Breast cancer is fairly heterogeneous; gene-expression profiling of breast cancer revealed six intrinsic molecular subtypes: luminal A (estrogen receptor (ER)+, progesterone receptor (PR)+, human epidermal growth factor receptor 2 (HER2)−, and Ki67−), luminal B (ER+, PR+, HER+/−, and Ki67+), HER2+, basal-like subtype (ER−, PR−, and HER2−), normal breast-like, and claudin-low (low expression of cellular adhesion genes) [5,6,7]. Here, MKI67 is linked to breast carcinoma.