Hostname: page-component-7c8c6479df-27gpq Total loading time: 0 Render date: 2024-03-27T16:48:22.142Z Has data issue: false hasContentIssue false

Symposium 1: Overnutrition: consequences and solutions Obesity and cancer risk

Conference on ‘Over- and undernutrition: challenges and approaches’

Published online by Cambridge University Press:  03 December 2009

Timothy J. Key*
Affiliation:
Cancer Epidemiology Unit, Nuffield Department of Clinical Medicine, University of Oxford, Richard Doll Building, Roosevelt Drive, OxfordOX3 7LF, UK
Elizabeth A. Spencer
Affiliation:
Cancer Epidemiology Unit, Nuffield Department of Clinical Medicine, University of Oxford, Richard Doll Building, Roosevelt Drive, OxfordOX3 7LF, UK
Gillian K. Reeves
Affiliation:
Cancer Epidemiology Unit, Nuffield Department of Clinical Medicine, University of Oxford, Richard Doll Building, Roosevelt Drive, OxfordOX3 7LF, UK
*
*Corresponding author: Professor Timothy J. Key, fax +44 1865 289610, email tim.key@ceu.ox.ac.uk
Rights & Permissions [Opens in a new window]

Abstract

Epidemiological studies have provided convincing evidence that obesity increases the risk for cancers of the oesophagus (adenocarcinoma), colon, pancreas, breast (post-menopausal), endometrium and kidney. The magnitude of the increase in risk varies between cancer sites. For an increase in BMI of 10 kg/m2 relative risks are approximately 2·3 for adenocarcinoma of the oesophagus, 1·5 for colon cancer in men, 1·2 for colon cancer in women, 1·4 for post-menopausal breast cancer, 2·9 for endometrial cancer and >1·5 for kidney cancer, while the size of the effect on cancer of the pancreas is uncertain. There is also evidence that obesity increases the risks for cancers of the gallbladder, malignant melanoma, ovary, thyroid, non-Hodgkin lymphoma, multiple myeloma and leukaemia. Estimates of the percentage of cancers that can be attributed to excess body weight suggest that in the UK and similar countries approximately 5% of all cancers are attributable to overweight and obesity.

Type
Research Article
Copyright
Copyright © The Authors 2009

There is now convincing evidence from epidemiological studies showing that obesity increases the risk for several types of cancer, and for the more common cancer sites the estimates of the size of the effect are reasonably precise. The present overview is based on recent reports from expert groups together with the results of meta-analyses and large prospective studies. In turn, the common cancer sites that are clearly related to obesity are discussed, giving examples of relative risk estimates from meta-analyses or large single studies, and some of the mechanisms that may underlie these associations are outlined.

Evidence and methods used

The association between overweight and obesity and cancer risk was evaluated by the International Agency for Research on Cancer in 2002(Reference Vainio and Bianchini1). This working group concludes that overweight and obesity definitely increase the risk for cancers of the oesophagus (adenocarcinoma), colon, breast (post-menopausal), endometrium and kidney. A more recent assessment by the World Cancer Research Fund has confirmed the effect of overweight and obesity on these cancer sites and also considers that the evidence for an adverse effect on cancer of the pancreas is convincing(2). The present overview discusses the effects of overweight and obesity on the risk for cancer at these six sites and also summarises the evidence for other types of cancer for which risk is probably also increased by obesity. Most of the estimates of relative risks associated with obesity that are cited in Table 1 are taken from a 2008 meta-analysis(Reference Renehan, Tyson and Egger3). For breast, endometrial and ovarian cancer in women the estimates are derived from the 2007 report of the Million Women Study, because this single very large study includes detailed adjustments for relevant reproductive and hormonal factors(Reference Reeves, Pirie and Beral4). The results of other large recent studies are discussed when appropriate. For estimates of attributable risks the prevalence of overweight and obesity among men and women aged 55–64 years in England in 2007(5) have been used.

Table 1. Estimates of the relative risks for cancer at different sites associated with an increase in BMI of 10 kg/m2 and of the attributable risks for each site for overweight and obesity in the UK

* Estimates from Renehan et al.(Reference Renehan, Tyson and Egger3) except for breast, endometrium, ovary and all cancers in women from Reeves et al.(Reference Reeves, Pirie and Beral4) and all cancers in men taken as risk for BMI >30 kg/m2v. BMI 18·5–24·9 kg/m2 from Samanic et al.(Reference Samanic, Chow and Gridley18).

