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Diet and cancer risk in Mediterranean countries: open issues

Published online by Cambridge University Press:  01 December 2006

Carlo La Vecchia*
Affiliation:
Istituto di Ricerche Farmacologiche, Mario Negri, Milano, Italy Istituto di Statistica Medica e Biometria, Università di Milano, Milano, Italy
Cristina Bosetti
Affiliation:
Istituto di Ricerche Farmacologiche, Mario Negri, Milano, Italy
*
*Corresponding author:[email protected]
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Abstract

Objective

To analyse various aspects of the Mediterranean diet in relation to the risk of several common cancers in Italy.

Design

Data from a series of case-control studies conducted in northern Italy between 1983 and 2004 on over 20 000 cases of several major cancers and 18 000 controls.

Results

For most digestive tract cancers, the risk decreased with increasing vegetable and fruit consumption, with relative risks between 0.3 and 0.7 for the highest level of intake, and the population-attributable risks for low intake of vegetables and fruit ranged between 15 and 40%. Less strong inverse relations were observed for other (epithelial) cancers, too. A number of micronutrients contained in vegetables and fruit showed an inverse relation with cancer risk. In particular, flavones, flavonols and resveratrol were inversely related to breast cancer risk. Olive oil, which is a typical aspect of the Mediterranean diet, has also been inversely related to cancers of the colorectum and breast, and mainly of the upper digestive and respiratory tract. Consumption of pizza, one of the most typical Italian foods, was related to a reduced risk of digestive tract cancers, although pizza may simply be an aspecific indicator of the Italian diet.

Conclusions

Adherence to the Mediterranean diet is a favourable indicator of the risk of several common epithelial cancers in Italy. A score summarising the major characteristics of the Mediterranean diet was related to a priori defined reduced risks of several digestive tract neoplasms by over 50%.

Type
Research Paper
Copyright
Copyright © The Authors 2006

Mediterranean diet is a general term indicating a complex of dietary patterns which includes different components in various regions of the Mediterranean, but is generally characterised by frequent consumption of fruit and vegetables, pulses and fish, low consumption of meat and cheese, and (as a major common characteristic) olive oil for seasoning.

Several aspects of the Mediterranean diet have been related to a reduced risk not only of cardiovascular disease, but also of several cancers, and it has been suggested that up to 25% of colorectal, 15% of breast and 10% of prostate, pancreas and endometrial cancers could be prevented by shifting to a Mediterranean dietReference Trichopoulou, Lagiou, Kuper and Trichoupulos1.

In the present paper, we will review the main findings on various aspects of Mediterranean diet and cancer risk from an integrated series of multicentric case-control studies conducted in Italy. This included over 20 000 cases of several major cancers and 18 000 controls collected since the early 1980s.

Vegetables and fruit

In this series of case-control studies, vegetable intake was inversely related to the risk of several common epithelial cancers: the relative risks (RRs) for digestive tract neoplasms ranged between 0.3 and 0.7 for the highest compared with the lowest tertile of vegetable intake (Fig. 1). Less consistent inverse relations were observed for some hormone-related neoplasms, such as breast and ovary. Fruit was associated in particular to reduced RRs of cancers of the upper digestive tract, stomach and urinary tract. For digestive tract cancers, population-attributable risks for low intake of vegetables and fruit ranged between 15 and 40%Reference La Vecchia, Chatenoud, Franceschi, Soler, Parazzini and Negri2. No material effect, however, was observed for fruit intake on neoplasms of the breast, the female genital tract or the prostate.

Fig. 1 RRs and 95% CI of selected cancers for the highest vs. the lowest levels of vegetable consumption. Italy, 1983–1997

