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Frontiers in Nutrition logoLink to Frontiers in Nutrition
. 2022 Mar 23;8:746944. doi: 10.3389/fnut.2021.746944

Allium Vegetables, Garlic Supplements, and Risk of Cancer: A Systematic Review and Meta-Analysis

Qifan Zhang 1, Qing Zhao 1, Yan Shen 1, Fuping Zhao 1, Yan Zhu 2,*
PMCID: PMC8985597  PMID: 35402472

Abstract

Purpose

The role of allium vegetables or garlic supplements on reducing cancer risk was inconsistent between laboratory study findings and related epidemiologic studies.

Methods

Studies assessing the effect of allium vegetables and garlic supplement consumption on cancer risk were included in our meta-analysis. We used fixed- or random-effects models to pool effect measures to evaluate the highest and lowest consumption. A dose-response regression analysis was used to assess the association between allium vegetables, garlic supplements, and cancer risk.

Results

In a pooled analysis of 22 studies with 25 reports on allium vegetables, a high consumption of allium vegetables showed no significant association with cancer risk (relative risk [RR] = 0.97, 95% confidence interval [CI] 0.92–1.03) in a fixed-effects model. Similarly, garlic supplements were not found to be significantly associated with an increased risk of cancer (RR = 0.97, 95% CI 0.84–1.12) in a random-effects model involving a pooled analysis of 10 studies with 11 reports. Consumption of allium vegetables did not significantly correspond with cancer risk (P for nonlinearity = 0.958, P for linearity = 0.907).

Conclusion

In this meta-analysis, we found no evidence that higher consumption of allium vegetables or garlic supplements reduced the risk of cancer; however, this finding requires further validation.

Systematic Review Registration

https://www.crd.york.ac.uk/prospero/#recordDetails, identifier: CRD42021246947.

Keywords: cancer risk, supplement, epidemiology, meta-analysis, allium vegetable

Introduction

The burden of cancer incidence and mortality is rapidly increasing worldwide. According to estimates from the World Health Organization (WHO), there were 19.3 million new cancer cases and almost 10.0 million cancer deaths in 2020 (https://gco.iarc.fr/today/home). Over the past decade, the search for dietary factors with effects on cancer prevention have led to the rapid expansion of the field of dietary patterns and cancer. Studies of individual nutrients and phytochemicals have revealed associations between certain dietary factors and cancer risk (1). Allium vegetables, mainly garlic, onion, and leeks, contained a high level of organosulfur compounds and flavonoids. Evidence from laboratory studies indicates that allium vegetables have anticancer effects through a variety of pathways (25). Therefore, allium vegetable consumption has been regarded as a potential dietary strategy for preventing pan-cancer. However, clinical findings examining the effects of allium vegetables on cancer risk reduction have been inconsistent. Previous systemic reviews and meta-analyses have shown that high consumption of allium vegetables might have a protective effect against cancer (6, 7). However, other studies have found no significant association between allium vegetable consumption and risk of cancer (7, 8).

Garlic supplements, as the most widely used type of allium vegetable-related supplements, were evaluated in the majority of previous meta-analyses. However, some studies have reported that garlic supplements were associated significantly with an increased risk of cancer growth (8, 9). Recently, an additional trial (10) with long-term follow-up assessed the effects of garlic supplements on cancer risk but did not detect any beneficial the benefits of garlic supplements on gastric cancer incidence.

Moreover, most previously published meta-analyses have focused on gastrointestinal cancers, like colorectal and stomach cancer (8, 11). However, to the best of our knowledge, no meta-analysis has comprehensively evaluated the role of allium vegetables or garlic supplements in total cancer prevention. Due to this conflicting evidence, as well as the limitations of previous reviews and the availability of new findings, the systematic review and meta-analysis was conducted to evaluate the effects of allium vegetables and garlic supplements on pan-cancer risk.

Methods

Protocol and Guidance

This study was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) (12). The protocol for this review was registered with PROSPERO (CRD42021246947).

Inclusion and Exclusion Criteria

After preliminary searches, we decided to include prospective studies, and took the pooled analysis of retrospective studies as our next work. Thus, we only considered trials to be eligible if they involved prospective study designs, including cohort, case-cohort, or intervention studies; if they investigated the relationship between allium vegetables or garlic supplements and malignancy risk; and if they provided or allowed for the calculation of relative risks (RR) with 95% confidence intervals (CIs).

We excluded studies if they were designed as nonhuman studies, case reports, or case series or had a retrospective study design, such as a case-control study; if they were editorials, or letters without the analyses of primary data; or, if they did not provide sufficient data; if they did not use an analytic epidemiologic design.

Data Sources and Searches

One of the authors (Q.F. Zhang) performed the search of several databases: Medline, Embase, and Web of Science from inception to May 1, 2021. The following combined search terms were used: MeSH headings and keywords relating to “neoplasms,” the MeSH heading “allium,” and keywords related to the allium vegetables and garlic supplements. Ongoing or unpublished eligible studies were also searched through ClinicalTrials.gov and the World Health Organization International Clinical Trials Registry Platform (WHO ICTRP). To maximize the identification of relevant studies, the reference lists of eligible studies were also reviewed. If multiple studies remained with the same or partially overlapping populations, we extracted the data with the largest sample size or the longest follow-up duration. If duplicate studies offered results related to different outcomes, we included them all in the pooled analysis of specific outcomes. An English-language restriction was also included in our search strategy.

Two researchers (Q. F. Zhang and Q. Zhao) independently screened all titles and abstracts of studies meeting the inclusion criteria. They then obtained full-text versions and performed further screening if studies were deemed eligible. We resolved any disagreements by consensus.

Data Extraction and Quality Assessment

Two independent researchers (Q.F. Zhang and Y. Shen) used a standard form to extract data from the included studies, including first author, publication year, study design, geographic region, sample size (number of cases and total participants), duration of follow-up, demographics of participants, tumor site, exposure, and effect sizes with 95% CIs of highest vs. lowest consumption category. We extracted effect sizes that represented the greatest degree of control for potential confounders. If person-years were not presented, they were using the number of subjects multiplied by the mean duration of follow-up. When a study reported an outcome of interest but without estimates, we tried to contact the author for related data. We resolved any disagreements by consensus.

