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Mitomycin c (MMC), a quinone-containing anticancer drug, is known to redox cycle and generate reactive oxygen species. A key enzyme mediating MMC redox cycling is cytochrome P450 reductase, a microsomal NADPH-dependent flavoenzyme. In the present studies, CHO cells overexpressing this enzyme (CHO-OR cells) and corresponding control cells (CHO-WT cells) were used to investigate the role of cytochrome P450 reductase in the actions of MMC. In lysates from both cell types, MMC was found to redox cycle and generate H2O2; this activity was greater in CHO-OR cells (Vmax = 1.2 ± 0.1 nmol H2O2/min/mg protein in CHO-WT cells vs. 32.4 ± 3.9 nmol H2O2/min/mg protein in CHO-OR cells). MMC was also more effective in generating superoxide anion and hydroxyl radicals in CHO-OR cells, relative to CHO-WT cells. Despite these differences in MMC redox cycling, MMC-induced cytotoxicity, as measured by growth inhibition, was similar in the two cell types (IC50 = 72 ± 20 nM for CHO-WT and 75 ± 23 nM for CHO-OR cells), as was its ability to induce G2/M and S phase arrest. Additionally, in 9 different tumor cell lines, although a strong correlation was observed between MMC-induced H2O2 generation and cytochrome P450 reductase activity, there was no relationship between redox cycling and cytotoxicity. Hypoxia, which stabilizes MMC radicals generated by redox cycling, also had no effect on the sensitivity of tumor cells to MMC-induced cytotoxicity. These data indicate that NADPH cytochrome P450 reductase-mediated MMC redox cycling is not involved in cytotoxicity of this chemotherapeutic agent.
Mitomycin c (MMC) is a quinone-containing alkylating agent widely used for the treatment of solid tumors (1). It has been postulated that bioreductive activation of MMC is responsible for its antitumor and cytotoxic properties. In this reaction, a one or two-electron enzymatic reduction of the quinone moiety in MMC generates a semiquinone free radical intermediate or a hydroquinone intermediate, respectively, both of which are potent DNA alkylating agents (2, 3). Under aerobic conditions, the semiquinone intermediate is oxidized back to the parent compound generating superoxide anion (see Fig. 1A for structure of MMC and redox cycling pathway). Superoxide anion then dismutates to H2O2; in the presence of trace metals, H2O2 forms hydroxyl radicals (4). These reactive oxygen species (ROS) can damage intracellular macromolecules including lipids, protein and DNA, resulting in oxidative stress and toxicity. Under hypoxic conditions, redox cycling is limited and the MMC semiquinone rearranges to form a DNA reactive hydroxyquinone intermediate (5–7).
Several different flavoenzymes have been shown to catalyze the one electron reduction of MMC including NADPH-cytochrome P450 reductase (EC 18.104.22.168), NADH-cytochrome b5 reductase, xanthine oxidase and nitric oxide synthase and it has been suggested that these enzymes are mediators of MMC-induced cytotoxicity (8–12). For example, Belcourt et al. (13) have shown that overexpression of cytochrome P450 reductase in Chinese hamster ovary (CHO) cells enhances their sensitivity to MMC under both oxygenated and hypoxic conditions. Increased sensitivity to MMC under these conditions has also been described in CHO cells engineered to express nuclear cytochrome P450 reductase (14). Similarly, viral delivery of cytochrome P450 reductase increases the sensitivity of human breast cancer cells to MMC, although this is only evident under oxygenated conditions (15). Martinez et al. (16) also reported increased sensitivity of human MDA 231 breast carcinoma cells overexpressing cytochrome P450 reductase to MMC. In contrast, Fitzsimmons et al. (17) found that there was no direct correlation between sensitivity to MMC and levels of cytochrome P450 reductase across 69 cell lines obtained from the National Cancer Institute Tumor Cell line panel. Findings in these studies that sensitivity to MMC correlated with DT-diaphorase, an obligate two electron reductase, suggested that the MMC-derived hydroquinone intermediate is more likely to mediate its antitumor activity.
