Since the groundbreaking work of Sørlie T and colleagues (2, 3) at the beginning of the 21st century, BC has been believed to consist of at least four different clinically relevant molecular subtypes, Luminal A, Luminal B, HER2 enriched, and triple-negative, classified according to the expression of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and Ki-67. This evidence concerns the gene PGR and breast cancer.