Table 4 Top ranked canonical pathways from IPA after performing basic core analysis.

From: Longitudinal genome-wide DNA methylation changes in response to kidney failure replacement therapy

 

Canonical pathway title

p-value

Controls vs dialysis patients baseline

Protein ubiquitination pathway

3.8 × 10–10

Cell cycle: G1/S checkpoint regulation

2 × 10–6

Role of BRCA1 in DNA damage response

1.1 × 10–5

Cell cycle control of chromosomal replication

1.3 × 10–5

Cell cycle: G2/M DNA damage checkpoint regulation

4.1 × 10–5

RAR activation

8.1 × 10–5

Controls vs KTx patients baseline

Molecular mechanisms of cancer

1.3 × 10–13

Axonal guidance signalling

3.1 × 10–10

Integrin signalling

6.9 × 10–9

Fcγ receptor-mediated phagocytosis in macrophages and monocytes

1.5 × 10–8

Protein kinase A signalling

1.7 × 10–8

G-protein coupled receptor signalling

3 × 10–8

Controls vs dialysis patients 12 months

Cyclins and cell cycle regulation

1.6 × 10–7

Cell cycle: G1/S checkpoint regulation

3.5 × 10–7

Small cell lung cancer signalling

2.9 × 10–6

Prostate cancer signalling

2 × 10–5

Chronic myeloid leukemia signalling

5.5 × 10–5

Molecular mechanisms of cancer

1.3 × 10–4

Controls vs KTx patients 12 months

Integrin signalling

9.3 × 10–9

Molecular mechanisms of cancer

1 × 10–8

Paxillin signalling

1.4 × 10–7

Tec kinase signalling

6.5 × 10–7

T cell receptor signalling

9.4 × 10–7

Role of NFAT in regulation of the immune response

1.1 × 10–6

Controls vs alla

IGF-1 signalling

3.3 × 10–5

Rac signalling

5.5 × 10–5

STAT3 pathway

1.3 × 10–4

Breast cancer regulation by Stathmin1

1.7 × 10–4

PTEN signalling

1.7 × 10–4

  1. aGene affiliations from all CpG sites displaying statistically significant differentially methylation in patients versus controls at both time points were entered into the analysis (see main text for more information).