In addition, given that cis-ATR is antiapoptotic, we hypothesize that cis-ATR may perform an oncogenic role, while Pin1 might be tumor suppressive in terms of ATR’s anti-apoptotic activity at the mitochondria. If cis-ATR is the dominant cytoplasmic form, it may block mitochondrial apoptosis and allow damaged cells to survive and mutate, even when DNA damage repair is insufficient and the abnormal cells are supposed to die via apoptosis. The gene discussed is ATR; the disease is neoplasm.