Salud Pública de México

Disponibilidad de alimentos en los hogares mexicanos de acuerdo con el grado de inseguridad alimentaria

The role of diet in cancer: the epidemiologic link

Magdalena Stepien, PhD,(1)Veronique Chajes,PhD,(1) Isabelle Romieu, MD, MPH, DSc.(1)

(1) International Agency for Research on Cancer (IARC). Lyon, France.


Diet is an important modifiable risk factor for cancer. Adequate diet modification may play a key role in reducing the incidence of some cancers. A growing body of epidemiological evidence suggested links of some nutritional exposures with individual cancers. This review updates and summarises the existing data on diet related factors for cancer prevention, evaluated in 2007 by World Cancer Research Fund/American Institute for Cancer Research and identifies the areas where more research is needed. Mechanisms of action of nutrients are iscussed.For cancer prevention, more apparent association pertains to the role of foods from plant origin, processed meat products and alcohol. There is a lack of evidence to clarify the relationship of dairy and cereal products, different types of carbohydrates, micronutrients naturally found in foods vs supplements, industrial trans-fats, food preparation and handling techniques and dietary patterns and cancer, in order to implement safe cancer prevention strategies.

Keywords: food; nutrition; cancer


La dieta es un factor de riesgo modificable importante para el cáncer. Una modificación adecuada puede jugar un papel clave en la reducción de la incidencia de algunos cánceres. La evidencia epidemiológica sugiere enlaces de algunas exposiciones nutricionales con cánceres específicos.Esta revisión actualiza y resume los datos existentes sobre factores de la dieta que se relacionan con la prevención del cáncer, que fueron evaluados en 2007 por el World Cancer Research Fund/American Institute for Cancer Research, e identifica áreas para profundizar en investigación. Se discuten mecanismos de acción de los nutrientes. Para la prevención del cáncer, la evidencia epidemiológica se relaciona con los alimentos de origen vegetal, carnes procesadas y alcohol. Se necesita más investigación para aclarar la relación que tienen con el cáncer ciertos alimentos como lácteos, granos, diferentes tipos de carbohidratos, y otros factores que podrían intervenir: micronutrientes presentes en los alimentos contra suplementos, grasas industriales trans, preparación de alimentos y hábitos alimentarios. Esto facilitaría la creación de estrategias seguras de prevención de cáncer.

Palabras clave: alimentos; nutrición; cáncer

Three decades ago it was estimated that in the United States over 30% of cancers could be prevented by modification of dietary habits.1In 2007, the World Cancer Research Fund and the American Institute for Cancer Research (WCRF/AICR) conducted an extensive literature review of epidemiological studies for dietary exposures in relation to cancer risks: Second Expert Report (SER).2The report led to the formulation of cancer prevention recommendations on food, nutrition and physical activity, based on epidemiological evidence linking dietary or nutritional components with individualcancer risks. Some dietary factors are believed to play a direct role in cancer prevention; while others are more likely to act through obesity-related mechanisms.2Despite the growing body of evidence, uncertainty remains for somefoods and nutrients; subsequent updates of the 2007 report (Continuous Update Projects, CUP) have further reviewed the evidence for individual cancer sites.3 The aim of this review was to combine the evidence for individual cancers, discuss and update existing data for the dietary factors rated as having strong (convincing or probable) or limited-suggestive evidence in relation to cancer prevention for at least one cancer. In the present revision recent reviews and key papers were searched for in PubMed with relevant keywords (cancer site/exposure) since the year when the relevant updated report was published, until June 2015. However, this paper did not involve a full systematic review. The review focuses on thirteen cancers with the highest incidence in men and women worldwide listed by Globocan 2012:4 breast, prostate, lung, colorectal, cervix uteri, stomach, liver,corpus uteri, ovary, oesophagus, bladder, kidney, pancreas. Cancers of non-Hodgkin’s lymphoma and leukaemia were excluded due to limited evidence for individual cancers; the WCRF/AICR report considered them jointly and concluded that more research is needed in order to be able to draw any conclusions.2Foods items that presented a protective effect in more than one cancersite were: fruits, vegetables, coffee and milk (figure 1).Consequently, nutrients for which the main dietary sources are fruit,vegetables or milk had an inverse association with cancer, including foods containing dietary fibre, selenium, calcium, some carotenoids,vitamins C, D, E, B6, folates and flavonoids.

Food items that presented an increased risk at several cancers sites were: alcoholic drinks, red and processed meat. Foods rich in animal fat, saturated fatty acids and iron were correspondingly positively related to cancer. Other factors may also play a role as a cancer trigger,such as food preparation (smoking, grilling or barbecuing),the use of partial hydrogenation of vegetable oils (shortenings containing trans fatty acids), dietary habits (salt addition), storage (aflatoxin), sourcing (arsenic in water) and preservation (salted foods). In addition, foods high in sugar or high glycaemic load have also been positively related to some cancers.

Foods and nutrients with a potential cancer protective effect

Fruits, vegetables and their constituents

There is epidemiologic evidence supporting inverse associations between fruits and/or vegetables intake and several cancers risk.5 According to WCRF/AICR, fruits were inversely associated with oesophageal cancer (based on case-control studies), stomach cancer (based on cohort studies) and lung cancer (based on cohort studies) (table I). There was also a suggestive, yet inconsistent, evidence for a protective role of fruits intake against colorectal cancer.Vegetableswere also negatively linked to colorectal and lung cancers; however most of the evidence was rated as limited-suggestive. A non-significantly decreased risk of oesophageal and stomach cancers was observed for intake of non-starchy vegetables (including green, leafy,cruciferous and allium vegetables) suggesting a strong probable association (table I).6-29

More recent data support some of these associations but not all. A meta-analysis of five cohort studies suggested an inverse association of fruits and vegetables with oesophageal cancer risk (RRfruits=0.80; 95%CI 0.61-1.07 and RRvegetables>=0.68; 95%CI 0.55-0.86).24 Similar results were obtained based on nine cohorts for oesophageal adenocarcinoma (RRfruit>=0.73; 95%CI 0.55-0.98 and RRvegetables=0.76, 95%CI 0.59-0.96)22and for lung cancer (RRfruits=0.80; 95%CI 0.74-0.88 and RRvegetables=0.74; 95%CI 0.67-0.82 and based on 30 case-control and cohort studies;6 however, divergent results were observed in the subgroup analysis by sex for vegetables, possibly due to confounding by smoking. In a recent meta-analysis of cohort studies a significant reduction in stomach cancer risk for fruits (RR=0.90; 95%CI 0.83-0.98, 22 studies) but not vegetables intake (RR=0.96; 95%CI 0.88-1.06, 19 studies).13 For colorectal cancers, recent results from three additional individual cohorts did not support a clear association with fruits,30vegetables31 and fruits or vegetables.32

