Background: Intake of cruciferous vegetables, a rich source of dietary isothiocyanates, has been inversely associated with risk of bladder cancer. Due to the potent antiproliferative effects of dietary isothiocyanates on bladder cancer in in vitro and in vivo models, cruciferous vegetable intake may also play a role in survival among patients with bladder cancer.

Methods: Using information obtained from the Roswell Park Cancer Institute Tumor Registry, patient medical records, and routinely collected questionnaire data, we examined potential associations between intake of cruciferous vegetables and survival among bladder cancer patients. As cooking can substantially reduce or destroy isothiocyanates, consumption of raw versus cooked cruciferous vegetables was examined separately. Hazard ratios (HR) and 95% confidence intervals (CI) were estimated using Cox proportional hazard models.

Results: A total of 239 bladder cancer patients were included in the study. After an average of 8 years of follow-up, 179 deaths occurred, with 101 deaths attributable to bladder cancer. After adjustment for other prognostic factors, a strong and significant inverse association was observed between bladder cancer mortality and broccoli intake, in particular raw broccoli intake (≥1 versus <1 serving per month; HR for overall death, 0.57; 95% CI, 0.39-0.83; HR for disease-specific death, 0.43; 95% CI, 0.25-0.74). There were no significant associations for total vegetables, total fruits, or other individual cruciferous vegetables.

Conclusions: Considering the strong preclinical evidence, intake of broccoli may improve bladder cancer survival.

Impact: Further prospective investigation is warranted to confirm the potential role of cruciferous vegetables in bladder cancer prognosis. Cancer Epidemiol Biomarkers Prev; 19(7); 1806–11. ©2010 AACR.

A challenge exists in the management of bladder cancer. Unlike many other cancers, the majority of bladder cancers (∼75%) are diagnosed early as superficial disease with tumors confined to the mucosa or submucosa. However, the cancer typically recurs (approximately 50-70%), and some patients further experience disease progression to a muscle-invasive stage with worse prognosis (1-3). Currently, several therapeutic agents are offered intravesically to high-risk patients to inhibit disease recurrence and progression. However, the cost of multiple use of clinical resources, frequent local side effects, and controversial long-term effects are all of concern (4, 5). Studies on promising dietary components may offer a new strategy for improvement of bladder cancer prognosis.

Intake of cruciferous vegetables has been associated with reduced risk of primary bladder cancer (6-9), which is believed to be at least partly attributed to the high content of glucosinolates, the precursors of isothiocyanates and indole-3-carbinol in cruciferous vegetables (10). Dietary isothiocyanates are a family of promising cancer chemopreventive agents with multifaceted anticancer mechanisms, including the induction of carcinogen-detoxification phase 2 enzymes, arrest of cell cycle progression, and induction of apoptosis. The potent antiproliferative activity of dietary isothiocyanates has been observed in a panel of cultured human bladder cancer cells that represent low-grade superficial, high-grade invasive, as well as doxorubicin-resistant bladder cancer (11-14). More importantly, urinary metabolites of isothiocyanates elicited the same anticancer response as their parent compounds in human bladder cancer cells, supporting the plausibility for a role of dietary isothiocyanates and/or isothiocyanate-rich cruciferous vegetables in bladder cancer prognosis. In an in vivo rat model in which N-butyl-N(4-hydroxybutyl)-nitrosamine was used to induce bladder carcinogenesis, orally ingested isothiocyanates in broccoli sprout extracts were rapidly and almost exclusively excreted into the bladder and significantly inhibited bladder tumor formation by 61% (15). Recently, in a rat orthotopic bladder cancer model, our group was able to show the inhibition of bladder cancer development and progression by low oral doses of allyl isothiocyanate (the isothiocyanate rich in mustard and horseradish). This activity seems to be bladder cancer–specific, as no effect was observed on the development of subcutaneous cancer at such low dose levels (16). Accordingly, two to three orders of magnitude higher concentration of isothiocyanate and their corresponding metabolites was found in the urine than in the plasma. This selectivity renders the bladder an ideal target for isothiocyanate as well as isothiocyanate-rich cruciferous vegetables. The rat orthotopic bladder cancer model resembles human bladder cancer development both in histology and behavior, and has been used to test therapeutic agents for bladder cancer treatment (17, 18). Therefore, these results provide preclinical evidence to support the potential role of isothiocyanate-rich cruciferous vegetables in bladder cancer prognosis. We applied this model to humans by examining associations between consumption of cruciferous vegetables as measured by a food frequency questionnaire among patients with bladder cancer at the Roswell Park Cancer Institute (RPCI), and disease-free survival and overall survival.

