- Open Access
The combination of olaparib and camptothecin for effective radiosensitization
© Miura et al.; licensee BioMed Central Ltd. 2012
- Received: 17 October 2011
- Accepted: 2 April 2012
- Published: 23 April 2012
Poly (ADP-ribose) polymerase-1 (PARP-1) is a key enzyme involved in the repair of radiation-induced single-strand DNA breaks. PARP inhibitors such as olaparib (KU-0059436, AZD-2281) enhance tumor sensitivity to radiation and to topoisomerase I inhibitors like camptothecin (CPT). Olaparib is an orally bioavailable inhibitor of PARP-1 and PARP-2 that has been tested in multiple clinical trials. The purpose of this study was to investigate the characteristics of the sensitizing effect of olaparib for radiation and CPT in order to support clinical application of this agent.
DLD-1 cells (a human colorectal cancer cell line) and H1299 cells (a non-small cell lung cancer cell line) with differences of p53 gene status were used. The survival of these cells was determined by clonogenic assay after treatment with drugs and X-ray irradiation. The γH2AX focus formation assay was performed to examine the influence of olaparib on induction and repair of double-stranded DNA breaks after exposure to radiation or CPT.
A radiosensitizing effect of olaparib was seen even at 0.01 μM. Its radiosensitizing effect after exposure for 2 h was similar to that after 24 h. H1299 cells with depletion or mutation of p53 were more radioresistant than H1299 cells with wild-type p53. However, similar enhancement of radiosensitization by olaparib was observed with all of the tested cell lines regardless of the p53 status. Olaparib also sensitized cells to CPT. This sensitizing effect was seen at low concentrations of olaparib such as 0.01 μM, and its sensitizing effect was the same at both 0.01 μM and 1 μM. The combination of olaparib and CPT had a stronger radiosensitizing effect. The results of the γH2AX focus assay corresponded with the clonogenic assay findings.
Olaparib enhanced sensitivity to radiation and CPT at low concentrations and after relatively short exposure times such as 2 h. The radiosensitizing effect of olaprib was not dependent on the p53 status of tumor cells. These characteristics could be advantageous for clinical radiotherapy since tumor cells may be exposed to low concentrations of olaparib and/or may have different levels of p53 mutation. The combination of olaparib and CPT had a stronger radiosensitizing effect, indicating that combining a PARP inihibitor with a topoiomerase I inhibitor could be promising for clinical radiosensitization.
- PARP inihibitor
- Topoisomerase I inhibitor
DNA is the principal target for the biologic effects of radiation. For radiotherapy, this comprises single strand breaks (SSB) and double-strand breaks (DSB) . SSB are not directly cytotoxic but during DNA replication may generate potentially lethal DSB by collapse of stalled replication forks . Radiation-induced SSB are primarily repaired by base excision repair , of which poly (ADP-ribose) polymerase-1 (PARP-1) is a key component. PARP-1 binds to SSB, activating poly ADP-ribosylation of itself and other proteins, triggering recruitment of repair factors and release of PARP-1 from the damaged site . PARP inhibitors inhibit SSB repair and the unrepaired SSB generate collapsed replication forks which give rise to potentially lethal DSB, leading to radiosensitization . Topoisomerase I poisons such as camptothecin (CPT) exert their cytotoxic effects by binding to and stabilizing the DNA helicase enzyme topoisomerase I. This enzyme plays a vital role in facilitating unwinding of the DNA double helix during DNA replication to relieve torsional strain. The mechanism involves temporary insertion of DNA breaks to allow unwinding, and an intermediate DNA/protein structure termed the ‘cleavable complex’ is generated. Topoisomerase I poisons stabilize the cleavable complex and extend the lifetime of the associated DNA strand breaks. PARP-1 is involved in the resolution of these DNA breaks, so inhibition of PARP activity increases the yield of unrepaired DNA damage and consequent cell death .
Olaparib (KU-0059436, AZD-2281) is an orally bioavailable inhibitor of PARP-1 and PARP-2 and a phase 1 trial using olaparib has been reported . The purpose of this study was to examine characteristics of sensitizing effects of olaparib to radiation and a topoisomerase I inhibitor, CPT for clinical application of olaparib.