Some individual vegetables were also listed by the report to have limited-suggestive protective effect (tableI). Carrots were the only factor that showed consistent protective evidence against cervical cancer. Allium vegetables were linked to lower risk of both stomach14 and colorectal cancers.3 Based on 2011 CUP, garlic was indicated as a probable colorectal cancer protective vegetable; two cohort and six case-control studies reported a non-significantly decreased risk (table I). However,in recent meta-analysis no significant association for garlic and colorectal cancers was observed (OR=0.93;95%CI 0.82-1.06).8 (OR=0.93; 95%CI 0.82-1.06).8





In the large European Prospective Investigation into Cancer and Nutrition (EPIC) of 10 European countries and close to 500 000 subjects analyses for fruit intake and total cancer risk showed a borderline protective effect (HR=0.99; 95%CI 0.98-1.00, per 100g/d).33 For vegetables this effect was slightly stronger (HR=0.98;95%CI 0.97-0.99). When cancers were considered separately,significant inverse trends were observed only for fruit but not vegetable intake and oesophageal and lung (in smokers only) cancers.34 A significant trend across quintiles was observed for combined fruit and vegetable intake for the risk of colorectal cancer (RR for highest vs lowest quintile=0.86; 95%CI0.75-1.00;P-trend=0.04).34Similarly, foods containing carotenoids (lung) or beta carotene (oesophagus), vitamin C (oesophagus),selenium (lung, stomach) and dietary fibre (colorectum,oesophagus) appeared as cancer protective food constituents (figure 1). A meta-analysis of prospective cohorts indicated an inverse correlation for carotenoidrich vegetables with lung cancer risk (RR=0.79; 95%CI0.71-0.87).35 Selenium, carotenoids nd vitamin C, but also flavonoids and vitamin E, are recognized antioxidants that naturally occur in fruits and vegetables. These micronutrients may play a protective role on cancer bytrapping free radicals, preventing lipid oxidation and protecting against DNA damage.36 Epidemiological evidence supports a protective role by dietary fibre against colorectal and oesophageal cancers (figure 1). Dietary fibre ecreases transit time and dilutes potentially toxic substances,37 limiting exposure of gastrointestinal tract to their possible carcinogenic effects. Another important cancer preventive characteristic of fibre could be its effect on modifying gut microbiota and alteration of icrobial metabolites.37 For example, high fibre intake may increase production of short chain fatty acids with antiapoptotic properties. In ddition, binding or diluting bile acids may reduce the potential carcinogenic effect of their metabolites.37 It has been suggested that the source of fibre may have divergent effects. For colorectal cancers, a meta-analysis of twenty-five prospective studies indicated a significant nverse association only for fibre coming from cereals (RR=0.90; 95%CI 0.83-0.97) or whole grains (RR=0.83; 95%CI 0.78-0.89), but not fruit, vegetable or legume fibre.38 However, as indicated by the expert report, no conclusion could be drawn based on the existing epidemiological vidence for cereal and grain products and cancer risk.2

A controversy pertains to the use of nutritional supplements as cancer-preventive measure. Epidemiological evidence indicates beta-carotene/ retinol supplementation as risk factors during supplementation for lung cancer in a specific population of heavy smokers or subjects exposed to asbestos.39,40 A meta-analysis of randomized controlled trials concluded that there is no clinical evidence to support preventive capacity of antioxidant supplements on cancer.41 Multivitamins were evaluated by WCRF/AICR for several other cancer sites (figure 1), but no sufficient evidence was present to draw any conclusion. Coffee Substantial amount of epidemiological evidence existed to suggest a strong probable dose-response relationshipbetween coffee and endometrial and liver cancers (table I). Both regular and decaffeinated coffee showed a protective effect against cancer development in endometrium. Three recent meta-analyses of observational studies confirmed this association.18,42,43 For liver cancers, meta-analysis based on six studies indicated 14% reduced risk with regular coffee intake (table I). Further three individually published meta-analyses found even stronger protective effect,16,17,44 while in the EPIC cohort a 72% risk reduction for hepatocellular carcinoma(HCC) for highest vs lowest quintile of regular coffee drinkers was observed (HR=0.28; 95%CI 0.16-0.50).45 A divergent effect in ubgroup analyses was observed: significantly inverse association was observed only for caffeinated coffee. Considering combined cancer sites a meta-analysis indicated that intake of regular coffee may significantly reduce the risk of total cancers (RR=0.97; 95%CI 0.96-0.98, per one cup/ day).46 The probable cancer protective effect of coffee may be attributed to caffeine but also other bioactive coffee components (e.g. chlorogenic acid, polyphenols and their metabolites).47 Coffee constituents may have antioxidant properties, play a role in the regulation of DNA repair, apoptosis and inflammation,47 have effects on hormonal activity,48-50 glucose tolerance51 and circulating levels of immune and inflammatory markers.52


Milk consumption has been shown to have a protective effect on colorectal and bladder cancers (table I). For colorectal cancer the inverse association for milk was confirmed in four meta- or pooled-analyses of observational studies.9,53-55 Higher calcium and vitamin D intake with milk may partly explain these findings by Artículo especial 268 salud pública de méxico / vol. 58, no. 2, marzo-abril de 2016 Stepien M y col. their action on inhibiting colonic neoplasia.56 Indeed, both dietary calcium and foods containing vitamin D had a protective effect for colorectal cancer (figure 1).Meta-analysis for both dietary calcium (RR=0.94, 95%CI 0.93-0.96; per 200 mg/day, five studies) and vitamin DRR=0.95, 95%CI 0.93-0.98; per 100 IU/d, ten studies) showed reduced risk of colorectal cancer.3 For bladder cancer a recent meta-analysis of sixteen studies supported a reduced risk with high milk intake (SRR=0.84; 95%CI 0.71-0.97).26 However, these results were not confirmed by another meta-analysis.27 Stronger heterogeneity in case-control studies and male subset and differences by geographic region were observed. Dietary calcium together with vitamin D and other bioactive milk components (e.g. lactoferrin, glycans) may mediate the protective effect of milk for some cancers through their antiproliferative, anti-inflammatory, antiviral and antimicrobial properties.56,57 However, for some other cancer sites some milk constituents may have an adverse effect. There was a limited-suggestive positive association for low fat milk and cheese and the risk of prostate cancer (table I) . In a recent study from EPIC,high dairy, milk, cheese and calcium, vitamin D, fat and protein coming from dairy but no other sources were all positively associated with liver cancer (HCC) risk.58 This could be related to the effect of high calcium intake on lowering circulating vitamin D59 or milk on increasing circulating Insulin-like growth factor 1 (IGF-1) levels associated with both HCC and prostate cancers.58,60 Interestingly,high IGF-1 levels were also linked to increased colorectal cancer risk,61 while milk had a protective effect,suggesting a more complex role of milk constituents on carcinogenesis processes at different sites.