Two researchers (Y. Shen and F.P. Zhao) independently assessed the quality of included studies by the Newcastle-Ottawa Scale (NOS; http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp). Publication bias was assessed qualitatively by visual estimation of funnel plots and quantitatively by calculation of Egger's test (13). We considered P-value less than to represent the possibility of small-study effects.

Data Synthesis and Analysis

The primary outcome for this meta-analysis was the incidence of cancer. We considered the RRs and 95% CI as the effect sizes for all studies. The association between allium vegetables/garlic supplements and cancer risk was quantified by pooling the RRs for the highest vs. lowest consumption category using random-effects or fixed-effects models according to the extent of between-study heterogeneity. The extent of heterogeneity was quantified by the Q test (14) and I2 score (15). If significant heterogeneity was not observed (I2 < 50%), we used a fixed-effects model to pool outcomes; otherwise, a random-effects model was used (I2 ≥ 50%).

Dose-Response Meta-Analysis

To precisely assess the effect of allium vegetable consumption on cancer risk, a random-effects dose-response meta-analysis was performed, as described previously (16). Moreover, we used the restricted cubic splines with four knots at fixed percentiles (5%, 35%, 65%, and 95%) of the distribution to assess the potential curve-linear relationship between allium vegetable consumption and cancer risk (17). For each study, we used the mean or median level of each category consumption for assigning to each corresponding RR. If data were not available, we assigned the midpoint of the upper and lower boundaries of each category as the average consumption.

Meta-Regression, Subgroup, and Sensitivity Analyses

Meta-regression and subgroup analyses were performed to identify potential sources of heterogeneity. We stratified included studies into different subgroups according to the number of cases, sex, location, follow-up period, allium vegetable species, and tumor sites. We conducted further sensitivity analyses by excluding one study per iteration. Because the probability of false-negative results is rather high after the adjustment of multiple testing, we did not adjust p values in the present meta-analysis.

Results

Eligible Studies and Study Characteristics

The search and selection procedures of literature are presented in Supplementary Figure 1. Finally, twenty-two studies on allium vegetables involving 13,677 patients and 10 studies on garlic supplements involving 6,555 patients were included in this meta-analysis. The main characteristics of included studies are summarized in Table 1.

Table 1.

Characteristics of studies included in the meta–analysis.

