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. Author manuscript; available in PMC: 2016 Mar 1.
Published in final edited form as: Prostate. 2014 Nov 18;75(4):360–369. doi: 10.1002/pros.22922

Figure 4.

Figure 4

Treatment with the Zn2+ chelator TPEN reduces viability for PC3 and C4-2 cells and TPEN cytotoxicity is completely reversed by exogenous Zn2+. (A) Reduced viability upon treatment with the indicated TPEN concentration. (B) Expanded scale differentiates sensitivity of PC3 and C4-2 cells to TPEN cytotoxic effects. (C) Rescue of TPEN cytotoxicity with exogenous ZnSO4 at the indicated concentration relative to TPEN (6 μM) and with the delay indicated. (D) NaPy but not DTPA displays rapid effects. Treatments were as indicated in Figure 1 except for 6 h followed by 72 h in drug-free media. Statistical significance, Student’s two-tailed test: *: p<0.05. (E,F) FluoZin fluorescence for PC3 cells: (E) Control (non-treated cells); (F) Treatment with TPEN (5 μM for 4 h) with identical settings as in (E).