- Research article
- Open Access
Purine Nucleoside Phosphorylase mediated molecular chemotherapy and conventional chemotherapy: A tangible union against chemoresistant cancer
BMC Cancer volume 11, Article number: 368 (2011)
Late stage Ovarian Cancer is essentially incurable primarily due to late diagnosis and its inherent heterogeneity. Single agent treatments are inadequate and generally lead to severe side effects at therapeutic doses. It is crucial to develop clinically relevant novel combination regimens involving synergistic modalities that target a wider repertoire of cells and lead to lowered individual doses. Stemming from this premise, this is the first report of two- and three-way synergies between Adenovirus-mediated Purine Nucleoside Phosphorylase based gene directed enzyme prodrug therapy (PNP-GDEPT), docetaxel and/or carboplatin in multidrug-resistant ovarian cancer cells.
The effects of PNP-GDEPT on different cellular processes were determined using Shotgun Proteomics analyses. The in vitro cell growth inhibition in differentially treated drug resistant human ovarian cancer cell lines was established using a cell-viability assay. The extent of synergy, additivity, or antagonism between treatments was evaluated using CalcuSyn statistical analyses. The involvement of apoptosis and implicated proteins in effects of different treatments was established using flow cytometry based detection of M30 (an early marker of apoptosis), cell cycle analyses and finally western blot based analyses.
Efficacy of the trimodal treatment was significantly greater than that achieved with bimodal- or individual treatments with potential for 10-50 fold dose reduction compared to that required for individual treatments. Of note was the marked enhancement in apoptosis that specifically accompanied the combinations that included PNP-GDEPT and accordingly correlated with a shift in the expression of anti- and pro-apoptotic proteins. PNP-GDEPT mediated enhancement of apoptosis was reinforced by cell cycle analyses. Proteomic analyses of PNP-GDEPT treated cells indicated a dowregulation of proteins involved in oncogenesis or cancer drug resistance in treated cells with accompanying upregulation of apoptotic- and tumour- suppressor proteins.
Inclusion of PNP-GDEPT in regular chemotherapy regimens can lead to significant enhancement of the cancer cell susceptibility to the combined treatment. Overall, these data will underpin the development of regimens that can benefit patients with late stage ovarian cancer leading to significantly improved efficacy and increased quality of life.
With the limitations of current monotherapies against the heterogeneity of cancer, the concept of combining new and traditional therapies to increase efficacy and lower side effects is generating significant clinical interest. Cancer targeted molecular chemotherapy, engendered by locally administered Gene Directed Enzyme Prodrug Therapy (GDEPT) provides a potent strategy for treating both local and metastatic disease [1, 2]., Combining GDEPT with conventional chemotherapy has the potential to increase treatment efficacy and is highly relevant clinically, given that the patients being enrolled in new trials often present with late stage cancer having failed previous chemotherapy . Such combinations are of particular relevance for ovarian cancer patients, most of whom present with late stage disease. With the current treatment option for these patients of platinum chemotherapy (cisplatin and carboplatin), only 20-30% of patients display 5-year survival  due to the development of chemo-resistant disease. Although combining platinum therapy with taxanes (paclitaxel, docetaxel) improves efficacy and survival, the development of the chemo-resistant phenotype remains an issue . Overall, combination treatments that are effective in platinum resistant or platinum sensitive patients are needed. Thus, we have evaluated the prospective synergies between Purine Nucleoside Phosphorylase (PNP) mediated GDEPT and chemotherapeutics, docetaxel and carboplatin in multidrug resistant ovarian cancer cells. PNP-GDEPT uses the E. coli enzyme, PNP, that can convert systemically administered, FDA approved pro-drug, Fludarabine Phosphate (Fludara), into active toxic metabolites (2-Fluoroadenine (2FA) . Particular advantages of using PNP-GDEPT include (1) its potential to kill both dividing and quiescent cells through 2FA incorporation into RNA and DNA [7, 8]; (2) the potency of "local bystander" cell killing effects due to passive, gap-junction independent diffusion of toxic metabolites to surrounding cells ; a strong bystander effect is seen even when only 1 in 100-1000 cells express the PNP transgene  and (3) PNP-GDEPT mediated regression of non-transduced cancer cells at distant sites, namely, 'distant bystander effect' in immunocompetent mouse models . Preclinically, activity of PNP-GDEPT against cancer (prostate, ovarian, melanoma, colon carcinoma, hepatocellular carcinoma and human glioma) has been proven [10, 12] "(reviewed in )" and its advantages over HSV/tk GDEPT have been shown [13, 14]. E. coli PNP has a different active site and substrate binding features from its mammalian counterpart ensuring its clinical relevance . However, the potential application of PNP-GDEPT for treating ovarian cancer remains relatively unexplored, with only one preclinical study being described .
Carboplatin displays similar efficacy to cisplatin but is better tolerated and in combination with paclitaxel has become the standard of care for ovarian cancer patients [16, 17]. However, this treatment can result in cumulative neurotoxicity and myelosupression which may limit further treatment of these patients. In this study, an alternative to paclitaxel, docetaxel, was investigated based on 1) its activity against relapsed ovarian cancer [18, 19] providing symptomatic and survival benefits to responsive patients , 2) lower neuropathy and hypersensitivity  and 3) its synergistic interactions with carboplatin in ovarian cancer cells . Though, docetaxel/carboplatin combination displayed good therapeutic outcome with relatively lower neuropathy, toxicities leading to grade 3-4 neutropenia and other neutropenic complications have been described [22, 23].
We report here the synergistic activity of Adenovirus (Ad)-mediated PNP-GDEPT and docetaxel and/or carboplatin against platinum resistant ovarian cancer cells in vitro. To attain a molecular insight into PNP-GDEPT actions and interactions, the protein profile of treated ovarian cancer cells was generated. The involvement of cellular apoptosis genes/proteins in the cytotoxicity of different treatments was assessed given their reported correlations with therapeutic toxicity [24, 25]. We anticipate that these data will form a basis for the development of future combination regimens involving PNP-GDEPT in the clinic.
Docetaxel (Commercial name: Taxotere) (Aventis, Pharmaceuticals Inc, NJ), Carboplatin (Pfizer, NSW, Australia) and Fludarabine Phosphate (Fludara), (Schering-Plough, Germany) were used. Antibodies to Bcl-2, Bik, Bax, Survivin, Caspase-7/9 and PARP were used (source, Additional file 1(Table S1).
2.2 Cell lines
Ovarian cancer cell lines were maintained either in Dulbecco's Modified Eagle Medium (DMEM) or Roswell Park Memorial Institute medium-1640 (RPMI) media supplemented with 10% foetal calf serum (FCS), 50 U/mL Penicillin and 50 μg/mL Streptomycin (GIBCO/Invitrogen, VIC, Australia) at 37°C, 5% CO2, in a humidified incubator.