Author Year Study design Location Cases Total participants Follow–up period (years) Sex Age at baseline Tumor site Exposure Effect Size (95%CI) Highest vs lowest consumption
Giovannucci (18) 1994 Cohort USA 205 47,949 6 Male 40–75 Colon Garlic 0.77 (0.51–1.16)
Dorant (19) 1994 Case-cohort Netherlands 484 120,852 3.3 Both Lung Onion 0.80 (0.52–1.24)
Leek 1.08 (0.80–1.45)
Garlic supplements 1.22 (0.81–1.86)
Steinmetz (20) 1994 Cohort USA 212 41,837 5 Female 55–69 Colon Garlic 0.68 (0.46–1.02)
Dorant (21) (1) 1996 Case-cohort Netherlands 152 120,852 3.3 Both 55–69 Stomach Garlic supplements 1.29 (0.62–2.67)
139 Stomach Onion 0.50 (0.26–0.95)
Leek 0.69 (0.42–1.14)
Dorant (22) (2) 1996 Case-cohort Netherlands 443 120,852 3.3 Both 55–69 Colon Garlic supplements 1.36 (0.79–2.35)
(293 colon, 150 rectum) Rectum 1.28 (0.63–2.60)
(243 male, 200 female) Male Colon Onion 0.87 (0.48–1.65)
Rectum 0.66 (0.28–1.52)
Female Colon 1.49 (0.79–2.81)
Rectum 1.34 (0.55–3.31)
Male Colon Leek 1.10 (0.71–1.70)
Rectum 0.72 (0.40–1.30)
Female Colon 1.18 (0.73–1.89)
Rectum 1.31 (0.60–2.85)
Schuurman (23) 1998 Case-cohort Netherlands 610 58,279 6.3 Male 55–69 Prostate Allium vegetables 0.95 (0.69–1.33)
Onion 0.93 (0.79–1.10)
Leek 1.38 (1.08–1.76)
Li (24) 2004 Intervention China 142 5,033 5 Both 35–74 All Garlic supplements 0.67 (0.43–1.03)
(107 male, 35 female) (2,526 intervention, 2,507 control) Stomach 0.48 (0.21–1.06)
(53 stomach, 48 liver) - Liver 0.78 (0.35–1.74)
(63 intervention, 79 control) Male All Garlic supplements 0.51 (0.30–0.85)
Stomach 0.36 (0.14–0.92)
Liver 0.71 (0.28–1.78)
Female All Garlic supplements 1.50 (0.62–3.61)
Stomach 1.14 (0.22–5.76)
Liver 1.17 (0.23–5.92)
Schulz (25) 2005 Cohort Europe 581 325,640 6.3 (mean) Female 19–98 Ovary Garlic/onion 0.79 (0.62–1.01)
Lin et al. (26) 2006 Cohort USA 878 107,401 10 Both 30–75 Colorectum Onion 1.03 (0.82–1.29)
380 35,425 Male 40–75 0.92 (0.65–1.29)
498 71,976 Female 30–55 1.13 (0.84–1.53)
Boeing (27) 2006 Cohort Europe 352 345,904 5.8 Both NA Upper aero-digestive tract Garlic/onion 1.17 (0.73–1.86)
255 130,633 Male 1.04 (0.79–1.36)
97 215,271 Female 1.20 (0.73–1.97)
Gonzalez (28) 2006 Cohort Europe 65 481,518 6.5 Both 35–70 Esophagus Garlic/onion 1.27 (0.59–2.73)
Larsson (29) 2006 Cohort Sweden 139 82,002 7.2 (mean) Both Stomach Allium vegetables 0.90 (0.58–1.41)
(36,664 female, 45,338 male)
Kirsh (30) 2007 Cohort USA 1,338 29,361 4.2 (mean) Male 55–74 Prostate Garlic 0.88 (0.76–1.03)
Onion 1.01 (0.88–1.17)
Satia (31) 2009 Cohort USA 428 77,512 5 Both 50–76 Colorectum Garlic supplements 1.35 (1.01–1.81)
665 77,125 Lung Garlic supplements 1.05 (0.83–1.34)
Epplein (32) 2010 Cohort China 206 73,064 12 Female 40–70 Stomach Allium vegetables 1.10 (0.74–1.63)
132 59,247 6 Male 40–74 0.92 (0.58–1.46)
Walter (33) 2010 Cohort USA 588 66,227 6.5 (mean) Both 50–76 Hematologic malignancies Garlic supplements 0.55 (0.34–0.87)
Gonzalez (34) 2011 Cohort Europe 1,070 299,651 9 (mean) Female 35–70 Cervix Garlic and onions 1.09 (0.85–1.40)
Brasky (35) 2011 Cohort USA 1,602 35,239 6.1 (median) Men 50–76 Prostate Garlic supplements 1.00 (0.85–1.17)
Steevens (36) 2011 Case-cohort Netherlands 824 120,852 16.3 Both 55–69 Esophageal squamous cell carcinoma Allium vegetables 1.64 (0.88–3.08)
Esophageal adenocarcinoma 0.84 (0.50–1.43)
Gastric cardia adenocarcinoma 1.55 (0.94–2.56)
Gastric noncardia adenocarcinoma 0.97 (0.69–1.35)
Esophageal squamous cell carcinoma Onion 1.10 (0.79–1.53)
Eesophageal adenocarcinoma 0.84 (0.65–1.09)
Gastric cardia adenocarcinoma 1.21 (0.95–1.53)
Gastric noncardia adenocarcinoma 0.91 (0.78–1.06)
McCullough (9) 2012 Cohort USA 1,130 99,700 7 Both 69 Colorectum Garlic 1.03 (0.77–1.37)
579 42,824 Male 1.19 (0.79–1.79)
551 56,876 Female 0.87 (0.58–1.32)
764 89,921 Both Colorectum Garlic supplements 1.03 (0.74–1.44)
390 38,053 Male 0.94 (0.57–1.53)
374 51,868 Female 1.09 (0.69–1.72)
Gonzalez (37) 2012 Cohort Europe 683 477,312 11.02 (mean) Both 35–70 Stomach Garlic/onion 0.97 (0.76–1.25)
Meng (38) 2013 Cohort USA 1,339 76,208 24 Female 30–55 Colorectum Garlic 1.21 (0.94–1.57)
1,029 45,592 22 Male 40–75 1.00 (0.71–1.42)
578 76,208 4 Female 30–55 Colorectum Garlic supplements 0.72 (0.49–1.07)
559 45,592 10 Male 40–75 1.22 (0.83–1.78)
Vogtmann (39) 2013 Cohort China 398 61,274 6.3 (median) Men 40–74 Colorectum Allium 0.99 (0.77–1.27)
Maasland (40) 2015 Case-cohort Netherlands 415 120,852 20.3 Both 55–69 Head and neck Allium 1.07 (0.76–1.50)
Onion 0.93 (0.77–1.11)
Kim (41) 2018 Cohort USA 292 123,484 Both Stomach Garlic 1.39 (0.89–2.17)
138 77,086 30 Female 1.34 (0.72–2.47)
154 46,398 28 Male 1.45 (0.76–2.78)
Li (10) 2019 Intervention China 150 3365 14.7 Both 35–64 Stomach Garlic supplements 0.81 (0.57–1.13)
(1678 intervention, 1687 control)
Yu (42) 2020 Cohort China 270 3199 10 Both 30–70 Liver Garlic 0.62 (0.42–0.93)

The assessment of risk of bias and quality showed that all included studies had NOS scores of ≥7, indicting a lower risk of bias and better quality.

Highest vs. Lowest Consumption Category

As shown in Figure 1, in the pooled analysis of the 22 studies (9, 1823, 2530, 32, 34, 3642) with 25 reports on allium vegetable consumption, no significant association was observed between a high consumption of allium vegetables and cancer risk (RR, 0.97; 95% CI, 0.92–1.03; P = 0.356; I2 = 22.0%; Ph = 0.161). Garlic supplements were also not found to be significantly associated with an increased risk of cancer (RR, 0.97; 95% CI, 0.84–1.12; P = 0.705; I2 =50.5%; Ph = 0.027) in a random-effects model involving a pooled analysis of 10 studies (9, 10, 19, 21, 22, 24, 31, 33, 35, 38) with 11 reports (Figure 2).

Figure 1.

Figure 1

Forest plot of the association between allium vegetable consumption and cancer risk (highest vs. lowest category of allium vegetable consumption).

Figure 2.

Figure 2

Forest plot of the association between garlic supplement consumption and cancer risk (highest vs. lowest category of supplement consumption).

Dose-Response Meta-Analysis

A random-effects, dose-response meta-analysis was performed to precisely assess the relationship between allium vegetable consumption and risk of cancer. A total of 14 studies (9, 19, 2123, 26, 29, 30, 32, 3842) with 20 reports were included. We did not find a curvilinear association between allium vegetable consumption and risk of cancer (P = 0.958 for nonlinearity; P = 0.907 for linearity) (Figure 3).

Figure 3.

Figure 3

Dose-response meta-analysis of the association between allium vegetable consumption and cancer risk. The solid line represents the linear relationship, and the short-dashed line represents the nonlinear relationship, with the long-dashed lines representing the 95% confidence intervals for the spline model.

Subgroup Analysis

In an analysis of individual allium vegetables, garlic intake was investigated in seven studies (9, 18, 20, 30, 38, 41, 42) with eight reports, which showed no association with cancer risk (RR, 0.93; 95% CI, 0.79–1.09). An analysis of eight studies (19, 2123, 26, 30, 36, 40) with nine reports related to onion consumption showed that a high amount of onion consumption was not associated with cancer risk (RR, 0.96; 95% CI, 0.90–1.03). Moreover, four studies (19, 2123) with five reports investigated the consumption of leeks and risk of cancer, with the pooled analysis showing no association between leek consumption and cancer risk (RR, 1.08; 95% CI, 0.88–1.34) (Table 2). Another subgroup analysis based on tumor site showed that allium vegetable consumption was not significantly associated with the risk of cancer in the digestive tract (RR, 1.01; 95% CI, 0.94–1.09) or the non-digestive tract (RR, 0.94; 95% CI, 0.87–1.01).

