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Short Communication |
USC/Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, Los Angeles, California 90089 [C-L. S., J-M. Y., K. A., M. C. Y.], and Department of Community, Occupational and Family Medicine, National University of Singapore, Singapore [S-H. L., H-P. L.]
| Abstract |
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92.5 g/1000 Kcal) was associated with a 2.3-fold increase in bladder cancer risk (95% confidence interval = 1.15.1) after adjustment for cigarette smoking and level of education. Similar results were obtained for intakes of soy protein and soy isoflavones. The soyfood-bladder cancer risk association did not differ significantly between men and women and was not explained by other dietary factors. The soy-cancer relationship became stronger when the analysis was restricted to subjects with longer (
3 years) duration of follow-up. To our knowledge, this is the first epidemiological report on the effect of dietary soy on bladder cancer risk. | Introduction |
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To our knowledge, there are no epidemiological data on the relationship between dietary soy and bladder cancer risk. There are limited data from in vitro and nonhuman in vivo studies suggesting that soy isoflavones may protect against bladder cancer development (4 , 5) . In this study, we examined adult soy intake in relation to bladder cancer risk within a prospective cohort study of Singapore Chinese whose intake levels of soy are among the highest in the world.
| Subjects and Methods |
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There are seven common soyfoods (all are nonfermented) in the Singapore Chinese diet, including plain tofu, taupok, taukwa, foopei, foojook, tofu-far, and soybean drink. Taupok is taukwa plus oil and tofu-far is tofu plus syrup. We used the following algorithm to estimate an overall soy intake for each study subject: water accounts for 89% of cooked plain-tofu by weight; 69% of cooked taukwa; 58% of cooked foopei; 54% of cooked foojook; and 92% of soybean drink. Thus, we determined that 1 g of taukwa is equivalent to 2.8 g (31/11) of plain tofu. Similarly, 1 g of foopei and foojook are equivalent to 3.8 g (42/11) and 4.2 g (46/11) of plain tofu, respectively. Finally, 1 g of soybean drink is equivalent to 0.73 g (8/11) of plain tofu. The total soy intake for a given subject was the summation of all soyfoods expressed in units of plain tofu equivalent. Previously, we had measured concentrations of genistein, daidzein, and glycitein in market samples of common soyfoods in Singapore (6) . Total soy isoflavone intake for a given subject was estimated from the summation of genistein, daidzein, and glycitein contents of all seven soyfoods. Likewise, total soy protein intake for each study subject was calculated from the protein contents of soyfoods listed in the Singapore Food Composition Table (6) .
Identification of incident cancer cases and deaths among cohort members was accomplished through regular record linkage of the cohort database with databases for the nationwide Singapore Cancer Registry and the Singapore Registry of Births and Deaths. The Singapore Cancer Registry was established in 1968 and since then has been continuously included in the "Cancer Incidence in Five Continents" serial publications by the International Agency for Research on Cancer in Lyon, France. As of December 31, 2000, 61 incident cases of bladder cancer were identified among cohort members. The observed number of incident bladder cancer was comparable with the corresponding expected number (64 bladder cancer cases) based on age- and sex-specific bladder cancer incidence rates for all Chinese in Singapore during 19921997 (7) . We reconfirmed the disease status of these 61 cases through manual review of their pathology reports.
For each study subject, person-years were counted from the date of baseline interview to the date of cancer diagnosis, date of death, or December 31, 2000, whichever occurred first. Eight hundred sixty-four cohort members with a personal history of cancer at baseline were excluded from the analysis. ANOVA was used to examine the associations between total soy intake and selected demographic/lifestyle characteristics and other dietary factors (8) . Cox proportional hazard regression method was used to estimate RRs3 and their corresponding 95% CIs and two-sided Ps, with adjustment for age at baseline (years), year of recruitment, sex, dialect group (Cantonese or Hokkien), and other potential confounders (9) . To adjust for energy intake, all foods and nutrients were expressed either as percentage of total energy or as weight/1000 Kcal. Intake levels of total soy, soy protein, and soy isoflavones were grouped in quartiles according to their distributions among all cohort subjects. All linear trend tests were based on the actual, continuous values of the dietary variables. Results in men and women were combined because the majority of the cases were men (77%) and no discernable difference in the soyfood-bladder cancer association was noted between the two sexes. Statistical computing was conducted using the SAS version 8.2 (SAS Institute, Inc.) and Epilog Windows version 1.0 (Epicenter Software).
| Results |
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Baseline characteristics of cohort subjects by quartiles of total soy intake are shown in Table 1
. Women reported significantly higher consumption of total soyfood compared with men. Statistically significant higher intakes of soyfoods also were observed among lifelong nonsmokers (versus smokers) and subjects with higher (versus lower) levels of education. There were statistically significant positive associations between intake of total soy and consumption of fish, nonsoy legumes, vegetables, fruits, total energy, total fat, total protein, total carotenoids, and vitamins A, C, and E. Conversely, statistically significant inverse associations were observed between total soy intake and consumption of grain products and carbohydrate. Table 1
also shows the means of total soy, soy protein, and soy isoflavones across the four quartiles of total soy in all cohort subjects.
