To develop more effective treatments for patients with HER2+ breast tumors, efforts have focused on the identification of genes that modify clinical response to trastuzumab including cyclin-dependent kinase inhibitor 1B (p27), phosphatase and tensin homolog (PTEN), insulin-like growth factor 1 receptor (IGF1R) and topoisomerase II α (TOP2A) [7-11]. Here, PTEN is linked to breast neoplasm.