The study population included 239 patients diagnosed with primary bladder cancer at RPCI between 1980 and 1998, who completed a comprehensive epidemiologic questionnaire. A detailed description of the study population and the epidemiologic data collection has been previously published (7). Briefly, a 44-item food frequency questionnaire was used to assess usual diet in the few years before diagnosis and queried intake of fruits and vegetables, cruciferous vegetables, and foods that are rich sources of vitamins A, C, and E, and fiber (19). Four food categories (fruits, vegetables, cruciferous vegetables, and raw cruciferous vegetables) were created by combining monthly frequency of use of each food item under the categories. The cruciferous vegetable category consisted of broccoli (raw and cooked), cabbage (raw and cooked), cauliflower (raw and cooked), Brussels sprouts, and greens including kale, turnip, collard, and mustard greens. The raw cruciferous vegetable consumption category, defined as raw broccoli, raw cabbage, and raw cauliflower, was created to more accurately represent dietary intake of isothiocyanates, as it is known that cooking substantially reduces isothiocyanate yield from cruciferous vegetables (20, 21). Intake of each food category was divided into tertiles, whereas for individual cruciferous vegetables, intake was divided into two categories (<1 or ≥1 servings per month). For each vegetable, a serving was defined to be equal to one-half cup.

Clinical information on tumor stage, grade, treatment, and survival was abstracted from the RPCI tumor registry, and medical records were reviewed to collect missing information. The two prognostic outcomes considered were as follows: overall death and death from bladder cancer. Overall death included death from any cause including bladder cancer. Death from bladder cancer included death attributable to bladder cancer as a primary or underlying cause on the death certificate. A total of 16 patients with unclear cause of death were included in the analysis of overall death but excluded from the analysis of death from bladder cancer. Disease recurrence was not included as an outcome in the current analysis due to incomplete information for majority of the patients. The conduct of the study was approved by the RPCI Institutional Review Board.

Survival time was calculated in months from date of diagnosis to date of death, loss to follow-up, or date of last contact (July 2007). Kaplan-Meier estimates of survival were generated, and a log-rank test was used to test the differences by each variable. For multivariable analysis, Cox proportional hazard regression models were used to calculate hazard ratios (HR) and 95% confidence intervals (95% CI). A set of potential confounders including age at diagnosis, tumor stage, grade, surgery, radiation, chemotherapy, immunotherapy, year of admission, gender, and smoking status was considered for inclusion in adjusted models using a forward selection technique. Patients were predominantly Caucasian (98%); therefore, race was not included as a potential confounder. As smoking is a major risk factor for bladder cancer, we included pack-years in the model, computed as the number of packs of cigarettes smoked per day times the number of years smoked. Total meat intake was also considered in the model to partially adjust for differences in dietary patterns associated with vegetable intake. The final model included covariates that were statistically significant (P < 0.05) when entered into the model individually. The proportional hazard assumption was confirmed for all covariates. All statistical analyses were conducted using SAS for Windows, version 9.1.

Of the 239 patients evaluated, 179 deaths (74.9%) were ascertained through July 2007. Mean follow-up time was 96 months (median, 77; range 1-301 mo). Among the 179 deaths, 101 (56.4%) were attributable to bladder cancer. Kaplan-Meier curves for overall survival and bladder cancer–specific survival are provided in Supplementary Figs. S1 and S2, respectively. As shown in Table 1, age at diagnosis, Surveillance Epidemiology and End Results stage, tumor grade, smoking status, gender, and treatment including surgery type, radiation, and chemotherapy were significantly associated with survival. However, only age at diagnosis, stage, smoking status, and radiation therapy remained significant in the multivariate models, indicating their independent prognostic roles in bladder cancer survival. Radiation therapy was associated with worse survival, likely due to the selection of patients with more advanced disease. Survival did not differ significantly by year of admission.

Table 1.