Selected micronutrients

The role of selected micronutrients contained in vegetables and fruit was also considered. Carotenoids, vitamin E and calcium showed an inverse relation with breast cancer riskReference Negri, La Vecchia, Franceschi, D'Avanzo, Talamini and Parpinel3. More important, ascorbic acid, carotenoids and other antioxidant vitamins were consistently and inversely related not only to upper digestive and respiratory tract neoplasmsReference Bidoli, Bosetti, La Vecchia, Levi, Parpinel and Talamini4, Reference Negri, Franceschi, Bosetti, Levi, Conti and Parpinel5, but also to gastric cancerReference La Vecchia, Ferraroni, D'Avanzo, Decarli and Franceschi6. Likewise, tomato intake, and hence lycopene, was inversely related to several digestive tract neoplasms, but not to breast, female genital tract and prostate cancersReference La Vecchia7, Reference Bosetti, Talamini, Montella, Negri, Conti and Franceschi8. For colorectal cancer, there was an apparently synergistic effect of calcium, vitamins D, E and carotenoids, the RR reaching 0.46 in subjects reporting high calcium/vitamin D and high antioxidant intake, as compared with those reporting low intake of both groups of micronutrientsReference La Vecchia, Braga, Negri, Franceschi, Russo and Conti9.

Folate is a micronutrient of special interest in relation to cancer risk, following the identification of a number of single nucleotide polymorphisms of vitamin B-related metabolic genes that are involved in the process of carcinogenesis. Folate level is thought to affect cancer risk through its role in both methylation and nucleotide synthesis of DNAReference Duthie10. Alcohol consumption, which is frequent in Italy, may interfere with folate absorption and increase folate excretion by the kidney, therefore causing relative folate deficiency.

In our series of data, folate was inversely associated with all cancer sites consideredReference Bidoli, Bosetti, La Vecchia, Levi, Parpinel and Talamini4, Reference Pelucchi, Talamini, Negri, Levi, Conti and Franceschi11Reference Pelucchi, Galeone, Talamini, Negri, Parpinel and Franceschi15 (Fig. 2). The strongest associations emerged for upper aerodigestive tract neoplasms (RRs between 0.4 and 0.6 for the highest level of intake), rectal (RR = 0.6) and prostate (RR = 0.7) cancers. For some of these cancer sites (i.e. colorectum, breast and prostate), there was some indication of an interaction between folate and alcohol consumption, i.e. the inverse relation was more evident among drinkers.

Fig. 2 RRs and 95% CI of selected cancers for the highest vs. the lowest levels of folate consumption. Italy, 1983–1997

Flavonoids, resveratrol and breast cancer risk

Flavonoids are polyphenols present in vegetables, fruit and beverages of plant origin, which have antioxidant, antimitogenic and antiproliferative potential. They may have therefore a protective role in various chronic diseases, including selected neoplasms.

We have applied data on the flavonoid content of several foods and beverages on dietary information collected in the context of a case-control study of 820 women with breast cancer and 1548 controls, conducted in GreeceReference Peterson, Lagiou, Samoli, Lagiou, Katsouyanni and La Vecchia16. The RR for an increment of 0.5 mg day− 1 of flavone was 0.87. The association persisted after controlling for fruit and vegetable consumption or for other flavonoid intake. This inverse association is compatible with the reported inverse association of breast cancer with consumption of vegetables, particularly leafy vegetables.

A similar investigation was conducted in Italy. The study included 2569 women with incident histologically confirmed breast cancer and 2588 hospital controlsReference Bosetti, Spertini, Parpinel, Gnagnarella, Lagiou and Negri17 After allowance for major potential confounding factors and energy intake, a reduced risk of breast cancer was found for increasing intake of flavones (RR = 0.81, for the highest vs. the lowest quintiles) and flavonols (RR = 0.80, Table 1). No consistent association was found for other flavonoids.

Table 1 Flavonoids and breast cancer risk in Italy. Data from a multicentric study of 2569 cases and 2558 controlsReference Bosetti, Spertini, Parpinel, Gnagnarella, Lagiou and Negri17

* Median intake among controls.

Reference category.

Estimates from multiple logistic regression models including terms for age, study centre, education, parity, alcohol consumption and non-alcohol energy intake.

# Odds ratio for a difference in intake equal to the difference between the upper cut-point of the fourth quintile and that of the first one.

We have also analysed the relation between dietary intake of resveratrol and breast cancer risk using data from a case-control study conducted between 1993 and 2003 in the Swiss Canton of Vaud on 369 cases and 602 controlsReference Levi, Pasche, Lucchini, Ghidoni, Ferraroni and La Vecchia18. Compared with the lowest tertile of resveratrol intake, the multivariate RRs were 0.50 for the intermediate and 0.39 for the highest tertile, and the trend in risk was significant. An inverse association was observed for resveratrol from grapes (RR = 0.64 and 0.55), but not from wine (Table 2).