As the association was not significant it was not reported.

Calculated using estimates of the prevalence of overweight and obesity in men and women aged 55–64 years in England in 2007(5).

Oesophageal cancer

Adenocarcinoma of the oesophagus

Obesity increases the risk of adenocarcinoma but not squamous cell carcinoma of the oesophagus. Relative risks for adenocarcinoma of the oesophagus for a 10 kg/m2 increase in BMI have been reported as 2·31 among men and 2·28 among women in the 2008 meta-analysis(Reference Renehan, Tyson and Egger3). Approximately 40% of adenocarcinomas of the oesophagus in the UK may be attributed to overweight and obesity (Table 1).

The mechanism by which obesity increases the risk for adenocarcinoma of the oesophagus is not fully understood, but probably involves an increase in the prevalence of chronic acid reflux from the stomach into the oesophagus, which damages the oesophageal epithelium(Reference Crowell, Bradley and Hansel6, Reference Lagergren, Bergström and Lindgren7).

Squamous cell carcinoma of the oesophagus

For squamous cell carcinoma of the oesophagus observational studies have reported that the risk is lower in obese subjects than in thin subjects; for example, relative risks for a 10 kg/m2 increase in BMI of 0·50 and 0·32 in men and women respectively(Reference Renehan, Tyson and Egger3). Squamous cell carcinoma of the oesophagus is strongly related to both smoking and alcohol intake. The Million Women Study investigators conclude that residual confounding by smoking and alcohol cannot easily explain the inverse association(Reference Reeves, Pirie and Beral4), but it is possible that the inverse association may be a result of weight loss several years before diagnosis among subjects with preclinical disease.

Colo-rectal cancer

For cancers of the colon and rectum there is strong evidence that the relationship between obesity and risk differs between men and women(Reference Renehan, Tyson and Egger3). In men the 2008 meta-analysis reports relative risks for a 10 kg/m2 increase in BMI of 1·54 for colon cancer and 1·19 for rectal cancer(Reference Renehan, Tyson and Egger3). The associations in women are much weaker; a relative risk of 1·19 for colon cancer and no significant association with rectal cancer. Furthermore, there are strongly significant differences in these associations between men and women (P<0·0001 for colon cancer and P=0·003 for rectal cancer). It is also clear that the increase in risk is greater for cancer of the colon than for cancer of the rectum. Furthermore, among women the effect of obesity may be greater among those who are premenopausal; in the Million Women Study the increase in risk for colo-rectal cancer associated with a 10 kg/m2 increase in BMI is 1·61 (95% CI 1·05, 2·48) among premenopausal women but 0·99 (95% CI 0·88, 1·12) among post-menopausal women(Reference Reeves, Pirie and Beral4).

Among men in the UK overweight and obesity are responsible for approximately 22% and 9% of cancers of the colon and rectum respectively. Among women overweight and obesity are responsible for approximately 8% of cancers of the colon, with no definite effect on cancers of the rectum (Table 1).

The biological mechanisms by which obesity increases risk of colo-rectal cancer are not understood. Possible mechanisms are that the relatively high circulating insulin levels associated with obesity contribute to increased cell division in the colon(Reference Becker, Dossus and Kaaks8) or that the relatively low levels of adiponectin associated with obesity allow increased angiogenesis(Reference Harriss, Atkinson and George9). Since the effect of obesity varies between men and women, sex hormones may also be involved.

Pancreatic cancer

The evidence on the association between overweight and obesity and the risk for cancer of the pancreas has some inconsistencies. The 2002 assessment by the International Agency for Research on Cancer does not include cancer of the pancreas among the cancers caused by obesity(Reference Vainio and Bianchini1), but the 2007 assessment by the World Cancer Research Fund was able to consider more studies and concludes that the evidence is convincing(2). The 2008 meta-analysis shows no significant association among men, whereas among women there is a relative risk of 1·25 for a 10 kg/m2 increase in BMI(Reference Renehan, Tyson and Egger3); however, the difference in associations between men and women is not itself significant. Among women the attributable risk for overweight and obesity in the UK is approximately 11% (Table 1).

