Cytotoxicity of Fumonisin [B.sub.1], Diethylnitrosamine, and Catechol on the SNO esophageal cancer cell line. (Articles).
Approximately 60-90% of human cancers are attributable to environmental factors, particularly chemical carcinogens (1). Two important groups of carcinogens that have emerged are the mycotoxins and N-nitrosamines.
Fumonisin [B.sub.1] (F[B.sub.1]) is a mycotoxin produced by the fungus Fusarium verticillioides, a ubiquitous soil-borne fungus that frequently contaminates maize and maize products. F[B.sub.1] is the most abundant and toxic of the known fumonisins and has been associated with many animal diseases, including equine leukoencephalomalacia (2), porcine pulmonary edema (3), and liver and kidney tumors in rats (4). The geographic areas where F[B.sub.1] occurs in high concentrations have been associated with high rates of esophageal cancer (EC) in humans (5). Although F[B.sub.1] has been classified by the International Agency for Research on Cancer as a type 2B carcinogen (6) and appears to be an initiator and promotor of carcinogenesis in rats (7), we have as yet no convincing evidence that F[B.sub.1] is a human carcinogen.
Minute quantities of nitrosamines are present in cigarette smoke, alcoholic beverages, and certain foods, but their cumulative effect over several years could play a role in cancer. N-nitrosamines are precarcinogens, giving rise to ultimate carcinogens only after enzymatic activation under acidic conditions in the stomach (8). A possible correlation exists between EC and gastrectomy, that is, alkaline reflux into the esophagus. This could account for the mechanism by which ultimate carcinogens of nitrosamines reach the esophagus.
N-nitrosamines are organ specific, and in this regard, asymmetrical nitrosamines (e.g., N-nitrosomethylalanine and N-nitrosopiperidine) have a tendency to induce tumors of the esophagus (1). Mingxin et al. (9) found that methylbenzylnitrosamine, nitrososarcosine ethyl ester, and other secondary amines induced carcinoma of the esophagus in rats. Harris et al. (10) reported that cultured human esophageal cells activated dimethylnitrosamine into DNA-binding metabolites.
F. verticillioides enhancement of nitrosamine-induced EC in rats has been reported by van Rensburg (11). Also, nitrosamines and their precursors have been found in foods from a high-EC area of China (12). These findings suggest that nitrosamines may play a role in the etiology of human esophageal carcinogenesis, possibly by acting synergistically with mycotoxins or other metabolites of F. verticillioides (13).
Excessive exposure to tobacco and alcohol has repeatedly been implicated as a principal factor in carcinoma of the esophagus (14,15). Tobacco and tobacco smoke contain many distinct classes of chemical carcinogens and cocarcinogens, including the N-nitrosamines, which are important environmental carcinogens. Dietary catechol (CAT), a constituent of cigarette smoke, was previously found to be a cocarcinogen with methyl-N-nitrosamine (MNAN) for inducing esophageal tumors in rats. CAT in drinking water was not significantly cocarcinogenic with MNAN, but ethanol and CAT given in the drinking water was cocarcinogenic with MNAN and tumorigenic when given without MNAN (16). The increased carcinogenicity by MNAN occurs because ethanol and CAT affect MNAN metabolism.
The human esophageal carcinoma cell line SNO was derived from a well-differentiated squamous cell carcinoma (6.5 cm long and metastatic to the lymph nodes) that was explanted from patient S.N., a 62-year-old Zulu male, in July 1972 (17).
There is sufficient evidence of the carcinogenicity of F[B.sub.1] in test animals, but not enough data to draw definite conclusions for humans (18). We undertook this study to investigate whether F[B.sub.1] is an etiologic agent in human esophageal carcinoma, as well as to review the cytotoxic effect of other etiologic factors in this disease. In this study we evaluated the cytotoxicity of F[B.sub.1], diethylnitrosamine (DEN), and CAT on the human SNO EC cell line.
Materials and Methods
Materials. We purchased all cell culture media and plasticware from Sterilin (Durban, South Africa). We obtained methylthiazol tetrazolium (MTT) salt, DEN, and CAT from Sigma Chemical Company (St. Louis, MO, USA) and F[B.sub.1] from the Programme on Mycotoxins and Experimental Carcinogenesis (Cape Town, South Africa). We purchased all solvents from Merck (Johannesburg, South Africa).