Baseline characteristics of bladder cancer patients (n = 239) by survival status, RPCI

CharacteristicNo. of participantsOverall deathDeath from bladder cancer
No. of eventsCrude HR (95% CI)No. of eventsCrude HR (95% CI)
Age at diagnosis, y 
    <60 75 46  32  
    60-70 103 77 1.41 (0.98-2.04) 46 1.11 (0.71-1.75) 
    >70 61 56 1.99 (1.34-2.96) 23 1.03 (0.60-1.76) 
SEER stage* 
    Localized 130 83  30  
    Advanced 108 95 2.04 (1.51-2.74) 71 3.90 (2.54-5.99) 
Tumor grade 
    I 84 58  29  
    II 112 86 1.62 (1.18-2.32) 53 1.24 (0.70-2.22) 
    Unspecified 43 35 1.18 (0.78-1.80) 19 1.73 (1.10-2.72) 
Surgery type 
    TURBT 154 120  64  
    Cystectomy 66 55 1.56 (1.13-2.15) 36 1.71 (1.13-2.57) 
    Unspecified 19 0.53 (0.20-1.45) 0.20 (0.03-1.47) 
Radiation therapy 
    No 191 132  67  
    Yes 48 47 1.93 (1.38-2.70) 34 2.53 (1.67-3.83) 
Chemotherapy 
    No 101 64  25  
    Yes 138 115 1.28 (0.95-1.74) 76 2.15 (1.37-3.39) 
Immunotherapy 
    No 187 139  80  
    Yes 52 40 0.79 (0.56-1.13) 21 0.73 (0.45-1.18) 
Smoking status 
    Never 47 28  10  
    Former 136 107 1.65 (1.09-2.50) 63 2.57 (1.32-5.02) 
    Current 56 44 1.77 (1.10-2.85) 28 2.75 (1.33-5.66) 
Gender 
    Male 186 144  84  
    Female 53 35 0.55 (0.38-0.80) 17 0.54 (0.32-0.91) 
Year of admission 
    ≤1990 132 106  53  
    >1990 107 73 1.01 (0.74-1.36) 48 1.19 (0.80-1.76) 
CharacteristicNo. of participantsOverall deathDeath from bladder cancer
No. of eventsCrude HR (95% CI)No. of eventsCrude HR (95% CI)
Age at diagnosis, y 
    <60 75 46  32  
    60-70 103 77 1.41 (0.98-2.04) 46 1.11 (0.71-1.75) 
    >70 61 56 1.99 (1.34-2.96) 23 1.03 (0.60-1.76) 
SEER stage* 
    Localized 130 83  30  
    Advanced 108 95 2.04 (1.51-2.74) 71 3.90 (2.54-5.99) 
Tumor grade 
    I 84 58  29  
    II 112 86 1.62 (1.18-2.32) 53 1.24 (0.70-2.22) 
    Unspecified 43 35 1.18 (0.78-1.80) 19 1.73 (1.10-2.72) 
Surgery type 
    TURBT 154 120  64  
    Cystectomy 66 55 1.56 (1.13-2.15) 36 1.71 (1.13-2.57) 
    Unspecified 19 0.53 (0.20-1.45) 0.20 (0.03-1.47) 
Radiation therapy 
    No 191 132  67  
    Yes 48 47 1.93 (1.38-2.70) 34 2.53 (1.67-3.83) 
Chemotherapy 
    No 101 64  25  
    Yes 138 115 1.28 (0.95-1.74) 76 2.15 (1.37-3.39) 
Immunotherapy 
    No 187 139  80  
    Yes 52 40 0.79 (0.56-1.13) 21 0.73 (0.45-1.18) 
Smoking status 
    Never 47 28  10  
    Former 136 107 1.65 (1.09-2.50) 63 2.57 (1.32-5.02) 
    Current 56 44 1.77 (1.10-2.85) 28 2.75 (1.33-5.66) 
Gender 
    Male 186 144  84  
    Female 53 35 0.55 (0.38-0.80) 17 0.54 (0.32-0.91) 
Year of admission 
    ≤1990 132 106  53  
    >1990 107 73 1.01 (0.74-1.36) 48 1.19 (0.80-1.76) 

Abbreviations: SEER, Surveillance Epidemiology and End Results; TURBT, transurethral resection of bladder tumor.

*Surveillance Epidemiology and End Results stage: Localized tumor included tumors in situ or confined to the bladder; Advanced tumor included tumors spreading regionally or distantly.

Tumor grade: Grade I tumor included well- or moderately differentiated tumors; grade II tumor included poor or undifferentiated tumors.

