Ma Huiyan, Xu Xinxin, Ursin Giske, Simon Michael S, Marchbanks Polly A, Malone Kathleen E, Lu Yani, McDonald Jill A, Folger Suzanne G, Weiss Linda K, Sullivan-Halley Jane, Deapen Dennis M, Press Michael F, Bernstein Leslie
Division of Cancer Etiology, Department of Population Sciences, Beckman Research Institute, City of Hope, Duarte, California, 91010.
Cancer Registry of Norway, PB 5313 Majorstuen, 0304, Oslo, Norway.
Cancer Med. 2015 Jul;4(7):1122-35. doi: 10.1002/cam4.465. Epub 2015 Apr 27.
Convincing epidemiologic evidence indicates that physical activity is inversely associated with breast cancer risk. Whether this association varies by the tumor protein expression status of the estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), or p53 is unclear. We evaluated the effects of recreational physical activity on risk of invasive breast cancer classified by the four biomarkers, fitting multivariable unconditional logistic regression models to data from 1195 case and 2012 control participants in the population-based Women's Contraceptive and Reproductive Experiences Study. Self-reported recreational physical activity at different life periods was measured as average annual metabolic equivalents of energy expenditure [MET]-hours per week. Our biomarker-specific analyses showed that lifetime recreational physical activity was negatively associated with the risks of ER-positive (ER+) and of HER2-negative (HER2-) subtypes (both Ptrend ≤ 0.04), but not with other subtypes (all Ptrend > 0.10). Analyses using combinations of biomarkers indicated that risk of invasive breast cancer varied only by HER2 status. Risk of HER2-breast cancer decreased with increasing number of MET-hours of recreational physical activity in each specific life period examined, although some trend tests were only marginally statistically significant (all Ptrend ≤ 0.06). The test for homogeneity of trends (HER2- vs. HER2+ ) reached statistical significance only when evaluating physical activity during the first 10 years after menarche (Phomogeneity = 0.03). Our data suggest that physical activity reduces risk of invasive breast cancers that lack HER2 overexpression, increasing our understanding of the biological mechanisms by which physical activity acts.
令人信服的流行病学证据表明,身体活动与乳腺癌风险呈负相关。这种关联是否因雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(HER2)或p53的肿瘤蛋白表达状态而异尚不清楚。我们评估了休闲身体活动对按这四种生物标志物分类的浸润性乳腺癌风险的影响,将多变量无条件逻辑回归模型应用于基于人群的女性避孕和生殖经历研究中1195例病例和2012例对照参与者的数据。不同生命时期自我报告的休闲身体活动以每周平均每年能量消耗代谢当量[MET]-小时来衡量。我们针对生物标志物的分析表明,终生休闲身体活动与ER阳性(ER+)和HER2阴性(HER2-)亚型的风险呈负相关(两者Ptrend≤0.04),但与其他亚型无关(所有Ptrend>0.10)。使用生物标志物组合的分析表明,浸润性乳腺癌风险仅因HER2状态而异。在每个特定生命时期,HER2-乳腺癌的风险随着休闲身体活动MET-小时数的增加而降低,尽管一些趋势检验仅具有边缘统计学意义(所有Ptrend≤0.06)。仅在评估初潮后前10年的身体活动时,趋势同质性检验(HER2-与HER2+)达到统计学意义(Phomogeneity=0.03)。我们的数据表明,身体活动可降低缺乏HER2过表达的浸润性乳腺癌的风险,增进了我们对身体活动作用的生物学机制的理解。