Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-12-03T19:16:28.931Z Has data issue: false hasContentIssue false

Cruciferous vegetable intake and the risk of human cancer: epidemiological evidence

Conference on ‘Multidisciplinary approaches to nutritional problems’ Symposium on ‘Nutrition and health’

Published online by Cambridge University Press:  08 December 2008

Mi Kyung Kim
Affiliation:
Carcinogenesis Branch, National Cancer Center, Kyunggido, Korea
Jung Han Yoon Park*
Affiliation:
Department of Food Science and Nutrition, Hallym University, Chuncheon, Korea
*
*Corresponding author: Professor Jung Han Yoon Park, fax +82 33 256 0199, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Over several decades a number of epidemiological studies have identified the inverse associations between cruciferous vegetables and the risk of several cancers, including gastric, breast, colo-rectal, lung, prostate, bladder and endometrial cancers, via plausible physiological mechanisms. Although retrospective case–control studies have consistently reported inverse associations between the risk of these cancers and the intake of cruciferous vegetables and isothiocyanate-containing plants, current prospective cohort studies have found these associations to be weaker and less consistent. Genetic variations affecting the metabolism of glucosinolate hydrolysis products may modulate the effects of cruciferous vegetable consumption on cancer risk, which may be one of the reasons for the discrepancies between retrospective and prospective studies. In addition, methodological issues such as measurement errors of dietary exposure, misclassification, recall bias, publication bias, confounding and study design should be carefully considered in interpreting the results of case–control and cohort studies and in drawing conclusions in relation to the potential effects of cruciferous vegetables on cancers. Although recent comprehensive reviews of numerous studies have purported to show the specific protective role of cruciferous vegetables, and particularly Brassicas, against cancer risk, the current epidemiological evidence suggests that cruciferous vegetable consumption may reduce the risk only of gastric and lung cancers. However, there is at present no conclusive evidence that the consumption of cruciferous vegetables attenuates the risk of all other cancers.

Type
Research Article
Copyright
Copyright © The Authors 2008

Abbreviations:
DIM

3,3′-diindolylmethane

GST

glutathione S-transferase

I3C

indole-3-carbinol

ITC

isothiocyanate

RR

relative risk

Abundant evidence derived from descriptive and analytical epidemiological studies has indicated that higher fruit and vegetable intake is associated with a reduced risk of a variety of cancers(1Reference Adlercreutz6), and several physiologically-plausible mechanisms have been suggested to explain these observations. The constituents of fruits and vegetables, including fibre, micronutrients (such as vitamins C and E and folate) and phytochemicals (such as carotenoids, phenolics, isoflavonoids, isothiocyanates (ITC) and indoles) demonstrate a range of physiological properties, including anticarcinogenic effects(Reference Stan, Kar and Stoner7). In particular, the phytochemicals have been reported to induce detoxification enzymes, scavenge free radicals, alleviate inflammation, inhibit malignant transformation, stimulate immune functions and regulate the growth of cancer cells(Reference Aggarwal and Shishodia8).

In 1997 an international panel of the American Institute for Cancer Research and the World Cancer Research Fund concluded that convincing evidence existed to suggest that higher consumption of vegetables, but not fruit, protects against several cancers(3). This conclusion was based principally on the results of case–control studies. Subsequently, however, several cohort studies have reported inconsistent results. In 2003, on the basis of all the published epidemiological evidence available, the Joint WHO/FAO Expert Consultation concluded that fruit and vegetables ‘probably,’ but not ‘convincingly,’ reduce cancer risk(5). A subsequent evaluation by the International Agency for Research on Cancer has confirmed that higher vegetable intake ‘probably’ lowers the risk of oesophageal and colo-rectal cancers, in addition to the conclusion that an increase in the consumption of vegetables ‘possibly’ reduces the risk of other cancers, including oral, pharynx, stomach, larynx, lung, ovary and kidney cancers(1).

Recently, the World Cancer Research Fund and American Institute for Cancer Research panels have issued a second report that concludes that the epidemiological findings from cohort studies conducted since the mid-1990s have rendered the overall evidence that fruits or vegetables protect against cancers somewhat less impressive. A number of studies have generated apparently conflicting results(Reference Stan, Kar and Stoner7). In no case now is the evidence of protection adjudged to be convincing. However, in many cases a judgment of ‘probable’ appears to be appropriate(4).

There may be many reasons why the protective role of vegetables against cancers remains inconclusive. Not all fruits and vegetables show the ability to suppress carcinogenesis, and there may be specific subtypes of fruits and vegetables that exhibit anticarcinogenic activity. Thus, it is crucial to determine which fruits and vegetables possess this ability. In addition, it is essential to determine which individual components present in fruit and vegetables play pivotal roles in cancer prevention. Thus, the present review has focused on the epidemiological evidence for the association between cruciferous vegetable intake and the risk of cancers. The mechanisms underlying the actions of cruciferous vegetable components are outlined and the epidemiological evidence for the effects of genetic polymorphisms on the response to cruciferous vegetable intake is discussed.

Constituents of cruciferous vegetables and mechanisms of their actions

Recently, cruciferous vegetables, rather than vegetables as a group, have drawn a great deal of attention in cancer research because of their potential protective properties. Cruciferous vegetables, including broccoli, cabbage, cauliflower, kale and mustard, are among the prevailing food crops worldwide. They are widely recognised as healthy foods, and have also been identified as rich sources of carotenoids, vitamin C, folate and soluble fibre, which may play an important role in cancer prevention(Reference Lampe9). In addition, the ability of cruciferous vegetables to protect against neoplastic diseases has been attributed to their high glucosinolate content(Reference Oganesian, Hendricks and Williams10). Glucosinolates are converted by myrosinase in plant cells and microflora in the gastrointestinal tract to indole-3-carbinol (I3C) and ITC(Reference Srivastava and Shukla11), two phytochemicals that exhibit anticarcinogenic effects in models of animal cancer.

