Table 4.
Proteins | Mutation type | n (%) | Fisher exact test p-value (vs. sporadics) | Fisher exact test p-value (BRCA1 vs. BRCA2) |
Nuclear CTSL >0 | BRCA1 mutation (−4) | 12 (85.7) | 0.0001 | 0.10 |
BRCA2 mutation (−1) | 7 (53.8) | 0.13 | ||
53BP1 <150 | BRCA1 mutation (−1) | 2 (11.8) | 0.0019 | 0.0001 |
BRCA2 mutation (−1) | 11 (84.6) | 0.0210 | ||
Nuclear VDR <120 | BRCA1 mutation (−1) | 3 (16.7) | 0.0027 | 0.0051 |
BRCA2 mutation (−1) | 8 (72.7) | 0.35 |
Values denote the absolute (n) and the relative (%) frequencies of BRCA1- or BRCA2-related tumors with Hscore values above (nuclear CTSL) or below (nuclear 53BP1 and VDR) the median Hscore values for each protein in sporadic breast tumors. Bolded p-values highlight the statistically significant difference measured by Fisher exact test comparing a molecular subtype with either the overall population of sporadic breast cancer or between tumors with BRCA1 versus BRCA2 germline mutations.