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. 2020 Dec 30;15(12):e0244558. doi: 10.1371/journal.pone.0244558

Table 4. Genomic covariate analysis of DACH1 mutated patients compared to wild-type at MCC (n = 65 patients).

Covariates DACH1
WT N = 53 M N = 12 Co-Occurrence P-valuea
PTEN (n = 40) 32/40 8/40 0.94
PIK3CA (n = 35) 26/35 9/35 0.191
TP53 (n = 31) 23/31 8/31 0.255
POLE Mutation (n = 28) 17/28 11/28 5.78E-04
MLH1 Mutation (n = 22) 12/22 10/22 2.39E-04
MSH2 Mutation (n = 25) 17/25 8/25 0.046
MSH6 Mutation (n = 28) 19/28 9/28 0.264
PMS2 Mutation (n = 12) 8/12 4/12 3.67E-07
Microsatellite Instability (n = 55) 0.1342b
 MSI-High (n = 7) 4/7 3/7
 Microsatellite Stable (n = 48) 40/48 8/48
Tumor Mutation Burden 6.02 24.0 4.29E-05c

a P-values were calculated using the Fisher’s exact test for categorical variables and using the student t-test for continuous variables. The co-occurrence analysis using Fisher’s exact test was performed to determine whether DACH1 mutations are mutually exclusive or tend to co-occur with other gene mutations.

b MSI data was only available for 11/12 DACH1 mutated patients and 44/53 of the DACH1 wild type patients.

c Tumor mutation burden p-value was calculated using the Wilcoxon rank sum test.