2.3 Viral vectors
Replication defective Ad vectors expressing either Green Fluorescent Protein (AdGFP) or PNP gene (AdPNP) under the control of cytomegalovirus (CMV) promoter were constructed (PNP or GFP genes are cloned in the E1 region of Ad5 genome), propagated and titrated in accordance with the instructions from the AdEasy™ adenoviral vector kit (Stratagene, TX, USA).
2.4 Assessment of gene expression of Ad-vector transduced ovarian cancer cells
Cells (24 well plates) infected with Ad-vectors at different multiplicities of infection (moi, plaque forming units (pfu)/cell) were assessed for gene expression at 48 h post infection (pi). GFP: For AdGFP infected cells, the GFP expression was determined by flow-cytometry using CellQuest™ (Version 3.0) software (Becton Dickinson, San Jose, CA). PNP: That the toxic effects of the PNP gene are only possible in the presence of Fludara has been shown unequivocally (with appropriate controls) in our previous studies and thus, is an acceptable measure of PNP activity [11, 26]. PNP activity, as determined by the enzymic assay, is accompanied by viral dose dependent ability of the prodrug, Fludara, to kill the transduced cells. The conversion of Fludara to its toxic metabolites by PNP in infected cells was shown by high performance liquid chromatography. Hence in this study, expression of PNP (same as used in our previous studies) in AdPNP infected cells was determined by assessment of cell killing in the presence of the prodrug, Fludara, given 48 h post infection using cell viability assays; after 3 to 7 days of incubation with the prodrug a colorimetric assay using the REDOX (4-[3-(4-Iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1, 3-benzene Disulfonate (WST-1) dye (Takara Pty Ltd. Otsu Shiga, Japan) was used. At relevant times, cells were incubated in media containing WST-1 (10: 1) for 2 h and the absorbance measured at 450 nm (Tecan Sunrise, Phoenix Research Products, USA).
2.5 Assessment of cytoxicity of docetaxel and/or carboplatin to ovarian cancer cells
Cells treated with different concentrations of docetaxel and/or carboplatin were assessed for cell viability using WST-1 assay at different times (see 2.4).
2.6 Evaluation of efficacy of combination of PNP-GDEPT with docetaxel and/or carboplatin
For synergy experiments, cells (plated in triplicate in 96 well plates, also see Additional file 2 (information, A1) were infected with either AdPNP or AdGFP. After 48 h, virus-containing media were replaced with Fludara and/or docetaxel and/or carboplatin containing media. The un-infected cells were treated with docetaxel and/or carboplatin. After 3 -5 days, cell viabilities were assessed by WST-1 assay.
2.6.1 Clonogenic assays to assess cytotoxicity of different treatments
Three days after combination or individual treatments, cells were re-plated in six-well plates. After 6-9 doublings (~2-3 weeks), cell colonies (≥ 50 cells) were stained with crystal violet (0.5% in absolute methanol) and counted.
2.6.2 Evaluation of therapeutic interactions between modalities
The therapeutic interactions between docetaxel, carboplatin and PNP-GDEPT were analysed using the CalcuSyn software (Biosoft, Cambridge, United Kingdom) developed by Chou and Talalay [27, 28] that allows statistical evaluation of interactions between 2 or more drugs. This methodology is based on the median effect equation correlating drug and its effects and is used to derive an accurate value of relative potencies of different drugs (e.g. IC50 etc). The median effect plot (based on the logarithmic form of Chou's median effect equation) forms the basis of quantification of synergism, summation and antagonism of drug combinations: log (fraction affected/fraction unaffected) vs. log (Dose). A value called Combination Index (CI) is generated that helps quantify the interactions for mutually exclusive and non-exclusive drugs (1983) : A CI < 0.9 implies synergism (> expected additive effect), CI = 0.90-1.10 implies additive and a CI > 1.10 shows antagonism (< expected additive effect) between drugs. Generation of a clinically significant value, 'Dose Reduction Index' (DRI) allows prediction of the fold reduction in individual modality dose when used in combination in comparison to when used alone .
2.7 Assessment of apoptosis in response to different treatments
Treated or untreated cells were analysed for apoptosis using the M30 CytoDEATH™assay kit (Additional file 1(Table S1) for source), based on binding of an antibody to a Caspase-cleaved epitope of cytokeratin 18-cytoskelatal protein in apoptotic cells and not in viable or necrotic cells (Peviva AB, Bromma, Sweden). Briefly, cells (1 × 105) (24 well plate) given PNP-GDEPT and/or docetaxel and/or carboplatin for 48 h were fixed in methanol (-20°C for 30 minutes), washed twice (PBS with 0.1% Tween 20 (PBST) and incubated with 100 μL of M30 CytoDEATH™ (1:100 dilution) or isotype control IgG2b (1:125) antibodies in incubation buffer (PBS with1% bovine serum albumin and 0.1% Tween 20). After a wash in PBST, cells were incubated for 1 h (4°C) with 100 μL of the fluorescein-labelled secondary antibody (FITC 1:70) (Silenus, Melbourne, Australia) and then analysed by flow cytometry (FlowJo Version 7.2.2 (Tree Star, Inc., CA).
2.8 Cell-cycle analysis of treated cells
Subconfluent OVCAR-3 cell cultures treated with different treatments were harvested at the indicated time points (0.025% EDTA), washed in ice-cold PBS and fixed using ice-cold ethanol at 4°C for 30 minutes. After two washes in PBS, cellular DNA was stained with propidium iodide solution (50 μg/mL propidium iodide, 0.1 mg/mL RNase A and 0.25% Tween 20 in PBS) for 1 h at 37°C. The percentage of cells in the G0/G1, S and G2/M phases was assessed using flow cytometry.
2.9 Protein expression by Western blot analyses
Proteins in cell lysates (50 μg) from variably treated cells were resolved on 10% polyacrylamide gel by SDS-PAGE and then blotted on to nitrocellulose membranes . The blots were incubated overnight in the relevant primary antibody at concentration recommended by the manufacturer (source, Additional file 1 (Table S1) followed by 1 h incubation with secondary antibody (anti-rabbit IgG Horse Radish Peroxidase (HRP) conjugated, 1:1000 or anti-mouse IgG HRP, 1:5000 (source, Additional file 1 (Table S1). The proteins were detected using an enhanced chemiluminescence (ECL) kit (Piercenet, Il, USA); treated membranes were exposed to X-ray film from 1-60 min (as required)-and developed using standard protocols. The protein bands were quantified from these films by densitometry using Quantity One software (Bio-Rad, Hercules, CA).