I3C affects the phase II enzyme systems in human subjects (for review, see Lampe(Reference Lampe9)), inhibits carcinogenesis in animal experiments(Reference Oganesian, Hendricks and Williams10, Reference Srivastava and Shukla11) and also inhibits the growth of a variety of human cancer cells(Reference Zhang, Hsu and Kinseth12, Reference Frydoonfar, McGrath and Spigelman13). When I3C is exposed to gastric acid it is converted to a number of self-condensation products, the major one of which is 3,3′-diindolylmethane (DIM)(Reference Grose and Bjeldanes14, Reference De Kruif, Marsman and Venekamp15). DIM is readily detected in the liver and faeces of rodents fed on I3C, whereas the ingested I3C is not detected in these animals(Reference Stresser, Williams and Griffin16). These results imply that DIM, and not I3C, may mediate the observed physiological effects of dietary I3C. The results of in vivo animal studies have indicated that DIM shows cancer-preventive effects(Reference Chang, Tou and Hong17, Reference Nachshon-Kedmi, Fares and Yannai18). One of the suggested mechanisms by which DIM exerts its anticarcinogenic effects is the stimulation of the aryl hydrocarbon receptor. The binding of DIM to aryl hydrocarbon receptor results in the translocation of the DIM–aryl hydrocarbon receptor complex to the nucleus and subsequent binding to xenobiotic response elements in the gene promoter, thereby resulting in transactivation(Reference Safe19). Aryl hydrocarbon receptor induces the transcription of the P4501A and 1B (CYP1A, CYP1B) enzyme families, glutathione S-transferase (GST) α, NAD(P)H:quinone oxidoreductase and UDP-glucuronosyltransferase(Reference Wolf20). In addition, DIM has been demonstrated to stimulate carcinogen detoxification(Reference Talalay and Fahey21), attenuate inflammation(Reference Cho, Seon and Lee22), enhance apoptosis(Reference Abdelrahim, Newman and Vanderlaag23, Reference Kim, Park and Shin24) and arrest the cell cycle(Reference Hong, Kim and Firestone25, Reference Firestone and Bjeldanes26) in cancer cell lines. Research has demonstrated that caspase-8 activation contributes to the DIM-induced apoptosis of colon cancer cells(Reference Kim, Park and Shin24). In addition, it has also been demonstrated that DIM suppresses the inflammatory response to lipopolysaccharide in murine macrophages via the inhibition of NF-κB and activator protein-1 signalling(Reference Cho, Seon and Lee22). Furthermore, DIM suppresses lung metastasis of 4T1 murine breast cancer cells when injected into the tail vein of syngeneic Balb/c mice (EJ Kim and JHY Park, unpublished results).

ITC formed from glucosinolates in cruciferous vegetables have been shown to effectively inhibit chemical carcinogenesis in animals. The chemopreventive effects of ITC observed in animal models is probably attributable, in part, to their ability to induce phase I activating enzymes (e.g. cytochrome P450) and phase II detoxifying enzymes (e.g. GST)(Reference Talalay and Fahey21). ITC are reported to activate gene transcription via an antioxidant/electrophile response element(Reference Bonnesen, Eggleston and Hayes27, Reference Kong, Owuor and Yu28). ITC dissociate the Kelch-like-ECH-associated protein 1 from nuclear factor-erythroid 2p45-related transcription factor in the cytoplasm. The released transcription factor translocates to the nucleus where it binds to small MAF (a term derived from musculoaponeurotic-fibrosarcoma virus), thereby forming a heterodimer that binds to the antioxidant/electrophile response element, resulting in transactivation(Reference Kong, Owuor and Yu28). The transcription factor/MAF target genes encode for phase II detoxification or antioxidant enzymes including GSTA2, NAD(P)H:quinone oxidoreductase, haem oxygenase-1 and γ-glutamate cysteine ligase (types C and M)(Reference Wolf20). Via this mechanism the increased production of phase II enzymes could result in more rapid and extensive excretion of reactive molecules, whether their source is reactive oxygen species, chemical carcinogens or hormone metabolites that are substrates for GST. GST catalyse the conjugation of glutathione to ITC(Reference Kolm, Danielson and Zhang29), thereby resulting in the formation of N-acetylcysteine conjugates that are later excreted by the kidney(Reference Shapiro, Fahey and Wade30). In addition, more current studies have demonstrated that ITC inhibit tumour cell proliferation both in vitro and in vivo via the inhibition of cell cycle progression and the stimulation of apoptosis via mechanisms distinct from effects on carcinogen metabolism (for review, see Zhang et al. (Reference Zhang, Yao and Li31)).

Epidemiological studies on cruciferous vegetable intake and cancer

Epidemiological investigations have previously identified associations between diets rich in cruciferous vegetables and other glucosinolate-containing plants and a reduced risk of several cancers(Reference Stan, Kar and Stoner7). A recent comprehensive review(Reference Higdon, Delage and Williams32), evaluation by the International Agency for Research on Cancer (33) and several pooled analyses(Reference Smith-Warner, Spiegelman and Yaun34Reference Lee, Giovannucci and Smith-Warner38) have suggested that higher intake of a specific subtype of vegetables such as cruciferous vegetables, but not vegetables as a whole, lowers the risk of a variety of cancers.

Gastric cancer

An initial review of case–control studies published up to 1996 has indicated consistent inverse associations between the intake of various vegetables and the risk of gastric cancer(Reference Steinmetz and Potter39). Eleven studies of total vegetables and eight studies of green vegetables have all reported inverse relationships. However, a panel assembled by the World Cancer Research Fund and American Institute for Cancer Research has recently concluded that vegetables ‘probably,’ but not ‘convincingly,’ reduce the risk of gastric cancer, based on a review of the results of ten large cohorts, forty-five case–control studies and nineteen ecological studies(4).

Few reports have investigated specifically the association between gastric cancer risk and cruciferous vegetable intake(Reference Hara, Hanaoka and Kobayashi40, Reference Chyou, Nomura and Hankin41). In a multi-centre hospital-based case–control study conducted in an agricultural area of Japan marginal associations were observed in the group with the highest consumption of Chinese cabbage (OR 0·61 (95% CI 0·35, 1·07)), broccoli (OR 0·60 (95% CI 0·34, 1·08)), Hypsizigus marmoreus (Bunashimeji) (OR 0·57 (95% CI 0·31,1·04)) and Pholita nameko (Nameko) (OR 0·56 (95% CI 0·30, 1·06))(Reference Hara, Hanaoka and Kobayashi40). Another case–cohort study conducted with a sample of Hawaiian men of Japanese descent has demonstrated that the consumption of cruciferous vegetables protects against gastric cancer(Reference Chyou, Nomura and Hankin41). A significant inverse trend was noted in the age-adjusted relative risk (RR; 0·60 (95% CI 0·4, 1·0); P=0·03 for trend) of gastric cancer with the intake of cruciferous vegetables.

A 2004 review by the International Agency for Research on Cancer has summarised the available results relating to gastric cancer(33). Overall, no association (OR 0·91 (95% CI 0·67, 1·23)) with cruciferous vegetable consumption was found in cohort studies, whereas a significant inverse association was shown (OR 0·71 (95% CI 0·73, 0·90)) in case–control studies. As was the case with other cancers, the inverse relationship between cruciferous vegetable consumption and the occurrence of gastric cancer from cohort studies was less pronounced than that reported in the case–control studies.