Table 2.

Subgroup analysis of the association between allium vegetable and supplement consumption and cancer risk.

Subgroup No of reports RR (95% CI) P for test I2 (%) P for heterogeneity P for meta–regression
Allium vegetables
Overall 25 0.97 (0.92–1.03) 0.356 22.0 0.161
No of cases
      ≥500 10 0.99 (0.93–1.06) 0.775 0.0 0.516 0.433
      <500 15 0.95 (0.86–1.04) 0.238 36.3 0.079
Sex
      Female 10 1.03 (0.93–1.14) 0.539 38.0 0.105
      Male 11 0.96 (0.89–1.04) 0.313 0.0 0.918 0.290
Location
      Europe and America 21 0.98 (0.93–1.04) 0.523 20.9 0.190 0.490
      China 4 0.92 (0.77–1.09) 0.314 38.8 0.179
Follow-up period
      ≥7 y 12 1.05 (0.96–1.14) 0.304 0.0 0.455 0.063
      <7 y 13 0.93 (0.87–1.00) 0.040 22.5 0.216
Type of intake
      Garlic 8 0.93 (0.79–1.09) 0.363 54.9 0.030
      Onion 9 0.96 (0.90–1.03) 0.285 7.8 0.370 0.637
      Leek 5 1.08 (0.88–1.34) 0.445 46.5 0.112 0.114
Tumor site
      Digestive tract 18 1.01 (0.94–1.09) 0.791 18.1 0.237
      Non-digestive tract 7 0.94 (0.87–1.01) 0.110 27.1 0.222 0.251
Garlic supplements
Overall 11 0.97 (0.84–1.12) 0.705 50.5 0.027
No of cases
      ≥500 5 0.96 (0.80–1.16) 0.689 59.9 0.029 0.840
      <500 6 0.99 (0.75–1.31) 0.957 47.4 0.107
Sex
      Female 3 0.95 (0.65–1.39) 0.783 37.8 0.200
      Male 4 0.92 (0.69–1.22) 0.569 59.4 0.060 0.885
Location
      Europe and America 9 1.03 (0.88–1.19) 0.727 46.2 0.062 0.141
      China 2 0.75 (0.58–0.99) 0.040 0.0 0.503
Follow-up period
      ≥5 y 7 0.94 (0.79–1.12) 0.473 58.6 0.025 0.475
      <5 y 4 1.07 (0.78–1.47) 0.661 45.7 0.137
Tumor site*
      Digestive tract 8 1.02 (0.83–1.26) 0.859 51.0 0.046
      Non-digestive tract 5 0.95 (0.78–1.17) 0.639 47.1 0.109 0.638
*

Two studies reported effect sizes of more than one disease subgroup.

The association between allium vegetable consumption and cancer risk were similarly nonsignificant in other subgroup analyses based on the number of cases, sex, and location. However, a stratified analysis based on the duration of follow-up period indicated that a high amount of allium vegetable consumption was marginally associated with a decreased risk of cancer in patients with a follow-up period of less than 7 years (RR, 0.93; 95% CI, 0.87–1.00) (Table 2).

Moreover, in the subgroup analysis of garlic supplements, the consumption of garlic supplements was not associated with cancer risk according to the number of cases, sex, follow-up period, or tumor site. Stratified by study location, however, garlic supplement consumption was marginally associated with a decreased cancer risk in Chinese patients (RR, 0.75; 95% CI, 0.58–0.99); however, only two reports were pooled in this subgroup.

Sensitivity Analysis

As shown in Figure 4, in our sensitivity analysis, the specific RRs from 25 reports for allium vegetable consumption ranged from a low of 0.96 (95% CI, 0.91–1.02; I2 = 17.6%; Ph = 0.219) after omitting the report by Meng, 2013 (1.1) (38) to a high of 0.99 (95% CI, 0.93–1.04; I2 = 17.2%; Ph = 0.225) after omitting the report by Schulz, 2005 (25), but they were, in general, similar. The 11 report-specific RRs for garlic supplement intake ranged from a low of 0.96 (95% CI, 0.86–1.06; I2 = 47.2%; Ph = 0.048) after omitting the report by Satia, 2009 (31) to a high of 1.03 (95% CI, 0.94-1.13; I2 = 34.2%; Ph = 0.134) after omitting the report by Walter, 2010 (33), which were again similar. The results of sensitivity analysis showed that there was no significant variation in the pooled RR after excluding any one of the studies, proving the stability of the overall results.

Figure 4.

Figure 4

Sensitivity analysis for cancer risk with allium vegetable (A) and garlic supplement (B).

Meta-Regressions

Our univariate meta-regression analysis found no statistically significant differences, revealing that the analyzed stratification factors were not a source of heterogeneity. However, we did find that the cancer risk was significantly higher in studies with allium vegetable consumption and a longer duration of follow-up (P for interaction = 0.017; Supplementary Figures 2, 3).

Publication Bias

No publication bias was observed in this meta-analysis. No asymmetry were found through a funnel plot analysis. Moreover, Egger's test (P = 0.910 for allium vegetables; P = 0.426 for garlic supplements) detected no significant small-study effects (Supplementary Figures 4, 5).

Discussion

Principal Findings

To our knowledge, the current meta-analysis was the first to assess the effects of allium vegetable and supplement consumption on pan-cancer risk. In our findings, there was no significant effect of higher consumption of allium vegetables on cancer risk. Furthermore, results from a dose-response meta-analysis revealed no nonlinear or linear relationship between allium vegetable consumption and cancer risk. Meanwhile, a subgroup analysis in patients with a follow-up duration of less than 7 years showed that a higher amount of allium vegetable consumption was marginally related to a decreased cancer risk. Our meta-regression analysis also revealed that the follow-up period might be a potential source of heterogeneity. Neither garlic and onion, nor leek consumption were associated with cancer risk. We also found that garlic supplements were not significantly associated with cancer risk. Our findings do not support the conclusion that allium vegetable or supplement intake are protective factors against cancer. Our comprehensive cancer risk assessment based on the consumption of allium vegetables or supplements enables a general understanding of the association between allium vegetable and supplement consumption and cancer risk.