2.10 Analysis of PNP-GDEPT treated samples by shot gun proteomics
Untreated OVCAR-3 cells and those treated with PNP-GDEPT (AdPNP at the moi of 10 pfu/cell for 48 hours and then incubation with Fludara at 1 μg/mL (2.7 μM) were lysed (3 cycles of freeze thawing) and cell lysates (50 μg protein) were resolved by SDS-PAGE using 10% polyacrylamide gel. After Coomassie blue staining (G-250 stain, Bio-Rad, NSW, Australia), from each lane ~ 10-20 gel pieces were excised and peptides extracted (trypsin digest) were processed as described  (Mass Spectrometry Unit, UNSW, Sydney, Australia). The digested peptides were separated using HPLC (Ultimate 3000 HPLC and autosampler system, Amsterdam, Netherlands), concentrated and desalted and then subjected to mass spectrometry (MS) (LTQ FT Ultra (Thermo Electron, Bremen, Germany).
2.10.1 Protein identification after mass spectrometry
Peptides and proteins in different samples were identified from extracted tandem mass spectra and peak lists were generated using Mascot Daemon/extract_msn (Matrix Science, London, England, Thermo) using the default parameters submitted to the database search program Mascot (version 2.1, Matrix Science). They were identified through searches on non-redundant NCBI protein database (September 2008, see Additional file 2 (information A2 for details of search parameters and hit criteria). Scaffold (version Scaffold_2.02.01, Proteome Software Inc., Portland, OR) was used to validate MS/MS based peptide and protein identifications (http://www.proteomesoftware.com/index.html). For statistical analyses, datasets (hit values based on scaffold analyses) representing PNP-GDEPT treated and un-treated samples were normalised by square root transformations; log2 transformation was carried out and the data plotted as treated vs. un-treated (data not shown). Subsequently, ratios of log2-transformed data of both samples were obtained to assess up or downregulated proteins. At 95% confidence interval, values of 232.9632 ± 123.8158 were considered significant.
To explore the potential synergies between PNP-GDEPT, docetaxel and carboplatin, ovarian cancer cell lines representing the most common, adenocarcinoma of epithelial OC, with variable levels of sensitivity to platinum drug treatment were selected (Additional file 3 (Table S2) Based on preliminary evaluations, plating densities that resulted in logarithmic growth at day 7 (maximum duration of our experiments) were used. This avoided potential cell death due to over-confluence/contact-inhibition of control treated cells prior to the termination of our experiments. In a 96 well format, the optimal numbers of cells/well were 7000 (OVCAR-3), 3000 (SKOV-3), 10,000 (A-2780 and 9,000 (Caov-3) (data not shown).
3.1 Efficiency of Ad-transduction in different ovarian cancer cell lines
Before evaluating the AdPNP-GDEPT, the permissivity of ovarian cancer cell lines to Ad transductions was evaluated by assessing the efficiency of Ad/CMV/GFP transductions in different cell types at 48 h post infection. This showed a variable level of Ad5-uptake (Figure 1A). At the moi of 100 pfu/cell, OVCAR-3 cells were the most permissive (% GFP expressing cells ± SEM: 80 ± 5) followed by A-2780 (15 ± 4) and SKOV-3 cells (12 ± 4). A highly permissive, lung cancer cell line, A-549, was used as a positive control. Overall, OVCAR-3 cells displayed the highest Ad-permissivity at all Ad/CMV/GFP-doses tested, whilst, Caov-3 cells were almost Ad-refractory with only 3% GFP expressing cells at the high moi of 500 pfu/cell.
3.2 Bystander effects of PNP-GDEPT correlate with the efficiency of gene transduction
Evaluation of AdPNP-GDEPT (Fludara: 1 μg/mL (~2.7 μM) in infected cells showed a dose dependent increase in cytotoxicity which correlated with the Ad-permissivity of cell lines (Figure 1B). The toxic effects (% cell death compared to untreated controls ± SEM) were maximal in OVCAR-3 cells (50% ± 5 at moi of 4 pfu/cell) followed by SKOV-3 (25% ± 5 at moi of 100 pfu/cell) and A-2780 (15% ± 7 at moi of 100 pfu/cell) with no effect in Ad-refractory Caov-3 cells. This was also reflected in the IC50 values (± SEM) [calculated as moi of AdPNP for 50% cytotoxicity]. Interestingly, the 'bystander effects' also correlated with the Ad-permissivity of cells; in highly permissive OVCAR-3 cells, a significant level of cell inhibition was observed at low viral doses of 1 or 2 moi and up to 90-100% cell growth inhibition was noted when only 12% (at moi of 10, Figure 1A) of cells expressed PNP. Whilst this differed from a previous report  that as low as 1% infection was required to kill all cells, the differences may be due to the expression system used, and the use of different cell lines.
3.3 Proteins implicated in actions of Ad-PNP GDEPT in ovarian cancer cells
An insight into the molecular changes underlying the cytotoxic effects of PNP-GDEPT may help to understand its interactions with other modalities. Shot-gun proteomics analyses were performed on proteins resolved by SDS-PAGE using cell lysates from untreated and treated (AdPNP at moi of 10 pfu/cell plus 2.7 μM Fludara) platinum-resistant OVCAR-3 cells (see section 2.10). From these, a list of up- and down-regulated proteins was generated (Tables 1 & 2); (Note: for description and potential roles of these proteins, see Additional file 4 (Tables S3 and S4). Normalisation of data showed symmetrical distribution, suggesting the similarity of the relative abundance of most proteins in both samples; however, clearly distinctive data points representing potentially unique or differentially abundant proteins were obvious. The stringency of analyses and the low level variation between the two data sets suggested the reliability of these data. Ratio values of treated to untreated cells (range 7925-26529, P < 0.01) indicated clear upregulation of 16 proteins, to levels significantly higher than those predicted for 99% confidence (232.9632 ± 163.636). The abundant expression of E. coli PNP, only in PNP-GDEPT treated samples (Scores: 26239 [treated] vs. none [untreated]) provided evidence of its production in Ad/CMV/PNP infected samples. Although, modulated expression of several proteins was seen, only those present in only one sample and which may have a potential role in cancer progression or apoptosis, are listed.
Overall, PNP-GDEPT treatment lead to general down-regulation of proteins involved in (1) cellular metabolism (lipid, amino acid, carbohydrate and glycolysis) (e.g. polymerase (RNA) II (DNA directed), dihydrolipoamide S-succinyltransferase (E2 component of 2-oxo-glutarate complex), ribosomal protein L4, mitochondrial trifunctional protein), (2) oncogenesis or cancer progression (cadherin, desmoplakin, plakoglobin, karyopherin, spondin, agrin, GTP binding protein and cadherin 6) and (3) drug resistance (antiquitin and epoxide hydrolase). An upregulation of proteins involved in apoptosis, tumour suppression Poly (ADP-ribose) polymerase (PARP) and dead box polypeptide 3) and general DNA synthesis was noted.
