Abstract
BACKGROUND/AIM: Methionine restriction selectively arrests cancer cells during the S-phase of the cell cycle. We hypothesized that DNA damage may occur in S-phase in cancer cells during methionine restriction. To determine if this occurs, we used MiaPaCa-2(Tet-On) 53BP1-green fluorescent protein (GFP) pancreatic cancer cells, which report GFP fluorescence in real time after DNA-damage response (DDR) in these cells. We also determined whether a chemotherapy drug in combination with methionine restriction increases the rate of DNA damage. MATERIALS AND METHODS: MiaPaCa-2(Tet-On) 53BP1-GFP cells were used for in vitro experiments. The 25% and 50% inhibitory concentrations (IC(25) and IC(50), respectively) of recombinant methioninase (rMETase) and paclitaxel on MiaPaCa-2(Tet-On) 53BP1-GFP pancreatic cancer cells were determined. Cell viability and DDR with rMETase alone, paclitaxel alone, and their combination were measured in MiaPaCa-2(Tet-On) 53BP1-GFP cells. RESULTS: The IC(25) of rMETase on MiaPaCa-2(Tet-On) 53BP1-GFP cells was 1.66 U/ml. The IC(25) for paclitaxel on MiaPaCa-2(Tet-On) 53BP1-GFP cells was 3.31 nM. The combination of rMETase and paclitaxel synergistically reduced the viability of MiaPaCa-2(Tet-On) 53BP1-GFP cells. The IC(50) of paclitacel on MiaPaCa-2(Tet-On) 53BP1-GFP cells was 5.1 nM. The IC(50) of rMETase on MiaPaCa-2(Tet-On) 53BP1-GFP cells was 2.3 U/ml. The combination of rMETase (IC(50)) plus paclitaxel (IC(50)) on MiaPaCa-2(Tet-On) 53BP1-GFP cells also caused more DNA damage than either agent alone. CONCLUSION: The present study suggests the synergy of methionine restriction and chemotherapy is due, at least in part, to DNA damage of cancer cells.