB2,MAPK1,EPHB3,EPHA1,RGS3,SEMA3F,PAK1,SEMA4G,NCK1,SEMA4B,CHP,FYN,GSK3B
ADCY8,ADCY6,PRKX,SGCG,MYL3,CACNB2,ITGB5,TPM4,SLC8A1,ITGA2,ATP2A2,ITGA7
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
BIOCARTA_AGR_PATHWAY | 36 | 12 | 1.9 | 0 | 0.0043 |
KEGG_ENDOCYTOSIS | 183 | 33 | 1.1 | 0 | 0.0043 |
KEGG_ARRHYTHMOGENIC_RIGHT_VENTRICULAR_CARDIOMYOPATHY_ARVC | 76 | 18 | 1.5 | 0 | 0.0044 |
KEGG_FOCAL_ADHESION | 201 | 34 | 0.95 | 0.0001 | 0.0072 |
BIOCARTA_INTRINSIC_PATHWAY | 23 | 8 | 2 | 0.0005 | 0.02 |
ITGB1,PXN,CDC42,PAK1,NRG2,ITGA1,DVL1,LAMA2,MAPK1,LAMA4,PSG1,MAPK8
PSD3,HLA-C,HLA-G,HLA-F,ARRB2,ERBB3,ASAP2,ASAP1,ASAP3,SNF8,AP2M1,GIT1,PARD6B,KDR,RABEP1,PIP4K2B,VPS37A,IL8RB,VPS37C,CDC42,BRD8,UNC45A,CXCR4,ADRB1,CHMP1B,IGF1R,HSPA2,SH3GLB1,IL2RG,EHD2,STAMBP,FAM125B,DNM3
ACTG1,DES,ACTN1,CACNB2,ITGB3,TCF7L2,ITGB1,ITGB7,CACNA2D1,TCF7,ITGA1,ITGA3,LAMA2,ITGA6,DSG2,ITGA8,ITGA7,DSC2
ACTG1,ILK,RAPGEF1,PIK3CG,BRAF,MAPK1,MAPK8,PXN,LAMB4,KDR,LAMA2,LAMA1,LAMA4,PTEN,CCND1,CAPN2,BIRC2,FYN,ACTN1,CAV2,ITGB3,ITGB1,DOCK1,ITGB7,ITGA1,ITGA3,ITGA6,ITGA8,ITGA7,CDC42,PAK1,IGF1R,PIK3R3,COL4A6
F12,F10,COL4A6,COL4A5,PROC,FGG,F5,FGA
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_BASAL_CELL_CARCINOMA | 55 | 16 | 2 | 0 | 0.0004 |
KEGG_WNT_SIGNALING_PATHWAY | 151 | 27 | 1.3 | 0 | 0.0021 |
KEGG_MELANOGENESIS | 102 | 20 | 1.4 | 0 | 0.0045 |
KEGG_PATHWAYS_IN_CANCER | 328 | 44 | 0.86 | 0.0001 | 0.0054 |
BIOCARTA_G1_PATHWAY | 28 | 9 | 2.1 | 0.0001 | 0.0066 |
WNT3A,WNT3,WNT10A,LEF1,SMO,WNT5A,TCF7L1,SUFU,FZD9,FZD4,FZD7,WNT2B,FZD6,WNT7B,FZD10,WNT7A
PPP2R5A,WNT3A,MMP7,WNT3,CUL1,WNT10A,WNT5A,DAAM2,RAC1,SMAD4,SFRP2,LEF1,CTNNBIP1,SUMO1,CCND1,TCF7L1,NFAT5,CSNK1A1,FZD9,GPI,FZD4,FZD7,WNT2B,FZD6,FZD10,WNT7B,WNT7A
ADCY3,ADCY5,WNT3A,WNT3,CREB3L1,CREB3L4,WNT10A,WNT5A,LEF1,TCF7L1,CALML3,CALML5,FZD9,FZD4,FZD7,FZD6,WNT2B,WNT7B,FZD10,WNT7A
WNT10A,MECOM,LAMC2,RAC1,FH,SMAD4,LAMA4,LAMA3,FGF8,NFKB1,TGFA,CCND1,SUFU,FZD9,FZD4,FZD7,FZD6,WNT7B,WNT7A,FGF19,WNT3A,TGFB3,FGF13,MMP1,WNT3,CDKN2B,CSF3R,STK4,WNT5A,ITGB1,ITGA2,BRCA2,CDKN1A,CDKN1B,HDAC1,ABL1,AKT3,LEF1,SMO,NCOA4,TCF7L1,MSH6,WNT2B,FZD10
TGFB3,CDKN2B,SMAD4,CCND1,CDKN1A,CDKN1B,DHFR,HDAC1,ABL1
Let genes with copy number alteration or mutation be query genes. Let marker genes of specific identified subtypes be query genes. The Enrichment is calculated as:
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Enrichment = log2 (# of query genes in the pathway/# No of query genes) - log2 (# of genes in the pathway/# of human genes)
The statistical signficance of the pathways that are enriched with genes with copy number alteration or mutation, and the pathways that are enriched with markers genes of specific identified subtypes is measured by P value.
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P value = Fisher exact P value
The Q value is for adjusting P value for multiple testing. A public available R package is used to calculate the Q value.
This is an experimental feature. The full results of the analysis summarized in this report can be downloaded from the TCGA Data Coordination Center.