The present studies were designed to further explore the role of cytochrome P450 reductase in the cytotoxicity of MMC under oxygenated and hypoxic conditions. For these studies, we compared MMC-induced cytotoxicity and redox cycling in cell lines varying in cytochrome P450 reductase activity including CHO cells constructed to overexpress the enzyme. Our results show that neither redox cycling nor stabilization of the MMC radical by hypoxia is correlated with cytotoxicity of MMC. These data provide further support for the concept that microsomal cytochrome P450 reductase plays a limited role in mediating the antitumor activity of MMC.
cDNA-expressed NADPH cytochrome P450 reductase from microsomal fractions of insect cells (Supersomes, cat. No. 456514) was obtained from BD Gentest (Woburn, MA). Amplex Red (10-acetyl-3, 7-dihydroxyphenoxazine) and 2',7'-dichlorofluorescein diacetate (DCFH-DA) were from Molecular Probes (Eugene, OR). Mouse monoclonal antibody to cytochrome P450 reductase was obtained from Santa Cruz (Santa Cruz, CA). MMC, NADPH, catalase and all other chemicals were from Sigma-Aldrich (St. Louis, MO).
Cytochrome P450 reductase-overexpressing CHO cells (CHO-OR) and control cells expressing empty vector (CHO-WT) were kindly provided by Dr. Jun Yan Hong at the University of Medicine and Dentistry of New Jersey (Piscataway, NJ). CHO-OR cells have been reported to express 30-fold more cytochrome P450 reductase relative to CHO-WT cells (18). We measured cytochrome P450 reductase activity in lysates of the cells using a cytochrome c reductase assay kit (Sigma-Aldrich), and found that CHO-WT cells contained 2.4 Units of cytochrome P450 reductase activity/mg protein and CHO-OR cells contained 83.7 Units of cytochrome P450 reductase activity/mg protein, where one unit will reduce one nmole of oxidized cytochrome c in the presence of 100 μM NADPH per min at pH 7.8 at 25 °C. This was confirmed by western blotting using antibody to cytochrome P450 reductase (not shown). Murine lung epithelial cells (MLE 15 cells) were obtained from Dr. Jacob N. Finkelstein (University of Rochester, NY). All other cell lines were from the American Type Culture Collection (Rockville, MD). Stocks of cells were maintained in liquid nitrogen and used fewer than 6 months after resuscitation. Cell lines were not further tested or authenticated. CHO-WT, CHO-OR and PC-3 cells were maintained in Ham's F12K medium. MLE 15, RAW 264.7, C2, S-180, B16, HL-60, HT-29 and HeLa cells were maintained in Dulbecco's modified Eagle's medium. All medium was supplemented with 10% fetal bovine serum, penicillin (100 units/ml) and streptomycin (100 μg/ml). For CHO cells, the growth medium was also supplemented with 500 μg/ml hygromycin B (Invitrogen, Carlsbad, CA). Cells were cultured at 37° C in 5% CO2 in a humidified incubator. Tissue culture reagents were from GIBCO BRL (Grand Island, NY).