Comparison With Other Studies

Many previous meta-analyses have focused on the association between allium vegetable consumption and risk of gastrointestinal cancers, including colorectal cancer (8, 43) and stomach cancer (6, 44) with inconsistent findings. In 2014, two meta-analyses involving observational studies found a higher consumption of allium vegetables was not associated with colorectal cancer risk (8, 43). Similar nonsignificant results was found in a meta-analysis assessing the effects of allium vegetables on esophageal cancer (7). However, consumption of a large amount of allium vegetables was found to reduce the risk of stomach cancer based on data mainly derived from case-control studies (6, 44). In our pooled analysis of only prospective studies, we found that higher allium vegetable consumption did not reduce the risk of cancer. A subgroup analysis also showed consistently nonsignificant results for different tumor sites, including the digestive tract and non-digestive tract. Though our study did suggest that higher allium vegetable consumption may have a protective role against cancer risk in patients with a follow-up duration of less than 7 years, the statistical difference was marginal for this finding. Our meta-regression analysis also found that cancer risk was significantly higher in studies with allium vegetable consumption in patients with a longer duration of follow-up. The follow-up period may therefore explain the heterogeneity in the pooled RR. We hypothesize that a longer follow-up period may have led to the development of cancer in more patients. Overall, allium vegetable consumption was not associated with cancer risk in the current meta-analysis.

Findings related to garlic, the mostly widely analyzed individual allium vegetable item, and its role in cancer risk has varied across studies and cancer types. A meta-analysis of 18 studies in 2018 revealed that high garlic consumption was associated with a reduced gastric cancer risk (11). Furthermore, its protective effect has been proven for upper aerodigestive tract cancer (7), esophageal cancer (7), and prostate cancer (45). However, conclusions from other meta-analyses did not support a protective role of garlic consumption in head and neck cancer (7), colorectal cancer (46). It is worth noting that previous meta-analyses always combined garlic and garlic supplements, however, garlic supplements have been proven to be significantly associated with an increased risk of certain cancer types, including colorectal cancer (8). In the current meta-analysis, we conducted a subgroup analysis exploring the role of garlic consumption on cancer prevention without garlic supplements, finding no association between higher garlic consumption and reduced cancer risk after pooling the results of eight reports, including five on colorectal cancer (9, 1820, 38) (1,2), one on stomach cancer [Kim, 2018 (41)], one on prostate cancer [Kirsh, 2007 (30)], and one on liver cancer[Yu, 2020 (42)]. It is worth exploring whether the addition of retrospective studies, such as case-control studies, would have led to different results. However, these pooled results did not support a protective role of garlic in cancer prevention.

In addition to garlic, other individual allium vegetable items have also been investigated for their effects on cancer risk. For example, onions have been demonstrated to be a protective factor against gastric cancer (6), esophageal cancer (7), and laryngeal cancer (7), but not colorectal (43) or prostate (45) cancers. As with garlic, the current meta-analysis showed no protective effects against cancer for onions or leeks.

Garlic supplements contains various mixture that must be prepared at a proper temperature, which have been demonstrated to be associated with toxicity (47). Accumulating evidence indicates important diversity between garlic supplements and raw/cooked garlic (48). Allicin, as the major biologically active element of garlic, is not present in garlic supplement (49). A previous meta-analysis that included five studies with 11 reports on the effects of garlic supplements showed that use of these supplements was significantly associated with an increased risk of colorectal cancer (8); however, another analysis comprising 10 reports demonstrated no significant association (46). In 2019, a blinded randomized placebo-controlled trial enrolled 3,365 residents in a region at high risk for gastric cancer in China (10). In a report of its long-term results, this study revealed that garlic supplements yielded a statistically significant decrease in gastric cancer mortality but a statistically insignificant decrease in incidence. By including the results of those recently published studies, the current meta-analysis provides an independent estimate of the effects of garlic supplements on cancer risk, showing that these supplements play neither a protective nor a harmful role in cancer. Notably, however, our pooled analysis of two reports from China showed inconsistent results, revealing that garlic supplement may decrease the risk of cancer incidence by 25%. However, we speculate that the small sample size with insufficient power generated less stable results.

Although many systematic reviews have studied the association between allium vegetable consumption and cancer risk, some issues still exist and need to be resolved, especially related to the discrepancies in their findings. First, retrospectively designed studies, such as case-control studies, have been enrolled in some previous meta-analyses. In general, case-control studies are more prone to recall and selection biases and are not entirely controlled for confounders, including those known to be protective factors, which may bias the results (8). Second, dietary factors are generally considered to be mainly related to gastrointestinal cancers, although laboratory evidence indicates that some ingredients in allium vegetables may also exert anticancer effects on other cancer types besides colorectal or stomach cancer (2, 5052). More epidemiologic studies, especially prospective studies, are required to further verify the role of allium vegetables in non-digestive tract cancers. Third, supplements provide the possibility of conducting randomized controlled trials for assessing the effects of allium vegetable on cancer. However, it remains unclear whether specific ingredients in allium vegetables play the major anticancer role or if supplements play the same role as raw allium vegetables. Both of these factors make the results of previously pooled analyses unreliable. To avoid the influence of these factors, the current meta-analysis included prospectively designed studies and separately pooled allium vegetables and supplements. We believe our findings offer more stable and comprehensive evidence about the role of allium vegetables.

