GAPDH suppressed cell apoptosis and prevented oxidative DNA damage via Ape1 endonuclease. WT or GAPDH-overexpressing R3 SMCs were transfected with GAPDH-targeted siRNA (A, B), Ape1-targeted siRNA (C, D), or with control (scrambled) siRNA, and cells were exposed to 110 μM H2O2 for 16 h. Cell death was measured with Cell Death ELISA (A, C), and AP site number was quantified by OxiSelect Oxidative DNA damage ELISA (B, D). Data from a representative experiment are shown. Each experiment was repeated at least 3 times. NS, not significant. *P < 0.05, ¶P < 0.01, §P < 0.005, ¥P < 0.001.