Cell growth inhibition was evaluated as previously described (19). Briefly, cells were plated at low density (2.5–10 × 104 cells/well) in 6-well tissue culture dishes and allowed to adhere overnight. The medium was then replaced with growth medium supplemented with increasing concentrations of MMC. To induce hypoxia, the cells were placed in an MIC-101 Modular Incubator Chamber (Billups-Rothenberg, Inc., Del Mar, CA), flushed with 95% N2/5% CO2 twice, and then incubated at 37 °C for 24 h. After an additional 3–5 days in culture, the cells were removed from the dishes with trypsin and counted using a Z1 Coulter Particle Counter (Beckman Coulter, Hialeah, FL). Concentrations of MMC that caused 50% growth inhibition (IC50) were then determined. In some experiments, hypoxia was induced using a two-enzyme system (glucose oxidase and catalase) as previously described (20) with some modifications. Briefly, cells were plated in 24-well tissue culture plates (5,000 cells/well) and allowed to adhere overnight. The medium was then replaced with 2 ml growth medium supplemented with 10 mM glucose with or without 2 U/ml glucose oxidase and 120 U/ml catalase. After 10 min, MMC was added and cells were incubated at 37 °C for 3 h. Cells were then washed and refed with fresh growth medium. After an additional 3 d at 37 °C, cells were trypsinized and counted as described above. Depletion of oxygen by the two-enzyme system was confirmed in an Oxygraph with a Clark-type electrode (Yellow Springs Instruments, Yellow Springs, OH). Earlier studies have suggested that, under hypoxic conditions, cell culture plasticware, but not glassware, can release trace amount of oxygen that can mediate redox cycling (21, 22). We found that there were no significant differences in the effects of MMC on cell growth under normoxic or hypoxic conditions when either plastic or glass culture dishes were used. Thus, using the Modular Incubator Chamber with CHO-OR cells on plastic dishes, the IC50 for MMC was 75 nM and 78 nM under normoxic and hypoxic conditions, respectively, while the IC50 for MMC was 75 nM and 80 nM, respectively, for glass dishes. Using the two enzyme hypoxia system with CHO-OR cells, for plastic dishes the IC50 for MMC was 3.0 μM and 2.0 μM under normoxic and hypoxic conditions, respectively, while the IC50 for MMC was 2.5 μM and 2.0 μM, respectively, for glass dishes.
To prepare lysates, cells were scraped from culture dishes in phosphate-buffered saline (PBS), washed and centrifuged (800 × g, 5 min). Cell pellets were stored at −70 °C until analysis. Prior to enzyme assays, cell pellets were resuspended in PBS (~107 cells/0.5 ml) and sonicated on ice using a sonic dismembrator (ARTEK Systems Inc., Farmingdale, NY). Homogenates were then sequentially centrifuged at 4 °C (3,000 × g and 12,000 × g, for removal of cellular debris and mitochondrial fractions, respectively). The resulting supernatant fractions were used in enzyme assays. Protein concentrations were quantified using the Dc protein assay kit (Bio-Rad, Hercules, CA) with bovine serum albumin as the standard.
Cell cycle analysis was performed as previously described with some modifications (23). Briefly, cells were seeded into 6-well plates at 2.5×105 cells/well and allowed to adhere overnight. The medium was then replaced with growth medium supplemented without or with MMC. After 24 h, cells were harvested, fixed in 70% ice-cold ethanol and stored at −20 °C until further processing. For DNA analysis, cells were treated with propidium iodide (10 μg/ml) and RNase (40 μg/ml) for 30 min and then analyzed on a Cytomics FC 500 flow cytometer (Beckman Coulter, Fullerton, CA). Data were analyzed by CXP software (Beckman Coulter).
Redox cycling of MMC in lysates was quantified by the formation of H2O2, hydroxyl radicals and superoxide anion. The Amplex Red/horse radish peroxidase (HRP) method was used to assay hydrogen peroxide production (24). Briefly, assays were run at 37° C in standard reaction mixes in 100 μl potassium phosphate buffer (50 mM, pH 7.8) containing 0–0.5 mM NADPH, 0–0.5 mM MMC, 25 μM Amplex Red, 1 unit/ml HRP and 1.25 μg/ml cytochrome P450 reductase or 100 μg/ml of cell lysate protein. The fluorescent product, resorufin was detected using an HTS 7000 Plus Bio Assay Reader (Perkin Elmer Life Sciences, Shelton, CT) with 540 nm excitation and 595 nm emission filters. Increases in fluorescence intensity were measured every 2.5 min for 30 min. Fluorescence was converted into amount of H2O2 based on calibration standards.