Strengths and Limitations

This present meta-analysis had several strengths. Because only prospective studies were included, our findings are unlikely to be influenced by recall or selection bias. Also, unlike most previous studies that assessed only specific cancer types, the associations between allium vegetables and multiple cancer types were examined in our study. Additionally, garlic supplements were analyzed separately from allium vegetables due to differences in their properties and effects. Moreover, our results based on pooled estimates were consistent in stratified analyses across various scenarios, indicating the robustness of our findings. Furthermore, we quantified the association between consumption of allium vegetables and cancer risks by performing linear and non-linear dose-response analyses. Finally, our subgroup, publication bias, and sensitivity analyses demonstrated the reliability and stability of the results.

However, some limitations existed the current meta-analysis. First, the measurements of dose level of allium vegetables or garlic supplements (daily, weekly, monthly, or gram, serving, clove) varied across the included studies, making it impossible to accurately compare equivalent consumption. Also, the included studies only reported use or nonuse, leading to the impossibility of assessing the dose-response relationship between garlic supplements and cancer risk. Second, although we pooled effect sizes adjusting for most established risk factors, the causes of cancer incidence are complicated and sometimes unclear, which may have introduced confounders that could have influenced our findings. Third, many laboratory studies have demonstrated the role of garlic components in inhibiting tumor growth and progression, suggesting that they might also play a role in prolonging the survival of cancer patients. However, whether allium vegetables or supplements could reduce cancer mobility was not analyzed in the current study, limiting the implications of our findings. Last, though prospective studies are less likely to be influenced by recall or selection bias, well-conducted retrospective studies provide less-biased evidence. The addition of retrospective studies in the pooled analysis was believed to provide more detailed information and strength the reliability of the findings, which was also our next work.

Implications

Cancer incidence and mortality is a major burden in most countries worldwide. Currently, not only treatment but also prevention of cancer has been of great concern to prolong lifespan of population. Considering the anticancer effects of certain active compounds present in allium vegetables, such as organosulfur, researchers have shown an increasingly interest in the ability of these substances to prevent cancer. Our findings suggest that neither allium vegetables or supplements have clinically relevant effects on cancer prevention; therefore, there is little evidence to support the idea that allium vegetables or supplements can reduce cancer in incidence. Additional large, randomized controlled trials are needed to confirm these results.

Conclusions

Overall, the current meta-analysis found that higher consumption of allium vegetables or garlic supplements were not associated with a decrease in cancer risk. Randomized controlled trials or well-designed cohort studies are warranted to confirm these findings.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author Contributions

Material preparation, data collection, and analysis were performed by QifZ, QinZ, YS, FZ, and YZ. The first draft of the manuscript was written by QifZ and QinZ. All authors commented on previous versions of the manuscript, read and approved the final manuscript, and contributed to the study conception and design.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2021.746944/full#supplementary-material