The mechanism for the effect of obesity on the risk for cancer of the pancreas is not understood. Diabetes mellitus is associated with an increased risk for pancreatic cancer(Reference Huxley, Ansary-Moghaddam and Berrington10) and obesity is a major cause of diabetes, but it is unclear whether diabetes contributes to the causation of pancreatic cancer or whether long-standing changes in the pancreas are precedents of both diabetes and cancer.

Breast cancer

Post-menopausal women

Obesity increases breast cancer risk in post-menopausal women. This relationship is strong among women not using hormone-replacement therapy, but is not evident among women using hormone-replacement therapy(Reference Lahmann, Hoffmann and Allen11). The Million Women Study investigators report a relative risk of 1·40 for a 10 kg/m2 increase in BMI among post-menopausal women who have never used hormone-replacement therapy(Reference Reeves, Pirie and Beral4). Approximately 16% of breast cancers among post-menopausal women in the UK who do not use hormone-replacement therapy are attributable to overweight and obesity (Table 1).

The increase in breast cancer risk associated with obesity among post-menopausal women is probably mediated by oestrogens. In post-menopausal women the main source of circulating oestrogens is conversion from androgens by the enzyme aromatase, which is present in the adipose tissue. Obese post-menopausal women have circulating oestradiol concentrations more than twice as high as those in thin post-menopausal women, and prospective analyses of circulating oestrogen concentrations and breast cancer risk have shown that the increase in risk observed with obesity can be completely explained by the increase in oestradiol concentrations(Reference Key, Appleby and Reeves12, Reference Rinaldi, Key and Peeters13). Obesity also causes a reduction in circulating concentrations of sex hormone-binding globulin, leading to an increase in the proportion of oestradiol that is free to leave the circulation(Reference Key, Appleby and Reeves12).

Premenopausal women

Obesity is associated with a reduction in breast cancer risk among premenopausal women. The Million Women Study investigators report a relative risk of 0·86 for a 10 kg/m2 increase in BMI among premenopausal women(Reference Reeves, Pirie and Beral4), and the results of the 2008 meta-analysis are almost identical(Reference Renehan, Tyson and Egger3).

The reason for the inverse association between obesity and breast cancer risk among premenopausal women is poorly understood. There is some evidence that obesity frequently leads to anovular menstrual cycles, which may reduce the risk for breast cancer as a result of lower exposure to progesterone(Reference Key and Pike14), but other mechanisms could be involved. It should also be noted that obesity in premenopausal women is likely to lead to obesity throughout life and therefore to an eventual increase in breast cancer risk.

Endometrial cancer

Obesity causes a large increase in the risk for endometrial cancer. The Million Women Study reports a relative risk for a 10 kg/m2 increase in BMI, with full adjustment for potential confounding factors including reproductive history, of 2·89(Reference Reeves, Pirie and Beral4). Analyses subdivided by menopausal status at recruitment show a relative risk of 1·77 among premenopausal women and 3·98 among post-menopausal women, and this difference in the size of the risks is significant (P=0·0001). Approximately 46% of endometrial cancers among post-menopausal women in the UK can be attributed to overweight and obesity (Table 1).

As with breast cancer, the effect of obesity in post-menopausal women on the risk for endometrial cancer is probably mediated by the increase in serum concentrations of oestradiol and the reduction in serum concentrations of sex hormone-binding globulin; in premenopausal women the mechanism may involve an increase in the incidence of anovulation and consequent increased exposure to oestradiol unopposed by progesterone(Reference Key and Pike15).

Kidney cancer

Overweight and obesity substantially increase the risk for kidney cancer. The 2008 meta-analysis estimates increases in risk per 10 kg/m2 increase in BMI of 1·54 and 1·80 in men and women respectively(Reference Renehan, Tyson and Egger3). Approximately one-quarter of kidney cancers in the UK may be attributable to overweight and obesity (22% in men and 27% in women; Table 1). Despite this well-established association the biological mechanism is not known. High blood pressure is strongly associated with obesity and is a risk factor for kidney cancer, but the evidence suggests that these factors may have independent effects on the risk for kidney cancer(Reference Chow, Gridley and Fraumeni16, Reference Weikert, Boeing and Pischon17).

