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. 2020 Jan 7;11:52. doi: 10.1038/s41467-019-13950-4

Fig. 6. BENSpm and MTDIA impact patient samples in ex vivo system.

Fig. 6

Ex vivo samples were collected from treatment naïve patients undergoing radical prostatectomy at Roswell Park Comprehensive Cancer Center. Tumors used for this study had at least 40% neoplastic involvement upon pathological review. Tumor samples were treated with vehicle control (vehicle), or combination treatment (1 nM MTDIA + 1 µM BENSpm or 10 nM MTDIA + 10 µM BENSpm) for 7 days in the presence of 20 µM MTA. Images from representative tumors 3, 8, and 10 from immunohistochemical stained slides for a cleaved caspase-3 (CC3) or b spermidine/spermine N1-acetyltransferase (SSAT) in both vehicle and the combination treated samples (B + M. Intratumoral (c) spermidine (Vehicle; n = 13, 1 + 1 BM; n = 13, and 10 + 10 BM; n = 7), d spermine (Vehicle; n = 12, 1 + 1 BM; n = 12, and 10 + 10 BM; n = 9), and e spermidine + spermine (Vehicle; n = 11, 1 + 1 BM; n = 11, and 10 + 10 BM; n = 9) levels normalized to protein concentrations for vehicle and combination (B + M) treated tumor samples. f The correlation between the change in SSAT IHC Score and the change in total spermidine + spermine levels measured by UPLC in the combination treated samples (n = 12). Pearson’s r values are indicated. Statistical analysis for polyamines was done using a paired t-test. *p < 0.05.