Colo-rectal cancer

The risk of colo-rectal cancer in relation to fruit and vegetable consumption has been reported in more than fifty epidemiological studies to date(Reference Steinmetz and Potter39, Reference Smith-Warner, Genkinger, Giovannucci, Heber, Blackburn, Go and Milner42). Earlier case–control studies conducted up to 1996 have shown that inverse associations between cruciferous vegetable intake and colon cancer risk have been relatively consistent, with eight case–control studies finding inverse associations, three finding no association and only one finding a positive association(Reference Steinmetz and Potter39). The evidence from case–control studies demonstrating a protective effect of cruciferous vegetables on rectal cancer is more consistent(Reference Steinmetz and Potter39). Five case–control studies have reported inverse associations, with marked reductions in risk for high cruciferous vegetable intake v. low intake. In a multi-centre Japanese study inverse associations were found in the group with the highest consumption of broccoli (OR 0·18 (95% CI 0·06, 0·58)) for the risk of colo-rectal cancer(Reference Hara, Hanaoka and Kobayashi40). These findings imply that cruciferous vegetables reduce the risk of colo-rectal cancer. However, in the Netherlands Cohort Study on Diet and Cancer(Reference Voorrips, Goldbohm and Verhoeven43) Brassica vegetables were shown to have inverse associations with colon cancer only in women (RR 0·51 (95% CI 0·33, 0·80); P=0·004 for trend), being stronger in the distal colon than in the proximal colon. For rectal cancer positive associations for Brassica vegetables of borderline significance were demonstrated in women (RR 1·66 (95% CI 0·94, 2·94); P=0·05 for trend).

In more recent studies the associations have been less consistent. In a recent review the weighted means of the RR reported for colo-rectal cancer were separately calculated for case–control and cohort studies(33). Data were selected only for cases in which the studies provided estimates of risk for cruciferous vegetable intake together with 95% CI. In the case–control studies a significant inverse association was detected (OR 0·73 (95% CI 0·63, 0·84)), whereas in the cohort studies no overall association with cruciferous vegetables intake was detected (OR 0·96 (95% CI 0·85, 1·09)). Similarly, a pooled analysis of fourteen prospective studies has shown that associations with colon cancer risk are not significant (pooled multivariate RR 0·99 (95% CI 0·93, 1·06) for the highest tertile v. the lowest tertile) for cruciferous vegetables(Reference Koushik, Hunter and Spiegelman37).

From the currently-available data it cannot be definitively concluded that the consumption of cruciferous vegetables is associated with the overall risk of colo-rectal cancer. However, inverse relationships have been demonstrated in subsites of the colo-rectum and by gender.

Lung cancer

The beneficial effect of cruciferous vegetable consumption on lung cancer risk is fairly consistent in several case–control studies that have demonstrated that higher intake of cruciferous vegetables lowers lung cancer risk(3). A recent review estimating the weighted means of the reported RR of lung cancer has shown a significant inverse association with cruciferous vegetables from both case–control (OR 0·76 (95% CI 0·65, 0·89)) and cohort studies (OR 0·86 (95% CI 0·75, 0·98))(33). However, several more recent cohort studies have reported conflicting results. Inverse associations between cruciferous vegetable consumption and lung cancer risk have been found in prospective studies of Finnish men(Reference Neuhouser, Patterson and Thornquist44), Dutch men and women(Reference Voorrips, Goldbohm and Verhoeven43) and US women(Reference Feskanich, Ziegler and Michaud45). In contrast, prospective studies of US men(Reference Feskanich, Ziegler and Michaud45) and European men and women(Reference Miller, Altenburg and Bueno-de-Mesquita46) have reported no such inverse association. Recently, the Pooling Project of Prospective Studies of Diet and Cancer(Reference Smith-Warner, Spiegelman and Yaun35) has evaluated the associations between specific and overall fruit and vegetable intakes and the risk of lung cancer by conducting a pooled analysis of cohort studies(Reference Smith-Warner, Spiegelman and Yaun35). In this project 3206 incident lung cancer cases developed among 430 281 women and men were followed for ⩽6–16 years across studies. Controlling for other lung cancer risk factors and smoking habits, a 16–23% reduction in the risk of lung cancer was detected for quintiles 2–5 of consumption for total vegetables and fruits v. the lowest quintile (RR 0·79 (95% CI 0·69, 0·90); P=0·001 for trend). A marginal association was detected between green leafy vegetable consumption (e.g. spinach (Spinacia oleracea), lettuce (Lactuca sativa), mustard and collard greens and kale) and lung cancer risk (pooled multivariate RR 0·93 (95% CI 0·81, 1·07) comparing intakes of ≥0·5 serving per d v. less than one serving per week; P=0·07 for trend; in the test for between-study heterogeneity P=0·45). However, none of the nine individual vegetables, including broccoli and cabbage, was found to be associated with the risk of lung cancer. Although the reason for discrepancies among the findings from prospective studies and between retrospective and prospective studies remains unclear, one possible explanation is that genetic variation, which affects the metabolism of glucosinolate hydrolysis products, may also influence the effects of cruciferous vegetable consumption on lung cancer risk.

Prostate cancer

Earlier epidemiological studies have suggested that a higher intake of cruciferous vegetables may lower prostate cancer risk (for review, see Verhoeven et al. (Reference Verhoeven, Goldbohm and van Poppel47)). A 2002 review has concluded that the epidemiological literature provides modest support for the premise that high cruciferous vegetable intake lowers prostate cancer risk(Reference Kristal and Lampe48). The examples are case–control studies(Reference Kolonel, Hankin and Whittemore49Reference Jain, Hislop and Howe52). Two studies have previously reported inverse associations for cruciferous vegetables, with marked reductions in risk for high cruciferous vegetable intake v. low intake(Reference Kolonel, Hankin and Whittemore49, Reference Jain, Hislop and Howe52). A population-based case–control study involving prostate cancer patients <65 years of age has reported that the adjusted OR for the comparison of twenty-eight or more servings of vegetables per week with fewer than fourteen servings per week is 0·65 (95% CI 0·45, 0·94; P=0·01 for trend; two-sided)(Reference Cohen, Kristal and Stanford50). For cruciferous vegetable consumption, adjusted for total vegetable intake and covariates, the OR for comparison of three or more servings per week with less than one serving per week is 0·59 (95% CI 0·39, 0·90; P=0·02 for trend). These results clearly show that high levels of consumption of vegetables, and in particular cruciferous vegetables, are associated with reduced prostate cancer risk(Reference Cohen, Kristal and Stanford50). Similarly, in a population-based case–control study that has evaluated the hypothesis that cruciferous vegetables contain potent anticarcinogenic ITC that may reduce the risk of prostate cancer, the intakes of cruciferous vegetables and broccoli, a good source of sulforaphane, were found to be associated with reduced prostate cancer risk at every level above that of the lowest consumers (adjusted 4th quartile OR 0·58 (95% CI 0·38, 0·89))(Reference Joseph, Moysich and Freudenheim51). This finding provides evidence suggesting that as little as two servings of cruciferous vegetables per month may reduce the risk of prostate cancer.