Other cancers

The 2008 meta-analysis reports significant associations between obesity and increased risks for cancers of the gallbladder (in women), malignant melanoma (in men), thyroid, non-Hodgkin lymphoma, multiple myeloma and leukaemia(Reference Renehan, Tyson and Egger3). The Million Women Study also reports a significant increase in the risk for ovarian cancer associated with obesity(Reference Reeves, Pirie and Beral4). The estimates of relative risks for these associations are shown in Table 1; further evaluation of these associations is required, but it is likely that obesity does increase the risk for most if not all these cancers.

Observational studies show that the risk for lung cancer is relatively high among individuals with a low BMI, but this finding may be a result of residual confounding by smoking and reverse causality(Reference Renehan, Tyson and Egger3, Reference Reeves, Pirie and Beral4). Obesity has little or no effect on the risk for stomach cancer or prostate cancer(Reference Renehan, Tyson and Egger3, Reference Reeves, Pirie and Beral4).

All cancers combined

Some studies have examined the association between obesity and the risk for any type of cancer. Two very large cohort studies provide reliable information. Among 360 000 Swedish men in the construction industry the relative risk in obese men compared with normal-weight men for any type of cancer is 1·10(Reference Samanic, Chow and Gridley18). In the Million Women Study in the UK the relative risk for any type of cancer (except non-melanoma skin cancer) associated with a 10 kg/m2 increase in BMI is 1·12(Reference Reeves, Pirie and Beral4). Thus, the attributable risks for all cancers in the UK are approximately 5% and 6% among men and women respectively (Table 1).

Reversing the effect of obesity on cancer risk

The clear evidence that overweight and obesity increase the risk for several types of cancer implies that weight loss should, at least to some extent, reverse this effect. There is some epidemiological evidence to support this notion; for example, the Nurses' Health Study has shown that women who lose weight after the menopause are at lower risk for breast cancer than women who maintain their weight(Reference Eliassen, Colditz and Rosner19). At a population level there is very little evidence that reducing obesity leads to reduced cancer rates, largely because of the lack of effective public health strategies to reduce obesity. There is some evidence from recent clinical studies that surgical procedures that cause substantial weight loss among morbidly-obese patients are associated with reduced cancer risk(Reference Adams, Stroup and Gress20, Reference Sjöström, Gummesson and Sjöström21).

Future research questions

More data are required on the possible associations between overweight and obesity and the risk for less-common types of cancer. There is also a need to explore further the importance of obesity at different ages in relation to lifetime risk for cancer and to better understand whether the distribution of body fat is important as well as the extent of adiposity.

Conclusions

Obesity is an important cause of cancer. The largest effects and greatest attributable risks are for adenocarcinoma of the oesophagus and for endometrial cancer. Current estimates suggest that approximately 5% of cancers in the UK are caused by overweight and obesity (Table 1). The percentage is likely to be similar in other Western countries with a similar prevalence of obesity and will increase if the prevalence of obesity increases. A reduction in cancer rates would be among the many benefits that would result if the prevalence of obesity can be reduced.

Acknowledgements

This work was supported by Cancer Research UK (CR-UK Programme Grant C570/A5028). The authors declare no conflicts of interest. T. J. K. was responsible for drafting the article. E. A. S. reviewed and revised the article and provided particular input for cancers of the gastrointestinal tract. G. K. R. reviewed and revised the article and provided particular input for hormone-related cancers.