We observed no associations between intake of total fruits, total vegetables, or total cruciferous vegetables and bladder cancer survival (Table 2). However, higher consumption of raw cruciferous vegetables was associated with a 33% reduction in overall mortality (HR, 0.67; 95% CI, 0.46-0.97), but not for disease-specific death.

Table 2.

Bladder cancer survival by fruit and vegetable intake, RPCI

No. of participantsOverall deathDeath from bladder cancer
No. of eventsAdjusted HR* (95% CI)No. of eventsAdjusted HR* (95% CI)
Fruits, servings/mo 
    <27.5 81 59  30  
    27.5-51 82 59 0.86 (0.59-1.24) 34 0.94 (0.57-1.55) 
    >51 76 61 0.91 (0.62-1.33) 37 1.09 (0.66-1.81) 
Vegetables, servings/mo 
    <52 83 60  32  
    52-85.5 80 61 0.90 (0.62-1.30) 36 0.95 (0.59-1.55) 
    >85.5 76 58 0.91 (0.62-1.36) 33 1.06 (0.63-1.78) 
Cruciferous, servings/mo 
    <5.5 76 58  31  
    5.5-14 80 59 0.96 (0.67-1.39) 37 1.05 (0.65-1.71) 
    >14 83 62 0.87 (0.60-1.26) 33 0.89 (0.53-1.48) 
Raw cruciferous, servings/mo 
    <1 66 56  32  
    1-3 99 68 0.67 (0.46-0.97) 39 0.67 (0.41-1.10) 
    >3 74 55 0.73 (0.50-1.06) 30 0.73 (0.44-1.21) 
No. of participantsOverall deathDeath from bladder cancer
No. of eventsAdjusted HR* (95% CI)No. of eventsAdjusted HR* (95% CI)
Fruits, servings/mo 
    <27.5 81 59  30  
    27.5-51 82 59 0.86 (0.59-1.24) 34 0.94 (0.57-1.55) 
    >51 76 61 0.91 (0.62-1.33) 37 1.09 (0.66-1.81) 
Vegetables, servings/mo 
    <52 83 60  32  
    52-85.5 80 61 0.90 (0.62-1.30) 36 0.95 (0.59-1.55) 
    >85.5 76 58 0.91 (0.62-1.36) 33 1.06 (0.63-1.78) 
Cruciferous, servings/mo 
    <5.5 76 58  31  
    5.5-14 80 59 0.96 (0.67-1.39) 37 1.05 (0.65-1.71) 
    >14 83 62 0.87 (0.60-1.26) 33 0.89 (0.53-1.48) 
Raw cruciferous, servings/mo 
    <1 66 56  32  
    1-3 99 68 0.67 (0.46-0.97) 39 0.67 (0.41-1.10) 
    >3 74 55 0.73 (0.50-1.06) 30 0.73 (0.44-1.21) 

*Adjusted for age at diagnosis (continuous), total meat intake (continuous), pack-years of smoking (continuous), tumor stage (localized or advanced), and radiation therapy (yes or no).

With regard to intake of individual cruciferous vegetables, we observed notable reductions in bladder cancer mortality with higher consumption of broccoli, particularly raw broccoli (survival curve is provided in Supplementary Fig. S3; Table 3). After adjustment for age at diagnosis, tumor stage, grade, pack-years of smoking, and total meat intake, higher consumption of raw broccoli was associated with a >2-fold reduction in risk of disease-specific death (HR, 0.43; 95% CI, 0.25-0.74), as well as reduction of overall mortality (HR, 0.57; 95% CI, 0.39-0.83). No associations were observed for other individual cruciferous vegetables. We further observed no statistically significant interactions by smoking status or by gender (data not shown).

Table 3.