Table 2 Resveratrol and breast cancer risk. Data from a study of 369 cases and 602 controlsReference Levi, Pasche, Lucchini, Ghidoni, Ferraroni and La Vecchia18

* Reference category: tertile of total resveratrol determined on controls distribution. The upper cut-points for the tertile of total resveratrol intake (μg per 100 g day− 1) ranged between 0.0 and 73.0 for the first tertile (lowest), 73.1 and 160.7 for the second tertile and >160.7 for the third tertile (highest); intake from wine was 0.0 for the first tertile, ranged between 0.1 and 176.8 for the second tertile and >176.8 for the third tertile; intake from grapes ranged between 0.0 and 72.2 for the first tertile, 72.3 and 126.4 for the second tertile and >126.4 for the third tertile.

The inverse relation of flavones and—to a lesser extent—flavonols and resveratrol with breast cancer risk may, at least in part, explain the inverse relation between vegetable consumption and breast cancer risk in this population.

Meat

Among various aspects of diet which appear to influence cancer risk, red meat is of specific relevance. In our integrated series of studies from Italy, the multivariate RRs for the highest tertile of meat intake ( ≥ 7 times per week) compared with the lowest one ( ≤ 3 times per week) were 1.7 for stomach, 2.0 for colon, 1.9 for rectal, 1.6 for pancreas, 1.5 for bladder, 1.5 for endometrial and 1.3 for ovarian cancers. This points to (red) meat as another important factor (after vegetables and fruits) in the nutritional aetiology of human cancerReference Tavani, La Vecchia, Gallus, Lagiou, Trichopoulos and Levi19. This finding has repeatedly been observed for colorectal cancer and is of particular importance for Mediterranean populations, whose traditional diet did not include high intake of red meat, but who are now changing this aspect of dietary habits in an unfavourable wayReference Trichopoulou, Lagiou, Kuper and Trichoupulos1.

Fish and n-3 fatty acids

Fish intake (a major source of n-3 polyunsaturated fatty acids, PUFA) has been shown to be a favourable indicator for several common cancersReference Fernandez, Chatenoud, La Vecchia, Negri and Franceschi20. In our dataset, first consumption was associated with a decreased risk for several digestive tract cancersReference Fernandez, Chatenoud, La Vecchia, Negri and Franceschi20. The RRs were consistently below unity for digestive tract cancers (RR between 0.7 and 0.8), as well as for gallbladder and laryngeal cancers. Inverse trends in risk were also observed for breast and female genital tract cancers, but not for bladder, urinary tract or lymphoid neoplasms.

The continuous RRs for an increase of 1 g week− 1 of n-3 PUFAs are reported in Fig. 3. The RRs were below unity for all cancers considered, except prostate: 0.7 for oral/pharyngeal and oesophageal cancers, and 0.9 for colon, rectal, breast and ovarian cancersReference Tavani, Pelucchi, Parpinel, Negri, Franceschi and Levi21. As n-3 PUFAs are incorporated into cell membranes and influence several biological responsesReference Alexander22, multiple mechanisms may be involved in their activity. These include suppression of neoplastic transformation, cell growth inhibition, influence on the immune system and inflammationReference Grimble23, Reference Grant24, enhanced apoptosis and antiangiogenesisReference Rose and Connolly25.

Fig. 3 RRs and 95% CI of selected cancers for an increase of 1 g week− 1 of n-3 polyunsaturated fatty acids (PUFA). Italy, 1992–2004

The data from this integrated network of studies confirm therefore that fish, and consequently n-3 PUFA consumption, is a favourable indicator of the risk of several common cancers, mainly those of the digestive tract. The results are less clear for breast and prostate cancers. The inverse relation between fish/n-3 PUFAs and cancers of the digestive tract was not explained by sociodemographic factors, total energy intake and selected other covariates. Together with the favourable effect of fish and n-3 PUFA intake on the cardiovascular systemReference Marckmann and Grønbaek26, 27, the results from these data indicate that fish is a preferable substitute for meat intake in our dietReference Tavani, La Vecchia, Gallus, Lagiou, Trichopoulos and Levi19.