We found that olaparib sensitized cells to radiation and also CPT, even at low concentrations such as 0.01 μM. The radiosensitizing effect of olaparib at exposure for 2 h was similar as for 24 h. These characteristics can be advantageous in radiotherapy since tumor cells may have low concentrations of olaparib due to the limited ability of drugs to penetrate tumor tissue. We also examined the radiosensitizing effects of the combined use of olaparib and CPT.
[Drugs, cells and cell culture]
Olaparib was obtained from JS Research Chemicals Trading (Germany). CPT was obtained from Sigma Chemical Company. DLD-1 is a human colorectal carcinoma cell line. H1299 is a p53-null non-small lung carcinoma cell line. H1299 cells were transfected with pCMV-Bam-Neo vector (neo) alone (as a control) and with wild-type p53 (wt) or mutated p53 gene [8, 9]. H1299/mp143 (m143), H1299/mp175 (m175), and H1299/mp248 (m248) were made with transfection of mutated p53 gene into codon 143, 175, 248 of H1299 cells, respectively. To determine whether p53 mRNA and the protein were stably expressed in these transfectants, we analyzed the reverse transcriptase-polymerase chain reaction restriction fragment length polymorphism on the sequence of transfected codon of the p53 gene for the mRNA. We also performed Western blot analysis for the protein. H1299 (wt, m248, m175, m143, neo) cells were cultured in MEM medium supplemented with 10% fetal calf serum. DLD-1 was cultured in RPMI-1640 medium supplemented with 10% fetal calf serum. All these cell lines were cultured at 37°C.
[Cell culture and clonogenic assay]
The survival of these cells after various treatments such as drug treatment and X-ray irradiation was determined as their colony-forming ability. The time between plating cells and treatments such as radiation and/or drug exposure was 24 h. Experiments were repeated three times. Mean values and standard error of the mean were expressed. We tested the significance at the p < 0.05 for our observations. The X-ray dose-survival curves were fitted to the linear quadratic equation, survival fraction = exp (−αD-βD2), where D is the X-ray dose. D37, the X-ray dose giving 37% survival was calculated from the fitted linear quadratic equation. Enhancement ratio was calculated as the D37 of untreated cells divided by that of treated cells. Since CPT have the cell killing effects, we excluded their cell killing effects in the calculation of enhancement ratio. We made the hypothetical survival curve in which the value of survival fraction was 1 at 0 Gy in the combined treatment of CPT and radiation.
[γH2AX focus assay]
Mouse monoclonal anti-γH2AX (Upstate, NY, USA) antibody and rabbit polyclonal anti- Rad51 (Oncogene, CA, USA) antibody were used. DLD-1 cells were exposed to olaparib (1 μM) for 8 h and/or CPT (0.01 μM) for 6 h. Since CPT has the cell killing effect, we used the shorter exposure time in CPT than olaparib. When cells were irradiated, 4 Gy of radiation was performed after 4 h exposure of olaparib and/or 2 h exposure of CPT. Then, cells were applied on slide glass at 24 h after irradiation. Cells diluted to appropriate numbers were grown on a glass slide and fixed with cold methanol for 20 min, rinsed with cold acetone for 10 seconds, and then air-dried. Above mentioned antibodies to γH2AX or Rad51 were used as the primary antibody. Alexa-546-conjugated anti-mouse IgG (Molecular Probes) were used for visualization of γH2AX and Rad51. Slides were mounted with antifade reagent (Mounting medium, DAKO). Foci were observed with an Olympus fluorescent microscope under 10 × 100 oil immersion. For quantification of foci, clear and easily distinguished dots of certain brightness were counted as positive foci. The number of foci was counted in 100 cells of sample each time point by visual inspection and average number of foci per cell was calculated. Cells that had 5 or more of Rad51 were considered as Rad51 positive.
For estimation of the distribution of cells in different phases of the cell cycle, FACS-analysis of cells stained with propidium iodide (PI) was performed. Harvested cells were fixed in 70% of ethanol and stored at 4°C until analysis. Fixed cells were washed once in PBS, incubated with PBS supplemented with RNase A (0.25 mg/ml) for 30 min at 37°C and stained in a PI-containing solution (50 μg PI/ml in PBS) for 10 min at 4°C. The cells were analyzed on a flowcytometer (FACS Calibur, Becton Dickinson, USA).