The generation of 2-hydroxyterephthalate from terephthalate was used as an indicator of hydroxyl radical production (25). Standard reaction mixes in 0.2 ml potassium phosphate buffer (20 mM, pH 7.4) contained 150 μg/ml cell protein from supernatant fractions, 1 mM terephthalate and 0.5 mM NADPH. Reactions were initiated by the addition of Fe3+/EDTA (100 μM/110 μM) to the assay mix. After incubation at 37° C for 1 h, reactions were stopped by adding an equal volume of ice-cold methanol. 2-Hydroxyterephthalate was quantified by HPLC with fluorescence detection as previously described (25). In these experiments, catalase (400 U/ml) was found to inhibit hydroxyl radical formation.
Superoxide anion was assayed by the formation of 2-hydroxyethidium from dihydroethidium (26). Standard reaction mixes described above were used except that Fe3+/EDTA was omitted and dihydroethidium (40 μM) was used in place of terephthalate. 2-Hydroxyethidium formation was detected using a Shimadzu HPLC (Kyoto, Japan) fitted with a Luna C18 column (250 mm × 2.0 mm, Phenomenex, Torrance, CA) and a fluorescence detector with excitation and emission wavelengths set at 510 nm and 595 nm, respectively. The mobile phase consisted of a linear (10–40%) gradient of acetonitrile in 0.1% trifluoroacetic acid and was run at a flow rate of 0.2 ml/min for 45 min. 2-Hydroxyethidium eluted from the column with a retention time of 40 min.
Oxygen consumption was determined using a Clark-type electrode in a mix of 50 mM potassium phosphate (pH 7.8), 0.5 mM NADPH, 10 mM glucose-6-phosphate, 0.5 U/ml glucose-6-phosphate dehydrogenase, 0.1 mg/ml of cell lysate protein, 0.5 mM MMC in a final volume of 1.2 ml. At the end of the experiment, several grains of sodium dithionite were added to deplete remaining oxygen for calibration. In some experiments, an Oxygraph system was used to quantify the effects of MMC (0.5 mM) on oxygen consumption in intact cells (2.5 × 106/ml). Disappearance of NADPH in enzyme reactions was assayed in 1 ml spectrophotometer cuvettes by quantifying decreases in absorbance at 340 nm as previously described (27).
Intracellular ROS were quantified using DCFH-DA in conjunction with flow cytometry as previously described (28). In brief, cells were suspended in PBS (1 × 106/ml) and incubated with 5 μM DCFH-DA at 37° C in a shaking water bath. After 15 min, MMC was added. After an additional 3 h, cellular fluorescence was analyzed by flow cytometry as described above.
Each determination was performed in duplicate or triplicate and repeated two or three times. Differences were analyzed for statistical significance using the one-way ANOVA or paired t-test with GraphPad Instat software (La Jolla, CA); p< 0.05 was considered significant. The GraphPad software was also used to calculate enzyme Kinetic parameters.
In initial studies we examined the cytotoxicity of MMC using CHO-WT cells. MMC was found to effectively inhibit the growth of these cells after short (3 h) and long term (4 d) exposure (Fig. 1 panel B and Table 1); greater cytotoxicity was observed after long term exposure. Growth inhibition by MMC was associated with arrest of cells in the G2/M and S phases of the cell cycle (Fig. 2, panels A and B). Previous work suggested that MMC-induced cytotoxicity was due, at least in part, to redox cycling via cytochrome P450 reductase (8, 29). Using recombinant cytochrome P450 reductase, we found that MMC was readily able to redox cycle, generating superoxide anion and H2O2 in the process (Fig. 3 panel A, and not shown). Redox cycling was time- and MMC-concentration-dependent; the Vmax for H2O2 production was 425.6 ± 34.6 nmol/min/mg protein, and the apparent Km, 272.2 ± 80.1 μM (n = 3, ± SEM). The reaction was also dependent on NADPH and inhibitable by diphenyleneiodonium (DPI, 10 μM) indicating a requirement for the flavin cofactors in cytochrome P450 reductase (Fig. 3 panel B, and data not shown). In the presence of MMC (100 μM), the Vmax for NADPH utilization for H2O2 generation by cytochrome P450 reductase was increased by approximately 9-fold with no major changes in Km (Table 2).