Foods and nutrients with a potential cancer promotive effect

Alcoholic drinks Alcohol is an established independent risk factor for cancers in liver (HCC), female breast, colorectal, oesophagus, oral cavity, pharynx and larynx.62 Based on fourteen cohorts, the estimate from a meta-analysis for liver cancers showed a 4% risk increase (per 10g/day= approximately 1 alcoholic drink) (table I). Chronic alcohol consumption may lead to systemic inflammation and metabolic ysregulation, leading to liver damage and progression to cirrhosis, key risk factors for liver cancers. Twenty case-control studies showed a 4% increased risk of oesophagus cancer for an increment of one drink a week. The estimate for one cohort analysed separately was stronger ( table I). Dose-response analyses for twelve cohorts showed an 8% increased risk of colorectal cancer, per 10g/day of ethanol, while each additional alcoholic drink a day was associatedwith a non-significant 11% increased risk (table I). The results for breast cancer are partly dependent on menopausal or hormonal status.63 Meta-analysis of thirteen studies indicated a dose-response 8% increased risk of postmenopausal breast cancer per 10g/day increase in alcohol consumption (table I). A dose-response metaanalysis of ten cohort and case-control studies indicatedthat ER- breast cancers may be less dependent on alcohol exposure than the hormone-positive cancers.64 However, recent data from the EPIC cohort reported a linear dose response relationship for alcohol intake and breast cancer with a 4.2% (95%CI 2.7%-5.8%, per 10 g/d) risk increase. Positive association was observed for both pre- and postmenopausal women and all types of receptor status. Exposure prior to first term pregnancywas related to a higher risk.65 Only heavy drinking was associated with an increased pancreatic cancer risk (RR=1.30; 95%CI 1.09-1.54), but no clear dose-responsewas observed (table I). However, for some cancers adverse effect of alcohol consumption was observed also for light drinking (≤12.5 g ethanol; ≤1 drink).66

According to the International Agency for Research on Cancer (IARC) alcohol is classified as a group 1 carcinogen to humans.67 Multiple biological mechanisms are proposed for the role of ethanol in the process of carcinogenesis. Ethanol and its intermediate metabolites demonstrated direct carcinogenic and/or genotoxic properties. Ethanol modulates activity of enzymes responsible for its detoxification and may act as a solvent for other carcinogenic molecules improving their cellular infiltration.68 Ethanol interacts with folate and tobacco affecting methylation processes and/or DNA modification by promoting genetic mutations.69 Ethanol is also a systemic pro-oxidant, leading to lipid peroxidation,production of prostaglandins, generation of free radicals and modulation of cellular regeneration.68

Animal products: red and processed meat and products high in fat

High intake of red or processed meat was associated with cancers in several sites (table I). Convincing and generally consistent evidence existed for increased risk of colorectal cancer. In dose-response analysis from nine cohort studies, 16% increased risk for each 100g/d increase in red and processed meat was observed and agreed with some other published meta-analyses.10,70-74 However uncertainties for a clear positive dose-response association exist. One study found evidence for a nonlinear shape association,11 confirmed by two other studies, but only for intakes higher than 90 or 140g/d,respectively.10,12 While for processed meat evidence is stronger, two recent comprehensive analyses by Alexander and colleagues put a doubt on a clear dose-response relationship between specifically red meat consumption and colorectal cancer risk,75,76 raising concerns on methodological differences between existing studies.

For lung, stomach, oesophagus and pancreas limited suggestive evidence was present (table I). For the association between red meat and lung cancer seven of nine case-control studies and a cohort study reported increased risk with increasing intakes, while a two-fold increased risk in highest vs lowest analyses based on three cohorts was observed (RR=2.10; 95%CI 1.00-4.42).2

A more recent meta-analysis (33 studies) showed a positive effect of both red and processed meat on lung cancer development.7 Stomach cancer was also linked to processed but not red meat intake (table I). A recent meta-analysis including eighteen studies indicated that each 100 g/day increment in red meat intake was associated with 17% increased risk of gastric cancer.15 For oesophageal cancer two cohort studies suggested a non-significant positive association with processed meatin extreme categories analyses, while for red meat the conclusions came from case-control studies, for which eight of ten found a positive association (table I). Another four meta-analyses confirmed an increased risk of both squamous and adenocarcinoma with higher red and/or processed meat intake,19,20,23,25 however, there is evidence for heterogeneity by the cancer subtype.21 For pancreatic cancer, red meat intake indicated a nonsignificantly increased risk, while for processed meat the association was significant (table I). This was confirmed in a meta-analysis based on eleven prospective studies.28

The definition of processed meat refers to meats preserved by smoking, curing, or salting, or addition of chemical preservatives. Therefore possible underlying mechanisms for cancer development may refer to the effect of carcinogenic compounds that are produced at high temperature ( heterocyclic amines and polycyclic aromatic hydrocarbons).77 Meats are often preserved with salt. Salt was positively associated with the risk of stomach cancer (table I). Seven prospective studies investigated salt intake from processed meat and accordingly found a statistically positive association(RR=1.24; 95%CI 1.06-1.46; for high consumers).78 Haem present in red meat may undergo conversion to other compounds with cancer-promotive effects, N-nitroso compounds and cytotoxic alkenals.77,79 Their precursor, nitrate, added as preservative may enhance this effect.80Evidence from animal and in vitro studies suggests the involvement of iron in gastrointestinal tract cancer development, caused by oxidative damage to colonic cells and promotion of cell growth.81,82

Some animal products (meat, cheese) high in fats were shown to increase risk of pancreatic cancer. 83 It is plausible that for pancreatic ancer dietary saturated fatty acids may be an important factor for cancer development.84 Total fat was also considered as a limited-suggestive risk factor for postmenopausal breast cancer (RR=1.06; 95%CI 0.99-1.14; per 20g/day; based on five cohort studies). For both cheese and animal fat positive association (suggestive) was found for colorectal cancer (figure 1).