In contrast, associations between prostate cancer risk and cruciferous vegetable intake derived from prospective studies have been less consistent, with some showing inverse associations(Reference Giovannucci, Rimm and Liu53, Reference Kirsh, Peters and Mayne54) and others finding no significant association(Reference Key, Allen and Appleby55). In a recent prospective study of the screening arm of the Prostate, Lung, Colo-rectal, and Ovarian Cancer Screening Trial vegetable consumption was not found to be associated with overall prostate cancer risk(Reference Kirsh, Peters and Mayne54). However, the risk of extraprostatic prostate cancer (stage III or IV tumours) was shown to be reduced with increasing vegetable intake (RR 0·41 (95% CI 0·22, 0·74) for high intake v. low intake; P=0·01 for trend). This association was explained principally by the intake of cruciferous vegetables (RR 0·60 (95% CI 0·36, 0·98) for high v. low intake; P=0·02 for trend), particularly, broccoli (RR 0·55 (95% CI 0·34, 0·89) for more than one serving per week v. less than one serving per month; P=0·02 for trend) and cauliflower (RR 0·48 (95% CI 0·25, 0·89) for more than one serving per week v. less than one serving per month; P=0·03 for trend). These results suggest that high intake of cruciferous vegetables, including broccoli and cauliflower, may be associated with a reduced risk of advanced prostate cancer, and in particular metastatic prostate cancer.

Multiple dietary evaluations of 2969 cases of prostate cancer from 1986 to 2000 have indicated no overall relationship between the baseline intake of cruciferous vegetables and prostate cancer risk(Reference Giovannucci, Rimm and Liu53). However, an inverse relationship between prostate cancer risk and cruciferous vegetable intake was found among men <65 years of age. Furthermore, when analysis was restricted to men who had undergone a prostate-specific antigen test and who had prostate gland-confined cancer the inverse relationship was shown to be stronger. The differential findings underlie the importance of control for screening, age of patients and stage of cancer (organ-confined or metastatic).

Breast cancer

Substantial epidemiological evidence of an inverse association between consumption of cruciferous vegetables and the risk of breast cancer has been derived from available case–control studies (overall OR 0·87 (95% CI 0·78, 0·96))(33). Additionally, other reports have suggested that the consumption of certain cruciferous vegetables may attenuate the risk. In the Western New York Diet Study, a case–control study of Caucasian women with incident breast cancer, a marginal inverse association has been shown between the consumption of cruciferous vegetables, particularly broccoli, and breast cancer risk in premenopausal women (4th quartile OR 0·6 (95% CI 0·40, 1·01); P=0·058), with weaker or non-existent associations among post-menopausal women(Reference Ambrosone, McCann and Freudenheim56). These data indicate that cruciferous vegetables may have a role in reducing the risk of premenopausal breast cancer. The association has also been assessed in a case–control study conducted in Sweden, a country with a wide range of cruciferous vegetable intake(Reference Terry, Wolk and Persson57). Brassica vegetable intake was found to be inversely associated with breast cancer risk (multivariate OR 0·76 (95% CI 0·62, 0·93) for highest quartile of intake v. lowest quartile; P=0·01 for trend). Further detailed analysis of the data shows that the OR among women in the highest decile (10%) of cruciferous vegetable consumption (median, 1·5 servings per d) v. the lowest decile (virtually no consumption) is 0·58 (95% CI 0·42, 0·79; P=0·003).

However, currently-available cohort studies have detected no association between cruciferous vegetable intake and breast cancer risk(33). A pooled analysis of eight cohort studies has reported no associations between the intakes of individual or overall fruit and vegetables and breast cancer risk(Reference Smith-Warner, Spiegelman and Yaun34). In this study 7377 incident invasive breast-cancer cases occurring among 351 825 women were followed for 6–16 years. Total fruit and vegetables were found to be marginally associated with the risk of breast cancer (pooled multivariate RR 0·93 (95% CI 0·86, 1·00); P=0·12 for trend) in comparisons of the highest intake quartile v. lowest intake quartile. However, the intake of cruciferous vegetables (broccoli, Brussels sprouts and cabbage) was not found to be significantly associated with breast cancer risk.

In summary, although several case–control and cohort studies have reported inverse relationships in a variety of populations, there is no conclusive epidemiological evidence to suggest that cruciferous vegetables have a causative function in reducing breast cancer risk.

Bladder cancer

To date, two prospective(Reference Michaud, Spiegelman and Clinton58, Reference Michaud, Pietinen and Taylor59) and one retrospective(Reference Zhao, Lin and Grossman60) epidemiological studies have assessed the specific role of cruciferous vegetables or dietary ITC against bladder cancer. The Health Professionals Follow-up Study(Reference Michaud, Spiegelman and Clinton58) has reported a weak non-significant inverse association between total fruit and vegetable intake and the risk of bladder cancer. However, a significant inverse association was found for cruciferous vegetables (RR 0·49 (95% CI 0·32, 0·75) for the highest category of cruciferous vegetable intake v. the lowest category). Among individual cruciferous vegetables broccoli (RR 0·61 (95% CI 0·42, 0·87)) and cabbage (RR 0·57 (95% CI 0·33, 0·97)) were found to be significantly associated with bladder cancer risk. These observations show that high cruciferous vegetable consumption may reduce bladder cancer risk, but other vegetables and fruits may not exert marked beneficial effects against this cancer.

In the Alpha-Tocopherol Beta-Carotene Cancer Prevention Study 27 111 male cigarette smokers aged 50–69 years were followed over a median of 11 years, during which 344 of the men developed bladder cancer(Reference Michaud, Pietinen and Taylor59). However, no associations between the consumption of cruciferous vegetables and bladder cancer risk were observed in this prospective cohort. These findings indicate that cruciferous vegetable intake is not likely to be associated with bladder cancer risk in smokers, but these results may not be generalisable to non-smokers.

In a recent case–control study involving 697 newly-diagnosed bladder cancer cases and 708 healthy controls matched by age, gender and ethnicity it has been shown that ITC from cruciferous vegetable consumption protect against bladder cancer(Reference Zhao, Lin and Grossman60). ITC intake was found to be associated inversely with bladder cancer risk (OR 0·71 (95% CI 0·57, 0·89)). This protective effect was found to be stronger in older individuals (64 years old), men, ever smokers and heavy smokers in stratified analysis.