We next compared the cytotoxicity of MMC in CHO-WT cells and CHO-OR cells. Surprisingly, overexpression of cytochrome P450 reductase had no effect on the sensitivity of the cells to MMC after 3 h incubation (IC50 = 2.5 μM for CHO-WT cells and 3 μM for CHO-OR cells) or 4 d incubation (IC50 = 72 nM for CHO-WT cells and 75 nM for CHO-OR cells) (Fig. 1, panel B and Table 1), or its ability to arrest cells in the G2/M and S phases of the cell cycle (Fig. 2, panels A and B). This is in contrast, menadione, a quinone known to effectively redox cycle (30), that was found to be more cytotoxic in CHO-OR cells, when compared to CHO-WT cells (Fig.1, panel C). In both CHO-WT and CHO-OR cells, the effects of MMC were concentration-dependent in the range of 0.003 to 3 μM. Maximal cell cycle arrest was evident at the highest concentration of MMC.
In further studies we characterized redox cycling in lysates of CHO-WT and CHO-OR cells. In the absence of MMC, low constitutive levels of H2O2 were generated by both cell types. Constitutive H2O2 levels were 2–3 fold greater in CHO-OR cells, when compared to CHO-WT cells (Fig. 3, panels C and D). The addition of MMC to the lysates resulted in a time- and concentration-dependent increase in H2O2 production in both cell types. Markedly greater maximal activity was detected in cells overexpressing cytochrome P450 reductase. The Vmax for these cells was approximately 27-fold greater than for wild type cells (32.4 nmol H2O2/min/mg protein vs 1.2 nmol H2O2/min/mg protein, respectively), while the Km values for MMC in CHO-OR cells was approximately 2.5-fold greater than in CHO-WT cells (Table 1). MMC-stimulated H2O2 production was also associated with increased metabolism of NADPH in both CHO-WT and CHO-OR cells (Table 2 and not shown). In the presence of 100 μM MMC, the Km for NADPH increased 4-fold in CHO-OR cells with no major changes in the Km for NADPH in CHO-WT cells. The Vmax for NADPH for H2O2 generation also increased 27-fold in CHO-OR cells and only 2-fold in CHO-WT cells (Table 2).
MMC was also more effective in stimulating superoxide anion and hydroxyl radical production by lysates of CHO-OR cells when compared to CHO-WT cells. As observed with H2O2, low constitutive amounts of superoxide anion and hydroxyl radicals were generated in both cell types. Whereas significant increases in production of superoxide anion were detected in lysates from CHO-OR cells treated with MMC, no significant effects were noted in CHO-WT cells (Fig. 3, panel E). In CHO-OR cell lysates, superoxide anion production was readily inhibited by superoxide dismutase (SOD) (Fig. 3, panel E). Approximately 2–4 times greater quantities of hydroxyl radicals were produced by CHO-OR cells when compared to CHO-WT cells when treated with MMC (Fig. 3, panel F). Hydroxyl radical formation was dependent on iron, and inhibited by catalase and DMSO (Fig. 3, panel F).
To confirm these findings in intact cells, we used techniques in flow cytometry in conjunction with the ROS-sensitive probe, DCFH-DA. Consistent with our findings using Amplex-Red in cell lysates, MMC was found to cause a 4-fold increase in H2O2 production in intact CHO-OR cells (p = 0.002, Fig. 4B, right panel); in contrast, relatively small effects were observed in CHO-WT cells (1.4-fold, p = 0.01, Fig. 4B, left panel).
Using mitochondria-free lysates, we observed that oxygen utilization was maintained at low levels in both CHO cell types. The addition of 0.5 mM MMC stimulated oxygen consumption in lysates of CHO-OR, but not CHO-WT cells (Fig. 4, panel A, tracings b and d). Increased oxygen utilization in CHO-OR cells was inhibited by DPI, a finding consistent with flavin-mediated MMC redox cycling by cytochrome P450 reductase (8, 11). We also found that MMC caused marked increases in oxygen consumption in intact CHO-OR cells, but not in intact CHO-WT cells (Fig. 4, panel A, tracings a and c).