Bladder cancer survival by individual cruciferous vegetable intake, RPCI

No. of participantsOverall deathDeath from bladder cancer
No. of eventsAdjusted HR* (95% CI)No. of eventsAdjusted HR* (95% CI)
Broccoli raw, servings/mo 
    <1 184 142  85  
    ≥1 (mean, 3.9) 55 37 0.57 (0.39-0.83) 16 0.43 (0.25-0.74) 
Broccoli cooked, servings/mo 
    <1 96 78  44  
    ≥1 (mean, 5.1) 143 101 0.67 (0.49-0.91) 57 0.68 (0.45-1.01) 
Cabbage raw, servings/mo 
    <1 128 94  54  
    ≥1 (mean, 4.1) 111 85 1.08 (0.79-1.46) 47 1.11 (0.74-1.66) 
Cabbage cooked, servings/mo 
    <1 155 114  66  
    ≥1 (mean, 4.1) 84 65 1.07 (0.77-1.48) 35 1.15 (0.75-1.77) 
Cauliflower raw, servings/mo 
    <1 182 140  80  
    ≥1 (mean, 5.1) 57 39 1.00 (0.69-1.46) 21 1.08 (0.66-1.77) 
Cauliflower cooked, servings/mo 
    <1 129 99  56  
    ≥1 (mean, 3.9) 110 80 0.92 (0.68-1.25) 45 0.95 (0.63-1.42) 
Brussels sprout, servings/mo 
    <1 176 132  73  
    ≥1 (mean, 4.3) 63 47 1.17 (0.82-1.68) 28 1.37 (0.86-2.18) 
Kale, turnip, collard, mustard greens, servings/mo 
    <1 194 144  81  
    ≥1 (mean, 5.1) 45 35 1.15 (0.78-1.69) 20 1.07 (0.63-1.79) 
No. of participantsOverall deathDeath from bladder cancer
No. of eventsAdjusted HR* (95% CI)No. of eventsAdjusted HR* (95% CI)
Broccoli raw, servings/mo 
    <1 184 142  85  
    ≥1 (mean, 3.9) 55 37 0.57 (0.39-0.83) 16 0.43 (0.25-0.74) 
Broccoli cooked, servings/mo 
    <1 96 78  44  
    ≥1 (mean, 5.1) 143 101 0.67 (0.49-0.91) 57 0.68 (0.45-1.01) 
Cabbage raw, servings/mo 
    <1 128 94  54  
    ≥1 (mean, 4.1) 111 85 1.08 (0.79-1.46) 47 1.11 (0.74-1.66) 
Cabbage cooked, servings/mo 
    <1 155 114  66  
    ≥1 (mean, 4.1) 84 65 1.07 (0.77-1.48) 35 1.15 (0.75-1.77) 
Cauliflower raw, servings/mo 
    <1 182 140  80  
    ≥1 (mean, 5.1) 57 39 1.00 (0.69-1.46) 21 1.08 (0.66-1.77) 
Cauliflower cooked, servings/mo 
    <1 129 99  56  
    ≥1 (mean, 3.9) 110 80 0.92 (0.68-1.25) 45 0.95 (0.63-1.42) 
Brussels sprout, servings/mo 
    <1 176 132  73  
    ≥1 (mean, 4.3) 63 47 1.17 (0.82-1.68) 28 1.37 (0.86-2.18) 
Kale, turnip, collard, mustard greens, servings/mo 
    <1 194 144  81  
    ≥1 (mean, 5.1) 45 35 1.15 (0.78-1.69) 20 1.07 (0.63-1.79) 

*Adjusted for age at diagnosis (continuous), total meat intake (continuous), pack-years of smoking (continuous), tumor stage (localized or advanced), and radiation therapy (yes or no).

In this study of 239 bladder cancer patients seen at RPCI between 1980 and 1998, survival was not associated with total fruits, total vegetables, or total cruciferous vegetable intake before diagnosis. However, intake of raw cruciferous vegetables was significantly associated with reduced disease-specific (57% reduction) and overall mortality (43% reduction), a result largely driven by raw broccoli intake. The reduction was observed with consumption of at least one serving raw broccoli per month (average intake 3.9 servings/mo), indicating the feasibility of this type of diet intervention strategy. Our findings are consistent with experimental evidence showing that isothiocyanate exposure, as measured by urinary metabolite concentrations, is 3- to 4-fold higher in individuals after consumption of raw compared with cooked broccoli (21). Experimental studies in animals and cell lines indicate that isothiocyanates may be promising chemopreventive agents against bladder cancer (10).

