At the onset of the 21st century, the classification of breast tumors into distinct molecular subtypes (luminal, HER2, or triple-negative breast cancer (TNBC)), based on the expression of hormone receptors for estrogen (ER) and progesterone (PR), and amplification of the HER2 oncogene, has changed the paradigm and oriented clinical decisions [59,60]. This evidence concerns the gene ERBB2 and triple-negative breast carcinoma.