3.4 Effects of docetaxel or carboplatin treatment on ovarian cancer cell lines
Growth inhibitory effects of docetaxel against all four ovarian cancer cells lines at different times were variable and dose and time dependent (Figures 2A, and Additional files 5 and 6 (Figure S1 & Table S5). Overall, A-2780 cells were the most sensitive followed by SKOV-3-, OVCAR-3- and Caov-3 cells. SKOV-3 and OVCAR-3 cells were chosen for the following experiments based on their mid-range sensitivity to docetaxel, variable Ad-permissivity and platinum resistance. This allowed us to test the synergies in different scenarios in cisplatin resistant ovarian cancer cells, which would be especially relevant for patients resistant to platinum treatment. The IC50 values for docetaxel (Figure 2A) showed SKOV-3 cells (0.31 nM ± 0.7; R2:0.96) (Figure 2) to be more docetaxel-sensitive compared to the OVCAR-3 cells (0.61 nM ± 1.1; R2:0.99).
Use of cisplatin resistant lines would be particularly relevant to studies involving carboplatin, given its efficacy against cisplatin resistant ovarian cancer . Using a range commonly used in other studies (IC50 range ~5 μM-35 μM , carboplatin efficacy was found to be dose dependent (Figure 2B). However, only a slight difference in the carboplatin sensitivity (IC50) was noted (OVCAR-3: 43.12 μM ± 6; R2:0.97 and SKOV-3: 38.73 μM ± 4; R2: 0.96) (Figure 2B).
3.5 PNP-GDEPT, docetaxel and/or carboplatin act synergistically in ovarian cancer cells in vitro
Cell viability (WST-1-based) evaluations of the cells treated with the combinations including docetaxel plus carboplatin, docetaxel plus PNP-GDEPT, carboplatin plus PNP-GDEPT and combination of all three, in general, showed a significant, dose dependent inhibition of cell growth (Additional file 7 (Figure A2) An assessment of interactions between modalities through CalcuSyn analysis [27, 28] (see methods for details) of cell viability data generated Combination Index-Fraction affected (CI-Fa) plots. These data showed that at the combination ratio (based on potency) of 1:1, the combined efficacy was additive for the docetaxel/carboplatin combination (Figure 3A and Table 3) (CI:0.89 at IC50 dose; R value 0.99), synergistic when PNP-GDEPT was combined with either docetaxel (Figure 3B and Table 3) (CI: 0.21 at IC50; R value 0.93) or carboplatin (Figure 3C and Table 3) (CI:0.28 at IC50; R value 0.96) and strongly synergistic when all three were combined (Figure 3D and Table 3) (CI:0.11 at IC50; R value 0.94). Statistical analyses further revealed the "Dose reduction Index (DRI)" values for each modality in combination to achieve a specific effect for the two cell lines (Additional file 8 (Table S6). In comparison to the individual doses, a dose reduction of up to ~20 fold for PNP-GDEPT, ~27 fold for docetaxel and ~31 fold for carboplatin was predicted to generate 50% cell killing when used in trimodal combination. In addition to evaluation of combinations at the ratio of 1:1, effects were also evaluated at other ratios e.g. 1:2, 2:1, 1:4 (Additional file 9 (Table S7, CI values). Overall, the trends were similar to those obtained when drugs were combined at 1:1 ratio with some variations. To assess whether the drug interactions lead to long term efficacy, clonogenic assays were performed comparing the effects of trimodal therapy with single treatments. Given the fact that carboplatin+docetaxel is the standard treatment for ovarian cancer patients, long term efficacy of the trimodal combination would have direct relevance to the clinic. Treatment of OVCAR-3 cells with, docetaxel (0.6 nM) or carboplatin (40 μM) or PNP-GDEPT (AdPNP at moi of 4 pfu/cell plus 2.7 μM Fludara) alone reduced the number of colonies to ~42%A, 36% and 22% respectively, compared with untreated controls (Figure 4A), whilst the combination of all three reduced colony growth to 2.3%+/-1.3% (13+/-7 cells vs. 560) (Figure 4A). This is slightly greater than an additive effect which would have yielded 3% (0.42 × 0.36 × 0.22 = 0.03) of the controls (17+/-13 cells compared to 560). Within the experimental errors of a clonogenic assay, where it is difficult to accurately assess clonal numbers especially in the untreated cells and due to other factors such as low plating efficiency, colony size and cancer heterogeneity, these results indicate an improvement over additive effects. Thus, though the trends are clear, statistical significance could not be achieved and the final confirmation of the potential of these combinations can only be drawn from exhaustive in vivo evaluations. While, these experiments were beyond the scope of this specific study, in another study, we have shown that our in vitro findings comparing synergistic responses of prostate cancer cells to PNP-GDEPT with docetaxel (including long term effects as evaluated by clonogenic assays) were supported by the in vivo outcomes (Singh et al, Clin Cancer Res. 2011, In press).
3.6 Evaluation of apoptosis in ovarian cancer cells after different treatments
For these assessments, time points beyond 48 h were not included as then the significant cellular toxicity (apoptosis/cell death) observed with combination regimens could potentially obscure the molecular responses to different treatments . Evaluation of apoptosis in SKOV-3 cells treated with docetaxel (1.5 nM), carboplatin (20 μM) and PNP-GDEPT (AdPNP moi: 150 pfu/cell, 2.7 μMFludara) (doses showing best efficacy) either alone or in combination showed that the numbers of apoptotic cells increased in a time dependent manner in tri-combination treated cells (Figure 4B). The percentage of M30 positive cells (a marker of early apoptosis) was maximal in tri-combination treated cells (49 ± 7) followed by bi-modal (docetaxel/carboplatin (17 ± 5), docetaxel/GDEPT (23 ± 6), carboplatin/GDEPT (31 ± 5), and then individual treatments (PNP-GDEPT (11 ± 4), docetaxel (14 ± 4), carboplatin (16 ± 6). As anticipated, apoptosis achieved in Fludara only treated cells was low (1.5 ± 1), In contrast, when the Fludara was converted by PNP as in cells treated with the combinations including PNP-GDEPT, there was a relatively higher number of apoptotic cells irrespective of the duration of the treatment.