We next compared MMC redox cycling and cytotoxicity in nine different mouse and human tumor cell lines that varied in cytochrome P450 reductase activity (27). MMC redox cycling was detectable in lysates from each of these tumor cell types. The greatest activity, as measured by H2O2 production, was observed in mouse MLE 15 cells, while human PC-3 and HL-60 cells and hamster CHO-WT cells contained the lowest activity. The apparent Km for MMC was also greatest in MLE 15 cells (Table 1). As observed with recombinant cytochrome P450 reductase, MMC (100 μM) increased the Vmax for NADPH for H2O2 generation in the cell lines with no major changes in the Km values (Table 2). In each of the tumor cell lines, a strong correlation (r2 = 0.996 including CHO-OR cells in the analysis and r2 = 0.929 without CHO-OR cells in the analysis) was observed between MMC-induced H2O2 generation during redox cycling and cytochrome P450 reductase activity (Fig. 2C, left panel). However, as observed with CHO-WT and CHO-OR cells, MMC-induced cytochrome P450 reductase activity and MMC redox cycling were not associated with cytotoxicity in the different tumor cell lines (Fig. 2C, right panel).
Several laboratories have suggested that the reaction of cells with MMC under hypoxic conditions increases its cytotoxicity due to stabilization of the highly reactive semiquinone free radical intermediate (31, 32). Interestingly, we found that exposure of CHO-WT and CHO-OR cells to MMC under hypoxic conditions for either 3 h or 24 h had no effect on their sensitivity to MMC (Fig. 1, panel B and Table 1). This is in contrast to menadione where increased cytotoxicity was observed in CHO-OR cells under hypoxic conditions (Fig. 1, panel C). Moreover, despite marked differences in the ability of the 9 tumor cell lines to redox cycle MMC, hypoxia caused no significant alterations in their sensitivity to the drug (Table 1).
NADPH-dependent one-electron reduction of MMC and subsequent generation of ROS have been demonstrated using reconstituted microsomal systems, purified cytochrome P450 reductase from rat liver (8, 11) and human recombinant enzyme (3). The present studies show that the rat recombinant enzyme is also highly effective in MMC redox cycling. Moreover, kinetic parameters for the recombinant enzyme, with respect to the generation of H2O2, were generally similar to the previous reports using purified rat cytochrome P450 reductase (11). MMC redox cycling initiated by the recombinant enzyme was due to an increase in the Vmax for NADPH for H2O2 generation with little or no change in affinity of the enzyme for the pyridine nucleotide. To further investigate the role of cytochrome P450 reductase in MMC-induced redox cycling, we analyzed this process in CHO wild type cells and CHO cells overexpressing cytochrome P450 reductase and in different mouse and human tumor cell lines varying in cytochrome P450 reductase content. Redox cycling of MMC was evident in all cell types; although none was as efficient as recombinant rat cytochrome P450 reductase in generating ROS. This is likely due to dilution of the reductase in tumor cell lysates and competition from other enzymes that either mediate redox cycling and/or detoxify ROS (9, 10, 29). The Km's and Vmax's for MMC redox cycling in most of the cell lines were generally in the same concentration range with the exception of CHO-OR cells. The higher Vmax in these cells can be attributed to greater expression of cytochrome P450 reductase. MMC metabolism in all tumor cells assayed increased the Vmax for NADPH for H2O2 generation; no major changes in the enzyme affinity for NADPH except in CHO-OR cells were noted. As observed with redox cycling, the kinetic parameters for NADPH for H2O2 generation in the different cell lines represent the specific characteristics of the enzyme activities mediating the one electron reduction of MMC. The mechanisms underlying the distinct reaction kinetics for NADPH in CHO-OR cells are not readily apparent and it will be of interest to further characterize the enzymes that are important in MMC metabolism in this and other cell lines.