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Compared with never smokers, ever smokers had a statistically significant 2-fold increased risk of bladder cancer after adjustment for level of education (RR = 2.12, 95% CI = 1.173.87). Among ever smokers, both duration and intensity of smoking were significantly related to risk (both sets of P for linear trend = 0.01). Smoking status (never, former, current) at baseline was the strongest predictor of bladder cancer risk in this study population; no other smoking variables contributed additionally toward risk once smoking status at baseline was included in the Cox regression model (all Ps > 0.50). Therefore, smoking status at baseline was used to adjust for cigarette smoking in subsequent dietary analyses.
Table 2
presents intake of total soy, soy protein, and soy isoflavones at baseline in relation to risk of bladder cancer. There was a statistically significant increase in risk with higher intakes of total soy, soy protein, or soy isoflavones. The relationship did not change after adjustment for cigarette smoking and level of education.
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There is a possibility that because of disease symptoms, soy intake patterns in bladder cancer patients were already modified before the time of cancer diagnosis. An increase in intake among these patients would result in an artifactual positive association between dietary soy and bladder cancer. If this were the case, the soy-bladder cancer association would be stronger in subjects with a shorter duration of follow-up. In fact, a stronger soy-bladder cancer risk association was observed for those with a longer (
3 years) duration of follow-up; the adjusted RRs (95% CI) for the 2nd, 3rd, and 4th quartile of total soy intake were 3.04 (0.8211.25), 2.87 (0.7610.86), and 4.02 (1.1014.69), respectively, relative to the lowest quartile.
We repeated all analyses on cases of transitional cell carcinoma only (n = 55 cases). Results remained unchanged. The adjusted RR (95% CI) for the highest versus lowest quartile of total soy intake was 2.25 (1.024.94).
| Discussion |
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The relationship between soyfood intake and risk of cancer in humans is unclear, even for breast cancer, the most studied site. Four epidemiological studies reported a statistically significant inverse relationship between dietary soy and risk of breast cancer (11) , whereas five others reported results compatible with a null association (12) . Results based on in vitro (breast cancer cells) or in vivo models are similarly mixed. The major constituent of soy isoflavones, genistein, was shown to have anticarcinogenic properties at high concentrations (13) but procarcinogenic activities at low concentrations (14) . In nude mice, genistein was found to both inhibit (15) and stimulate breast tumor growth (16) .
To our knowledge, this study is the first epidemiological investigation on dietary soy and bladder cancer risk. The data from in vitro and whole animal studies have yielded conflicting results on the role of dietary soy in bladder carcinogenesis. Mokhtar et al. (4) reported that dietary soy reduced nitrosamine-induced bladder tumors in mice. Soy isoflavones or soy concentrate inhibited both growth of human bladder cancer cells in vitro and growth of implanted murine or human bladder cancer in nude mice (5) . On the other hand, laboratory studies involving human bladder cancer cells (17) and whole animals (18) have supported a role of insulin-like growth factor-1 in bladder carcinogenesis, and a recent randomized, double-blind, placebo-controlled feeding experiment observed that men given soy protein supplements exhibited significant increase in serum insulin-like growth factor-1 level (19) .
Results regarding the association between dietary soy and other cancers are equally conflicting. Soy was shown to inhibit growth of colon cancer cells (20) and the development of chemically induced colon cancer in rats (21) . However, administration of genistein to male rats treated with a colon carcinogen led to enhanced colon cancer development (22) . Available epidemiological data indicate that dietary soy has no effect on colon cancer risk (23) . Additionally, genistein was shown to promote growth of human pancreatic tumor cells (24) and induce chromosomal aberrations in human peripheral blood lymphocytes (25) .
It is possible that some unidentified substances in soyfoods are responsible for the observed adverse effect on the development of bladder cancer. In fact, our data showed a stronger positive association with total soy than with soy protein or soy isoflavones. It is also conceivable that soyfood is a surrogate of some other as-yet-unidentified constituents in the diet that relate to an increased risk of bladder cancer.
Since 1999, when the Food and Drug Administration concluded that soy protein included in a diet low in saturated fat and cholesterol may reduce the risk of coronary heart disease, there has been a noticeable increase in the consumption and production of soyfoods in the United States. According to national surveys conducted by the United Soybean Board, 27% of Americans reported using soy products at least once a week in the year 2000, up from 15% in the year 1998 (26) . Therefore, the risk versus benefit of dietary soy in disease causation carries important public health implications.
Urine is an important route for the excretion of soy constituents such as genistein, daidzein, and their metabolites. In fact, the concentration of genistein in the urine is considerably higher than that in blood (27) . Thus, a possible effect of dietary soy on bladder cancer risk warrants further study. We caution that our novel finding of a positive association between soy and bladder cancer risk is based on a relatively short period of follow-up and a modest number of cancer cases. If this provocative observation is confirmed by others, laboratory studies to delineate possible mechanisms will be needed.
| Footnotes |
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1 The Singapore Chinese Health Study has been supported by NIH Grants R01 CA55069, R53 CA53890, and R01 CA80205 from the National Cancer Institute, Bethesda, Maryland. ![]()
2 To whom requests for reprints should be addressed, at USC/Norris Comprehensive Cancer Center, MC 9175, University of Southern California Keck School of Medicine, 1441 Eastlake Avenue, Los Angeles, CA 90089-9176. Phone: (323) 865-0827; Fax: (323) 865-0136; E-mail: canlan{at}hsc.usc.edu ![]()
3 The abbreviations used are: RR, relative risk; CI, confidence interval. ![]()
Received 4/18/02; revised 8/20/02; accepted 9/16/02.
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