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 9 genes with significant mutation (Q value <= 0.1) and 503 genes with significant copy number alteration (Q value <= 0.25). The identified marker genes (Q value <= 0.01 or within top 2000) are 2000 for subtype 1, 2000 for subtype 2, 2000 for subtype 3. Pathways significantly enriched with these genes (Q value <= 0.01) are identified :
0 pathways significantly enriched with genes with copy number alteration or mutation.
4 pathways significantly enriched with marker genes of gene expression subtype 1
1 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_ENDOMETRIAL_CANCER | 52 | 8 | 2.6 | 0 | 0.012 |
BIOCARTA_CHEMICAL_PATHWAY | 22 | 5 | 3.2 | 0.0002 | 0.013 |
BIOCARTA_IGF1MTOR_PATHWAY | 20 | 5 | 3.4 | 0.0001 | 0.013 |
KEGG_NOTCH_SIGNALING_PATHWAY | 47 | 7 | 2.6 | 0.0001 | 0.013 |
KEGG_SPLICEOSOME | 126 | 10 | 1.8 | 0.0005 | 0.03 |
MLH1,PTEN,AKT1,CASP9,PIK3CD,TP53,GRB2,GSK3B
TP53,AKT1,CASP9,EIF2S1,PARP1
RPS6KB1,PTEN,AKT1,GSK3B,EIF2S1
NUMB,DLL1,SNW1,DVL1,NCSTN,NOTCH2,HDAC2
RBM8A,SLU7,SNRPE,CCDC12,CDC40,DHX8,SNW1,DDX5,EIF4A3,SYF2
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_SPLICEOSOME | 126 | 24 | 1.3 | 0 | 0.0029 |
KEGG_ENDOCYTOSIS | 183 | 33 | 1.1 | 0 | 0.0029 |
KEGG_CHEMOKINE_SIGNALING_PATHWAY | 190 | 33 | 0.99 | 0.0001 | 0.0042 |
KEGG_PATHWAYS_IN_CANCER | 328 | 48 | 0.74 | 0.0002 | 0.0095 |
KEGG_B_CELL_RECEPTOR_SIGNALING_PATHWAY | 75 | 16 | 1.3 | 0.0007 | 0.021 |
NCBP2,NCBP1,SNRPD2,CTNNBL1,DDX23,DHX38,U2AF1,SNRPA1,HNRNPU,SNRPB,HNRNPM,PRPF40A,PPIE,BUD31,PRPF6,SNRNP200,THOC2,PRPF38B,TRA2B,SF3B5,SF3B3,PRPF19,SF3A3,RBM17
DAB2,ITCH,PLD2,PSD4,HLA-E,HLA-G,ACAP1,FGFR4,FGFR3,ERBB4,ASAP1,ADRBK1,EGF,IQSEC3,KDR,GRK7,PARD6G,PIP4K2B,CLTA,VPS37A,BRD8,CXCR4,AGAP1,RAB11FIP5,SH3KBP1,KIT,SH3GLB2,SH3GLB1,VPS36,DNM3,CBL,AP2A1,ARAP2
ADCY3,ADCY4,FOXO3,GNG7,BRAF,NCF1,ROCK2,PIK3CD,ADRBK1,CX3CL1,RAC2,VAV1,CXCL14,CXCL13,GRK7,XCL2,NFKB1,PLCB3,CXCR4,RHOA,PLCB2,AKT3,LYN,GNB1,GNB4,CXCL2,GNG12,ENC1,SOS2,PIK3R1,STAT3,CCL17,JAK3
