In the present study we investigated the
protein expression of
claudins 1, 3, and 4 and their relationship to clinical variables and outcome in a cohort of ER-ve and ER+ve human invasive breast
cancers. Immunohistochemical analysis was performed on tissue microarrays representing a total of 412
tumors and interpretable data was derived from 314, 299, and 306
tumors for
claudins 1, 3, and 4, respectively. In the ER+ve subset, 5%, 89%, and 52%, and in the ER-ve subset, 39%, 79%, and 79% of
tumors stained positively for
claudins 1, 3, and 4, respectively (p < 0.0001, p = 0.026, p < 0.0001). Thus, in the two subsets, a significantly higher number of
tumors were positive for
claudins 3 and 4, compared to
claudin 1. In addition,
protein expressions of
claudins 1 and 4 were significantly higher in those
tumors that displayed characteristics of the basal-like subtype of breast
cancers (ER-ve, Her-2-ve, EGFR+ve, CK5/6+ve). This study shows a unique pattern of expression for the different
claudins in ER-ve and ER+ve
tumors. Our data also suggests that increased expression of
claudins 1 and 4 was associated with the basal-like subtype of breast
cancers, a subtype generally linked to poor outcome.