3.7 Effects of different treatments on cell cycle in treated cells
Cell cycle analyses of OVCAR-3 cells treated for 48 h with docetaxel (0.6 nM), carboplatin (10 μM) and PNP-GDEPT (AdPNP moi: 10 pfu/cell, 1 μg/mL(2.7 μM) Fludara) either alone or in combination showed a decline in percentage of cells in G1 phase (20-35%) relative to controls, irrespective of the treatments applied (Figure 4C). As expected [35, 36] carboplatin (G2/M: 33% ± 9) and docetaxel (G2/M: 43% ± 8) treatments led to an increase in G2/M populations. The percentage of apoptotic cells (sub-G1phase) for different treatments was maximal in tri-combination treated cells (37% ± 6) followed by bi-modal (carboplatin/docetaxel (28% ± 6) < PNP-GDEPT/docetaxel (32% ± 6) < PNP-GDEPT/carboplatin (34% ± 7) and then least in single agent treated cells (carboplatin (9% ± 3) < docetaxel (12% ± 6) < PNP-GDEPT (20% ± 5) with negligible apoptosis in control treated cells. As with M30 analysis, the percentage apoptosis was greater when treatments included PNP-GDEPT. Results were statistically significant when combination treatment was compared with single treatment or control treatment (P ≤ 0.05).
3.8 Treatment related effects on pro- and anti-apoptotic proteins
Mutations in pathways involved in apoptosis modulate their responses to therapy (e.g. chemoresistance) [reviewed in . Apoptosis involves initiation (apoptotic stimulus, e.g., chemotherapeutic or biological agent), effector and execution phases (which decide the fate of the cell) . Thus, relative expressions of protein members representing effector phase [Bcl-2, Bik, Bax, Inhibitor of apoptosis (survivin) and execution phase (caspase-7/9, PARP) were evaluated in the treated cells (Figure 5A & 5B) (See Additional file 10 (Table S8) for their correlation with ovarian cancer outcomes). A significant but variable down-regulation of anti-apoptotic genes/proteins (Bcl-2) and up-regulation of pro-apoptotic genes (Bax, Bik and Bok) was achieved when modalities were combined, especially when PNP-GDEPT was included (Figure 5, Additional file 11 (Table S9). Their expression was relatively little affected by either carboplatin or docetaxel used alone or together. Survivin was down-regulated by all combination treatments. Evaluation of PARP (cleaved and un-cleaved) expression in differentially treated cells showed the upregulation of un-cleaved (especially 116 kDa band) and cleaved PARP in response to all treatments; this was even more in the case with combination treatments, and highest when PNP-GDEPT was involved. As Caspase-mediated proteolysis of PARP is a biochemical marker of apoptosis that denotes the final stages of apoptosis leading to DNA fragmentation , this indicates that cell killing was occurring in the treated cells.
This study is the first demonstration of potential synergistic anti-tumour interactions between PNP-GDEPT based molecular chemotherapy with docetaxel and carboplatin in cisplatin-resistant ovarian cancer cells. The data are significant given that the ovarian cancer cell lines tested represented subtypes of the epithelial adenocarcinomas encountered in over 80% of patients. Synergy evaluations in complex biological systems such as cells grown in culture can be affected by biological variability, desired dose levels, experimental conditions, such as, temperature, oxygen tension, pH and finally whether synergy is treatment schedule dependent or combination ratio dependent . To address the differences between measurement units of PNP-GDEPT and chemotherapeutic drugs, the combination ratios were based on the potency of the individual components (i.e. doses to achieve a particular effect e.g. IC50). We minimised the variability and error in data interpretation by evaluating IC50 values in each experiment for individual modalities and evaluating potential synergy using the well-recognized Chou and Talalay's statistical analyses (CalcuSyn software). For simplicity, mutual exclusivity of the component drugs was assumed, as recommended when more than two drugs are involved [27, 40].
The efficiency of docetaxel and carboplatin against the chosen ovarian cancer cell lines correlated with preclinical and clinical reports [21, 33]. The use of PNP-GDEPT to treat ovarian cancer has been reported in only one study; this was against SKOV-3 cells/tumours, although, the prodrug, 6-methylpurine-2'-deoxyriboside (MePdR), which is yet to be FDA approved, was used . Our in vitro data correlated with their outcomes. The use of FDA approved Fludara in our study yields a greater clinical relevance to our findings.
A synergy between modalities means greater efficacy than the two added together. Synergy between PNP-GDEPT and docetaxel and/or carboplatin has important clinical implications; in particular, the ability to use lower doses of each modality should translate in the clinic to decreased side effects and an improved quality of life. An estimation of clinically relevant Dose Reduction Indices made using the CalcuSyn software (Additional file 8 (Table S6) indicated that significant lowering of individual doses when used in combination is possible. This is especially relevant when PNP-GDEPT is given to patients who have had prior- or are undergoing chemotherapy with docetaxel and/or carboplatin treatment. Dose reduction of docetaxel (ranging from ~4-45 fold and carboplatin (from 3-56 fold) was predicted in the trimodal combination with PNP-GDEPT in the multidrug resistant ovarian cancer cells under study. Given the toxicities associated with high dosing of carboplatin or docetaxel alone and in combination [41, 42], these are valuable outcomes especially, for treating patients with drug refractory cancer. A decrease in therapeutic doses of PNP-GDEPT could also lower the total Fludara required; this is important given its potential immunosuppressive effects. The data obtained in this study warrant further confirmation in vivo. However, we have previously ratified the in vitro synergy found between PNP-GDEPT and docetaxel treatment against prostate cancer cells by in vivo studies, where a decrease in tumour load both in the prostate and at distant sites in immunocompetent mice was achieved [Singh P et al, 2011, In press, Clin Can Res]. Although, synergies were undeniably proven using combinations in multiple ratios, an assessment of sequential administration of different treatments was not done. Further exploration of treatments given in tandem may lead to better synergies; it has been indicated that a tumour containing both wild-type p53 cells as well as p53 mutants could be treated with platinum followed by a taxane. In such a tumour, platinum would first eradicate the wild-type p53 cells after which the taxane would kill those with mutant p53 .
Synergies between AdPNP-GDEPT and docetaxel could be partly explained by mutual enhancement stimulated by Ad transduction and docetaxel [44, 45]. However, interactions between PNP/Fludara and docetaxel or those between carboplatin and AdPNP-GDEPT are not yet fully understood. Overall, it appears as though the levels of synergies vary between cell types and that trimodal therapy may not be as beneficial for some cell types as expected (e.g. in SKOV-3 cells, bimodal + PNP-GDEPT was as effective as trimodal treatment). A better understanding of these interactions will help in the design of new regimens in cohorts who have undergone pre-existing treatment.