Fibres, whole and refined cereals

In the Italian network of case-control studies, the RRs for the highest consumption level of whole-grain foods were 0.2–0.3 for upper digestive and respiratory tract neoplasms, 0.5 for stomach, colon and gallbladder, 0.7 for rectum, 0.6 for liver, 0.8 for pancreas and prostate, 0.9 for breast and endometrium, 0.6 for ovary, 0.4 for bladder and kidney and around 0.5 for lymphomas and myelomas. Thus, in this population, high frequency of whole-grain food intake is an indicator of reduced cancer riskReference Chatenoud, Tavani, La Vecchia, Jacobs, Negri and Levi28.

With reference to fibres and colorectal carcinogenesis, in our dataReference Negri, Franceschi, Parpinel and La Vecchia29 from an area with intermediate colorectal cancer incidence and mortality on a European levelReference Fernandez, La Vecchia, Gonzalez, Lucchini, Negri and Levi30, the RR of colon and rectal cancers was below unity for most types of fibres, and no appreciable differences emerged between the two sites. The RRs for colorectal cancer for an increment equal to the difference between the 80th and the 20th percentiles were 0.68 for total fibres, 0.67 for soluble non-cellulose polysaccharides (NCP), 0.71 for total insoluble fibre, 0.67 for cellulose, 0.82 for insoluble NCP and 0.88 for lignin. When fibre was classified according to the source, the RR was 0.75 for vegetable fibre, 0.85 for fruit fibre, but 1.09 for cereal fibre.

In contrast, refined grain intake was associated with an increased risk of stomach, colorectal, breast, upper digestive sites and thyroid cancers in studies conducted in Mediterranean populationsReference Franceschi, Russo and La Vecchia31, Reference Chatenoud, La Vecchia, Franceschi, Tavani, Jacobs and Parpinel32. Glycaemic index (GI) and glycaemic load (GL) are indicators of the rate of adsorption of carbohydrates, and hence measures of insulin demand, and have been suggested to be relevant factors in gastric, colorectal, breast, female genital tract and prostatic carcinogenesis. The points to a potential role of insulin and hence insulin-like growth factors (IGFs) in cancer promotionReference Franceschi, Russo and La Vecchia31Reference Augustin, Gallus, Bosetti, Levi, Negri and Franceschi39. The RRs for the highest levels of GI/GL vs. the lowest ones were around 2 for various cancers considered.

Whole-grain foods should therefore replace refined cereal ones. This is of specific relevance in countries like Italy, where white bread and pasta are major components of the diet.

Olive oil and fats

The possible relation between total fats, and specific types of fats, and cancer risk remains a major open issue. In large studies from Italy, isocaloric substitution of 5% of total calories as saturated fats by unsaturated ones was associated with reductions in breast (RR = 0.67) and colorectal (RR = 0.78) cancer risk. Replacement of complex carbohydrates by unsaturated fats was associated with similar risk reductions. Part of the benefit for monounsaturated and polyunsaturated fats in the Mediterranean diet may be due to the positive correlation between (olive) oil and vegetable intakeReference Franceschi, Russo and La Vecchia31. It seems, therefore, that substituting olive oil for other seasoning fats has favourable effects on the risk of breastReference Franceschi, Russo and La Vecchia31, Reference La Vecchia, Negri, Franceschi, Decarli, Giacosa and Lipworth40Reference Bosetti, Micelotta, Dal Maso, Talamini, Montella and Negri43 and colorectalReference Braga, La Vecchia, Franceschi, Negri, Parpinel and Decarli44 cancers, as well as upper digestive tract neoplasms, with RRs for the highest consumption level of olive oil of 0.7 for oral/pharyngealReference Trichopoulou42 and laryngeal neoplasmsReference Bosetti, La Vecchia, Talamini, Negri, Levi and Dal Maso46, and of 0.4 for oesophagealReference Bosetti, La Vecchia, Talamini, Simonato, Zambon and Negri47 cancer.