Endometrial cancer

A recent systematic review of literature and meta-analysis(Reference Bandera, Kushi and Moore61) has summarised the current evidence for a relationship between fruit and vegetable intake and endometrial cancer by utilising data from pertinent cohort and case–control studies published up to June 2006(Reference Littman, Beresford and White62Reference Goodman, Hankin and Wilkens64). The summary OR for the highest category of intake v. the lowest category were 0·71 (95% CI 0·55, 0·91) for total vegetables and 0·85 (95% CI 0·74, 0·97) for cruciferous vegetables. Summary OR for increasing intake levels at 100 g/d were 0·90 (95% CI 0·86, 0·95) for total vegetables and 0·79 (95% CI 0·69, 0·90) for cruciferous vegetables. Currently-available results, derived exclusively from case–control studies, appear to suggest that high consumption of vegetables, specifically cruciferous vegetables, may moderately reduce endometrial cancer risk. To date, no cohort study has been conducted to evaluate the relationship between endometrial cancer and individual fruit and vegetables. Additional prospective data from well-conducted population-based studies will be necessary before a firm conclusion can be drawn.

Genetic polymorphisms and response to cruciferous vegetable intake for cancer risk

Although a comprehensive review of epidemiological evidence relating to the protective role of cruciferous vegetables and/or ITC against cancers suggests a putative protective role, as discussed earlier, it remains an open question as to whether consumption of cruciferous vegetables and/or ITC may reduce the risk. One possible explanation for the inconsistent evidence across epidemiological studies may be variations in genes that are directly and indirectly involved in carcinogenesis in relation to cancer risk. Genetic polymorphisms associated with the exposure to environmental risk factors for cancer can affect the cancer susceptibility of each individual, when coupled with the relevant carcinogen exposures. It has recently been shown that genetic polymorphisms of phase I and phase II enzymes, which are components of the biotransformation pathways, alter an individual's response to cancer chemopreventive foods, including cruciferous vegetables(Reference Lampe and Peterson65, Reference Seow, Vainio and Yu66). ITC from cruciferous vegetables both induce and are substrates for the GST, a family of phase II enzymes involved in the detoxification of carcinogens, environmental toxins and oxidative stress products, by catalysing conjugation with glutathione(Reference Ahn, Gammon and Santella67). Several genetic polymorphisms (GSTM1, GSTM3, GSTT1, GSTP1, GSTA1) of GST that exert an effect on GST enzyme activity have been assessed in relation to human cancers(Reference Ahn, Gammon and Santella67, Reference Ye, Song and Higgins68). It is reported that the enzyme activities are reduced or completely absent in individuals with null genotypes of GSTM1 and/or GSTT1 (Reference Seow, Vainio and Yu66). Lower and/or absent GST activity in such individuals could result in slower elimination of and more extended exposure to ITC following the ingestion of cruciferous vegetables.

Numerous epidemiological studies have assessed whether inverse associations between ITC intake from cruciferous vegetables and cancer risk are altered in individuals with GST gene polymorphisms in relation to colo-rectal(Reference Seow, Yuan and Sun69), lung(Reference Wang, Giovannucci and Hunter70, Reference London, Yuan and Chung71), breast(Reference Ambrosone, McCann and Freudenheim56, Reference Ahn, Gammon and Santella67, Reference Steck, Gaudet and Britton72), head and neck(Reference Gaudet, Olshan and Poole73), kidney(Reference Moore, Brennan and Karami74) and bladder cancer(Reference Zhao, Lin and Grossman60) and colo-rectal adenoma(Reference Tijhuis, Wark and Aarts75, Reference Lin, Probst-Hensch and Louie76). Overall, associations between ITC intake and the risk of lung, kidney and colo-rectal cancer are modified by the GSTM1 and/or GSTT1 genotypes.

A meta-analysis using results from 130 genetic association studies of five GST variants (GSTM1-null, GSTT1-null, I105V, and A114V polymorphisms in the GSTP1 gene, and GSTM3 intron 6 polymorphism) and lung cancer risk published before 2005 (a total of 30 397 controls and 23 452 lung cancer cases), has reported RR for lung cancer of 1·18 (95% CI 1·14, 1·23) and 1·09 (95% CI 1·02, 1·16) for the GSTM1-null and GSTT1-null polymorphisms respectively(Reference Ye, Song and Higgins68). However, no significant associations were found when analysis was restricted to the larger studies with ≥500 cases (RR 1·04 (95% CI 0·95, 1·14) for GSTM1 and 0·99 (95% CI 0·86, 1·11) for GSTT1).

Higher consumption of ITC or a higher level of urinary ITC have been found to be inversely related to lung cancer risk, particularly among GSTM1-null and/or GSTT1-null individuals in a nested case–control study within a prospective cohort of Chinese men and women (Shanghai, China)(Reference Wang, Giovannucci and Hunter70, Reference London, Yuan and Chung71) and a hospital-based case–control study of Singaporean Chinese women(Reference Zhao, Seow and Lee77). Among those with GSTM1- and/or GSTT1-null genotypes the risk of lung cancer associated with ITC level was predominant.

Increased renal cell carcinoma risk has been observed for GSTT1-null or both GSTM1/T1-null carriers compared with GSTM1-present and GSTT1-present carriers among individuals with a low intake of cruciferous vegetables in the Central and Eastern European Kidney Cancer Study(Reference Moore, Brennan and Karami74).

A prospective study of 63 257 middle-aged women and men in the Singapore Chinese Health Study has shown a 57% reduction in colo-rectal cancer risk in high-ITC consumers v. low-ITC consumers (OR 0·31 (95% CI 0·12, 0·84)) among subjects with both GSTM1- and GSTT1-null genotypes(Reference Seow, Yuan and Sun69). Furthermore, inverse relationships between broccoli consumption and the risk of colo-rectal adenomas have been found in subsets of GST genotypes (GSTM1-null and GSTM1/T1-null genotypes).

The Western New York Diet Study has reported a marginal reduction in breast cancer risk with high cruciferous vegetable intake only in premenopausal women (OR 0·60 (95% CI 0·40, 1·01); P=0·058)(Reference Ambrosone, McCann and Freudenheim56). Modification of the association by GSTM1 and/or GSTT1 genotypes was not found to be significant for either the post- or premenopausal group. More recently, possible associations between GSTA1 polymorphisms and breast cancer risk in relation to cruciferous vegetable consumption has been evaluated in the Long Island Breast Cancer Study Project(Reference Ahn, Gammon and Santella67), a population-based case–control study (1089 controls and 1036 cases)(Reference Gammon, Neugut and Santella78). Although breast cancer risk was not affected by these genotypes among women who consumed smaller amounts of cruciferous vegetables, the risk was found to be elevated significantly in those with the GSTA1 *B/*B genotypes as compared with those with the common *A/*A genotypes.

Concluding remarks

Over several decades, a number of epidemiological studies have identified associations between dietary components such as vegetables and fruits and reduced risk of several cancers. More specifically, a variety of vegetables and fruits have been individually assessed in order to identify the most effective cancer-preventing components. Although relatively-few retrospective and prospective studies have evaluated the associations between cruciferous vegetables and other glucosinolate-containing plants and the risk of cancers, the results indicate that higher intake of specific types of vegetables such as cruciferous vegetables, but not vegetables as a whole, may lower the risk of several cancers(Reference Smith-Warner, Spiegelman and Yaun34Reference Lee, Giovannucci and Smith-Warner38).

