In our current study we aimed to further investigate the correlation between these nuclear protein markers either expressed throughout (Ki67, MCM2), from post G1 (Cyclin A) or in M-phase (PHH3) of the cell cycle and the routinely examined clinicopathological factors of breast cancers undergoing PST (i.e. histological type, tumor grade, cTNM stage, biological behavior and tumor subtypes). This evidence concerns the gene MKI67 and neoplasm.