Trans fatty acids

Some recent epidemiological studies indicate that a high intake of Industrial trans fatty acids (ITFA) from industrially-produced hydrogenated vegetable oils mayincrease risks of different types of cancer, but studies are still scarce. These studies reported evidence of increase drisks of postmenopausal breast,85,86 prostate,87 ovarian,88 distal colorectal89 cancers and colorectal adenomas90 associated with increasing dietary intake or biomarkers of ITFA. Thus, prevention of cancer should consider suppressing ITFA in highly processed foods.

Glycaemic index/load or high in sugar foods

An important role in most cancers’ development is attributed to body fatness.91 Diets high in some fats, but also sugars postprandially converted to fat may indirectly contribute to increased body adipose tissue content. Diet high in sugar may results in hyperinsulinemia and increased levels of circulating tumour promoter IGF-1.92 Sugar (including sucrose and fructose) and/or high glycaemic index (GI) or load (GL) that reflect postprandial increase in blood sugar levels, were positively associated with some IGF-1-related cancers.92 Notably, pancreatic cancer that is strongly related to body fatness showed some evidence for association with foods and beverages containing fructose; 22% statistically significant increased risk of pancreatic cancer per 25g/day of fructose was observed in a meta-analysis of six cohort studies (RR=1.22; 95%CI 1.08-1.37).2 Foods containing sugars were also listed as limited-suggestive risk factor for colorectal cancer (figure 1), however no significant associations were reported between GI or GL and cancers of digestive tract, including colorectal.29,93 In turn, based on summary report of four cohort studies, GL was positively associated with endometrial cancer risk (table I). Lower but statistically significant estimates were obtained in another study (RR=1.06; 95%CI 1.01-1.11; per 50 unit/day).94 High GL was related to postmenopausal breast cancer in the EPIC cohort study. A stronger effect was observed among ER- tumors (HR= 1.36; 95%CI 1.02-1.82; 5th vs 1st quintile).95 Nowadays popular sources of fructose include sugary drinks. A suggestive, modest positive association between sugary drinks and pancreatic cancer was observed in a pooled analysis of fourteen cohort studies (RR=1.19; 95%CI 0.98-1.46; comparing ≥250 to 0 g/d).96 Recent evidence also suggests a possible risk association between liver cancer (HCC) and both sugar and sugary drinks intake.97,98 Direct mechanisms for carcinogenesis related to high dietary sugar intake and high glycemic load may be related to insulin resistance,99 promotion of systemic inflammation and increased levels of ro-inflammatory factors,100 that may promote cell proliferation (e.g. tumor necrosis factor alpha, interleukin-6 and C-reactive protein).91

Indices of lifestyle, dietary patterns and cancer risk

Foods are consumed in combination and several factors may affect consumer’s dietary choices. Important impact on the foods consumed may erive from geographical location, cultural dietary habits, socioeconomic status, religion and underlying diseases.101 WCRF/AICR report investigated the relationship of several dietary patterns and specific diets but no conclusion could be reached in relation to any of the cancers studied. However, morerecent evidence form cohort studies suggested protective effect of: a) healthy lifestyle index score, combining healthy diet, physical activity, low alcohol intake, no smoking and healthy BMI, on gastric adenocarcinoma, breast (in postmenopausal women) and colorectal cancers;102,104 b) adherence to the Mediterranean dietary pattern on overall cancer risk;105 c) healthy dietary pattern derived from factor analysis on breast106 and colorectal cancer risk,107 and d) concordance with a score based on WCRF/AICR recommendations on total, colorectal,stomach, breast, endometrium, lung, kidney, upper aerodigestive tract, liver, and esophagus cancers.108

Limitations and conclusion

In this report we updated the epidemiological evidence on the association of dietary factors and cancer. However,as new studies are conducted some of the results may be modified in particular with regards to factors with probable or limited evidence. In addition, it is important to remember that the estimation of the true intake of some nutrients is limited by imprecise dietary measurements, Other factors including potential recall bias in case-control studies or in more health conscious populations, unmeasured or residual confounding factors(such as food processing or preparation) may also alter the results. Dietary pattern analyses may partly deal with interaction between dietary nutrients but are difficult to interpret in etiological studies. Taken together, favourable diet in relation to cancer prevention should be based on plant foods (fruits and vegetables) and be rich in dietary fibre and naturally occurring antioxidants. More evidence is needed on the protective effects of cereal products, legumes and coffee. Consumption of red and processed meat, energy-dense and high in sugars foods, as well as alcoholic and possibly sugary drinks should be limited. Adherence to dietary recommendations should be complemented by lifestyle modification, such as maintaining healthy body weight and being physically active. It is also important that the recommendations be applicable considering geographical region, economic development, and dietary cultural habits. Lastly, diet-gene interactions should be taken into account and personalised nutrition considered, especially in high risk individuals.109 In 2014, the 4th edition of European Code Against Cancer was launched by IARC indicating twelve lifestyle behaviours to lower the risk of developing cancer.110 One of the recommendations refers to maintaining a healthy diet: eating of plenty of whole grains, pulses, vegetable and fruits, limiting intake of red meat, high-calorie and high in salt foods, and avoiding sugary drinks and processed meat. Additional evidence, particularly based on existing ohorts, is continuously accumulating and changing, especially concerning the strength of observed associations. New WCRF/AICR global evaluation s ongoing and expected to be released in 2017.

Declaration of conflict of interests. The authors declare that they have no conflict of interests.


1. Doll R, Peto R. The causes of cancer: quantitative estimates of avoidable risks of cancer in the United States today. J Natl Cancer Inst 1981;66(6):1191-1308.

2.World Cancer Research Fund/American Institute for Cancer Research. Food,nutrition, physical activity, and the prevention of cancer: a global perspective. Washington DC:World Cancer Research Fund, 2007.

3.WCRF/AICR. Continous Update Project findings & reports [internet document]. Washington DC: WCRF/AICR, 2010-1015 [accessed: July 1, 2015]. Avilable at:

4.Globocan.Estimated age-standardised incidence and mortality rates: both sexes [internet document]. Lyon: Globocan, 2012 [accessed: July 1, 2015].Avilable at:

5.Riboli E, Norat T. Epidemiologic evidence of the protective effect of fruit and vegetables on cancer risk. Am J Clin Nutr 2003;78(3 suppl):559S-569S.

