An inverse association between physical activity and risk for breast cancer has been proposed and available evidence indicates that protection against cancer is due to effects of physical activity that are distinct from as well as related to its effects on adult weight gain. Little is know about how physical activity per se affects the risk for cancer. Given current trends towards reduced occupational activity, most women will need to use recreational activity to experience health benefits. This subset of physical activity is generally referred to as exercise. In this application we propose to study the influence of three principal components of exercise, its intensity, duration, and frequency, on the development of breast cancer in a widely used experimental model system. Our objectives are described in the following aims: 1) Determine the exercise intensity, duration, and frequency that inhibits the post initiation stage of mammary carcinogenesis. For those individuals who are maintaining body weight in an acceptable range for cancer risk reduction, but who also wish to exercise for further reduction in risk, the relative importance of exercise intensity, duration and frequency for cancer prevention is unclear and requires investigation. A newly developed model for exercise in which running behavior is maintained by food reinforcement will be used for this work. This approach not only circumvents the use of adverse stimuli to maintain compliance to an exercise protocol, but also permits manipulation of the ratio of dietary energy ingested relative to the amount of energy expended during exercise. 2) Investigate the effects of exercise per the conditions described in Aim 1 on insulin-like growth factor (IGF) and corticosterone and a signaling pathway they may affect in mammary tissue and in pre-malignant and malignant mammary pathologies. We hypothesize that the effects of exercise on insulin-like growth factor (IGF) and corticosterone are likely to account, at least in part, for inhibitory activity. Therefore, the proposed experiments will focus on the investigation of these molecules. 3) Evaluate whether exercise-related alterations in cell proliferation, apoptosis and/or angiogenesis are likely to account for cancer inhibitory activity. Based on those results and findings from Aim 2, investigate the molecular pathway(s) most likely to account for the cancer inhibitory activity of exercise. Little information exists concerning the effects of exercise on the misregulation of cellular processes involved in carcinogenesis. For the cellular process (proliferation, apoptosis or angiogenesis) identified, molecular studies will be conducted. The preclinical experiments proposed should provide critical information concerning the effects of exercise on biomarkers and mechanisms in relation to cancer endpoints. These data should facilitate the translation of pre-clinical and clinical research to public health recommendations for cancer risk reduction.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA100693-04
Application #
7253429
Study Section
Chemo/Dietary Prevention Study Section (CDP)
Program Officer
Perloff, Marjorie
Project Start
2004-07-01
Project End
2009-03-31
Budget Start
2007-07-01
Budget End
2009-03-31
Support Year
4
Fiscal Year
2007
Total Cost
$225,478
Indirect Cost
Name
Colorado State University-Fort Collins
Department
Miscellaneous
Type
Schools of Earth Sciences/Natur
DUNS #
785979618
City
Fort Collins
State
CO
Country
United States
Zip Code
80523
Thompson, Henry J; Jones, Lee W; Koch, Lauren G et al. (2017) Inherent aerobic capacity-dependent differences in breast carcinogenesis. Carcinogenesis 38:920-928
Jiang, Weiqin; Zhu, Zongjian; Thompson, Henry J (2013) Effects of limiting energy availability via diet and physical activity on mammalian target of rapamycin-related signaling in rat mammary carcinomas. Carcinogenesis 34:378-87
Zhu, Zongjian; Jiang, Weiqin; Zacher, Jarrod H et al. (2012) Effects of energy restriction and wheel running on mammary carcinogenesis and host systemic factors in a rat model. Cancer Prev Res (Phila) 5:414-22
Thompson, Henry J; McTiernan, Anne (2011) Weight cycling and cancer: weighing the evidence of intermittent caloric restriction and cancer risk. Cancer Prev Res (Phila) 4:1736-42
Mann, Phillip B; Jiang, Weiqin; Zhu, Zongjian et al. (2010) Wheel running, skeletal muscle aerobic capacity and 1-methyl-1-nitrosourea induced mammary carcinogenesis in the rat. Carcinogenesis 31:1279-83
Thompson, Henry J; Wolfe, Pamela; McTiernan, Anne et al. (2010) Wheel running-induced changes in plasma biomarkers and carcinogenic response in the 1-methyl-1-nitrosourea-induced rat model for breast cancer. Cancer Prev Res (Phila) 3:1484-92
Thompson, Henry J; Jiang, Weiqin; Zhu, Zongjian (2009) Candidate mechanisms accounting for effects of physical activity on breast carcinogenesis. IUBMB Life 61:895-901
Jiang, Weiqin; Zhu, Zongjian; Thompson, Henry J (2009) Effects of physical activity and restricted energy intake on chemically induced mammary carcinogenesis. Cancer Prev Res (Phila) 2:338-44
Zhu, Zongjian; Jiang, Weiqin; McGinley, John N et al. (2009) Energetics and mammary carcinogenesis: effects of moderate-intensity running and energy intake on cellular processes and molecular mechanisms in rats. J Appl Physiol (1985) 106:911-8
Zhu, Zongjian; Jiang, Weiqin; Sells, Jennifer L et al. (2008) Effect of nonmotorized wheel running on mammary carcinogenesis: circulating biomarkers, cellular processes, and molecular mechanisms in rats. Cancer Epidemiol Biomarkers Prev 17:1920-9

Showing the most recent 10 out of 12 publications