References

  • 1.Steck SE, Murphy EA. Dietary patterns and cancer risk. Nat Rev Cancer. (2020) 20:125–38. 10.1038/s41568-019-0227-4 [DOI] [PubMed] [Google Scholar]
  • 2.Chu Q, Lee DT, Tsao SW, Wang X, Wong YC. S-allylcysteine, a water-soluble garlic derivative, suppresses the growth of a human androgen-independent prostate cancer xenograft, CWR22R, under in vivo conditions. BJU Int. (2007) 99:925–32. 10.1111/j.1464-410X.2006.06639.x [DOI] [PubMed] [Google Scholar]
  • 3.Xiao J, Xing F, Liu Y, Lv Y, Wang X, Ling MT, et al. Garlic-derived compound S-allylmercaptocysteine inhibits hepatocarcinogenesis through targeting LRP6/Wnt pathway. Acta pharmaceutica Sinica B. (2018) 8:575–86. 10.1016/j.apsb.2017.10.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Katsuki T, Hirata K, Ishikawa H, Matsuura N, Sumi S, Itoh H. Aged garlic extract has chemopreventative effects on 1,2-dimethylhydrazine-induced colon tumors in rats. J Nutr. (2006) 136:847S–51S. 10.1093/jn/136.3.847S [DOI] [PubMed] [Google Scholar]
  • 5.Tung YC, Tsai ML, Kuo FL, Lai CS, Badmaev V, Ho CT, et al. Se-Methyl-L-selenocysteine Induces Apoptosis via Endoplasmic Reticulum Stress and the Death Receptor Pathway in Human Colon Adenocarcinoma COLO 205 Cells. J Agric Food Chem. (2015) 63:5008–16. 10.1021/acs.jafc.5b01779 [DOI] [PubMed] [Google Scholar]
  • 6.Turati F, Pelucchi C, Guercio V, La Vecchia C, Galeone C. Allium vegetable intake and gastric cancer: a case-control study and meta-analysis. Mol Nutr Food Res. (2015) 59:171–9. 10.1002/mnfr.201400496 [DOI] [PubMed] [Google Scholar]
  • 7.Guercio V, Turati F, La Vecchia C, Galeone C, Tavani A. Allium vegetables and upper aerodigestive tract cancers: a meta-analysis of observational studies. Mol Nutr Food Res. (2016) 60:212–22. 10.1002/mnfr.201500587 [DOI] [PubMed] [Google Scholar]
  • 8.Zhu B, Zou L, Qi L, Zhong R, Miao X. Allium vegetables and garlic supplements do not reduce risk of colorectal cancer, based on meta-analysis of prospective studies. Clin Gastroenterol Hepatol. (2014) 12:1991–2001 e1–4. 10.1016/j.cgh.2014.03.019 [DOI] [PubMed] [Google Scholar]
  • 9.McCullough ML, Jacobs EJ, Shah R, Campbell PT, Gapstur SM. Garlic consumption and colorectal cancer risk in the CPS-II Nutrition Cohort. Cancer Causes Control: CCC. (2012) 23:1643–51. 10.1007/s10552-012-0042-7 [DOI] [PubMed] [Google Scholar]
  • 10.Li WQ, Zhang JY, Ma JL Li ZX, Zhang L, Zhang Y, et al. Effects of Helicobacter pylori treatment and vitamin and garlic supplementation on gastric cancer incidence and mortality: follow-up of a randomized intervention trial. BMJ. (2019) 366:l5016. 10.1136/bmj.l5016 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Li Z, Ying X, Shan F, Ji J. The association of garlic with Helicobacter pylori infection and gastric cancer risk: A systematic review and meta-analysis. Helicobacter. (2018) 23:e12532. 10.1111/hel.12532 [DOI] [PubMed] [Google Scholar]
  • 12.Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ. (2009) 339:b2700. 10.1136/bmj.b2700 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. (1997) 315:629–34. 10.1136/bmj.315.7109.629 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. (2002) 21:1539–58. 10.1002/sim.1186 [DOI] [PubMed] [Google Scholar]
  • 15.Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. (2003) 327:557–60. 10.1136/bmj.327.7414.557 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Greenland S, Longnecker MP. Methods for trend estimation from summarized dose-response data, with applications to meta-analysis. Am J Epidemiol. (1992) 135:1301–9. 10.1093/oxfordjournals.aje.a116237 [DOI] [PubMed] [Google Scholar]
  • 17.Harrell FE. Jr, Lee KL, Pollock BG Regression models in clinical studies: determining relationships between predictors and response. J Natl Cancer Inst. (1988) 80:1198–202. 10.1093/jnci/80.15.1198 [DOI] [PubMed] [Google Scholar]
  • 18.Giovannucci E, Rimm EB, Stampfer MJ, Colditz GA, Ascherio A, Willett WC. Intake of fat, meat, and fiber in relation to risk of colon cancer in men. Cancer Res. (1994) 54:2390–7. [PubMed] [Google Scholar]
  • 19.Dorant E, van den Brandt PA, Goldbohm RA. A prospective cohort study on Allium vegetable consumption, garlic supplement use, and the risk of lung carcinoma in The Netherlands. Cancer Res. (1994)54:6148–53. [PubMed] [Google Scholar]
  • 20.Steinmetz KA, Kushi LH, Bostick RM, Folsom AR, Potter JD. Vegetables, fruit, and colon cancer in the Iowa Women's Health Study. Am J Epidemiol. (1994) 139:1–15. 10.1093/oxfordjournals.aje.a116921 [DOI] [PubMed] [Google Scholar]
  • 21.Dorant E, van den Brandt PA, Goldbohm RA, Sturmans F. Consumption of onions and a reduced risk of stomach carcinoma. Gastroenterology. (1996) 110:12–20. 10.1053/gast.1996.v110.pm8536847 [DOI] [PubMed] [Google Scholar]
  • 22.Dorant E, van den Brandt PA, Goldbohm RA. A prospective cohort study on the relationship between onion and leek consumption, garlic supplement use and the risk of colorectal carcinoma in The Netherlands. Carcinogenesis. (1996) 17:477–84. 10.1093/carcin/17.3.477 [DOI] [PubMed] [Google Scholar]
  • 23.Schuurman AG, Goldbohm RA, Dorant E, van den Brandt PA. Vegetable and fruit consumption and prostate cancer risk: a cohort study in The Netherlands. Cancer Epidemiol Biomarkers Prev. (1998) 7:673–80. [PubMed] [Google Scholar]
  • 24.Li H, Li HQ, Wang Y, Xu HX, Fan WT, Wang ML, et al. An intervention study to prevent gastric cancer by micro-selenium and large dose of allitridum. Chin Med J. (2004) 117:1155–60. [PubMed] [Google Scholar]
  • 25.Schulz M, Lahmann PH, Boeing H, Hoffmann K, Allen N, Key TJ, et al. Fruit and vegetable consumption and risk of epithelial ovarian cancer: the European Prospective Investigation into Cancer and Nutrition. Cancer Epidemiol Biomarkers Prev. (2005) 14:2531–5. 10.1158/1055-9965.EPI-05-0159 [DOI] [PubMed] [Google Scholar]
  • 26.Lin J, Zhang SM, Wu K, Willett WC, Fuchs CS, Giovannucci E. Flavonoid intake and colorectal cancer risk in men and women. Am J Epidemiol. (2006) 164:644–51. 10.1093/aje/kwj296 [DOI] [PubMed] [Google Scholar]
  • 27.Boeing H, Dietrich T, Hoffmann K, Pischon T, Ferrari P, Lahmann PH, et al. Intake of fruits and vegetables and risk of cancer of the upper aero-digestive tract: the prospective EPIC-study. Cancer Causes Control: CCC. (2006) 17:957–69. 10.1007/s10552-006-0036-4 [DOI] [PubMed] [Google Scholar]
  • 28.Gonzalez CA, Pera G, Agudo A, Bueno-de-Mesquita HB, Ceroti M, Boeing H, et al. Fruit and vegetable intake and the risk of stomach and oesophagus adenocarcinoma in the European Prospective Investigation into Cancer and Nutrition (EPIC-EURGAST). Int J Cancer. (2006) 118:2559–66. 10.1002/ijc.21678 [DOI] [PubMed] [Google Scholar]