6.Wang M, Qin S, Zhang T, Song X, Zhang S. The effect of fruit and vegetable intake on the development of lung cancer: a meta-analysis of 32 publications and 20 414 cases. Eur J Clin Nutr 2015:1-9.

7.Xue XJ, Gao Q, Qiao JH, Zhang J, Xu CP, Liu J. Red and processed meat consumption and the risk of lung cancer: a dose-response meta-analysis of 33 published studies. Int J Clin Exp Med 2014;7(6):1542-1553.

8.Chiavarini M, Minelli L, Fabiani R. Garlic consumption and colorectal cancer risk in man: a systematic review and meta-analysis. Public Health Nutr 2015:1-10.

9.Ralston RA, Truby H, Palermo CE, Walker KZ. Colorectal cancer and nonfermented milk, solid cheese, and fermented milk consumption: asystematic review and meta-analysis of prospective studies. Crit Rev Food Sci Nutr 2014;54(9):1167-1179.

10. Chan DS, Lau R, Aune D, Vieira R, Greenwood DC, Kampman E,. Red and processed meat and colorectal cancer incidence: meta-analysis of prospective studies. PloS One 2011;6(6):e20456.

11. Aune D, Chan DS, Vieira AR, Navarro-Rosenblatt DA, Vieira R, Greenwood DC,et al.Red and processed meat intake and risk of colorectal adenomas: asystematic review and meta-analysis of epidemiological studies. Cancer Causes Control 2013;24(4):611-627.

12. Xu X, Yu E, Gao X, Song N, Liu L, Wei X,et al. Red and processed meat intake and risk of colorectal adenomas: a meta-analysis of observational studies. Int J Cancer 2013;132(2):437-448.

13.Wang Q, Chen Y, Wang X, Gong G, Li G, Li C. Consumption of fruit, but not vegetables, may reduce risk of gastric cancer: results from a meta-analysis of cohort studies. Eur J Cancer 2014;50(8):1498-1509.

14.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(1):80-89.

15. Song P, Lu M, Yin Q, Wu L, Zhang D, Fu B, et al. Red meat consumption and stomach cancer risk: a meta-analysis. J Cancer Res Clin Oncol 2014;140(6):979-992.

16.Bravi F, Bosetti C, Tavani A, Gallus S, La Vecchia C. Coffee reduces risk for hepatocellular carcinoma: an updated meta-analysis. Clin Gastroenterol Hepatol 2013;11(11):1413-1421.

17. Sang LX, Chang B, Li XH, Jiang M. Consumption of coffee associated with reduced risk of liver cancer: a meta-analysis. BMC Gastroenterol 2013;13:34.

18.Yang TO, Crowe F, Cairns BJ, Reeves GK, Beral V. Tea and coffee and risk of endometrial cancer: cohort study and meta-analysis. Am J Clin Nutr 2015;101(3):570-578.

19.Choi Y, Song S, Song Y, Lee JE. Consumption of red and processed meat and esophageal cancer risk: meta-analysis. World J Gastroenterol 2013;19(7):1020-1029.

20.Zhu HC, Yang X, Xu LP, Zhao LJ, Tao GZ, Zhang C, et al.Meat consumption is associated with esophageal cancer risk in a meat- and cancer-histological-type dependent manner. Dig Dis Sci2014;59(3):664-673.

21.Salehi M, Moradi-Lakeh M, Salehi MH, Nojomi M, Kolahdooz F. Meat, fish,and esophageal cancer risk: a systematic review and dose-response meta-analysis. Nutr Rev 2013;71(5):257-267.

22. Li B, Jiang G, Zhang G, Xue Q, Zhang H, Wang C, et al. Intake of vegetables and fruit and risk of esophageal adenocarcinoma: a meta-analysis of observational studies. Eur J Nutr 2014;53(7):1511-1521.

23.Huang W, Han Y, Xu J, Zhu W, Li Z. Red and processed meat intake and risk of esophageal adenocarcinoma: a meta-analysis of observational studies. Cancer Causes Control 2013;24(1):193-201.

24.Liu J, Wang J, Leng Y, Lv C. Intake of fruit and vegetables and risk of esophageal squamous cell carcinoma: a meta-analysis of observational studies. Int J Cancer 2013;133(2):473-485.

25.Qu X, Ben Q, Jiang Y. Consumption of red and processed meat and risk for esophageal squamous cell carcinoma based on a meta-analysis. Ann Epidemiol 2013;23(12):762-770.

26.Mao QQ, Dai Y, Lin YW, Qin J, Xie LP, Zheng XY. Milk consumption and bladder cancer risk: a meta-analysis of published epidemiological studies. Nutr Cancer 2011;63(8):1263-1271.

27. Li F, An SL, Zhou Y, Liang ZK, Jiao ZJ, Jing YM, et al. Milk and dairy consumption and risk of bladder cancer: a meta-analysis. Urology 2011;78(6):1298-1305.

28.Larsson SC, Wolk A. Red and processed meat consumption and risk of pancreatic cancer: meta-analysis of prospective studies. Br J Cancer 2012;106(3):603-607.

29. Aune D, Chan DS, Lau R, Vieira R, Greenwood DC, Kampman E, et al.Carbohydrates, glycemic index, glycemic load, and colorectal cancer risk: a systematic review and meta-analysis of cohort studies. Cancer Causes Control 2012;23(4):521-535.

30.Ruder EH, Thiebaut AC, Thompson FE, Potischman N, Subar AF, Park Y,et al. Adolescent and mid-life diet: risk of colorectal cancer in the NIH-AARP Diet and Health Study. Am J Clin Nutr 2011;94(6):1607-1619.

31. 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 2013;24(11):1935-1945.

32. Leenders M, Siersema PD, Overvad K, Tjonneland A, Olsen A, Boutron-Ruault MC, et al. Subtypes of fruit and vegetables, variety in consumption and risk of colon and rectal cancer in the European Prospective Investigation into Cancer and Nutrition. International J Cancer 2015/06/17 [E-pub ahead of print]

33. Boffetta P, Couto E, Wichmann J, Ferrari P, Trichopoulos D, Bueno-de-Mesquita HB, et al.Fruit and vegetable intake and overall cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC). J Natl Cancer Inst 2010;102(8):529-537.