[Radiosensitizing effect of olaparib at various exposure times and concentrations]
Additional file 1 shows the relationship between the olaparib concentration and its radiosensitizing effect on DLD-1 cells. These cells were treated with 4 Gy of radiation and were exposed to various concentrations of olaparib for 1 h before irradiation and 24 h after irradiation. Additional file 2 shows the relationship between the olaparib exposure time and its radiosensitizing effect on DLD-1 cells. The results displayed in Additional file 1 and Additional file 2 correspond with those shown in Figure 1a and 1b. Cells were treated with 4 Gy of radiation and were exposed to 1 μM olaparib for 1 h before irradiation and various times after irradiation. In these experiments, a radiation dose of 4 Gy was used since it killed more cells than 2 Gy, and the difference between various treatments was clearer at 4 Gy.
Olaparib did not decrease plating efficiency at any of the exposure times or concentrations examined in this study.
[Radiosensitizing effect of olaparib on human cancer cells with different p53 statuses]
We examined whether the p53 status of tumor cells influenced the enhancement of radiosensitivity by olaparib. To assess the influence of p53 status, we used five human lung cancer cell lines with identical genotypes except for p53 (wt, m143, m175, m248, and neo) and found that wt cells were significantly more radiosensitive than m143 and neo cells (p < 0.01). Conversely, m143 cells were significantly more radioresistant than m248 and wt cells (p < 0.01). These results indicated that the p53 status influenced the radiosensitivity of H1299 cell lines.
Radiation enhancement ratio by olaparib
[Sensitization to CPT by olaparib]
We also examined the influence of the concentration of olaparib on its sensitizing effect, especially in regard to low concentrations (Figure 2b). A sensitizing effect was evident at only 0.01 μM and the strength of the sensitizing effect was the same at both 0.05 μM and 1 μM.
[Radiosensitization with olaparib plus CPT]
As shown in Figure 3b, the surviving fraction of cells exposed to CPT at 0 Gy of irradiation has been adjusted to 1. It can be seen that the combination of olaparib and CPT had the strongest effect since olaparib increased sensitivity to both radiation and CPT. The enhancement ratio (D37) for 0.1 μM olaparib and CPT was 1.37, while that for 1 μM olaparib and CPT was 1.45. In addition, the enhancement ratio (D37) for 1 μM olaparib alone was 1.20 and that for CPT alone was 1.33.
[γH2AX focus formation assay after irradiation or CPT]
Figure 4a shows the γH2AX and Rad51 foci in untreated DLD-1 cells, cells treated with irradiation (IR), and cells treated with CPT. Figure 4b presents the results for cells with Rad51 foci. There was no significant difference between the control cells (Ola-, CPT-, IR-) and cells treated with olaparib (Ola+, CPT-, IR-), suggesting that olaparib alone did not induce DSB. Cells treated with radiation (Ola-, CPT-, IR+) had significantly more foci than control cells (Ola-, CPT-, IR-) as did cells treated with CPT (Ola-, CPT+, IR-), indicating that radiation or CPT induced DSB. Cells exposed to radiation combined with olaparib (Ola+, CPT-, IR+) had significantly more foci than cells treated with radiation alone (Ola-, CPT-, IR+). In addition, cells exposed to CPT combined with olaparib (Ola+, CPT+, IR-) showed significantly more foci than cells treated with CPT alone (Ola-, CPT+, IR-), revealing that olaparib enhanced the induction of DSB by radiation or CPT. Cells exposed to radiation combined with olaparib (Ola+, CPT-, IR+) had a similar number of foci as cells exposed to radiation combined with CPT (Ola-, CPT+, IR+), showing that olaparib and CPT caused similar enhancement of the induction of DSB by radiation. Cells exposed to radiation combined with olaparib and CPT (Ola+, CPT+, IR+) had the most foci among all of the treatment groups.
Figure 4c presents the results for cells without Rad51 foci. The findings are similar to those shown in Figure 4b. However, the enhancement of radiation-induced DSB by olaparib and/or CPT was less marked in cells without Rad51 foci than in cells with Rad51 foci. There was no significant difference between radiation combined with olaparib (Ola+, CPT-, IR+) and radiation alone (Ola-, CPT-, IR+) in cells without Rad51 foci.
