Skip to main content
. Author manuscript; available in PMC: 2013 Aug 31.
Published in final edited form as: Oncogene. 2012 Oct 8;32(35):4120–4129. doi: 10.1038/onc.2012.423

Table 2. Subclassification of breast cancers studied and relationship with hDMP1 and p53 LOH.

All the breast cancer cases (n=104, enough information was not available in 6 cases) have been subclassified into luminal A, luminal B, HER2, triple-negative/basal type, and unclassified/normal-type based on the data from histochemical studies for ER, PR, HER2, Ki67, cytokeratin, and morphology of tumor cells as described in the Materials and Methods. The percentage of our breast cancer samples in each category was very close to those reported in the literature. hDMP1 LOH(+) breast cancers were significantly associated with luminal A category while p53 LOH(+) breast cancers were associated with non-luminal A subtype.

hDMP1 LOH(+) hDMP1 LOH(−) Pecentage p values
Luminal A 19 13 45.2 0.0085
Luminal B 8 15 19.0 0.5350
HER2 5 17 21.1 0.0573
Triple-negative 6 12 11.9 0.5026
Normal/unclassified 4 5 9.5 0.7951
Not evaluated 4 2
total 46 64
p53 LOH(+) p53 LOH(−) Pecentage p values
Luminal A 6 26 16.7 0.0234
Luminal B 8 15 22.2 0.9848
HER2 10 12 27.8 0.2288
Triple-negative 8 10 22.2 0.3342
Normal/unclassified 4 5 11.1 0.5546
Not evaluated 2 4
total 38 72
All cases Pecentage Reported percentage
Luminal A 32 29.1 28
Luminal B 23 20.9 19
HER2 22 20.0 17
Triple-negative 18 16.4 27
Normal/unclassified 9 8.2 8
unknown 6 5.4
total 110