In an effort to understand these interactions, protein studies were performed. Apoptosis was shown to play a significant role in cell death triggered by combining two or three modalities (Figure 5). The most effective apoptotic stimulus (M30 positive cells, sub G1 phase) occurred when bimodal combinations involved PNP-GDEPT or tri-combination treatment was given, accordingly reflected in the cell killing observed in our studies. Interference with cell cycle through processes like DNA damage/microtubule-stabilisation initiates apoptosis. Both carboplatin and docetaxel led to an accumulation of cells in G2/M as shown previously [35, 36, 46]; combining them led to increased apoptosis (sub G0/G1 phase) suggesting irreversible DNA damage. This may explain the success of carboplatin/taxane combinations in the clinic although, long-term data on the development of the chemoresistant phenotype of ovarian cancers is as yet inadequate [22, 47]. Increasing involvement of pro-/anti-apoptotic proteins and caspases which generally regulate the effector phase of apoptosis was observed with multimodal treatments in accordance with the corresponding cell killing synergies. Overall, pro-apoptotic proteins Bax, Bik, Bok, Cleaved Caspase-7 & -9 were up regulated and anti-apoptotic, Bcl-2 and Survivin were down regulated when modalities were combined, albeit to variable levels. A strong protein expression of both caspase-7 and -9 in responses to combination therapies suggests that pathways involving these Caspases (initiated through release of cytochrome c from mitochondria) involving the Bcl-2 family of pro- and anti-apoptotic proteins may be more active in these synergies.
This is the first study to identify protein changes in response to PNP-GDEPT as obtained in OVCAR-3 cells using Shotgun Proteomics [47, 48]. That PNP-GDEPT may be acting through involvement in numerous processes ultimately leading to shutdown of cell metabolism, downregulation of some key oncogenes (e.g. cadherin, desmoplakin, plakoglobin, karyopherin, spondin, agrin) and genes involved in drug detoxification (e.g. antiquitin, epoxide hydrolase) with final upregulation of apoptosis (e.g. PARP) or tumour suppressor proteins (e.g. Dead box polypeptide 3) is suggestive of pro-apoptotic effects (Table 3 and Additional file 4 (Tables S3 & S4). Of interest was the downregulation of genes involved in detoxification or drug resistance, which may account for the increased sensitivity of drug resistant OVCAR-3 cells to docetaxel and carboplatin and for enhanced apoptosis observed when PNP-GDEPT was included in combination regimens. This is predictive of its promise for synergies with chemotherapy in the clinic.
Another observation of note is the downregulation of proteins representing "a desmosome model of carcinogenesis" (including desmoplakin, cadherins, plakoglobin, filaggerin) proposed by Chidgey et al , in which upregulation of c-myc or Bcl-2 promotes uncontrolled cell growth. This was supported by the Bcl-2 downregulation associated with PNP-GDEPT treatment (Figure 5) in our study. Hence, downregulation of this pathway may be one of the major features of PNP-GDEPT efficacy. There was also a possible stress response, with upregulation of proteins involved in purine and pyrimidine metabolism coupled with the downregulation of metabolic pathways. This upregulation of DNA synthesis proteins could also be Ad-transduction mediated, as this is known to trigger the cells into synthesis phase.
In conclusion, the data indicate that the apoptosis induced by the three way synergy between docetaxel, carboplatin and PNP-GDEPT involves the effector phase mediated by the Bcl-2 family of proteins (pro- and anti-apoptotic) and execution phase involving cleaved Caspase 9, Caspase 7 and PARP. Overall, there is a strong indication that involvement of PNP-GDEPT correlates with a more active involvement of pathways involving downregulation of Bcl-2, survivin and drug resistance proteins, leading to a high apoptotic index as achieved in the synergies involving PNP-GDEPT. These data strongly support the use of PNP-GDEPT in synergistic treatments in the clinic for ovarian cancers that show drug resistance to first line therapies. We anticipate that the information generated in this study will have potential applications against other types of cancers.
6. Conflict of interest statement
The authors declare that they have no competing interests.
Russell PJ, Khatri A: Novel gene-directed enzyme prodrug therapies against prostate cancer. Expert Opin Investig Drugs. 2006, 15: 947-961. 10.1517/13543722.214.171.1247.
Nawa A, Tanino T, Luo C, Iwaki M, Kajiyama H, Shibata K, Yamamoto E, Ino K, Nishiyama Y, Kikkawa F: Gene directed enzyme prodrug therapy for ovarian cancer: could GDEPT become a promising treatment against ovarian cancer?. Anticancer Agents Med Chem. 2008, 8: 232-239. 10.2174/187152008783497000.
Singh P, Yam M, Russell PJ, Khatri A: Molecular and traditional chemotherapy: a united front against prostate cancer. Cancer Lett. 2010, 293: 1-14. 10.1016/j.canlet.2009.11.019.
Vasey PA: Ovarian cancer: front-line standard treatment in 2008. Ann Oncol. 2008, 19 (Suppl 7): vii61-66.
Han LY, Kipps E, Kaye SB: Current treatment and clinical trials in ovarian cancer. Expert Opin Investig Drugs. 2010, 19: 521-534. 10.1517/13543781003647966.
Zhang Y, Parker WB, Sorscher EJ, Ealick SE: PNP anticancer gene therapy. Curr Top Med Chem. 2005, 5: 1259-1274. 10.2174/156802605774463105.
Parker WB, Allan PW, Shaddix SC, Rose LM, Speegle HF, Gillespie GY, Bennett LL: Metabolism and metabolic actions of 6-methylpurine and 2-fluoroadenine in human cells. Biochem Pharmacol. 1998, 55: 1673-1681. 10.1016/S0006-2952(98)00034-3.
Sorscher EJ, Peng S, Bebok Z, Allan PW, Bennett LL, Parker WB: Tumor cell bystander killing in colonic carcinoma utilizing the Escherichia coli DeoD gene to generate toxic purines. Gene Ther. 1994, 1: 233-238.
Hughes BW, King SA, Allan PW, Parker WB, Sorscher EJ: Cell to cell contact is not required for bystander cell killing by Escherichia coli purine nucleoside phosphorylase. J Biol Chem. 1998, 273: 2322-2328. 10.1074/jbc.273.4.2322.
Gadi VK, Alexander SD, Kudlow JE, Allan P, Parker WB, Sorscher EJ: In vivo sensitization of ovarian tumors to chemotherapy by expression of E. coli purine nucleoside phosphorylase in a small fraction of cells. Gene Ther. 2000, 7: 1738-1743. 10.1038/sj.gt.3301286.
Martiniello-Wilks R, Wang XY, Voeks DJ, Dane A, Shaw JM, Mortensen E, Both GW, Russell PJ: Purine nucleoside phosphorylase and fludarabine phosphate gene-directed enzyme prodrug therapy suppresses primary tumour growth and pseudo-metastases in a mouse model of prostate cancer. J Gene Med. 2004, 6: 1343-1357. 10.1002/jgm.629.