Thus, neoplasms of the upper digestive and respiratory tract appear to be specifically and favourably influenced by olive oil. Frequent consumption of butter and other saturated fats, in contrast, was directly related to the risk of these neoplasmsReference Braga, La Vecchia, Franceschi, Negri, Parpinel and Decarli44Reference Franceschi, Favero, Conti, Talamini, Volpe and Negri45.

Pizza as an indicator of Mediterranean diet on cancer risk

Pizza is one of the most typical and representative foods of the Italian diet. An inverse association was found between regular pizza consumption ( ≥ 1 portion of pizza per week) and the risk of cancers of the digestive tractReference Gallus, Bosetti, Negri, Talamini, Montella and Conti48, with RRs of 0.66 for oral and pharyngeal cancers, 0.41 for oesophageal, 0.82 for laryngeal, 0.74 for colon and 0.93 for rectal cancers. The RRs for most cancers considered, and the corresponding trends in risk, were significant. However, pizza was not associated with the risk of sex hormone-related cancers, such as breast, ovarian and prostate cancersReference Gallus, Talamini, Bosetti, Negri, Montella and Franceschi49. The favourable influence of pizza on the risk of several digestive tract neoplasms may be related to tomatoes or olive oil, which have been inversely related to the risk of the cancers considered. However, evaluating the biological effect of specific components of pizza remains difficult, and pizza may simply represent a general and aspecific indicator of a favourable Mediterranean diet.

A Mediterranean diet score

A simple and intuitive scoreReference Bosetti, Gallus, Trichopoulou, Talamini, Franceschi and Negri50, summarising eight of the major characteristics of the Mediterranean diet, i.e. high consumption of cereals, legumes, fruit, vegetables, low consumption of meat, milk or dairy products, high monounsaturated/saturated fat ratio and moderate alcohol intake, was used to define a dietary pattern reflecting favourable aspects of diet. The relation between this a priori defined nutritional pattern and the risk of cancers of the upper aerodigestive tract has been evaluated using data from three case-control studies conducted in Italy. For all cancers considered, a significant reduced risk was found for increasing levels of the Mediterranean score: the multivariate RRs for subjects with ≥ 6 Mediterranean characteristics, compared with those with < 3, were 0.40 for oral and pharyngeal, 0.26 for oesophageal and 0.23 for laryngeal cancers.

This provides therefore additional evidence that the combination of various food items reflecting the Mediterranean diet favourably affects the risk of several common cancersReference Gallus, Bosetti and La Vecchia51.

Acknowledgements

Ms Ivana Garimoldi provided editorial assistance. This work was conducted with the contribution of the Italian Association for Cancer Research, the Italian League against Cancer and the Italian Ministry of Education and Research (COFIN 2005).