  • 29.Larsson SC, Bergkvist L, Wolk A. Fruit and vegetable consumption and incidence of gastric cancer: a prospective study. Cancer Epidemiol Biomarkers Prev. (2006) 15:1998–2001. 10.1158/1055-9965.EPI-06-0402 [DOI] [PubMed] [Google Scholar]
  • 30.Kirsh VA, Peters U, Mayne ST, Subar AF, Chatterjee N, Johnson CC, et al. Prospective study of fruit and vegetable intake and risk of prostate cancer. J Natl Cancer Inst. (2007) 99:1200–9. 10.1093/jnci/djm065 [DOI] [PubMed] [Google Scholar]
  • 31.Satia JA, Littman A, Slatore CG, Galanko JA, White E. Associations of herbal and specialty supplements with lung and colorectal cancer risk in the VITamins and Lifestyle study. Cancer Epidemiol Biomarkers Prev. (2009) 18:1419–28. 10.1158/1055-9965.EPI-09-0038 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Epplein M, Shu XO, Xiang YB, Chow WH, Yang G, Li HL, et al. Fruit and vegetable consumption and risk of distal gastric cancer in the Shanghai Women's and Men's Health studies. Am J Epidemiol. (2010) 172:397–406. 10.1093/aje/kwq144 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Walter RB, Brasky TM, Milano F, White E. Vitamin, mineral, and specialty supplements and risk of hematologic malignancies in the prospective VITamins And Lifestyle (VITAL) study. Cancer Epidemiol Biomarkers Prev. (2011) 20:2298–308. 10.1158/1055-9965.EPI-11-0494 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Gonzalez CA, Travier N, Lujan-Barroso L, Castellsague X, Bosch FX, Roura E, et al. Dietary factors and in situ and invasive cervical cancer risk in the European prospective investigation into cancer and nutrition study. Int J Cancer. (2011) 129:449–59. 10.1002/ijc.25679 [DOI] [PubMed] [Google Scholar]
  • 35.Brasky TM, Kristal AR, Navarro SL, Lampe JW, Peters U, Patterson RE, et al. Specialty supplements and prostate cancer risk in the VITamins and Lifestyle (VITAL) cohort. Nutr Cancer. (2011) 63:573–82. 10.1080/01635581.2011.553022 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Steevens J, Schouten LJ, Goldbohm RA, van den Brandt PA. Vegetables and fruits consumption and risk of esophageal and gastric cancer subtypes in the Netherlands Cohort Study. Int J Cancer. (2011) 129:2681–93. 10.1002/ijc.25928 [DOI] [PubMed] [Google Scholar]
  • 37.Gonzalez CA, Lujan-Barroso L, Bueno-de-Mesquita HB, Jenab M, Duell EJ, Agudo A, et al. Fruit and vegetable intake and the risk of gastric adenocarcinoma: a reanalysis of the European Prospective Investigation into Cancer and Nutrition (EPIC-EURGAST) study after a longer follow-up. Int J Cancer. (2012) 131:2910–9. 10.1002/ijc.27565 [DOI] [PubMed] [Google Scholar]
  • 38.Meng S, Zhang X, Giovannucci EL, Ma J, Fuchs CS, Cho E. No association between garlic intake and risk of colorectal cancer. Cancer Epidemiol. (2013) 37:152–5. 10.1016/j.canep.2012.11.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Vogtmann E, Xiang YB Li HL, Levitan EB, Yang G, Waterbor JW, et al. Fruit and vegetable intake and the risk of colorectal cancer: results from the Shanghai Men's Health Study. Cancer Causes Control: CCC. (2013) 24:1935–45. 10.1007/s10552-013-0268-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Maasland DH, van den Brandt PA, Kremer B, Goldbohm RA, Schouten LJ. Consumption of vegetables and fruits and risk of subtypes of head-neck cancer in the Netherlands Cohort Study. Int J Cancer. (2015) 136:E396–409. 10.1002/ijc.29219 [DOI] [PubMed] [Google Scholar]
  • 41.Kim H, Keum N, Giovannucci EL, Fuchs CS, Bao Y. Garlic intake and gastric cancer risk: Results from two large prospective US cohort studies. Int J Cancer. (2018) 143:1047–53. 10.1002/ijc.31396 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Yu CX, Chen YS, Ge ZJ, Zhang YH, Xu X, Tian T, et al. Dietary habits and risk of hepatocellular carcinoma among hepatitis B surface antigen carriers: A prospective cohort study in China. J Dig Dis. (2020) 21:406–15. 10.1111/1751-2980.12878 [DOI] [PubMed] [Google Scholar]
  • 43.Turati F, Guercio V, Pelucchi C, La Vecchia C, Galeone C. Colorectal cancer and adenomatous polyps in relation to allium vegetables intake: a meta-analysis of observational studies. Mol Nutr Food Res. (2014) 58:1907–14. 10.1002/mnfr.201400169 [DOI] [PubMed] [Google Scholar]
  • 44.Zhou Y, Zhuang W, Hu W, Liu GJ, Wu TX, Wu XT. Consumption of large amounts of Allium vegetables reduces risk for gastric cancer in a meta-analysis. Gastroenterology. (2011) 141:80–9. 10.1053/j.gastro.2011.03.057 [DOI] [PubMed] [Google Scholar]
  • 45.Zhou XF, Ding ZS, Liu NB. Allium vegetables and risk of prostate cancer: evidence from 132,192 subjects. Asian Pac J Cancer Prev. (2013) 14:4131–4. 10.7314/APJCP.2013.14.7.4131 [DOI] [PubMed] [Google Scholar]
  • 46.Chiavarini M, Minelli L, Fabiani R. Garlic consumption and colorectal cancer risk in man: a systematic review and meta-analysis. Public Health Nutr. (2016) 19:308–17. 10.1017/S1368980015001263 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Rahman K, Lowe GM. Garlic and cardiovascular disease: a critical review. J Nutr. (2006) 136:736S–40S. 10.1093/jn/136.3.736S [DOI] [PubMed] [Google Scholar]
  • 48.Fleischauer AT, Arab L. Garlic and cancer: a critical review of the epidemiologic literature. J Nutr. (2001) 131:1032S–40S. 10.1093/jn/131.3.1032S [DOI] [PubMed] [Google Scholar]
  • 49.Lawson LD, Wang ZJ. Low allicin release from garlic supplements: a major problem due to the sensitivities of alliinase activity. J Agric Food Chem. (2001) 49:2592–9. 10.1021/jf001287m [DOI] [PubMed] [Google Scholar]
  • 50.Tang FY, Chiang EP, Chung JG, Lee HZ, Hsu CY. S-allylcysteine modulates the expression of E-cadherin and inhibits the malignant progression of human oral cancer. J Nutr Biochem. (2009) 20:1013–20. 10.1016/j.jnutbio.2008.09.007 [DOI] [PubMed] [Google Scholar]
  • 51.Xu YS, Feng JG, Zhang D, Zhang B, Luo M, Su D, et al. S-allylcysteine, a garlic derivative, suppresses proliferation and induces apoptosis in human ovarian cancer cells in vitro. Acta Pharmacol Sin. (2014) 35:267–74. 10.1038/aps.2013.176 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Tang FY, Chiang EP, Pai MH. Consumption of S-allylcysteine inhibits the growth of human non-small-cell lung carcinoma in a mouse xenograft model. J Agric Food Chem. (2010) 58:11156–64. 10.1021/jf102539k [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.


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