Hong JS, Waud WR, Levasseur DN, Townes TM, Wen H, McPherson SA, Moore BA, Bebok Z, Allan PW, Secrist JA, et al: Excellent in vivo bystander activity of fludarabine phosphate against human glioma xenografts that express the escherichia coli purine nucleoside phosphorylase gene. Cancer Res. 2004, 64: 6610-6615. 10.1158/0008-5472.CAN-04-0012.
Lockett LJ, Molloy PL, Russell PJ, Both GW: Relative efficiency of tumor cell killing in vitro by two enzyme-prodrug systems delivered by identical adenovirus vectors. Clin Cancer Res. 1997, 3: 2075-2080.
Mohr L, Shankara S, Yoon SK, Krohne TU, Geissler M, Roberts B, Blum HE, Wands JR: Gene therapy of hepatocellular carcinoma in vitro and in vivo in nude mice by adenoviral transfer of the Escherichia coli purine nucleoside phosphorylase gene. Hepatology. 2000, 31: 606-614. 10.1002/hep.510310310.
Bzowska A, Kulikowska E, Shugar D: Properties of purine nucleoside phosphorylase (PNP) of mammalian and bacterial origin. Z Naturforsch [C]. 1990, 45: 59-70.
du Bois A, Luck HJ, Meier W, Adams HP, Mobus V, Costa S, Bauknecht T, Richter B, Warm M, Schroder W, et al: A randomized clinical trial of cisplatin/paclitaxel versus carboplatin/paclitaxel as first-line treatment of ovarian cancer. J Natl Cancer Inst. 2003, 95: 1320-1329.
Ozols RF, Bundy BN, Greer BE, Fowler JM, Clarke-Pearson D, Burger RA, Mannel RS, DeGeest K, Hartenbach EM, Baergen R: Phase III trial of carboplatin and paclitaxel compared with cisplatin and paclitaxel in patients with optimally resected stage III ovarian cancer: a Gynecologic Oncology Group study. J Clin Oncol. 2003, 21: 3194-3200. 10.1200/JCO.2003.02.153.
Oishi T, Kigawa J, Fujiwara K, Fujiwara M, Numa F, Aotani E, Katsumata N, Kohno I, Kato H, Terakawa N: A feasibility study on biweekly administration of docetaxel for patients with recurrent ovarian cancer. Gynecol Oncol. 2003, 90: 421-424. 10.1016/S0090-8258(03)00322-6.
Rose PG, Blessing JA, Ball HG, Hoffman J, Warshal D, DeGeest K, Moore DH: A phase II study of docetaxel in paclitaxel-resistant ovarian and peritoneal carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2003, 88: 130-135. 10.1016/S0090-8258(02)00091-4.
Markman M: Taxanes in the management of gynecologic malignancies. Expert Rev Anticancer Ther. 2008, 8: 219-226. 10.1586/14737126.96.36.199.
Engblom P, Rantanen V, Kulmala J, Grenman S: Carboplatin-paclitaxel- and carboplatin-docetaxel-induced cytotoxic effect in epithelial ovarian carcinoma in vitro. Cancer. 1999, 86: 2066-2073. 10.1002/(SICI)1097-0142(19991115)86:10<2066::AID-CNCR26>3.0.CO;2-1.
Vasey PA, Jayson GC, Gordon A, Gabra H, Coleman R, Atkinson R, Parkin D, Paul J, Hay A, Kaye SB: Phase III randomized trial of docetaxel-carboplatin versus paclitaxel-carboplatin as first-line chemotherapy for ovarian carcinoma. J Natl Cancer Inst. 2004, 96: 1682-1691. 10.1093/jnci/djh323.
Escobar PF, Rose PG: Docetaxel in ovarian cancer. Expert Opin Pharmacother. 2005, 6: 2719-2726. 10.1517/146565188.8.131.5219.
MacKenzie SH, Clark AC: Targeting cell death in tumors by activating caspases. Curr Cancer Drug Targets. 2008, 8: 98-109. 10.2174/156800908783769391.
LaCasse EC, Mahoney DJ, Cheung HH, Plenchette S, Baird S, Korneluk RG: IAP-targeted therapies for cancer. Oncogene. 2008, 27: 6252-6275. 10.1038/onc.2008.302.
Voeks D, Martiniello-Wilks R, Madden V, Smith K, Bennetts E, Both GW, Russell PJ: Gene therapy for prostate cancer delivered by ovine adenovirus and mediated by purine nucleoside phosphorylase and fludarabine in mouse models. Gene Ther. 2002, 9: 759-768. 10.1038/sj.gt.3301698.
Chou TC, Talalay P: Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul. 1984, 22: 27-55.
Chou TC, Hayball MP: Calcusyn: Windows software for dose effect analysis. 1996, Cambridge (England): Anonymous Biosoft
Chou J, Chou TC: Computerized simulation of dose reduction index (DRI) in synergistic drug combinations. Pharmacologist. 1988, 30:
Towbin H, Staehelin T, Gordon J: Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA. 1979, 76: 4350-4354. 10.1073/pnas.76.9.4350.
Shevchenko A, Wilm M, Vorm O, Mann M: Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels. Anal Chem. 1996, 68: 850-858. 10.1021/ac950914h.
See HT, Freedman RS, Kudelka AP, Burke TW, Gershenson DM, Tangjitgamol S, Kavanagh JJ: Retrospective review: re-treatment of patients with ovarian cancer with carboplatin after platinum resistance. Int J Gynecol Cancer. 2005, 15: 209-216. 10.1111/j.1525-1438.2005.15205.x.
Smith JA, Ngo H, Martin MC, Wolf JK: An evaluation of cytotoxicity of the taxane and platinum agents combination treatment in a panel of human ovarian carcinoma cell lines. Gynecol Oncol. 2005, 98: 141-145. 10.1016/j.ygyno.2005.02.006.
Konstantinopoulos PA, Fountzilas E, Pillay K, Zerbini LF, Libermann TA, Cannistra SA, Spentzos D: Carboplatin-induced gene expression changes in vitro are prognostic of survival in epithelial ovarian cancer. BMC Med Genomics. 2008, 1: 59-10.1186/1755-8794-1-59.
Fabbri F, Carloni S, Brigliadori G, Zoli W, Lapalombella R, Marini M: Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: a cytometric study. BMC Cell Biol. 2006, 7: 6-10.1186/1471-2121-7-6.
Nguyen HN, Sevin BU, Averette HE, Perras J, Ramos R, Donato D, Ochiai K, Penalver M: Cell cycle perturbations of platinum derivatives on two ovarian cancer cell lines. Cancer Invest. 1993, 11: 264-275. 10.3109/07357909309024851.