Several methodological issues such as measurement errors of dietary exposure, misclassification, recall bias, publication bias, confounding and study design should be carefully considered in interpreting the findings from the case–control and cohort studies, and in reaching a conclusion about the potential effects of cruciferous vegetables on cancers.

Although recent comprehensive reviews of numerous studies purport to show a specific protective effect of cruciferous vegetables, particularly Brassicas, on cancer risk, the currently-available epidemiological evidence suggests that cruciferous vegetable consumption may reduce the risk of gastric and lung cancers. However, it would still be premature to conclude that the consumption of cruciferous vegetables reduces the risk for all other cancers.

Acknowledgements

This study was supported by the Korea Research Foundation Grant funded by the Korean Government (MOEHRD; KRF-2006–311-C00176) and by the KOSEF (Korea Science and Engineering Foundation) under grant no. R01–2006–000–10621–0. The authors declare no conflict of interest.

References

1. International Agency for Research on Cancer (2003) Fruit and Vegetables. IARC Handbooks of Cancer Prevention, vol. 8. Lyon, France: IARC Press.Google Scholar
2. Anand, P, Kunnumakara, AB, Sundaram, C et al. (2008) Cancer is a preventable disease that requires major lifestyle changes. Pharm Res 25, 20972116.CrossRefGoogle ScholarPubMed
3. World Cancer Research Fund and American Institute for Cancer Research (1997) Food, Nutrition and the Prevention of Cancer: A Global Perspective. Washington, DC: American Institute for Cancer Research.Google Scholar
4. World Cancer Research Fund and American Institute for Cancer Research (2007) Food, Nutrition, Physical Activity and the Prevention of Cancer: A Global Perspective. Washington, DC: American Institute for Cancer Research.Google Scholar
5. World Health Organization (2003) Diet, Nutrition and the Prevention of Chronic Diseases. WHO Technical Report Series no. 916. Geneva: WHO.Google Scholar
6. Adlercreutz, H (2002) Phyto-oestrogens and cancer. Lancet Oncol 3, 364373.CrossRefGoogle ScholarPubMed
7. Stan, SD, Kar, S, Stoner, GD et al. (2007) Bioactive food components and cancer risk reduction. J Cell Biochem 104, 339356.CrossRefGoogle Scholar
8. Aggarwal, BB & Shishodia, S (2006) Molecular targets of dietary agents for prevention and therapy of cancer. Biochem Pharmacol 71, 13971421.CrossRefGoogle ScholarPubMed
9. Lampe, JW (1999) Health effects of vegetables and fruit: assessing mechanisms of action in human experimental studies. Am J Clin Nutr 70, 475S490S.CrossRefGoogle ScholarPubMed
10. Oganesian, A, Hendricks, JD & Williams, DE (1997) Long term dietary indole-3-carbinol inhibits diethylnitrosamine-initiated hepatocarcinogenesis in the infant mouse model. Cancer Lett 118, 8794.CrossRefGoogle ScholarPubMed
11. Srivastava, B & Shukla, Y (1998) Antitumour promoting activity of indole-3-carbinol in mouse skin carcinogenesis. Cancer Lett 134, 9195.CrossRefGoogle ScholarPubMed
12. Zhang, J, Hsu, BAJ, Kinseth, BAM et al. (2003) Indole-3-carbinol induces a G1 cell cycle arrest and inhibits prostate-specific antigen production in human LNCaP prostate carcinoma cells. Cancer 98, 25112520.CrossRefGoogle ScholarPubMed
13. Frydoonfar, HR, McGrath, DR & Spigelman, AD (2002) Inhibition of proliferation of a colon cancer cell line by indole-3-carbinol. Colorectal Dis 4, 205207.CrossRefGoogle ScholarPubMed
14. Grose, KR & Bjeldanes, LF (1992) Oligomerization of indole-3-carbinol in aqueous acid. Chem Res Toxicol 5, 188193.CrossRefGoogle ScholarPubMed
15. De Kruif, CA, Marsman, JW, Venekamp, JC et al. (1991) Structure elucidation of acid reaction products of indole-3-carbinol: detection in vivo and enzyme induction in vitro. Chem Biol Interact 80, 303315.CrossRefGoogle ScholarPubMed
16. Stresser, DM, Williams, DE, Griffin, DA et al. (1995) Mechanisms of tumor modulation by indole-3-carbinol. Disposition and excretion in male Fischer 344 rats. Drug Metab Dispos 23, 965975.Google ScholarPubMed
17. Chang, X, Tou, JC, Hong, C et al. (2005) 3,3′-Diindolylmethane inhibits angiogenesis and the growth of transplantable human breast carcinoma in athymic mice. Carcinogenesis 26, 771778.CrossRefGoogle ScholarPubMed
18. Nachshon-Kedmi, M, Fares, FA & Yannai, S (2004) Therapeutic activity of 3,3′-diindolylmethane on prostate cancer in an in vivo model. Prostate 61, 153160.CrossRefGoogle ScholarPubMed
19. Safe, S (2001) Molecular biology of the Ah receptor and its role in carcinogenesis. Toxicol Lett 120, 17.CrossRefGoogle Scholar
20. Wolf, CR (2001) Chemoprevention: increased potential to bear fruit. Proc Natl Acad Sci U S A 98, 29412943.CrossRefGoogle ScholarPubMed
21. Talalay, P & Fahey, JW (2001) Phytochemicals from cruciferous plants protect against cancer by modulating carcinogen metabolism. J Nutr 131, 3027S3033.CrossRefGoogle ScholarPubMed
22. Cho, HJ, Seon, MR, Lee, YM et al. (2008) 3,3′-Diindolylmethane suppresses the inflammatory response to lipopolysaccharide in murine macrophages. J Nutr 138, 1723.CrossRefGoogle ScholarPubMed
23. Abdelrahim, M, Newman, K, Vanderlaag, K et al. (2006) 3,3′-diindolylmethane (DIM) and its derivatives induce apoptosis in pancreatic cancer cells through endoplasmic reticulum stress-dependent upregulation of DR5. Carcinogenesis 27, 717728.CrossRefGoogle ScholarPubMed
24. Kim, EJ, Park, SY, Shin, HK et al. (2007) Activation of caspase-8 contributes to 3,3′-diindolylmethane-induced apoptosis in colon cancer cells. J Nutr 137, 3136.CrossRefGoogle ScholarPubMed
