Since increased FGF3/4/19 copy number is frequently detected and highly related to the initiation and progression of many tumors including urothelial carcinoma, multiple myeloma, prostate cancer, and hepatocellular carcinoma (Xie et al., 2020), we believe that our finding will also benefit other anti-cancer therapies targeting FGF3/4/19 variated tumors. The gene discussed is FGF3; the disease is prostate cancer.