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. 2021 May 11;125(2):247–254. doi: 10.1038/s41416-021-01398-7

Fig. 3. Prostate cancer database expression data and patient microarray staining demonstrate significant EZH2 and NSD2 correlation within individual tumours and NSD2 and EZH2 expression predicts biochemical recurrence in PC.

Fig. 3

ac For individual tissue samples with expression for both enzymes available, mRNA expression values plotted for each marker. a TCGA (n = 491) consisting of hormone-sensitive primary PC. b MSKCC (n = 128) consisting of primary and metastatic PC samples. c SU2C (n = 270) consists of metastatic CRPC patients. RNA expression data were queried and downloaded using the cBioPortal platform. As sample distribution was found to be non-Gaussian, Spearman correlation coefficients were calculated. d, e Kaplan–Meier analysis performed using clinical outcome data available on cBioPortal for d TCGA (n = 498) and e MSKCC (n = 140). Progression-free time defined as time to biochemical recurrence as determined by PSA cut-offs. In each dataset, samples were assigned individual quartile rank for NSD2 and EZH2. Samples containing top quartile ranks for both NSD2 and EZH2 (n = 70; 21) were compared to all remaining samples in their respective cohorts (n = 428;119). P values are documented.