34.Bradbury KE, Appleby PN, Key TJ. Fruit, vegetable, and fiber intake in relation to cancer risk: findings from the European Prospective Investigation into Cancer and Nutrition (EPIC). Am J Clin Nutr 2014;100 Suppl 1:394S-398S. 10.3945/ajcn.113.071357

35. Gallicchio L, Boyd K, Matanoski G, Tao XG, Chen L, Lam TK, et al. Carotenoids and the risk of developing lung cancer: a systematic review. Am J Clin Nutr 2008;88(2):372-383.

36. O’Brien PJ. Antioxidants and cancer: molecular mechanisms. Adv Exp Med Biol 1994;366:215-239.

37.Zeng H, Lazarova DL, Bordonaro M. Mechanisms linking dietary fiber, gut microbiota and colon cancer prevention. World J Gastrointest Oncol 2014;6(2):41-51.

38. Aune D, Chan DS, Lau R, Vieira R, Greenwood DC, Kampman E, et al.Dietary fibre, whole grains, and risk of colorectal cancer: systematic review and dose-response meta-analysis of prospective studies. BMJ 2011;343:d6617.

39. Goodman GE, Thornquist MD, Balmes J, Cullen MR, Meyskens FL, Jr., Omenn GS, et al. The Beta-Carotene and Retinol Efficacy Trial: incidence of lung cancer and cardiovascular disease mortality during 6-year follow-up after stopping beta-carotene and retinol supplements. J Natl Cancer Inst 2004;96(23):1743-1750.

40. Albanes D, Heinonen OP, Taylor PR, Virtamo J, Edwards BK, Rautalahti M, et al. Alpha-Tocopherol and beta-carotene supplements and lung cancer incidence in the alpha-tocopherol, beta-carotene cancer prevention study: effects of base-line characteristics and study compliance. J Natl Cancer Inst 1996;88(21):1560-1570.

41. Bjelakovic G, Nikolova D, Simonetti RG, Gluud C. Antioxidant supplements for preventing gastrointestinal cancers. Cochrane Database Syst Rev 2008(3):CD004183.

42. Bravi F, Scotti L, Bosetti C, Gallus S, Negri E, La Vecchia C, et al. Coffee drinking and endometrial cancer risk: a metaanalysis of observational studies. Am J Obstet Gynecol 2009;200(2):130-135.

43. Je Y, Giovannucci E. Coffee consumption and risk of endometrial cancer: findings from a large up-to-date meta-analysis. Int J Cancer 2012;131(7):1700-1710.

44. Larsson SC, Wolk A. Coffee consumption and risk of liver cancer: a meta-analysis. Gastroenterology 2007;132(5):1740-1745. 10.1053/j.gastro.2007.03.044

45. Bamia C, Lagiou P, Jenab M, Trichopoulou A, Fedirko V, Aleksandrova K, et al. Coffee, tea and decaffeinated coffee in relation to hepatocellular carcinoma in a European population: multicentre, prospective cohort study. Int J Cancer 2015;136(8):1899-1908.

46. Yu X, Bao Z, Zou J, Dong J. Coffee consumption and risk of cancers: a meta-analysis of cohort studies. BMC Cancer 2011;11:96. 10.1186/1471-2407-11-96

47. Bohn SK, Blomhoff R, Paur I. Coffee and cancer risk, epidemiological evidence, and molecular mechanisms. Mol Nutr Food Res 2014;58(5):915-930.

48. Kotsopoulos J, Eliassen AH, Missmer SA, Hankinson SE, Tworoger SS. Relationship between caffeine intake and plasma sex hormone concentrations in premenopausal and postmenopausal women. Cancer 2009;115(12):2765-2774.

49. Ferrini RL, Barrett-Connor E. Caffeine intake and endogenous sex steroid levels in postmenopausal women. The Rancho Bernardo Study. Am J Epidemiol 1996;144(7):642-644.

50. Rossi T, Gallo C, Bassani B, Canali S, Albini A, Bruno A. Drink your prevention: beverages with cancer preventive phytochemicals. Pol Arch Med Wewn 2014;124(12):713-722.

51. Tunnicliffe JM, Shearer J. Coffee, glucose homeostasis, and insulin resistance: physiological mechanisms and mediators. Appl Physiol Nutr Metab 2008;33(6):1290-1300.

52. Loftfield E, Shiels MS, Graubard BI, Katki HA, Chaturvedi AK, Trabert B, et al. Associations of Coffee Drinking with Systemic Immune and Inflammatory Markers. Cancer Epidemiology, Biomarkers & Prevention: A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology 2015;24(7):1052-1060.

53. Aune D, Lau R, Chan DS, Vieira R, Greenwood DC, Kampman E, et al. Dairy products and colorectal cancer risk: a systematic review and meta-analysis of cohort studies. Ann Oncol 2012;23(1):37-45.

54. Huncharek M, Muscat J, Kupelnick B. Colorectal cancer risk and dietary intake of calcium, vitamin D, and dairy products: a meta-analysis of 26,335 cases from 60 observational studies. Nutr Cancer 2009;61(1):47-69.

55. Cho E, Smith-Warner SA, Spiegelman D, Beeson WL, van den Brandt PA, Colditz GA, et al. Dairy foods, calcium, and colorectal cancer: a pooled analysis of 10 cohort studies. J Natl Cancer Inst 2004;96(13):1015-1022.

56. Lamprecht SA, Lipkin M. Cellular mechanisms of calcium and vitamin D in the inhibition of colorectal carcinogenesis. Ann N Y Acad Sci 2001;952:73-87.

57. Hill DR, Newburg DS. Clinical applications of bioactive milk components. Nutr Rev 2015;73(7):463-476.

58. Duarte-Salles T, Fedirko V, Stepien M, Trichopoulou A, Bamia C, Lagiou P, et al. Dairy products and risk of hepatocellular carcinoma: the European Prospective Investigation into Cancer and Nutrition. Int J Cancer 2014;135(7):1662-1672.

59. Tao ZQ, Shi AM, Wang KX, Zhang WD. Epidemiology of prostate cancer: current status. Eur Rev Med Pharmacol Sci 2015;19(5):805-812.

60. Renehan AG, Zwahlen M, Minder C, O’Dwyer ST, Shalet SM, Egger M. Insulin-like growth factor (IGF)-I, IGF binding protein-3, and cancer risk: systematic review and meta-regression analysis. Lancet 2004;363(9418):1346-1353.

