Efficacy and Mechanisms of Aerobic Exercise on Cancer Initiation, Progression, and Metastasis: A Critical Systematic Review of In Vivo Preclinical Data

被引:173
作者
Ashcraft, Kathleen A. [1 ]
Peace, Ralph M. [1 ]
Betof, Allison S. [2 ]
Dewhirst, Mark W. [1 ]
Jones, Lee W. [3 ]
机构
[1] Duke Univ, Med Ctr, Durham, NC 27710 USA
[2] Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10017 USA
关键词
INDUCED MAMMARY CARCINOGENESIS; INDUCED COLON CARCINOGENESIS; HIGH-INTENSITY EXERCISE; HEALTHY FOOD CHOICES; PHYSICAL-ACTIVITY; BREAST-CANCER; TUMOR-GROWTH; VOLUNTARY EXERCISE; POSTMENOPAUSAL WOMEN; NATURAL CYTOTOXICITY;
D O I
10.1158/0008-5472.CAN-16-0887
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
A major objective of the emerging field of exercise-oncology research is to determine the efficacy of, and biological mechanisms by which, aerobic exercise affects cancer incidence, progression, and/or metastasis. There is a strong inverse association between self-reported exercise and the primary incidence of several forms of cancer; similarly, emerging data suggest that exercise exposure after a cancer diagnosis may improve outcomes for early-stage breast, colorectal, or prostate cancer. Arguably, critical next steps in the development of exercise as a candidate treatment in cancer control require preclinical studies to validate the biological efficacy of exercise, identify the optimal "dose", and pinpoint mechanisms of action. To evaluate the current evidence base, we conducted a critical systematic review of in vivo studies investigating the effects of exercise in cancer prevention and progression. Studies were evaluated on the basis of tumor outcomes (e.g., incidence, growth, latency, metastasis), dose-response, and mechanisms of action, when available. A total of 53 studies were identified and evaluated on tumor incidence (n = 24), tumor growth (n = 33), or metastasis (n = 10). We report that the current evidence base is plagued by considerable methodologic heterogeneity in all aspects of study design, endpoints, and efficacy. Such heterogeneity precludes meaningful comparisons and conclusions at present. To this end, we provide a framework of methodologic and data reporting standards to strengthen the field to guide the conduct of high-quality studies required to inform translational, mechanism-driven clinical trials. (C)2016 AACR.
引用
收藏
页码:4032 / 4050
页数:19
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