In addition to generating H2O2 during MMC redox cycling, cell lysates from CHO-OR cells produced superoxide anion and, in the presence of redox active iron, hydroxyl radicals. As expected, this was associated with increased oxygen consumption, due to the rapid reaction of the MMC semiquinone radical with molecular oxygen. MMC was also found to be active in redox cycling in intact CHO-OR cells, as evidenced by increased H2O2 formation and oxygen consumption. Both the generation of ROS and increased oxygen utilization can contribute to cellular oxidative stress (33).
MMC was also found to be a potent growth inhibitor for CHO cells. Despite marked differences in cytochrome P450 reductase content and redox cycling in CHO-WT and CHO-OR cells, no significant differences were noted between the cell types in their sensitivity to the growth inhibitory actions of MMC, or its ability to arrest cells in the G2/M and S phases of the cell cycle. These unexpected findings prompted us to compare cytochrome P450 reductase activity, redox cycling and sensitivity to MMC in other tumor cell types varying in cytochrome P450 reductase. Indeed, despite a direct correlation between cytochrome P450 reductase activity and redox cycling in nine different mouse and human tumor cell lines, there was no correlation between redox cycling and growth inhibition. These data are consistent with Fitzsimmons et al. (17), who compared the activities of cytochrome P450 reductase, cytochrome b5 reductase and DT-diaphorase and cytotoxicity of MMC and a related indolequinone EO9 (3-hydroxy-5-aziridinyl-1-methyl-2[indole-4,7-dione]–prop-β-en-(-ol) in 69 NCI tumor cell lines. In these studies, the sensitivity of the cells to MMC and EO9 correlated with DT-diaphorase, which mediates the two-electron reduction of MMC, but not with cytochrome P450 reductase and cytochrome b5 reductase which mediate redox cycling. A number of other laboratories have similarly described a correlation between DT-diaphorase expression and sensitivity to MMC or related indoloquinones in different tumor cell lines, breast tumor xenographs and DT-diaphorase overexpressing cells (15, 34, 35). Resistance to MMC has also been correlated with reduced DT-diaphorase activity (36).
In contrast to our studies, a direct correlation between expression of cytochrome P450 reductase and sensitivity to MMC has been described in cells lines and tumor tissue by several laboratories. This includes breast tumor cells in culture and maintained as xenographs (15, 16), as well as variant CHO cell lines overexpressing cytochrome P450 reductase (13, 14). Differences between our findings and previous reports using CHO cells, with respect to sensitivity to MMC and cytochrome P450 reductase expression, may be due to methods used to assess cytotoxicity. While our growth inhibition assays showed no differences in MMC sensitivity between CHO-WT and CHO-OR cells following either a 3 h or a 4 day exposure, Belcourt et al. (13) and Seow et al. (14) reported increased sensitivity of their cytochrome P450 reductase overexpressing CHO cells when treated with MMC for 1 h. One can speculate that the sensitivity of the different cells to MMC may be due to differences in uptake and/or metabolism of the drug during the exposure. Belcourt et al. (13) and Seow et al. (14) also used clonogenic assays to assess cytotoxicity and it may be that this assay selects for cells with altered sensitivity to the drug. Selected clones may express other enzymes reported to activate MMC such as DT-diaphorase (17, 35), NRH:quinone oxidoreductase 2 (37, 38), NADPH-ferrodoxin reductase (39) or cytochrome b5 reductase (9); they may also express antioxidants that detoxify and protect against ROS-induced damage. In this regard, antioxidant enzymes including glutathione peroxidase, superoxide dismutase and catalase have all been shown to reduce or abolish MMC cytotoxicity in tumor cells in vitro (29, 40).