61. Rinaldi S, Cleveland R, Norat T, Biessy C, Rohrmann S, Linseisen J, et al. Serum levels of IGF-I, IGFBP-3 and colorectal cancer risk: results from the EPIC cohort, plus a meta-analysis of prospective studies. Int J Cancer 2010;126(7):1702-1715.

62. Scoccianti C, Cecchini M, Anderson AS, Berrino F, Boutron-Ruault MC, Espina C, et al. European Code against Cancer 4th Edition: Alcohol drinking and cancer. Cancer Epidemiol 2015 Jun 24 [Epub ahead of print].

63. Scoccianti C, Lauby-Secretan B, Bello PY, Chajes V, Romieu I. Female breast cancer and alcohol consumption: a review of the literature. Am J Prev Med 2014;46(3 Suppl 1):S16-S25.

64. Suzuki R, Orsini N, Mignone L, Saji S, Wolk A. Alcohol intake and risk of breast cancer defined by estrogen and progesterone receptor status--a meta-analysis of epidemiological studies. Int J Cancer 2008;122(8):1832-1841.

65. Romieu I, Scoccianti C, Chajes V, de Batlle J, Biessy C, Dossus L, et al. Alcohol intake and breast cancer in the European Prospective investigation into Cancer and Nutrition: Short title: Alcohol intake and breast cancer: Alcohol intake and breast cancer. Int J Cancer 2015;137(8):1921-1930.

66. Bagnardi V, Rota M, Botteri E, Tramacere I, Islami F, Fedirko V, et al. Light alcohol drinking and cancer: a meta-analysis. Ann Oncol 2013;24(2):301-308.

67. Baan R, Straif K, Grosse Y, Secretan B, El Ghissassi F, Bouvard V, et al. Carcinogenicity of alcoholic beverages. Lancet Oncol 2007;8(4):292-293.

68. Seitz HK, Mueller S. Alcohol and cancer: an overview with special emphasis on the role of acetaldehyde and cytochrome P450 2E1. Adv Exp Med Biol 2015;815:59-70.

69. Giovannucci E. Alcohol, one-carbon metabolism, and colorectal cancer: recent insights from molecular studies. J Nutr 2004;134(9):2475S-2481S.

70. Huxley RR, Ansary-Moghaddam A, Clifton P, Czernichow S, Parr CL, Woodward M. The impact of dietary and lifestyle risk factors on risk of colorectal cancer: a quantitative overview of the epidemiological evidence. Int J Cancer 2009;125(1):171-180.

71. Larsson SC, Wolk A. Meat consumption and risk of colorectal cancer: a meta-analysis of prospective studies. Int J Cancer 2006;119(11):2657-2664.

72. Norat T, Lukanova A, Ferrari P, Riboli E. Meat consumption and colorectal cancer risk: dose-response meta-analysis of epidemiological studies. Int J Cancer 2002;98(2):241-256.

73. Sandhu MS, White IR, McPherson K. Systematic review of the prospective cohort studies on meat consumption and colorectal cancer risk: a meta-analytical approach. Cancer Epidemiol Biomarkers Prev 2001;10(5):439-446.

74. Smolinska K, Paluszkiewicz P. Risk of colorectal cancer in relation to frequency and total amount of red meat consumption. Systematic review and meta-analysis. Arch Med Sci 2010;6(4):605-610.

75. Alexander DD, Weed DL, Miller PE, Mohamed MA. Red Meat and Colorectal Cancer: A Quantitative Update on the State of the Epidemiologic Science. J Am Coll Nutr 2015:1-23.

76. Alexander DD, Weed DL, Cushing CA, Lowe KA. Meta-analysis of prospective studies of red meat consumption and colorectal cancer. Eur J Cancer Prev 2011;20(4):293-307.

77. Chiang VS, Quek SY. The Relationship of Red Meat with Cancer: Effects of Thermal Processing and Related Physiological Mechanisms. Crit Rev Food Sci Nutr 2015 Jun 15:0 [Epub ahead of print].

78. D’Elia L, Rossi G, Ippolito R, Cappuccio FP, Strazzullo P. Habitual salt intake and risk of gastric cancer: a meta-analysis of prospective studies. Clin Nutr 2012;31(4):489-498.

79. Loh YH, Jakszyn P, Luben RN, Mulligan AA, Mitrou PN, Khaw KT. N-Nitroso compounds and cancer incidence: the European Prospective Investigation into Cancer and Nutrition (EPIC)-Norfolk Study. Am J Clin Nutr 2011;93(5):1053-1061.

80. Walker R. Nitrates, nitrites and N-nitrosocompounds: a review of the occurrence in food and diet and the toxicological implications. Food Additi Contam 1990;7(6):717-768.

81. Padmanabhan H, Brookes MJ, Iqbal T. Iron and colorectal cancer: evidence from in vitro and animal studies. Nutr Rev 2015;73(5):308-317.

82. Ward MH, Cross AJ, Abnet CC, Sinha R, Markin RS, Weisenburger DD. Heme iron from meat and risk of adenocarcinoma of the esophagus and stomach. Eur J Cancer Prev 2012;21(2):134-138.

83. Shen QW, Yao QY. Total fat consumption and pancreatic cancer risk: a meta-analysis of epidemiologic studies. Eur J Cancer Prev 2015;24(4):278-285.

84. Jansen RJ, Robinson DP, Frank RD, Anderson KE, Bamlet WR, Oberg AL, et al. Fatty acids found in dairy, protein and unsaturated fatty acids are associated with risk of pancreatic cancer in a case-control study. Int J Cancer 2014;134(8):1935-1946.

85. Chajes V, Thiebaut AC, Rotival M, Gauthier E, Maillard V, Boutron-Ruault MC, et al. Association between serum trans-monounsaturated fatty acids and breast cancer risk in the E3N-EPIC Study. Am J Epidemiol 2008;167(11):1312-1320.

86. Kim EH, Willett WC, Colditz GA, Hankinson SE, Stampfer MJ, Hunter DJ, et al. Dietary fat and risk of postmenopausal breast cancer in a 20-year follow-up. Am J Epidemiol 2006;164(10):990-997.

87. Chavarro JE, Stampfer MJ, Campos H, Kurth T, Willett WC, Ma J. A prospective study of trans-fatty acid levels in blood and risk of prostate cancer. Cancer Epidemiol Biomarkers Prev 2008;17(1):95-101.