[Effects of olaparib, CPT and radiation on the cell cycle]
Figure 4d shows the cell cycle after the same treatments as Figure 4b and c. There was no difference between the control cells (Ola-, CPT-, IR-) and cells treated with olaparib (Ola+, CPT-, IR-), indicating that olaparib alone did not change cell cycle distributions. Cells treated with radiation (Ola-, CPT-, IR+) or CPT (Ola-, CPT+, IR-) tended to have more S phase cells than the control cells (Ola-, CPT-, IR-). Radiation and olaparib (Ola+, CPT-, IR+) had the similar cell cycle distribution to radiation alone (Ola-, CPT-, IR+). In contrast, cells treated with CPT and olaparib (Ola+, CPT+, IR-) tended to have reduced S phase cells, compared with CPT alone (Ola-, CPT+, IR-). Cells treated with olaparib, CPT and radiation (Ola+, CPT+, IR+) had increased G2/M phase cells and reduced S phase cells, compared with the other treatments.
PARP inhibitors such as olaparib increase sensitivity to radiation and to topoisomerase I inhibitors such as CPT . The concentration of olaparib tested in previous studies was 0.5 or 1 μM [5, 11]. In a clinical study, the plasma concentration of olaparib reached 11.5 μM (5 μg/ml) after oral administration of 100 or 200 mg, which are doses that do not cause dose-limiting toxicity . The present findings support the clinical usefulness of olaparib at oral doses of 100 to 200 mg. However, the ability of drugs to penetrate tumor tissue in vivo is often limited, so that some tumor cells may not be exposed to effective concentrations . Therefore, it is possible that tumor cells may be exposed to much lower olaparib concentrations than 0.5 or 1 μM. For this reason, we examined the sensitizing effect of olaparib for radiation and CPT at very low concentrations.
Figure 1a demonstrates the relationship between the olaparib concentration and its radiosensitizing effect on DLD-1 cells. Although the radiosensitizing effect of olaparib showed a concentration-dependent increase, low concentrations (such as 0.01 μM) still had a radiosensitizing effect, indicating that effective radiosensitization achieved even for tumor cells exposed to low concentrations of this agent.
We also examined the relationship between the exposure time and the radiosensitizing effect of olaparib. Figure 1b demonstrates that the radiosensitizing effect of olaparib after exposure for 2 h was similar to that at 24 h, demonstrating that effective radiosensitization could be achieved even for tumor cells with a short exposure time. Olaparib enhances radiosensitivity by inhibiting the repair of SSB. Unrepaired SSB lead to collapse of replication forks that give rise to potentially lethal DSB, leading to radiosensitization . Thus, SSB are converted to DSB during replication after exposure to olaparib . Longer incubation times than 2 h after irradiation might be required to convert SSB to DSB since the cell cycle of DLD1 cells lasts for 24 h or longer. However, we found that 2 h of incubation with olaparib after irradiation is sufficient for radiosensitization and that exposure to this agent throughout the entire period of SSB repair is not necessary to enhance the generation of DSB.
In order to test the potential clinical value of olaparib, we also examined whether the p53 status of tumor cells influenced the enhancement of radiosensitization using five human lung cancer cell lines with identical genotypes except for p53 (wt, m143, m175, m248, and neo). We found that H1299 cells with depletion or mutation of p53 were more radioresistant than H1299 cells with wild-type p53, showing that p53 status influenced the radiosensitivity of these cell lines. There have been conflicting reports concerning the relationship between p53 status and radiosensitivity. Some authors have reported that p53 gene mutation decreases radiosensitivity , while others have reported an increase of radiosensitivity  or no correlation with radiosensitivity . Because p53 regulates multiple aspects of the cell cycle, DNA repair, and apoptosis after irradiation , this protein not only determines cell death but also cell survival. Accordingly, cells with various p53 statuses could be more radiosensitive or radioresistant . In the present study, the surviving fraction was reduced by exposure to olaparib for all of the cell lines tested with various p53 statuses. Enhancement of radiosensitization was similar for all of the cell lines regardless of p53 status (Table 1), indicating that the radiosensitizing effect of olaparib is independent of p53.
