PARP and CHK inhibitors interact to cause DNA damage and cell death in mammary carcinoma cells

摘要

The present studies examined viability and DNA damage levels in mammary carcinoma cells following PA RP1 and CHK1 inhibitor drug combination exposure. PA RP1 inhibitors [AZD2281; ABT888; NU1025; AG014699] interacted with CHK1 inhibitors [UCN-01; AZD7762; LY2603618] to kill mammary carcinoma cells. PA RP1 and CHK1 inhibitors interacted to increase both single strand and double strand DNA breaks that correlated with increased ?H2AX phosphorylation. Treatment of cells with CHK1 inhibitors increased the phosphorylation of CHK1 and ERK1/2. Knock down of ATM suppressed the drug-induced increases in CHK1 and ERK1/2 phosphorylation and enhanced tumor cell killing by PA RP1 and CHK1 inhibitors. Expression of dominant negative MEK1 enhanced drug-induced DNA damage whereas expression of activated MEK1 suppressed both the DNA damage response and tumor cell killing. Collectively our data demonstrate that PA RP1 and CHK1 inhibitors interact to kill mammary carcinoma cells and that increased DNA damage is a surrogate marker for the response of cells to this drug combination.