25. Hong, C, Kim, HA, Firestone, GL et al. (2002) 3,3′-Diindolylmethane (DIM) induces a G(1) cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression. Carcinogenesis 23, 12971305.CrossRefGoogle Scholar
26. Firestone, GL & Bjeldanes, LF (2003) Indole-3-carbinol and 3-3′-diindolylmethane antiproliferative signaling pathways control cell-cycle gene transcription in human breast cancer cells by regulating promoter-Sp1 transcription factor interactions. J Nutr 133, 2448S2455S.CrossRefGoogle ScholarPubMed
27. Bonnesen, C, Eggleston, IM & Hayes, JD (2001) Dietary indoles and isothiocyanates that are generated from cruciferous vegetables can both stimulate apoptosis and confer protection against DNA damage in human colon cell lines. Cancer Res 61, 61206130.Google ScholarPubMed
28. Kong, AN, Owuor, E, Yu, R et al. (2001) Induction of xenobiotic enzymes by the MAP kinase pathway and the antioxidant or electrophile response element (ARE/EpRE). Drug Metab Rev 33, 255271.CrossRefGoogle ScholarPubMed
29. Kolm, RH, Danielson, UH, Zhang, Y et al. (1995) Isothiocyanates as substrates for human glutathione transferases: structure-activity studies. Biochem J 311, 453459.CrossRefGoogle ScholarPubMed
30. Shapiro, TA, Fahey, JW, Wade, KL et al. (1998) Human metabolism and excretion of cancer chemoprotective glucosinolates and isothiocyanates of cruciferous vegetables. Cancer Epidemiol Biomarkers Prev 7, 10911100.Google ScholarPubMed
31. Zhang, Y, Yao, S & Li, J (2006) Vegetable-derived isothiocyanates: anti-proliferative activity and mechanism of action. Proc Nutr Soc 65, 6875.CrossRefGoogle ScholarPubMed
32. Higdon, JV, Delage, B, Williams, DE et al. (2007) Cruciferous vegetables and human cancer risk: epidemiologic evidence and mechanistic basis. Pharmacol Res 55, 224236.CrossRefGoogle ScholarPubMed
33. International Agency for Research on Cancer (2004) Cruciferous vegetables, isothiocyanates and Indoles. IARC Handbooks of Cancer Prevention, vol. 9. Lyon, France: IARC.Google Scholar
34. Smith-Warner, SA, Spiegelman, D, Yaun, S-S et al. (2001) Intake of fruits and vegetables and risk of breast cancer: a pooled analysis of cohort studies. JAMA 285, 769776.CrossRefGoogle ScholarPubMed
35. Smith-Warner, SA, Spiegelman, D, Yaun, S-S et al. (2003) Fruits, vegetables and lung cancer: A pooled analysis of cohort studies. Int J Cancer 107, 10011011.CrossRefGoogle ScholarPubMed
36. Koushik, A, Hunter, DJ, Spiegelman, D et al. (2005) Fruits and vegetables and ovarian cancer risk in a pooled analysis of 12 cohort studies. Cancer Epidemiol Biomarkers Prev 14, 21602167.CrossRefGoogle Scholar
37. Koushik, A, Hunter, DJ, Spiegelman, D et al. (2007) Fruits, vegetables, and colon cancer risk in a pooled analysis of 14 cohort studies. J Natl Cancer Inst 99, 14711483.CrossRefGoogle Scholar
38. Lee, JE, Giovannucci, E, Smith-Warner, SA et al. (2006) Intakes of fruits, vegetables, vitamins a, c, and e, and carotenoids and risk of renal cell cancer. Cancer Epidemiol Biomarkers Prev 15, 24452452.CrossRefGoogle Scholar
39. Steinmetz, KA & Potter, JD (1996) Vegetables, fruit, and cancer prevention: A review. J Am Diet Assoc 96, 10271039.CrossRefGoogle ScholarPubMed
40. Hara, M, Hanaoka, T, Kobayashi, M et al. (2003) Cruciferous vegetables, mushrooms, and gastrointestinal cancer risks in a multicenter, hospital-based case-control study in Japan. Nutr Cancer 46, 138147.CrossRefGoogle Scholar
41. Chyou, P-H, Nomura, AMY, Hankin, JH et al. (1990) A case-cohort study of diet and stomach cancer. Cancer Res 50, 75017504.Google ScholarPubMed
42. Smith-Warner, SA, Genkinger, J & Giovannucci, E (2006) Fruit and vegetable intake and cancer. In Nutritional Oncology, 2nd ed., pp. 97173 [Heber, D, Blackburn, GL, Go, VL and Milner, J editors]. Burlington, MA: Elsevier.CrossRefGoogle Scholar
43. Voorrips, LE, Goldbohm, RA, Verhoeven, DTH et al. (2000) Vegetable and fruit consumption and lung cancer risk in the Netherlands Cohort Study on Diet and Cancer. Cancer Causes Control 11, 101115.CrossRefGoogle ScholarPubMed
44. Neuhouser, ML, Patterson, RE, Thornquist, MD et al. (2003) Fruits and vegetables are associated with lower lung cancer risk only in the placebo arm of the beta-carotene and retinol efficacy trial (CARET). Cancer Epidemiol Biomarkers Prev 12, 350358.Google ScholarPubMed
45. Feskanich, D, Ziegler, RG, Michaud, DS et al. (2000) Prospective study of fruit and vegetable consumption and risk of lung cancer among men and women. J Natl Cancer Inst 92, 18121823.CrossRefGoogle ScholarPubMed
46. Miller, AB, Altenburg, HP, Bueno-de-Mesquita, B et al. (2004) Fruits and vegetables and lung cancer: Findings from the European prospective investigation into cancer and nutrition. Int J Cancer 108, 269276.CrossRefGoogle ScholarPubMed
47. Verhoeven, DT, Goldbohm, RA, van Poppel, G et al. (1996) Epidemiological studies on brassica vegetables and cancer risk. Cancer Epidemiol Biomarkers Prev 5, 733748.Google ScholarPubMed
48. Kristal, AR & Lampe, JW (2002) Brassica vegetables and prostate cancer risk: a review of the epidemiological evidence. Nutr Cancer 42, 19.CrossRefGoogle Scholar
49. Kolonel, LN, Hankin, JH, Whittemore, AS et al. (2000) Vegetables, fruits, legumes and prostate cancer: a multiethnic case-control study. Cancer Epidemiol Biomarkers Prev 9, 795804.Google ScholarPubMed
50. Cohen, JH, Kristal, AR & Stanford, JL (2000) Fruit and vegetable intakes and prostate cancer risk. J Natl Cancer Inst 92, 6168.CrossRefGoogle ScholarPubMed
51. Joseph, MA, Moysich, KB, Freudenheim, JL et al. (2004) Cruciferous vegetables, genetic polymorphisms in glutathione S-transferases M1 and T1, and prostate cancer risk. Nutr Cancer 50, 206213.CrossRefGoogle ScholarPubMed