References

1Trichopoulou, A, Lagiou, P, Kuper, H, Trichoupulos, D. Cancer and Mediterranean dietary traditions. Cancer Epidemiology, Biomarkers & Prevention 2000; 9: 869–73.Google ScholarPubMed
2La Vecchia, C, Chatenoud, L, Franceschi, S, Soler, M, Parazzini, F, Negri, E. Vegetables and fruit and human cancer: update of an Italian study. International Journal of Cancer 1999; 82: 151–2.3.0.CO;2-9>CrossRefGoogle ScholarPubMed
3Negri, E, La Vecchia, C, Franceschi, S, D'Avanzo, B, Talamini, R, Parpinel, M, et al. . Intake of selected micronutrients and the risk of breast cancer. International Journal of Cancer 1996; 65: 140–4.3.0.CO;2-Z>CrossRefGoogle ScholarPubMed
4Bidoli, E, Bosetti, C, La Vecchia, C, Levi, F, Parpinel, M, Talamini, R, et al. . Micronutrients and laryngeal cancer risk in Italy and Switzerland: a case-control study. Cancer Causes Control 2003; 14: 477–84.Google Scholar
5Negri, E, Franceschi, S, Bosetti, C, Levi, F, Conti, E, Parpinel, M, et al. . Selected micronutrients and oral and pharyngeal cancer. International Journal of Cancer 2000; 86: 122–7.Google Scholar
6La Vecchia, C, Ferraroni, M, D'Avanzo, B, Decarli, A, Franceschi, S. Selected micronutrient intake and the risk of gastric cancer. Cancer Epidemiology, Biomarkers & Prevention 1994; 3: 393–8.Google ScholarPubMed
7La Vecchia, C. Tomatoes, lycopene intake, and digestive tract and female hormone-related neoplasms. Experimental Biology and Medicine (Maywood) 2002; 227: 860–3.CrossRefGoogle ScholarPubMed
8Bosetti, C, Talamini, R, Montella, M, Negri, E, Conti, E, Franceschi, S, et al. . Retinol, carotenoids and the risk of prostate cancer: a case-control study from Italy. International Journal of Cancer 2004; 112: 689–92.CrossRefGoogle ScholarPubMed
9La Vecchia, C, Braga, C, Negri, E, Franceschi, S, Russo, A, Conti, E, et al. . Intake of selected micronutrients and the risk of colorectal cancer. International Journal of Cancer 1997; 73: 525–30.3.0.CO;2-8>CrossRefGoogle ScholarPubMed
10Duthie, SJ. Folic acid deficiency and cancer: mechanisms of DNA instability. British Medical Bulletin 1999; 55: 578–92.CrossRefGoogle ScholarPubMed
11Pelucchi, C, Talamini, R, Negri, E, Levi, F, Conti, E, Franceschi, S, et al. . Folate intake and risk of oral and pharyngeal cancer. Annals of Oncology 2003; 14: 1677–81.CrossRefGoogle ScholarPubMed
12Franceschi, S, Bidoli, E, Negri, E, Zambon, P, Talamini, R, Ruol, A, et al. . Role of macronutrients, vitamins and minerals in the aetiology of squamous-cell carcinoma of the oesophagus. International Journal of Cancer 2000; 86: 626–31.Google Scholar
13La Vecchia, C, Negri, E, Pelucchi, C, Franceschi, S. Dietary folate and colorectal cancer. International Journal of Cancer 2002; 102: 545–7.CrossRefGoogle ScholarPubMed
14Negri, E, La Vecchia, C, Franceschi, S. Dietary folate consumption and breast cancer risk (reply to). Journal of the National Cancer Institute 2000; 92: 1270–1.CrossRefGoogle Scholar
15Pelucchi, C, Galeone, C, Talamini, R, Negri, E, Parpinel, M, Franceschi, S, et al. . Dietary folate and risk of prostate cancer in Italy. Cancer Epidemiology, Biomarkers & Prevention 2005; 14: 944–8.CrossRefGoogle ScholarPubMed
16Peterson, J, Lagiou, P, Samoli, E, Lagiou, A, Katsouyanni, K, La Vecchia, C, et al. . Flavonoid intake and breast cancer risk: a case-control study in Greece. British Journal of Cancer 2003; 89: 1255–9.Google Scholar
17Bosetti, C, Spertini, L, Parpinel, M, Gnagnarella, P, Lagiou, P, Negri, E, et al. . Flavonoids and breast cancer risk in Italy. Cancer Epidemiology, Biomarkers & Prevention 2005; 14: 805–8.Google Scholar