It is well recognized that hypoxia can enhance the biological activity of redox active chemotherapeutic agents; presumably via the stabilization of the one electron reduced drug (32). In the case of MMC, this is the highly reactive MMC semiquinone radical (Fig. 1A) (32). Under hypoxic conditions, the MMC semiquinone radical can also rearrange to form the more stable hydroquinone (5, 7). Increased cytotoxicity of MMC under hypoxic conditions has been reported previously. For example, Keyes et al. (41) found that hypoxia enhanced the sensitivity of EMT6 mouse breast carcinoma cells and V79 Chinese hamster lung fibroblasts to MMC. Belcourt et al. (13, 42) and Seow et al. (14) reported in that MMC was more cytotoxic in CHO cells overexpressing cytochrome P450 reductase under hypoxic conditions. Interestingly, these investigators found little or no differences in the cytotoxicity of MMC in parental CHO cells under hypoxic and aerobic conditions, despite the fact that these cells readily redox cycle MMC. In contrast, in our studies, we found no differences in the cytotoxicity of MMC under hypoxic conditions in CHO-WT or CHO-OR cells, or in the different tumor cell lines which varied in cytochrome P450 reductase activity. Each cell type can mediate the one electron reduction of MMC and it is presumed that this process occurs in the cells under hypoxic conditions. If semiquinone radicals are in fact stabilized in cells under hypoxia, they do not appear to mediate MMC-induced growth inhibition. Our results are in accord with earlier studies showing no significant differences in cytotoxicity of MMC or the related analog EO9 under aerobic and hypoxic conditions in A2780 human ovarian tumor cells or HT-29 colon tumor cells (43–45).
The precise mechanisms mediating the distinct sensitivities of the different tumor cell lines to MMC under aerobic and hypoxic conditions are not known. One and two electron reduction of MMC occurs in both the presence and absence of oxygen, and electrophilic intermediates formed as a result are active alkylating species that can modify DNA forming monoadducts, intrastrand cross-links and DNA-DNA interstrand cross-links (46). The relative formation of the different reduced species of MMC at different oxygen tensions and their contribution to toxicity in each cell line has not been determined. In the presence of oxygen, MMC redox cycling generates ROS which can contribute to the biological effects of MMC. Whether or not ROS contribute to the actions of MMC may depend, as indicated above, not only on antioxidant enzymes (29, 40), but also small molecular weight antioxidants such as glutathione, alpha-tocopherol and ascorbic acid which can detoxify oxidants. However, it is important to note that MMC-induced ROS formation does not appear to directly mediate cytotoxicity as evidenced by the fact that no correlation was observed between the capacity of the different cells to generate ROS and cell growth inhibition. Our previous work showing that cytochrome P450 reductase activity and ROS generation by nitrofurantoin redox cycling does not correlate with cell growth inhibition in the tumor cell lines suggest that the present findings are not specific for MMC (27). In this regard, Ramji et al. (47) have shown that redox cycling of doxorubicin is also not correlated with cytotoxicity in cytochrome P450 reductase overexpressing breast cancer cell lines. It has previously been reported that MMC-induced cytotoxicity is correlated with the activity of enzymes mediating its two electron reduction (15, 17, 34, 35). This suggests that the MMC hydroquinone intermediate may be important in growth inhibition observed in our studies including CHO-OR cells which are highly efficient in generating ROS. This is supported by our findings that hypoxia has no effect on MMC-induced cytotoxicity. Other enzymes in CHO-OR cells that can mediate the two electron reduction of MMC include NRH:quinone oxidoreductase (37, 38). We also cannot exclude the possibility that other enzymes mediating the one electron reduction of MMC including NADH-cytochrome b5 reductase, xanthine oxidase and nitric oxide synthase also mediate cytotoxicity in these cells. Further studies are needed to more precisely characterize the metabolism of MMC under aerobic and hypoxic conditions in order to identify the enzymes mediating this process, and to better define MMC-induced growth limiting events in the different tumor cell lines.
Financial support: This work was supported in part by National Institutes of Health grants CA100994 (JDL), CA093798 (DEH), ES005022 (JDL, DLL), ES004738 (DLL, JDL), CA132624 (DLL, JDL), AR055073 (JDL, DLL, DEH) and GM034310 (DLL, JDL). This work was also funded in part by the National Institutes of Health CounterACT Program through the National Institute of Arthritis and Musculoskeletal and Skin Diseases (award #U54AR055073 to JDL). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the federal government.