88. Merritt MA, Cramer DW, Missmer SA, Vitonis AF, Titus LJ, Terry KL. Dietary fat intake and risk of epithelial ovarian cancer by tumour histology. Br J Cancer 2014;110(5):1392-1401.

89. Vinikoor LC, Millikan RC, Satia JA, Schroeder JC, Martin CF, Ibrahim JG, et al. trans-Fatty acid consumption and its association with distal colorectal cancer in the North Carolina Colon Cancer Study II. Cancer Causes Control 2010;21(1):171-180.

90. Vinikoor LC, Schroeder JC, Millikan RC, Satia JA, Martin CF, Ibrahim J, et al. Consumption of trans-fatty acid and its association with colorectal adenomas. Am J Epidemiol 2008;168(3):289-297.

91. Ungefroren H, Gieseler F, Fliedner S, Lehnert H. Obesity and cancer. Hor Mol Biol Clin Inves 2015;21(1):5-15.

92. Kaaks R. Nutrition, insulin, IGF-1 metabolism and cancer risk: a summary of epidemiological evidence. Novartis Found Symp 2004;262:247-260; discussion 60-68.

93. Mulholland HG, Murray LJ, Cardwell CR, Cantwell MM. Glycemic index, glycemic load, and risk of digestive tract neoplasms: a systematic review and meta-analysis. Am J Clin Nutr 2009;89(2):568-576.

94. Nagle CM, Olsen CM, Ibiebele TI, Spurdle AB, Webb PM. Glycemic index, glycemic load and endometrial cancer risk: results from the Australian National Endometrial Cancer study and an updated systematic review and meta-analysis. Eur J Nutr 2013;52(2):705-715.

95. Romieu I, Ferrari P, Rinaldi S, Slimani N, Jenab M, Olsen A, et al. Dietary glycemic index and glycemic load and breast cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC). Am J Clin Nutr 2012;96(2):345-355.

96. Genkinger JM, Li R, Spiegelman D, Anderson KE, Albanes D, Bergkvist L, et al. Coffee, tea, and sugar-sweetened carbonated soft drink intake and pancreatic cancer risk: a pooled analysis of 14 cohort studies. Cancer Epidemiol Biomarkers Prev 2012;21(2):305-318.

97. Laguna JC, Alegret M, Roglans N. Simple sugar intake and hepatocellular carcinoma: epidemiological and mechanistic insight. Nutrients 2014;6(12):5933-5954.

98. Stepien M, Duarte-Salles T, Fedirko V, Trichopoulou A, Lagiou P, Bamia C, et al. Consumption of soft drinks and juices and risk of liver and biliary tract cancers in a European cohort. Eur J Nutr 2014 Dec 21 [Epub ahead of print].

99. Calle EE, Kaaks R. Overweight, obesity and cancer: epidemiological evidence and proposed mechanisms. Nat Rev Cancer 2004;4(8):579-591.

100. Ludwig DS. The glycemic index: physiological mechanisms relating to obesity, diabetes, and cardiovascular disease. Jama 2002;287(18):2414-2423.

101. Hawkes C, Asfaw A, Bauman AE, Bull FC, Eckhardt C, Leroy J, Smith M. Evidence on the determinants of dietary patterns, nutrition and physical activity, and the interventions to maintain or to modify them: a systematic review. London: International Food Policy Research Institute to the World Cancer, 2006.

102. Aleksandrova K, Pischon T, Jenab M, Bueno-de-Mesquita HB, Fedirko V, Norat T, et al. Combined impact of healthy lifestyle factors on colorectal cancer: a large European cohort study. BMC Med 2014;12:168.

103. Buckland G, Travier N, Huerta JM, Bueno-de-Mesquita HB, Siersema PD, Skeie G, et al. Healthy lifestyle index and risk of gastric adenocarcinoma in the EPIC cohort study. Int J Cancer 2015;137(3):598-606.

104. McKenzie F, Ferrari P, Freisling H, Chajes V, Rinaldi S, de Batlle J, et al. Healthy lifestyle and risk of breast cancer among postmenopausal women in the European Prospective Investigation into Cancer and Nutrition cohort study. Int J Cancer 2015;136(11):2640-2648.

105. Grosso G, Buscemi S, Galvano F, Mistretta A, Marventano S, La Vela V, et al. Mediterranean diet and cancer: epidemiological evidence and mechanism of selected aspects. BMC Surg 2013;13 Suppl 2:S14.

106. Catsburg C, Kim RS, Kirsh VA, Soskolne CL, Kreiger N, Rohan TE. Dietary patterns and breast cancer risk: a study in 2 cohorts. Am J Clin Nutr 2015;101(4):817-823.

107. Randi G, Edefonti V, Ferraroni M, La Vecchia C, Decarli A. Dietary patterns and the risk of colorectal cancer and adenomas. Nutr Rev 2010;68(7):389-408.

108. Romaguera D, Vergnaud AC, Peeters PH, van Gils CH, Chan DS, Ferrari P, et al. Is concordance with World Cancer Research Fund/American Institute for Cancer Research guidelines for cancer prevention related to subsequent risk of cancer? Results from the EPIC study. Am J Clin Nutr 2012;96(1):150-163.

109. Hesketh J. Personalised nutrition: how far has nutrigenomics progressed? Eur J Clin Nutr 2013;67(5):430-435.

110. IARC. European Code Against Cancer. 12 ways to reduce your cancer risk. Lyon, France: IARC, 2015 [accessed on July 1, 2015]. Available at:

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Salud Pública de México es una publicación periódica electrónica, bimestral, publicada por el Instituto Nacional de Salud Pública (con domicilio en Avenida Universidad núm. 655, col. Santa María Ahuacatitlán, Cuernavaca, Morelos, C.P. 62100, teléfono 329-3000, página web,, con ISSN: 1606-7916 y Reserva de Derechos al Uso Exclusivo con número: 04-2012-071614550600-203, ambos otorgados por el Instituto Nacional del Derecho de Autor. Editor responsable: Carlos Oropeza Abúndez. Responsable de la versión electrónica: Subdirección de Comunicación Científica y Publicaciones, Avenida Universidad núm. 655, planta baja, col. Santa María Ahuacatitlán, Cuernavaca, Morelos, C.P. 62100, teléfono 329 3000. Fecha de última modificación: 7 de junio de 2018. D.R. © por el sitio: Instituto Nacional de Salud Pública.

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