The Effects of Exercise Duration and Intensity on Breast Cancer-Related DNA Methylation: A Randomized Controlled Trial

被引:16
作者
Gillman, Arielle S. [1 ,3 ]
Helmuth, Timothy [1 ]
Koljack, Claire E. [2 ]
Hutchison, Kent E. [1 ]
Kohrt, Wendy M. [2 ]
Bryan, Angela D. [1 ]
机构
[1] Univ Colorado, Ctr Hlth & Neurosci Genes & Environm CUChange, Dept Psychol & Neurosci, Boulder, CO 80309 USA
[2] Univ Colorado, Anschutz Med Campus, Aurora, CO 80045 USA
[3] NCI, Basic Biobehav & Psychol Sci Branch, Behav Res Program, Div Canc Control & Populat Sci, Bethesda, MD 20892 USA
关键词
breast cancer; exercise; physical activity; methylation; PHYSICAL-ACTIVITY; PROMOTER HYPERMETHYLATION; SPORADIC BREAST; EXPRESSION; GENES; MECHANISMS; PREVENTION; BRCA1; INFLAMMATION; ASSOCIATION;
D O I
10.3390/cancers13164128
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary While physical activity has been associated with reduced cancer risk, it is not well understood why this is the case. One possible reason is that physical activity affects DNA methylation-a process that functions to turn certain genes "on" or "off"-which can affect cancer-related processes in the body. We tested this in an experimental study, where women aged 30-45 were randomly assigned to complete 16 weeks of exercise of varying intensity and duration. We hypothesized that higher levels of exercise would lead to changes in DNA methylation that would be associated with reduced cancer risk. Contrary to our hypotheses, we found that the total amount of exercise completed was not associated with changes in DNA methylation, though we did find that increases in VO(2)max, a marker of physical fitness, were associated with decreases in methylation of the BRCA1 gene, and higher levels of exercise during a follow-up period were associated with lower levels of methylation of the GALNT9 gene. This study provides preliminary evidence that increased exercise behavior or fitness may affect the methylation of some genes that are related to breast cancer. Emerging research suggests that one mechanism through which physical activity may decrease cancer risk is through its influence on the methylation of genes associated with cancer. The purpose of the current study was to prospectively test, using a rigorous experimental design, whether aerobic exercise affects DNA methylation in genes associated with breast cancer, as well as whether quantity of exercise completed affects change in DNA methylation in a dose-response manner. 276 women (M age = 37.25, SD = 4.64) were recruited from the Denver metro area for a randomized controlled trial in which participants were assigned to a supervised aerobic exercise program varying in a fully crossed design by intensity (55-65% versus 75-85% of VO(2)max) and duration (40 versus 20 min per session). DNA methylation was assessed via blood samples provided at baseline, after completing a 16-week supervised exercise intervention, and six months after the intervention. 137 participants completed the intervention, and 81 had viable pre-post methylation data. Contrary to our hypotheses, total exercise volume completed in kcal/kg/week was not associated with methylation from baseline to post-intervention for any of the genes of interest. An increase in VO(2)max over the course of the intervention, however, was associated with decreased post-intervention methylation of BRCA1, p = 0.01. Higher levels of self-reported exercise during the follow-up period were associated with lower levels of GALNT9 methylation at the six-month follow-up. This study provides hypothesis-generating evidence that increased exercise behavior and or increased fitness might affect methylation of some genes associated with breast cancer to reduce risk.
引用
收藏
页数:14
相关论文
共 61 条
[31]   Genetic polymorphisms in DNA repair genes XRCC1 and 3 are associated with increased risk of breast cancer in Bangladeshi population [J].
Howlader, Nupur Rani ;
Rahman, Md. Mostafizur ;
Hossain, Md. Amir ;
Sultana, Razia ;
Hossain, Syed Mozammel ;
Mazid, Md. Abdul ;
Rahman, Md. Mustafizur .
BREAST CANCER RESEARCH AND TREATMENT, 2020, 182 (03) :739-750
[32]   N-acetylgalactosaminyltransferases in cancer [J].
Hussain, Muhammad Ramzan Manwar ;
Hoessli, Daniel C. ;
Fang, Min .
ONCOTARGET, 2016, 7 (33) :54067-54081
[33]   DNA methylation marker to estimate the breast cancer cell fraction in DNA samples [J].
Ishihara, Hiroki ;
Yamashita, Satoshi ;
Fujii, Satoshi ;
Tanabe, Kazunari ;
Mukai, Hirofumi ;
Ushijima, Toshikazu .
MEDICAL ONCOLOGY, 2018, 35 (11)
[34]   The fundamental role of epigenetic events in cancer [J].
Jones, PA ;
Baylin, SB .
NATURE REVIEWS GENETICS, 2002, 3 (06) :415-428
[35]   Inhibition of breast cancer growth and invasion by single-minded 2s [J].
Kwak, Hyeong-Il ;
Gustafson, Tanya ;
Metz, Richard P. ;
Laffin, Brian ;
Schedin, Pepper ;
Porter, Weston W. .
CARCINOGENESIS, 2007, 28 (02) :259-266
[36]   RUNX3 is frequently inactivated by dual mechanisms of protein mislocalization and promoter hypermethylation in breast cancer [J].
Lau, Quek Choon ;
Raja, Erna ;
Salto-Terez, Manuel ;
Liu, Qiang ;
Ito, Kosei ;
Inoue, Masafumi ;
Putti, Thomas Choudary ;
Loh, Marie ;
Ko, Tun Kiat ;
Huang, Canhua ;
Bhalla, Kapil N. ;
Zhu, Tao ;
Ito, Yoshiaki ;
Sukumar, Saraswati .
CANCER RESEARCH, 2006, 66 (13) :6512-6520
[37]  
Lynch BM, 2011, RECENT RESULTS CANC, V186, P13, DOI 10.1007/978-3-642-04231-7_2
[38]   Methylation Landscape of Human Breast Cancer Cells in Response to Dietary Compound Resveratrol [J].
Medina-Aguilar, Rubiceli ;
Perez-Plasencia, Carlos ;
Marchat, Laurence A. ;
Gariglio, Patricio ;
Garcia Mena, Jaime ;
Rodriguez Cuevas, Sergio ;
Ruiz-Garcia, Erika ;
Astudillo-de la Vega, Horacio ;
Hernandez Juarez, Jennifer ;
Flores-Perez, Ali ;
Lopez-Camarillo, Cesar .
PLOS ONE, 2016, 11 (06)
[39]   Physical activity and breast cancer - A systematic review [J].
Monninkhof, Evelyn M. ;
Elias, Sjoerd G. ;
Vlems, Femke A. ;
van der Tweel, Ingeborg ;
Schuit, A. Jantine ;
Voskuil, Dorien W. ;
van Leeuwen, Flora E. .
EPIDEMIOLOGY, 2007, 18 (01) :137-157
[40]  
Nakajima N, 2009, INT J SPORTS MED, V30, P1