Contrary to the findings observed with broccoli intake, no associations were observed with other individual cruciferous vegetables regardless of whether they were consumed raw or cooked. As usual consumption of individual cruciferous vegetables in the study was similar (means of broccoli, cabbage, and cauliflower consumption were 4.1, 3.9, and 3.3 servings per month, respectively), it is unlikely that this null association was the result of the small range of exposure. It is unclear whether the differential associations observed between individual cruciferous vegetables and bladder cancer survival are related to specific types of isothiocyanates or the amount of isothiocyanates derived from each vegetable. For example, the major isothiocyanate derived from broccoli is sulforaphane, whereas cabbage and cauliflower are abundant in allyl isothiocyanate (22). The two isothiocyanates share the characteristic -N = C = S structure but differ in their side chains, resulting in varied anticancer potencies as well as the underlying mechanisms observed in human bladder cancer cells (12, 13). Investigation of the in vivo efficacy of individual isothiocyanates against bladder cancer would offer more clues to understanding these observed associations. Moreover, isothiocyanate yield differs substantially among different cruciferous vegetables due to their wide range of glucosinolate concentration. Jiao et al. (23) showed that total isothiocyanate yield from nine types of cruciferous vegetables in Singapore varied as much as 16-fold. The isothiocyanate content in broccoli was 40% higher than that in cabbage and 2.3-fold higher than that in cauliflower. Furthermore, it is noteworthy that, in addition to isothiocyanates, cruciferous vegetables contain many other compounds with anticancer potential including indoles, vitamins, dietary fiber, and other phytochemicals, which could also contribute to the observed associations either independently and/or in combination with isothiocyanates.

Several limitations need to be taken into consideration in this study. First, questionnaire data, including cruciferous vegetable intake, were collected at the time of diagnosis, which may not represent dietary habits after the disease diagnosis. Cancer survivors are often motivated to modify their diet with the hope of improving prognosis (18). However, such diet modifications tend to be healthy changes such as eating less meat and fat and increasing vegetable and fruit intake (24). Therefore, it is possible that our findings have been underestimated. Validation of the findings in a prospective study using cruciferous vegetable intake after diagnosis would provide more conclusive evidence.

Second, due to the relatively small sample size, we have limited statistical power to examine potential interactions between cruciferous vegetable and other prognostic factors. Cigarette smoking is the strongest risk factor of bladder cancer. Consistent with the potent detoxification effect of isothiocyanates on cigarette-related carcinogens, a strong inverse association was observed between cruciferous vegetable intake and bladder cancer risk among smokers (7). Smoking was an independent prognostic factor for bladder cancer survival in the current study. It is possible that cruciferous vegetable intake may modify the associations between cigarette smoking and bladder cancer survival.

Third, outcome data were collected retrospectively, which could introduce the possibility of misclassification. Moreover, due to the incomplete recurrence data, we were unable to investigate the associations between cruciferous vegetable intake and bladder cancer recurrence, whereas high risk of recurrence is the most common event occurring in bladder cancer patients. Therefore, such information may have a great effect on bladder cancer survivorship.

To our knowledge, this is the first study to investigate the role of cruciferous vegetables in bladder cancer survival. A strong inverse association between broccoli intake and bladder cancer mortality was observed. The strong preclinical evidence of broccoli sprout extract in in vitro and in vivo bladder cancer models supports the validity of this association. Further large-scale prospective studies are warranted to confirm the potential role of cruciferous vegetables in bladder cancer prognosis.

No potential conflicts of interest were disclosed.

Grant Support: National Cancer Institute (R25 CA114101).

