Fig. 3.
FGFR3 gene body hypomethylation and FGFR3 overexpression are characteristic for CN. A Clustering the methylation values of the FGFR3 locus of primary tumors and control tissue from Capper et al. 2018 revealed severe hypomethylation at the gene body as a distinct feature of CN. However, individual FGFR3 CpG sites, especially three sites denoted as CN specific in a previous study by Lee et al. 2024 showed high variance. FGFR3 methylation levels did not correspond to FGFR3 staining intensity. B-C FGFR3 staining intensity ranged from strong in 30/71 (42%) cases to intermediate in 41/71 (58%) cases. D FGFR3 immunohistochemistry often demonstrated a gradient effect with stronger staining intensity at the periphery with progressively weaker staining towards the center due to a fixation artifact. E Kaplan-Meier estimates did not show a significant PFS difference between cases with strong (+ +) and intermediate (+) staining intensity. F FGFR3 demethylation was consistent across primary and recurrent samples and did not show any association with sample material, the development of a recurrence, or age