Boehrer S, Nowak D, Hoelzer D, Mitrou PS, Chow KU: Novel agents aiming at specific molecular targets increase chemosensitivity and overcome chemoresistance in hematopoietic malignancies. Curr Pharm Des. 2006, 12: 111-128. 10.2174/138161206780574588.
Eastman A, Rigas JR: Modulation of apoptosis signaling pathways and cell cycle regulation. Semin Oncol. 1999, 26: 7-16. discussion 41-12
Oliver FJ, de la Rubia G, Rolli V, Ruiz-Ruiz MC, de Murcia G, Murcia JM: Importance of poly(ADP-ribose) polymerase and its cleavage in apoptosis. Lesson from an uncleavable mutant. J Biol Chem. 1998, 273: 33533-33539. 10.1074/jbc.273.50.33533.
Chou TC: Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacol Rev. 2006, 58: 621-681. 10.1124/pr.58.3.10.
Kaye SB, Vasey PA: Docetaxel in ovarian cancer: phase III perspectives and future development. Semin Oncol. 2002, 29: 22-27.
Markman M: Managing taxane toxicities. Support Care Cancer. 2003, 11: 144-147.
Wahl AF, Donaldson KL, Fairchild C, Lee FY, Foster SA, Demers GW, Galloway DA: Loss of normal p53 function confers sensitization to Taxol by increasing G2/M arrest and apoptosis. Nat Med. 1996, 2: 72-79. 10.1038/nm0196-72.
Li Y, Okegawa T, Lombardi DP, Frenkel EP, Hsieh JT: Enhanced transgene expression in androgen independent prostate cancer gene therapy by taxane chemotherapeutic agents. J Urol. 2002, 167: 339-346. 10.1016/S0022-5347(05)65465-1.
Yoo GH, Piechocki MP, Oliver J, Lonardo F, Zumstein L, Lin HS, Kim H, Shibuya TY, Shehadeh N, Ensley JF: Enhancement of Ad-p53 therapy with docetaxel in head and neck cancer. Laryngoscope. 2004, 114: 1871-1879. 10.1097/01.mlg.0000147914.51239.ed.
Johnson SW, Stevenson JP, O'Dwyer VT: Cisplatin and its analogues. Cancer: Principles and Practice of Oncology. Edited by: DeVita VT, Hellman S, Rosenberg SA. 2001, Philadelphia: Lippincott, Williams & Wilkins, 376-88.
Vasey PA, Atkinson R, Coleman R, Crawford M, Cruickshank M, Eggleton P, Fleming D, Graham J, Parkin D, Paul J, et al: Docetaxel-carboplatin as first line chemotherapy for epithelial ovarian cancer. Br J Cancer. 2001, 84: 170-178. 10.1054/bjoc.2000.1572.
Chidgey M, Dawson C: Desmosomes: a role in cancer?. Br J Cancer. 2007, 96: 1783-1787. 10.1038/sj.bjc.6603808.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/11/368/prepub
We gratefully acknowledge the funding support from National Health and Medical Research Council, Australia (grant #510238) & The Sydney Foundation Australia. We are also grateful to Dr Nirupama Vema for her timely help towards completion of this manuscript.
7. Authors' contributions
PS is responsible for the completion of all the experimental work. He was involved in the design and development of this study (and in conducting experiments. He contributed significantly to drafting and writing of this manuscript. SJ was responsible for the western blotting/densitometry studies, and participated in general, in all aspects of this study (experimental planning and conducting) and helped with literature searches, experimental design and data interpretation. PJR provided the overall infrastructural, financial and intellectual support for this study. She was actively involved in the conception, design and development of this work and contributed towards writing and editing of the manuscript. SN provided resources and intellectual input for design and data interpretation of the shotgun proteomic analyses. He was involved in the writing/editing of this manuscript and provided the critical feedback for shotgun proteomics analyses. AK is responsible for the conception, design and development of this study. In addition to coordinating the research, she contributed significantly towards data interpretation and final analyses. She also contributed significantly to literature searches, drafting and writing of this manuscript. All authors have read and approved the manuscript in its final form.
Electronic supplementary material
Additional file 4: Tables S3 & S4. Table S3: List of proteins significantly down-regulated in PNP-GDEPT treated samples compared to untreated control cells and their role in cancer. Table S4: List of proteins significantly up regulated in PNP-GDEPT treated samples compared to untreated control cells and their role in cancer. (DOC 228 KB)
Additional file 5: Figure S1. Response of ovarian cancer cells to docetaxel treatment: Four ovarian cancer cell lines were exposed to a range of docetaxel concentrations (0.1-316 nM). WST-1 assay was performed to analyse cell viability on days 2, 3, 4 and 5. Cell viability was plotted as the percentage of vehicle control cells (cells treated with corresponding concentrations of polysorbate 80+ethanol) using GraphPad Prism. Dose response curves for A-2780, SKOV-3, OVCAR-3 and Caov-3 as generated on days 2 (black line), 3 (red line), 4 (purple line) and 5 (brown line) are shown. (EPS 986 KB)
Additional file 6: . Docetaxel (nM) needed to kill 50% of ovarian cancer cells (IC50). (DOC 37 KB)
Additional file 7: . Evaluation of cell growth inhibitory effects of different combinations in OVCAR-3 cells: Cells treated with different doses of A. docetaxel and/or carboplatin, B. PNP-GDEPT (Fludara (1 μg/mL, 2.7 μM) and/or docetaxel, C. PNP-GDEPT and/or carboplatin D. PNP-GDEPT (Fludara (1 μg /mL, 2.7 μM) and/or docetaxel and/or carboplatin were analysed for cell viability using WST-1 assay on day 5. Graphs representing inhibition of cell growth plotted as a function of increasing doses of docetaxel and/or carboplatin and/or PNP-GDEPT for OVCAR-3 cells are shown. Some combinations led to slightly greater cell growth inhibition compared with either alone. Values represent mean (± SEM) of three independent experiments. The P values on the graph indicate the significance of trends at various time points calculated using Two Way Anova analyses. (EPS 1 MB)
About this article
Cite this article
Singh, P.P., Joshi, S., Russell, P.J. et al. Purine Nucleoside Phosphorylase mediated molecular chemotherapy and conventional chemotherapy: A tangible union against chemoresistant cancer. BMC Cancer 11, 368 (2011). https://doi.org/10.1186/1471-2407-11-368
- Molecular chemotherapy
- Purine nucleoside phosphorylase (PNP)
- Fludarabine Phosphate (Fludara)
- Gene directed enzyme prodrug therapy (GDEPT)
- Ovarian cancer