Preparation of toxin stock solutions. We prepared stock solutions of F[B.sub.1], DEN, and CAT by dissolving 0.5 mg of each toxin in 30 [micro]L ethanol, 170 [micro]L dimethyl sulfoxide (DMSO), and 4.8 mL complete culture medium (CCM; minimum essential medium supplemented with 5% fetal calf serum, 1% Penstrep fungizone, and 1% L-glutamine), thus yielding a toxin concentration of 100 [micro]M. The control stock solution contained ethanol, DMSO, and CCM. For the cytotoxicity assay, we used serial dilutions (2.165-34.64 [micro]M) prepared from the stock solution.
Preparation of the MTT salt. We dissolved MTT salt (5 mg) in 1 mL Hank's balanced salt solution (HBSS) to give a concentration of 5 mg/mL. We then filtered the suspension through a 0.45-[micro]m filter and stored it in the dark at room temperature until use.
The MTT assay. We determined the cytotoxic effect of the toxins on SNO cells using the MTT assay. We washed two confluent monolayers in 75-c[m.sup.3] culture flasks in CCM with HBSS, which we then trypsinized to detach cells from the flask. We removed the trypsin and replaced it with 15 mL CCM and gently shook the flasks to dislodge the cells. We assessed cell viability using trypan blue, determined cell numbers using a hemocytometer (19), and resuspended cells to give a cell count of 4.5 x [10.sup.6] cells. We aliquoted the cell suspension (100 pL) into each well of two 96-well tissue culture plates and incubated them at 37[degrees]C.
After 24 hr, we replaced the CCM with 100 [micro]L toxin at concentrations ranging from 2.165 to 34.64 [micro]M, using five replicates for each serial dilution. After a 48-hr incubation at 37[degrees]C, we removed the toxin and replaced it with 10 [micro]L MTT (5 mg/mL) and 100 [micro]L CCM, and then incubated the mixture for a further 4 hr. We subsequently removed the supernatant and aliquoted 100 [micro]L DMSO into each well to solubilize any resulting formazan crystals. After 1 hr, we determined the optical density of the resulting solution spectrophotometrically using a Bio-Rad (Johannesburg, South Africa) multiwell plate reader at 595 nm and a reference wavelength of 630 nm. We calculated cell viability from the absorbance values obtained.
We then statistically analyzed the results using one-way analysis of variance (ANOVA) for multiple comparisons and Student's t-test and the Mann-Whitney rank sum test for two-group comparisons. We constructed graphs to illustrate cell viability after calculation of the standard deviation. We considered data comparisons significant if p < 0.05.
Results and Discussion
In this study we evaluated the cytotoxic effect of F[B.sub.1] and other etiologic agents (DEN and CAT) on SNO cells using the MTT assay.
We observed minimal cytotoxicity in SNO cells exposed to F[B.sub.1] over 48 hr compared with control cells (Figures 1 and 2), with F[B.sub.1]-treated cells showing a 23% cell mortality after 48-hr incubation with 34.64 [micro]M F[B.sub.1] (p < 0.022). The low cytotoxic response by SNO cells at the concentrations tested is in agreement with other studies. Cawood et al. (20) noted a low cytotoxic response in primary hepatocytes. However, F[B.sub.1] has been shown to be cytotoxic to certain mammalian cell lines (21,22), suggesting that some tissue may accumulate F[B.sub.1] over time or may be more susceptible to the cancer-promoting ability of F[B.sub.1]. The effects of F[B.sub.1] are chronic, as suggested by the late age of onset of EC (between 40 and 60 years). F[B.sub.1] is also poorly absorbed (experiments show that 90% of F[B.sub.1] is directly excreted), which explains why F[B.sub.1] is a slow-acting carcinogen (23).
[FIGURES 1-2 OMITTED]
Apart from a chronic effect, the low toxic response over 48 hr by cells treated with F[B.sub.1] may suggest that F[B.sub.1] is more effective as a cancer promoter than an initiator of EC in humans. This disagrees with studies that show a toxic effect by F[B.sub.1] in rat liver and kidney. The presence of an amino group and the location of the hydroxyl on [C.sub.14]/[C.sub..sub.15] may also play an important role in both the toxic and cancer-initiating activities of F[B.sub.1]. The presence of the amino group facilitates the conjugation of F[B.sub.1] via gluteraldehyde to protein carriers (24). This would provide a plausible mechanism by which F[B.sub.1] exerts its mitogenic effect.