References

1.International Agency for Research on Cancer (2002) Weight Control and Physical Activity. IARC Handbooks of Cancer Prevention, vol. 6 [Vainio, H and Bianchini, F, editors]. Lyon, France: IARC Press.Google Scholar
2.World Cancer Research Fund/American Institute for Cancer Research (2007) Food, Nutrition, Physical Activity, and the Prevention of Cancer: a Global Perspective. Washington, DC: AICR.Google Scholar
3.Renehan, AG, Tyson, M, Egger, M et al. (2008) Body-mass index and incidence of cancer: a systematic review and meta-analysis of prospective observational studies. Lancet 371, 569578.CrossRefGoogle Scholar
4.Reeves, GK, Pirie, K, Beral, V et al. (2007) Cancer incidence and mortality in relation to body mass index in the Million Women Study: cohort study. Br Med J 335, 11341139.CrossRefGoogle ScholarPubMed
5.The Information Centre for Health and Social Care (2009) Statistics on obesity, physical activity and diet: England, February 2009. http://www.ic.nhs.uk/statistics-and-data-collections/health-and-lifestyles/obesity/statistics-on-obesity-physical-activity-and-diet:-england-february-2009 (accessed June 2009).Google Scholar
6.Crowell, MD, Bradley, A, Hansel, S et al. (2009) Obesity is associated with increased 48-h esophageal acid exposure in patients with symptomatic gastroesophageal reflux. Am J Gastroenterol 104, 553559.Google ScholarPubMed
7.Lagergren, J, Bergström, R, Lindgren, A et al. (1999) Symptomatic gastroesophageal reflux as a risk factor for esophageal adenocarcinoma. N Engl J Med 340, 825831.CrossRefGoogle ScholarPubMed
8.Becker, S, Dossus, L & Kaaks, R (2009) Obesity related hyperinsulinaemia and hyperglycaemia and cancer development. Arch Physiol Biochem 115, 8696.CrossRefGoogle ScholarPubMed
9.Harriss, DJ, Atkinson, G, George, K et al. (2009) Lifestyle factors and colorectal cancer risk (1): systematic review and meta-analysis of associations with body mass index. Colorectal Dis 11, 547563.CrossRefGoogle ScholarPubMed
10.Huxley, R, Ansary-Moghaddam, A, Berrington, de González A et al. (2005) Type-II diabetes and pancreatic cancer: a meta-analysis of 36 studies. Br J Cancer 92, 20762083.CrossRefGoogle ScholarPubMed
11.Lahmann, PH, Hoffmann, K, Allen, N et al. (2004) Body size and breast cancer risk: findings from the European Prospective Investigation into Cancer and Nutrition (EPIC). Int J Cancer 111, 762771.CrossRefGoogle ScholarPubMed
12.Key, TJ, Appleby, PN, Reeves, GK et al. (2003) Body mass index, serum sex hormones, and breast cancer risk in postmenopausal women. J Natl Cancer Inst 95, 12181226.Google ScholarPubMed
13.Rinaldi, S, Key, TJ, Peeters, PH et al. (2006) Anthropometric measures, endogenous sex steroids and breast cancer risk in postmenopausal women: a study within the EPIC cohort. Int J Cancer 118, 28322839.CrossRefGoogle ScholarPubMed
14.Key, TJ & Pike, MC (1988) The role of oestrogens and progestagens in the epidemiology and prevention of breast cancer. Eur J Cancer Clin Oncol 24, 2943.CrossRefGoogle ScholarPubMed
15.Key, TJ & Pike, MC (1988) The dose-effect relationship between ‘unopposed’ oestrogens and endometrial mitotic rate: its central role in explaining and predicting endometrial cancer risk. Br J Cancer 57, 205212.CrossRefGoogle ScholarPubMed
16.Chow, WH, Gridley, G, Fraumeni, JF Jr et al. (2000) Obesity, hypertension, and the risk of kidney cancer in men. N Engl J Med 343, 13051311.CrossRefGoogle ScholarPubMed
17.Weikert, S, Boeing, H, Pischon, T et al. (2008) Blood pressure and risk of renal cell carcinoma in the European prospective investigation into cancer and nutrition. Am J Epidemiol 167, 438446.CrossRefGoogle ScholarPubMed
18.Samanic, C, Chow, WH, Gridley, G et al. (2006) Relation of body mass index to cancer risk in 362,552 Swedish men. Cancer Causes Control 17, 901909.CrossRefGoogle ScholarPubMed
19.Eliassen, AH, Colditz, GA, Rosner, B et al. (2006) Adult weight change and risk of postmenopausal breast cancer. JAMA 296, 193201.CrossRefGoogle ScholarPubMed
20.Adams, TD, Stroup, AM, Gress, RE et al. (2009) Cancer incidence and mortality after gastric bypass surgery. Obesity 17, 796802.CrossRefGoogle ScholarPubMed
21.Sjöström, L, Gummesson, A, Sjöström, CD et al. (2009) Effects of bariatric surgery on cancer incidence in obese patients in Sweden (Swedish Obese Subjects Study): a prospective, controlled intervention trial. Lancet Oncol 10, 653662.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Estimates of the relative risks for cancer at different sites associated with an increase in BMI of 10 kg/m2 and of the attributable risks for each site for overweight and obesity in the UK