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. 2021 Sep 15;22(18):9970. doi: 10.3390/ijms22189970

Table 2.

The top two significant genes across five CRC relevant signalling pathways from the TCGA Legacy dataset. A Kaplan–Meier estimate and log-rank test were used to compute the association between patient event-free survival and gene expressions. The associated hazard ratio, 95% confidence interval, p-value, mafdr (estimate positive false discovery rate for multiple hypothesis testing), and standard error are apparent. “Patient” indicates the number of patients for which data were available. The last column, “significant”, indicates the number of significant genes out of the total number of genes for this pathway. The fold change and p-value cut-off used were 0.5 and 0.05, respectively.

Genes Hazard Ratio 95% Confidence
Interval
p-Value mafdr Standard
Error
Patient Significant
(1) WNT 53/119
DVL3 2.8158 (1.6159–4.9066) 2.58×104 1.37×102 0.2833 329
VANGL2 2.7692 (1.5039–5.0992) 1.08×103 1.40×102 0.3115 329
(2) PI3K-Akt 159/340
EFNA1 3.2860 (1.8496–5.8377) 4.96×105 9.92×105 0.2932 329
KRAS 0.2853 (0.1502–0.5418) 1.27×104 1.26×104 0.3272 329
(3) TP53 11/38
BCL2 0.4610 (0.2960–0.7179) 6.12×104 0.0012 0.2260 329
CDKN2A 1.8156 (1.1931–2.7629) 5.36×103 0.0054 0.2142 329
(4) MAPK 113/252
KRAS 0.2853 (0.1502–0.5418) 1.27×104 2.09×104 0.3272 329
CACNA1I 2.7685 (1.6159–4.7432) 2.10×104 2.09×104 0.2747 313
(5) TGF-Beta 53/135
TERT 2.8734 (1.6639–4.96201) 1.53×104 3.05×104 0.2787 328
TGFB1I1 2.2381 (1.3807–3.6281) 1.08×103 0.0011 0.2465 329