The oncogenic function of mutp53 is mainly caused by altered structure and properties of mutp53 to bind with other oncogenic (e.g., Ets2, SREBPs, vitamin D receptor, NF-Y, AMPK) or tumor suppressive (e.g., TP63, TP73, Mre11) proteins [7,9,10,11,12,13,14]. Here, TP73 is linked to neoplasm.