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1
Josephson
DY
,
Pasin
E
,
Stein
JP
. 
Superficial bladder cancer: part 1. Update on etiology, classification and natural history
.
Expert Rev Anticancer Ther
2006
;
6
:
1723
34
.
2
Colquhoun
AJ
,
Mellon
JK
. 
Epidermal growth factor receptor and bladder cancer
.
Postgrad Med J
2002
;
78
:
584
9
.
3
Botteman
MF
,
Pashos
CL
,
Redaelli
A
,
Laskin
B
,
Hauser
R
. 
The health economics of bladder cancer: a comprehensive review of the published literature
.
PharmacoEconomics
2003
;
21
:
1315
30
.
4
Patard
JJ
,
Rodriguez
A
,
Lobel
B
. 
The current status of intravesical therapy for superficial bladder cancer
.
Curr Opin Urol
2003
;
13
:
357
62
.
5
Hendricksen
K
,
Witjes
JA
. 
Current strategies for first and second line intravesical therapy for nonmuscle invasive bladder cancer
.
Curr Opin Urol
2007
;
17
:
352
7
.
6
Zeegers
MP
,
Goldbohm
RA
,
van den Brandt
PA
. 
Consumption of vegetables and fruits and urothelial cancer incidence: a prospective study
.
Cancer Epidemiol Biomarkers Prev
2001
;
10
:
1121
8
.
7
Tang
L
,
Zirpoli
GR
,
Guru
K
, et al
. 
Consumption of raw cruciferous vegetables is inversely associated with bladder cancer risk
.
Cancer Epidemiol Biomarkers Prev
2008
;
17
:
938
44
.
8
Michaud
DS
,
Spiegelman
D
,
Clinton
SK
,
Rimm
EB
,
Willett
WC
,
Giovannucci
EL
. 
Fruit and vegetable intake and incidence of bladder cancer in a male prospective cohort
.
J Natl Cancer Inst
1999
;
91
:
605
13
.
9
Mettlin
C
,
Graham
S
. 
Dietary risk factors in human bladder cancer
.
Am J Epidemiol
1979
;
110
:
255
63
.
10
Tang
L
,
Zhang
Y
. 
Isothiocyanates in the chemoprevention of bladder cancer
.
Curr Drug Metab
2004
;
5
:
193
201
.
11
Tang
L
,
Zhang
Y
,
Jobson
HE
, et al
. 
Potent activation of mitochondria-mediated apoptosis and arrest in S and M phases of cancer cells by a broccoli sprout extract
.
Mol Cancer Ther
2006
;
5
:
935
44
.
12
Tang
L
,
Zhang
Y
. 
Mitochondria are the primary target in isothiocyanate-induced apoptosis in human bladder cancer cells
.
Mol Cancer Therap
2005
;
4
:
1250
9
.
13
Tang
L
,
Zhang
Y
. 
Dietary isothiocyanates inhibit the growth of human bladder carcinoma cells
.
J Nutr
2004
;
134
:
2004
10
.
14
Tang
L
,
Li
G
,
Song
L
,
Zhang
Y
. 
The principal urinary metabolites of dietary isothiocyanates, N-acetylcysteine conjugates, elicit the same anti-proliferative response as their parent compounds in human bladder cancer cells
.
Anticancer Drugs
2006
;
17
:
297
305
.
15
Munday
R
,
Mhawech-Fauceglia
P
,
Munday
CM
, et al
. 
Inhibition of urinary bladder carcinogenesis by broccoli sprouts
.
Cancer Res
2008
;
68
:
1593
600
.
16
Bhattacharya
A
,
Tang
L
,
Li
Y
, et al
. 
Inhibition of bladder cancer development by allyl isothiocyanate
.
Carcinogenesis
2010
;
31
:
281
6
.
17
Xiao
Z
,
McCallum
TJ
,
Brown
KM
, et al
. 
Characterization of a novel transplantable orthotopic rat bladder transitional cell tumour model
.
Br J Cancer
1999
;
81
:
638
46
.
18
Hanel
EG
,
Xiao
Z
,
Wong
KK
,
Lee
PW
,
Britten
RA
,
Moore
RB
. 
A novel intravesical therapy for superficial bladder cancer in an orthotopic model: oncolytic reovirus therapy
.
J Urol
2004
;
172
:
2018
22
.
19
Byers
T
,
Marshall
J
,
Fiedler
R
,
Zielezny
M
,
Graham
S
. 
Assessing nutrient intake with an abbreviated dietary interview
.
Am J Epidemiol
1985
;
122
:
41
50
.
20
Getahun
SM
,
Chung
FL
. 
Conversion of glucosinolates to isothiocyanates in humans after ingestion of cooked watercress
.
Cancer Epidemiol Biomarkers Prev
1999
;
8
:
447
51
.
21
Conaway
CC
,
Getahun
SM
,
Liebes
LL
, et al
. 
Disposition of glucosinolates and sulforaphane in humans after ingestion of steamed and fresh broccoli
.
Nutr Cancer
2000
;
38
:
168
78
.
22
Kushad
MM
,
Brown
AF
,
Kurilich
AC
, et al
. 
Variation of glucosinolates in vegetable crops of Brassica oleracea
.
J Agric Food Chem
1999
;
47
:
1541
8
.
23
Jiao
D
,
Yu
MC
,
Hanker
JH
,
Low
SH
,
Chung
FL
. 
Total isothiocyanate contents in cooked vegetables frequently consumed in Singapore
.
J Agric Food Chem
1998
;
46
:
1055
8
.
24
Maskarinec
G
,
Murphy
S
,
Shumay
DM
,
Kakai
H
. 
Dietary changes among cancer survivors
.
Eur J Cancer Care
2001
;
10
:
12
20
.

Supplementary data