52. Jain, MG, Hislop, GT, Howe, GR et al. (1999) Plant foods, antioxidants, and prostate cancer risk: findings from case-control studies in Canada. Nutr Cancer 34, 173184.CrossRefGoogle ScholarPubMed
53. Giovannucci, E, Rimm, E, Liu, Y et al. (2003) A prospective study of cruciferous vegetables and prostate cancer. Cancer Epidemiol Biomarkers Prev 12, 14031409.Google ScholarPubMed
54. Kirsh, VA, Peters, U, Mayne, ST et al. (2007) Prospective study of fruit and vegetable intake and risk of prostate cancer. J Natl Cancer Inst 99, 12001209.CrossRefGoogle ScholarPubMed
55. Key, TJ, Allen, N, Appleby, P et al. (2004) Fruits and vegetables and prostate cancer: no association among 1104 cases in a prospective study of 130544 men in the European Prospective Investigation into Cancer and Nutrition (EPIC). Int J Cancer 109, 119124.CrossRefGoogle Scholar
56. Ambrosone, CB, McCann, SE, Freudenheim, JL et al. (2004) Breast cancer risk in premenopausal women is inversely associated with consumption of broccoli, a source of isothiocyanates, but is not modified by GST genotype. J Nutr 134, 11341138.CrossRefGoogle Scholar
57. Terry, P, Wolk, A, Persson, I et al. (2001) Brassica vegetables and breast cancer risk. JAMA 285, 29752977.Google ScholarPubMed
58. Michaud, DS, Spiegelman, D, Clinton, SK et al. (1999) Fruit and vegetable intake and incidence of bladder cancer in a male prospective cohort. J Natl Cancer Inst 91, 605613.CrossRefGoogle Scholar
59. Michaud, DS, Pietinen, P, Taylor, PR et al. (2002) Intakes of fruits and vegetables, carotenoids and vitamins A, E, C in relation to the risk of bladder cancer in the ATBC cohort study. Br J Cancer 87, 960965.CrossRefGoogle Scholar
60. Zhao, H, Lin, J, Grossman, HB et al. (2007) Dietary isothiocyanates, GSTM1, GSTT1, NAT2 polymorphisms and bladder cancer risk. Int J Cancer 120, 22082213.CrossRefGoogle ScholarPubMed
61. Bandera, EV, Kushi, LH, Moore, DF et al. (2007) Fruits and vegetables and endometrial cancer risk: a systematic literature review and meta-analysis. Nutr Cancer 58, 621.CrossRefGoogle Scholar
62. Littman, AJ, Beresford, SA & White, E (2001) The association of dietary fat and plant foods with endometrial cancer (United States). Cancer Causes Control 12, 691702.CrossRefGoogle ScholarPubMed
63. Tao, MH, Xu, WH, Zheng, W et al. (2005) A case-control study in Shanghai of fruit and vegetable intake and endometrial cancer. Br J Cancer 92, 20592064.CrossRefGoogle ScholarPubMed
64. Goodman, MT, Hankin, JH, Wilkens, LR et al. (1997) Diet, body size, physical activity, and the risk of endometrial cancer. Cancer Res 57, 50775085.Google ScholarPubMed
65. Lampe, JW & Peterson, S (2002) Brassica, biotransformation and cancer risk: genetic polymorphisms alter the preventive effects of cruciferous vegetables. J Nutr 132, 29912994.CrossRefGoogle ScholarPubMed
66. Seow, A, Vainio, H & Yu, MC (2005) Effect of glutathione-S-transferase polymorphisms on the cancer preventive potential of isothiocyanates: an epidemiological perspective. Mutat Res 592, 5867.CrossRefGoogle ScholarPubMed
67. Ahn, J, Gammon, MD, Santella, RM et al. (2006) Effects of glutathione S-transferase A1 (GSTA1) genotype and potential modifiers on breast cancer risk. Carcinogenesis 27, 18761882.CrossRefGoogle ScholarPubMed
68. Ye, Z, Song, H, Higgins, JPT et al. (2006) Five glutathione S-transferase gene variants in 23,452 cases of lung cancer and 30,397 controls: meta-analysis of 130 studies. PLoS Med 3, 524534.CrossRefGoogle Scholar
69. Seow, A, Yuan, JM, Sun, CL et al. (2002) Dietary isothiocyanates, glutathione S-transferase polymorphisms and colorectal cancer risk in the Singapore Chinese Health Study. Carcinogenesis 23, 20552061.CrossRefGoogle ScholarPubMed
70. Wang, LI, Giovannucci, EL, Hunter, D et al. (2004) Dietary intake of cruciferous vegetables, glutathione S-transferase (GST) polymorphisms and lung cancer risk in a Caucasian population. Cancer Causes and Control 15, 977985.CrossRefGoogle Scholar
71. London, SJ, Yuan, JM, Chung, FL et al. (2000) Isothiocyanates, glutathione S-transferase M1 and T1 polymorphisms, and lung-cancer risk: a prospective study of men in Shanghai, China. Lancet 356, 724729.CrossRefGoogle Scholar
72. Steck, SE, Gaudet, MM, Britton, JA et al. (2007) Interactions among GSTM1, GSTT1 and GSTP1 polymorphisms, cruciferous vegetable intake and breast cancer risk. Carcinogenesis 28, 19541959.CrossRefGoogle ScholarPubMed
73. Gaudet, MM, Olshan, AF, Poole, C et al. (2004) Diet, GSTM1 and GSTT1 and head and neck cancer. Carcinogenesis 25, 735740.CrossRefGoogle ScholarPubMed
74. Moore, LE, Brennan, P, Karami, S et al. (2007) Glutathione S-transferase polymorphisms, cruciferous vegetable intake and cancer risk in the Central and Eastern European Kidney Cancer Study. Carcinogenesis 28, 19601964.CrossRefGoogle ScholarPubMed
75. Tijhuis, MJ, Wark, PA, Aarts, JMMJG et al. (2005) GSTP1 and GSTA1 polymorphisms interact with cruciferous vegetable intake in colorectal adenoma risk. Cancer Epidemiol Biomarkers Prev 14, 29432951.CrossRefGoogle ScholarPubMed
76. Lin, HJ, Probst-Hensch, NM, Louie, AD et al. (1998) Glutathione transferase null genotype, broccoli, and lower prevalence of colorectal adenomas. Cancer Epidemiol Biomarkers Prev 7, 647652.Google ScholarPubMed
77. Zhao, B, Seow, A, Lee, EJ et al. (2001) Dietary isothiocyanates, glutathione S-transferase-M1, -T1 polymorphisms and lung cancer risk among Chinese women in Singapore. Cancer Epidemiol Biomarkers Prev 10, 10631067.Google ScholarPubMed
78. Gammon, MD, Neugut, AI, Santella, RM et al. (2002) The Long Island Breast Cancer Study Project: description of a multi-institutional collaboration to identify environmental risk factors for breast cancer. Breast Cancer Res Treat 74, 235254.CrossRefGoogle Scholar