Fig. 3From: RAD51 is a poor prognostic marker and a potential therapeutic target for oral squamous cell carcinomaB02 significantly enhanced cytotoxicity of cisplatin in both OECM1 EV cells and RAD51 OE cells. (A) XTT assay in OECM1 EV and OECM1 RAD51 OE cells at 48 h after B02 treatment. B02 decreased cell viability both in control and RAD51 OE cells, (B) XTT assay in OECM1 EV and OECM1 RAD51 OE cells at 72 h after B02 treatment, (C) XTT assay in OECM1 EV cells at 48 h after cisplatin treatment with/without B02 and B02 enhanced cytotoxicity of cisplatin, (D) XTT assay in OECM1 EV cells at 72 h after cisplatin treatment with/without B02 and B02 enhanced cytotoxicity of cisplatin, (E) XTT assay in OECM1 RAD51 OE cells at 48 h after cisplatin treatment with/without B02 and B02 enhanced cytotoxicity of cisplatin, (F) XTT assay in OECM1 RAD51 OE cells at 72 h after cisplatin treatment with/without B02 and B02 enhanced cytotoxicity of cisplatinOECM1 EV, control; OECM1 RAD51 OE, overexpression; *, P < 0.05; **, P < 0.01; ***, P < 0.001Back to article page