Next, we investigated the effect of olaparib on sensitivity to CPT. Figure 2a shows the relationship between the olaparib concentration and its CPT-sensitizing effect. Olaparib sensitized cells to the cytotoxic effect of CPT, even at a CPT concentration of only 0.005 μM. The combination of olaparib with CPT significantly reduced the surviving fraction over the range of CPT concentrations from 0.005 to 0.02 μM. We also examined the relationship between the sensitizing effect of olaparib and its concentration, especially at low concentrations (Figure 2b). A sensitizing effect was still apparent at a concentration of 0.01 μM and the effect seen at this level was similar to that obtained at 1 μM.
We then investigated the combined effects of olaparib, CPT, and radiation. Figure 3a displays the surviving fraction of DLD-1 cells after treatment with olaparib and/or CPT. The combination of radiation with olaparib or CPT significantly increased the lethal effect of radiation (p < 0.01), except when olaparib was combined with 2 Gy. The cytotoxic effect of olaparib, CPT, and radiation all together was much greater than that of radiation alone.
In order to compare the radiosensitizing effect of CPT with that of olaparib, we adjusted the surviving fraction at 0 Gy to 1 in Figure 3b, since CPT itself had a cytotoxic effect. Then we assessed the radiosensitivity of DLD-1 cells after treatment with olaparib or CPT. The radiosensitizing effect of 1 μM olaparib was similar to that of CPT at 4 Gy and greater than that of CPT at 6 and 8 Gy (p < 0.01). Since olaparib increased sensitivity to both radiation and CPT, the combination of olaparib and CPT had the strongest radiosensitizing effect. The enhancement ratio (D37) of olaparib plus CPT was larger than that for either olaparib alone or CPT alone. Thus, combination therapy with PARP inhibitors and topoisomerase I inhibitors may be a promising strategy for enhancing the effects of radiotherapy.
After DSB are induced by irradiation or cytotoxic drugs, H2AX is rapidly phosphorylated and there is always a constant number or percentage of γH2AX formed per DSB. Therefore, γH2AX is a sensitive and early indicator of DSB in vitro and in vivo. Furthermore, residual γH2AX at 24 h after irradiation can be used to assess the radiosensitivity of cells or their ability to recover from damage and the efficiency of the cellular repair process . Accordingly, we investigated residual γH2AX foci after exposure of cells to radiation, olaparib, and CPT. Olaparib alone did not increase γH2AX foci, while radiation or CPT did so. Radiation combined with olaparib and CPT produced the most foci among all of the treatment groups. These findings agreed with the results of clonogenic assays, suggesting that the sensitizing effect of olaparib for radiation or CPT is related to induction of DSB or to inhibiting the repair of DSB. We also used radiation-induced Rad51 foci to investigate the cell cycle dependence of γH2AX focus formation after various treatments. We found that enhancement of radiation-induced DSB by olaparib and CPT was greater in cells with Rad51 foci than in cells without Rad51 foci, indicating that olaparib had a stronger effect on the induction of DSB by radiation or CPT in the S and G2/M phases than in the G1 phase.
Figure 4d shows the cell cycle after the treatments with olaparib, CPT, or radiation.
Olaparib alone did not change cell cycle distributions. Cells treated with radiation or CPT had more S phase cells than the control cells, corresponding to that radiation  or CPT  arrests or delays cell cycle progression during the S phase. Cells treated with CPT and olaparib had less S phase cells than CPT alone. This might suggest that olaparib enhances the S phase specific cell killing effect of CPT . The combination of olaparib, CPT and radiation reduced S phase and increased G2/M phase. This effect might result from S phase specific cell killing with CPT and G2/M arrest with radiation.
Olaparib enhanced the sensitivity of radiation and CPT, even at low concentrations, such as 0.01 μM. The radiosensitizing effects of olaparib at exposure for 2 h had the similar as for 24 h. The radiosensitizing effect of olaprib did not depend on p53 status. These characteristics can be advantageous in clinical radiotherapy since tumor cells may have low concentrations of olaparib and/or p53 mutation. The combination of olaparib and CPT had the good radiosensitizing effects, indicating that the combination of PARP inhibitor and topoiomerase I inhibitor can be promising as a method of clinical radiosensitization.
The research were supported in part by a Grant-in Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan and by a grant from program for developing the supporting system for upgrading the education and research in Sapporo Medical University.
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