18Levi, F, Pasche, C, Lucchini, F, Ghidoni, R, Ferraroni, M, La Vecchia, C. Resveratrol and breast cancer risk. European Journal of Cancer Prevention 2005; 14: 139–42.CrossRefGoogle ScholarPubMed
19Tavani, A, La Vecchia, C, Gallus, S, Lagiou, P, Trichopoulos, D, Levi, F, et al. . Red meat intake and cancer risk: a study in Italy. International Journal of Cancer 2000; 86: 425–8.3.0.CO;2-S>CrossRefGoogle Scholar
20Fernandez, E, Chatenoud, L, La Vecchia, C, Negri, E, Franceschi, S. Fish consumption and cancer risk. The American Journal of Clinical Nutrition 1999; 70: 8590.CrossRefGoogle ScholarPubMed
21Tavani, A, Pelucchi, C, Parpinel, M, Negri, E, Franceschi, S, Levi, F, et al. . N-3 Polyunsaturated fatty acid intake and cancer risk in Italy and Switzerland. International Journal of Cancer 2003; 105: 113–6.Google Scholar
22Alexander, JW. Immunonutrition: the role of omega-3 fatty acids. Nutrition 1998; 14: 627–33.CrossRefGoogle ScholarPubMed
23Grimble, RF. Nutritional modulation of immune function. The Proceedings of the Nutrition Society 2001; 60: 389–97.CrossRefGoogle ScholarPubMed
24Grant, WB. Fish consumption, cancer, and Alzheimer disease. The American Journal of Clinical Nutrition 2000; 71: 599603.CrossRefGoogle ScholarPubMed
25Rose, DP, Connolly, JM. Omega–3 fatty acids as cancer chemopreventive agents. Pharmacology & Therapeutics 1999; 83: 217–44.Google Scholar
26Marckmann, P, Grønbaek, M. Fish consumption and coronary heart disease mortality: a systematic review of prospective cohort studies. European Journal of Clinical Nutrition 1999; 53: 585–90.Google Scholar
27GISSI-Prevenzione Investigators (Gruppo Italiano per lo Studio della Sopravvivenza nell'Infarto Miocardico). Dietary supplementation with n–3 polyunsaturated fatty acids and vitamin E after myocardial infarction: results of the GISSI-prevenzione trial. Lancet 1999; 354: 447–55.CrossRefGoogle Scholar
28Chatenoud, L, Tavani, A, La Vecchia, C, Jacobs, DR Jr, Negri, E, Levi, F, et al. . Whole grain food intake and cancer risk. International Journal of Cancer 1998; 77: 24–8.3.0.CO;2-1>CrossRefGoogle ScholarPubMed
29Negri, E, Franceschi, S, Parpinel, M, La Vecchia, C. Fibre intake and risk of colorectal cancer. Cancer Epidemiology, Biomarkers & Prevention 1998; 7: 667–71.Google Scholar
30Fernandez, E, La Vecchia, C, Gonzalez, JR, Lucchini, F, Negri, E, Levi, F. Converging patterns of colorectal cancer mortality in Europe. European Journal of Cancer 2005; 41: 430–7.Google Scholar
31Franceschi, S, Russo, A, La Vecchia, C. Carbohydrates, fat and cancer of the breast and colon-rectum. Journal of Epidemiology and Biostatistics 1998; 3: 217–8.Google Scholar
32Chatenoud, L, La Vecchia, C, Franceschi, S, Tavani, A, Jacobs, DR Jr, Parpinel, MT, et al. . Refined-cereal intake and risk of selected cancers in Italy. The American Journal of Clinical Nutrition 1999; 70: 1107–10.CrossRefGoogle ScholarPubMed
33Franceschi, S, Dal Maso, L, Augustin, L, Negri, E, Parpinel, M, Boyle, P, et al. . Dietary glycaemic load and colorectal cancer risk. Annals of Oncology 2001; 12: 173–8.Google Scholar
34Augustin, LS, Dal Maso, L, La Vecchia, C, Parpinel, M, Negri, E, Vaccarella, S, et al. . Dietary glycemic index and glycemic load, and breast cancer risk: a case-control study. Annals of Oncology 2001; 12: 1533–8.CrossRefGoogle ScholarPubMed
35Augustin, LS, Gallus, S, Negri, E, La Vecchia, C. Glycemic index, glycemic load and risk of gastric cancer. Annals of Oncology 2004; 15: 581–4.CrossRefGoogle ScholarPubMed
36Augustin, LS, Galeone, C, Dal Maso, L, Pelucchi, C, Ramazzotti, V, Jenkins, DJ, et al. . Glycemic index, glycemic load and the risk of prostate cancer. International Journal of Cancer 2004; 112: 446–50.Google Scholar