Cytotoxicity depends on the ability of a molecule to bind cellular receptors and/or penetrate the cell membrane (dependent on size, structural conformation, and polarity of the compound). Polarity appears to be an important determinant in the cytotoxic behavior of F[B.sub.1]. In general, less polar molecules have higher cytotoxicity (25). F[B.sub.1] is a strongly polar compound (26). This explains the low cytotoxic response observed on treatment with F[B.sub.1].
Another possibility is that F[B.sub.1] acts in synergy with a cocarcinogen that forms part of the etiology of EC. It therefore appears that SNO cells are more susceptible to combined treatment with DEN and F[B.sub.1]. Oneway ANOVA revealed a significant difference between treatment with F[B.sub.1] alone compared with treatment with DEN + F[B.sub.1] at 34.64 [micro]m (p < 0.043), 17.32 [micro]M (p < 0.008), 8.66 [micro]M (p < 0.005), and 4.33 [micro]M (p < 0.03). A cell mortality of 37% occurred upon treatment with DEN +. F[B.sub.1] (34.64 [micro]M). At the same concentration, we observed only 9% cell mortality upon treatment with DEN alone. Figure 1 shows the differences observed in cell viability after treating SNO cells with F[B.sub.1], DEN, and DEN + F[B.sub.1].
DEN is part of a widely acting group of potent carcinogens. Nitrosamines are metabolized by mixed-function oxidase enzymes to a chemically active alkylating agent in the rat and possibly in the human esophagus (27). This reaction produces alkylating intermediates that can form [O.sup.6]-alkylguanines from DNA guanine. DNA guanine then pairs with thymine rather than cytosine. It is thought that this mispairing produces a mutation that initiates carcinogenesis (28). In support of this view, we detected elevated levels of [O.sup.6]-methylguanine in esophageal DNA extracted from EC patients in China (29). When nitrosamines alkylate rat esophageal DNA and thereby initiate cancer, they are presumably activated by microsomes in the rat esophagus because the active metabolites do not travel in the blood from other organs to the esophagus (24). The same may apply to nitrosamine induction of EC in humans. The results suggest that DEN acts in concert with F[B.sub.1] and may act as a cancer initiator to promote the activity of F[B.sub.1].
The cytotoxicities of F[B.sub.1], CAT, and CAT + F[B.sub.1] are shown in Figure 2. CAT is cytotoxic to SNO cells, producing 44% cell mortality at 34.64 [micro]M (p < 0.03). This agrees with epidemiologic studies that have clearly demonstrated a strong positive association of chronic tobacco smoking with EC (14). We also observed a significant difference between F[B.sub.1] treatment and F[B.sub.1] + CAT at 4.33 F[B.sub.1]M (p < 0.01) and 2.165 [micro]M (p < 0.038). However, we found no significant differences in cytotoxic activity between treatment with F[B.sub.1] alone and F[B.sub.1] + CAT (23% and 28% cell death, respectively) when we assessed the entire range of concentrations against each other. When CAT and F[B.sub.1] co-occur, there seems to be a stimulation of cell growth or a reduction in mitochondrial dehydrogenase activity. The results of this study suggest that F[B.sub.1] inhibits the effect of CAT on the cells, possibly by reducing binding sites for the toxin.
[FIGURE 2 OMITTED]
The results show that F[B.sub.1] alone is not overtly cytotoxic in humans, but that it may act as a promotor or initiator of carcinogenesis in synergy with certain cocarcinogens. Future studies will involve the treatment and immunolocalization of F[B.sub.1] in SNO cells, using light and electron microscopy. In addition, we know that F[B.sub.1] alters sphingolipid metabolism. We will therefore expose SNO cells to sphinganine and F[B.sub.1] to determine the cytotoxic effect on this cell line.
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Address correspondence to R.B. Myburg, Department of Physiology, School of Medical Sciences, Nelson R. Mandela School of Medicine, Private Bag 7, Congella, 4013, South Africa. Telephone: +27-31-260-4404. Fax: +27-31-260-4455. E-mail: firstname.lastname@example.org
We thank the University of Natal Research Fund and the Cancer Association of South Africa for funding this study.
Received 18 July 2001; accepted 17 December 2001.
Rene B. Myburg, Michael F. Dutton, and Anil A. Chuturgoon
Department of Physiology, School of Medical Sciences, Nelson R. Mandela School of Medicine, Congella, South Africa
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|Author:||Chuturgoon, Anil A.|
|Publication:||Environmental Health Perspectives|
|Date:||Aug 1, 2002|
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