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 161 genes with significant mutation (Q value <= 0.1) and 454 genes with significant copy number alteration (Q value <= 0.25). The identified marker genes (Q value <= 0.01 or within top 2000) are 19 for subtype 1, 19 for subtype 2, 19 for subtype 3. Pathways significantly enriched with these genes (Q value <= 0.01) are identified :
3 pathways significantly enriched with genes with copy number alteration or mutation.
0 pathways significantly enriched with marker genes of gene expression subtype 1
2 pathways significantly enriched with marker genes of gene expression subtype 2
0 pathways significantly enriched with marker genes of gene expression subtype 3
Pathway | Nof Genes | Nof CNV_Mut | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_WNT_SIGNALING_PATHWAY | 151 | 16 | 1.9 | 0 | 0.0028 |
KEGG_PARKINSONS_DISEASE | 130 | 12 | 1.9 | 0.0001 | 0.0099 |
KEGG_COLORECTAL_CANCER | 62 | 9 | 2.3 | 0.0001 | 0.0099 |
KEGG_ENDOMETRIAL_CANCER | 52 | 8 | 2.4 | 0.0001 | 0.01 |
KEGG_OOCYTE_MEIOSIS | 114 | 11 | 1.7 | 0.0004 | 0.024 |
MAPK9,PPP2R5E,DVL2,DVL3,RHOA,PPP2R1B,SUMO1,PSEN1,PPP2CA,PPP2CB,PPP3CC,CHP,PPP3CA,FBXW11,APC,CSNK1A1
VDAC3,COX6A1,UQCRC1,PINK1,NDUFS5,CASP3,NDUFS4,CASP9,PARK7,SDHB,SDHD,SLC18A1
CASP3,CASP9,RHOA,BRAF,MAPK9,BCL2,APC,MSH3,RAF1
CASP9,ILK,EGFR,BRAF,CTNNA2,APC,RAF1,NRAS
CDC16,PPP1CC,PPP2R5E,PPP2R1B,PPP2CA,PPP2CB,PPP3CC,CHP,PPP3CA,FBXW11,RPS6KA1
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
BIOCARTA_RELA_PATHWAY | 16 | 0 | 0 | 1 | 1 |
BIOCARTA_NO1_PATHWAY | 31 | 0 | 0 | 1 | 1 |
BIOCARTA_CSK_PATHWAY | 24 | 0 | 0 | 1 | 1 |
BIOCARTA_AMI_PATHWAY | 20 | 0 | 0 | 1 | 1 |
BIOCARTA_ARAP_PATHWAY | 18 | 0 | 0 | 1 | 1 |
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_CELL_CYCLE | 128 | 18 | 2.9 | 0 | 0 |
KEGG_SYSTEMIC_LUPUS_ERYTHEMATOSUS | 140 | 11 | 2.1 | 0 | 0.0066 |
KEGG_HOMOLOGOUS_RECOMBINATION | 28 | 5 | 3.2 | 0.0002 | 0.021 |
BIOCARTA_MCM_PATHWAY | 18 | 4 | 3.5 | 0.0004 | 0.025 |
KEGG_OOCYTE_MEIOSIS | 114 | 9 | 2 | 0.0004 | 0.025 |
DBF4,TTK,CCNA2,MAD2L1,ORC6L,CDC20,CDC27,CDC45L,CDC6,CDC2,MCM4,CCND3,BUB1B,ORC2L,BUB3,CDC25C,CDC25A,CCNB2
H2AFZ,H2AFX,HIST1H2AD,HIST2H2AB,C7,C3,HIST1H2AG,HIST1H2AE,HIST1H2AI,HIST1H2AH,HIST1H2AL
BLM,SHFM1,ATRX,RAD51,RAD54B
CDC6,MCM4,ORC2L,ORC6L
AURKA,SGOL1,MAD2L1,FBXO5,CDC20,CDC27,CDC2,CDC25C,CCNB2
Pathway | Nof Genes | Nof Marker | Enrichment | P value | Q value |
---|---|---|---|---|---|
KEGG_FOCAL_ADHESION | 201 | 10 | 2.2 | 0.0001 | 0.014 |
KEGG_ECM_RECEPTOR_INTERACTION | 84 | 7 | 2.9 | 0 | 0.014 |
KEGG_PATHOGENIC_ESCHERICHIA_COLI_INFECTION | 59 | 5 | 3 | 0.0003 | 0.037 |
KEGG_TRYPTOPHAN_METABOLISM | 40 | 4 | 3.2 | 0.0008 | 0.069 |
KEGG_HYPERTROPHIC_CARDIOMYOPATHY_HCM | 85 | 5 | 2.4 | 0.0024 | 0.16 |
LAMC2,RAC2,SPP1,COL11A1,PARVB,COL6A3,COL6A1,COL1A1,ITGA2,ACTB
COL11A1,LAMC2,COL1A1,COL6A3,COL6A1,SPP1,ITGA2
TUBB6,NCK1,TUBA3C,TUBA3D,ACTB
AADAT,MAOA,INMT,ALDH1B1
TPM2,TPM4,ACTB,ITGA2,CACNA2D4
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:
-
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.
-
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.