BRAF,RXRA,PIK3CD,LAMC1,LAMB2,RAC2,RAC3,BMP2,HGF,DVL1,LAMA4,MITF,SPI1,NFKB1,GLI1,MYC,CTBP2,KIT,SOS2,FZD1,STAT3,FGF18,TGFB3,FGF13,CDKN2B,RALB,STK4,EP300,HIF1A,TRAF2,FGFR3,RBX1,EGF,HDAC1,PLCG1,RHOA,TPR,AKT3,CDK6,RB1,DAPK1,CKS1B,TCF7L2,TPM3,PIK3R1,MSH2,CBL,HSP90B1
NFKB1,AKT3,LYN,PIK3CD,CARD11,CD72,RAC2,DAPP1,RASGRP3,RAC3,SOS2,CHP,PIK3R1,CR2,MALT1,VAV1
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_SPLICEOSOME | 126 | 24 | 1.3 | 0 | 0.0089 |
KEGG_GLYOXYLATE_AND_DICARBOXYLATE_METABOLISM | 16 | 6 | 2.1 | 0.0015 | 0.12 |
KEGG_ADHERENS_JUNCTION | 75 | 15 | 1.2 | 0.0012 | 0.12 |
KEGG_HUNTINGTONS_DISEASE | 183 | 27 | 0.86 | 0.0013 | 0.12 |
KEGG_LEUKOCYTE_TRANSENDOTHELIAL_MIGRATION | 118 | 20 | 0.98 | 0.002 | 0.13 |
LSM7,SNRPD2,SMNDC1,RBM8A,LSM5,U2AF1,SNRPB,HNRNPC,CCDC12,HSPA1L,HNRNPM,HNRNPK,DDX5,MAGOHB,PRPF3,SNRNP200,PRPF38B,TRA2B,SF3B3,PRPF19,SF3B1,DHX15,RBM25,RBM17
CS,MTHFD1L,HYI,GLYCTK,MTHFD1,PGPEP1
WASF2,CSNK2A2,EGFR,PTPRM,ACTN4,CTNNA2,EP300,CTNND1,ACP1,TCF7L2,PVRL4,YES1,CREBBP,CSNK2B,TJP1
TBP,COX5A,COX5B,CREB3L3,TAF4B,POLR2J2,EP300,COX6B2,HIP1,NDUFA4L2,CREBBP,COX8A,HDAC1,CLTB,UQCRC1,UQCRQ,SLC25A5,CYCS,COX4I2,COX4I1,POLR2J,ATP5G1,DNAH2,NDUFA9,CREB1,SOD1,AP2A2
ACTN4,ROCK2,CTNNA2,MYL5,GNAI2,ITGB1,PTK2,ITGA4,CLDN7,CXCR4,ESAM,MSN,CLDN2,CTNND1,CLDN10,CLDN11,VCAM1,EZR,PTK2B,MAPK14
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_HEMATOPOIETIC_CELL_LINEAGE | 88 | 24 | 1.7 | 0 | 0 |
KEGG_CELL_CYCLE | 128 | 28 | 1.3 | 0 | 0.0003 |
KEGG_PATHOGENIC_ESCHERICHIA_COLI_INFECTION | 59 | 17 | 1.8 | 0 | 0.0003 |
BIOCARTA_MCM_PATHWAY | 18 | 9 | 2.5 | 0 | 0.0005 |
KEGG_NOD_LIKE_RECEPTOR_SIGNALING_PATHWAY | 62 | 16 | 1.5 | 0.0001 | 0.0039 |
GYPA,CD44,IL4R,CSF3R,CD3G,IL11RA,CD36,IL1R2,CSF2,CSF1,KIT,ITGAM,CD9,FCGR1A,CD2,CD4,CD5,CD7,IL6,IL2RA,ITGA3,CD19,ITGA5,CD14
PTTG2,TGFB1,CCNA2,ESPL1,SKP1,ORC1L,ANAPC13,SMAD4,CDC20,CDC26,MAD1L1,CDC14A,CDC14B,CCNE1,CDC45L,CDC7,CDC6,CDC2,MCM2,MCM4,MCM5,MCM6,CDC25C,YWHAE,CDC25B,CCNB1,CCNB2,ORC3L
OCLN,TLR5,CTNNB1,RHOA,TUBB6,TUBA1A,TUBA1B,TUBB3,LY96,WAS,ARPC1B,WASL,ARPC5,ARPC2,TUBA3C,TUBA3D,CD14
CDC6,MCM2,MCM4,MCM5,ORC1L,MCM6,CDT1,CCNE1,ORC3L
CASP5,NLRC4,NOD2,CASP8,HSP90AA1,MAPK8,CCL5,PYDC1,PYCARD,PSTPIP1,TRAF6,IL6,CARD9,BIRC3,HSP90B1,TRIP6
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.