37Augustin, LS, Polesel, J, Bosetti, C, Kendall, CW, La Vecchia, C, Parpinel, M, et al. . Dietary glycemic index, glycemic load and ovarian cancer risk: a case-control study in Italy. Annals of Oncology 2003; 14: 7884.CrossRefGoogle Scholar
38Augustin, LS, Gallus, S, Franceschi, S, Negri, E, Jenkins, DJ, Kendall, CW, et al. . Glycemic index and load and risk of upper aero-digestive tract neoplasms (Italy). Cancer Causes Control 2003; 14: 657–62.Google Scholar
39Augustin, LS, Gallus, S, Bosetti, C, Levi, F, Negri, E, Franceschi, S, et al. . Glycemic index and glycemic load in endometrial cancer. International Journal of Cancer 2003; 105: 404–7.Google Scholar
40La Vecchia, C, Negri, E, Franceschi, S, Decarli, A, Giacosa, A, Lipworth, L. Olive oil, other dietary fats, and the risk of breast cancer (Italy). Cancer Causes Control 1995; 6: 545–50.Google Scholar
41Prieto-Ramos, F, Serra-Majem, L, La Vecchia, C, Ramon, JM, Tresserras, R, Salieras, L. Mortality trends and past and current dietary factors of breast cancer in Spain. European Journal of Epidemiology 1996; 12: 141–8.Google Scholar
42Trichopoulou, A. Olive oil and breast cancer. Cancer Causes Control 1995; 6: 545–50.Google Scholar
43Bosetti, C, Micelotta, S, Dal Maso, L, Talamini, R, Montella, M, Negri, E, et al. . Food groups and risk of prostate cancer in Italy. International Journal of Cancer 2004; 110: 424–8.Google Scholar
44Braga, C, La Vecchia, C, Franceschi, S, Negri, E, Parpinel, M, Decarli, A, et al. . Olive oil, other seasoning fats, and the risk of colorectal carcinoma. Cancer 1998; 82: 448–53.3.0.CO;2-L>CrossRefGoogle ScholarPubMed
45Franceschi, S, Favero, A, Conti, E, Talamini, R, Volpe, R, Negri, E, et al. . Food groups, oils and butter and cancer of the oral cavity and pharynx. British Journal of Cancer 1999; 80: 614–20.CrossRefGoogle ScholarPubMed
46Bosetti, C, La Vecchia, C, Talamini, R, Negri, E, Levi, F, Dal Maso, L, et al. . Food groups and laryngeal cancer risk: a case-control study from Italy and Switzerland. International Journal of Cancer 2002; 100: 355–60.Google Scholar
47Bosetti, C, La Vecchia, C, Talamini, R, Simonato, L, Zambon, P, Negri, E, et al. . Food groups and risk of squamous cell esophagel cancer in Northern Italy. International Journal of Cancer 2000; 87: 289–94.Google Scholar
48Gallus, S, Bosetti, C, Negri, E, Talamini, R, Montella, M, Conti, E, et al. . Does pizza protect against cancer? British Journal of Cancer 2003; 107: 283–4.Google ScholarPubMed
49Gallus, S, Talamini, R, Bosetti, C, Negri, E, Montella, M, Franceschi, S, et al. . Pizza consumption and the risk of breast, ovarian and prostate cancer. European Journal of Cancer Prevention 2006; 15: 74–6.Google Scholar
50Bosetti, C, Gallus, S, Trichopoulou, A, Talamini, R, Franceschi, S, Negri, E, et al. . Influence of the mediterranean diet on the risk of cancers of the upper aerodigestive tract. Cancer Epidemiology, Biomarkers & Prevention 2003; 12: 1091–4.Google ScholarPubMed
51Gallus, S, Bosetti, C, La Vecchia, C. Mediterranean diet and cancer risk. European Journal of Cancer Prevention 2004; 13: 447–52.Google Scholar
Figure 0

Fig. 1 RRs and 95% CI of selected cancers for the highest vs. the lowest levels of vegetable consumption. Italy, 1983–1997

Figure 1

Fig. 2 RRs and 95% CI of selected cancers for the highest vs. the lowest levels of folate consumption. Italy, 1983–1997

Figure 2

Table 1 Flavonoids and breast cancer risk in Italy. Data from a multicentric study of 2569 cases and 2558 controls17

Figure 3

Table 2 Resveratrol and breast cancer risk. Data from a study of 369 cases and 602 controls18

Figure 4

Fig. 3 RRs and 95% CI of selected cancers for an increase of 1 g week− 1 of n-3 polyunsaturated fatty acids (PUFA). Italy, 1992–2004