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      Dietary Walnut Suppressed Mammary Gland Tumorigenesis in the C(3)1 TAg Mouse

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      Nutrition and Cancer
      Taylor & Francis

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          Abstract

          Walnuts contain multiple ingredients that, individually, have been shown to slow cancer growth, including omega-3 fatty acids, antioxidants, and phytosterols. In previous research, consumption of walnuts has slowed the growth of implanted breast cancers. We wanted to determine whether regular walnut consumption might reduce the risk for developing cancer. Homozygous male C(3)1 TAg mice were bred with female SV129 mice consuming either the control AIN-76 diet or the walnut-containing diet. At weaning, the female hemizygous pups were randomized to control or walnut-containing diets and followed for tumor development. Compared to a diet without walnuts, consumption of walnuts significantly reduced tumor incidence (fraction of mice with at least one tumor), multiplicity (number of glands with tumor/mouse), and size. Gene expression analyses indicated that consumption of the walnut diet altered expression of multiple genes associated with proliferation and differentiation of mammary epithelial cells. A comparison with another dietary intervention indicated that the omega 3 content alone did not account for the extent of tumor suppression due to the walnut. The results of this study indicate that walnut consumption could contribute to a healthy diet to reduce risk for breast cancer.

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          Most cited references41

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          Food, Nutrition, Physical Activity, and the Prevention of Cancer: a Global Perspective,

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            Report of the American Institute of Nurtition ad hoc Committee on Standards for Nutritional Studies.

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              Mediterranean dietary pattern and prediction of all-cause mortality in a US population: results from the NIH-AARP Diet and Health Study.

              The Mediterranean diet has been suggested to play a beneficial role for health and longevity. However, to our knowledge, no prospective US study has investigated the Mediterranean dietary pattern in relation to mortality. Study participants included 214,284 men and 166,012 women in the National Institutes of Health (NIH)-AARP (formerly known as the American Association of Retired Persons) Diet and Health Study. During follow-up for all-cause mortality (1995-2005), 27,799 deaths were documented. In the first 5 years of follow-up, 5,985 cancer deaths and 3,451 cardiovascular disease (CVD) deaths were reported. We used a 9-point score to assess conformity with the Mediterranean dietary pattern (components included vegetables, legumes, fruits, nuts, whole grains, fish, monounsaturated fat-saturated fat ratio, alcohol, and meat). We calculated hazard ratios (HRs) and 95% confidence intervals (CIs) using age- and multivariate-adjusted Cox models. The Mediterranean diet was associated with reduced all-cause and cause-specific mortality. In men, the multivariate HRs comparing high to low conformity for all-cause, CVD, and cancer mortality were 0.79 (95% CI, 0.76-0.83), 0.78 (95% CI, 0.69-0.87), and 0.83 (95% CI, 0.76-0.91), respectively. In women, an inverse association was seen with high conformity with this pattern: decreased risks that ranged from 12% for cancer mortality to 20% for all-cause mortality (P = .04 and P < .001, respectively, for the trend). When we restricted our analyses to never smokers, associations were virtually unchanged. These results provide strong evidence for a beneficial effect of higher conformity with the Mediterranean dietary pattern on risk of death from all causes, including deaths due to CVD and cancer, in a US population.
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                Author and article information

                Journal
                Nutr Cancer
                Nutr Cancer
                hnuc
                Nutrition and Cancer
                Taylor & Francis
                0163-5581
                1532-7914
                20 July 2011
                August 2011
                : 63
                : 6
                : 960-970
                Affiliations
                Department of Biochemistry and Microbiology, Marshall University School of Medicine, Huntington, West Virginia, USA
                Author notes
                Address correspondence to W. Elaine Hardman, Ph.D., Department of Biochemistry and Microbiology, Marshall University School of Medicine, 1700 3rd Ave., Huntington, WV 25701. Phone: 304-696-3721. Fax: 304-696-7204. E-mail: hardmanw@ 123456marshall.edu
                Article
                10.1080/01635581.2011.589959
                3474134
                21774594
                5461bfa8-47cd-484f-baff-b54942655879
                Copyright © 2011, Taylor & Francis Group, LLC

                This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Taylor & Francis journals , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 5 August 2010
                : 6 April 2012
                Categories
                Research Article

                Oncology & Radiotherapy
                Oncology & Radiotherapy

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