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Table 3 Pathway Enrichment analysis

From: Evaluation of copy number variation and gene expression in neurofibromatosis type-1-associated malignant peripheral nerve sheath tumours

 

Pathway name

P value

Genes

Fold change (3 benign vs. 3 malignant)

Fold change (4 benign vs. 5 malignant

1

Glutathione metabolism

0.00056

GSTM1

−3.25

−2.27

GSTM2

−3.25

−2.27

GSTM4

−3.25

−2.27

2

Glutathione metabolism/human version

0.00059

GSTM1

−3.25

−2.27

GSTM2

−3.25

−2.27

GSTM4

−3.25

−2.27

3

Glutathione metabolism/rodent version

0.00073

GSTM1

−3.25

−2.27

GSTM2

−3.25

−2.27

GSTM4

−3.25

−2.27

4

Development: Wnt signalling pathway. Degradation of beta-catenin in the absence Wnt signalling

0.00106

CSNK1D

2.42

1.99

DAB2

3.46

2.65

5

Cell adhesion: PLAU signalling

0.00445

HGF

7.80

10.97

SERPINE1

5.74

4.54

6

Role of alpha-6/beta-4 integrins in carcinoma progression

0.00589

HGF

7.80

10.97

LIMK1

2.04

2.23

7

Development: TGF-beta-dependent induction of EMT via MAPK

0.00641

DAB2

3.46

2.65

SERPINE1

5.74

4.54

8

Transport: macropinocytosis regulation by growth factors

0.01130

HGF

7.80

10.97

LIMK1

2.04

2.23

9

Development: regulation of epithelial-to-mesenchymal transition (EMT)

0.01165

HGF

7.80

10.97

SERPINE1

5.74

4.54

10

Transport: clathrin-coated vesicle cycle

0.01421

PREB

1.45

1.43

DAB2

3.46

2.65

  1. The pathways were ranked by hypergeometric P values, and a summary of the top ten pathways is reported. The P value represents the probability that a gene set of this size would co-occur by chance alone. Network objects represent the ratio of the number of genes from the list compared to the total number of genes known to be associated with the pathway.