Jiang Weiqin, Zhu Zongjian, Thompson Henry J
Cancer Prevention Laboratory, Colorado State University, Fort Collins, CO 80523, USA.
Cancer Prev Res (Phila). 2009 Apr;2(4):338-44. doi: 10.1158/1940-6207.CAPR-08-0169. Epub 2009 Mar 31.
In the field of energetics and cancer, little attention has been given to whether energy balance directed interventions designed to regulate body weight by increasing energy expenditure versus reducing energy intake have an equivalent effect on the development of breast cancer. The objective of this experiment was to determine the effects on mammary carcinogenesis of physical activity (PA), achieved via running on an activity wheel, or restricted energy intake (RE). Food intake of PA and RE rats was controlled so that both groups had the same net energy balance determined by growth rate, which was 92% of the sedentary control group (SC). A total of 135 female Sprague-Dawley rats were injected with 1-methyl-1-nitrosourea (50 mg/kg) and 7 days thereafter were randomized to either SC, PA, or RE. Mammary cancer incidence was 97.8%, 88.9%, and 84.4% and cancer multiplicity was 3.66, 3.11, and 2.64 cancers/rat in SC, RE, and PA, respectively (SC versus PA, P = 0.02 for incidence and P = 0.03 for multiplicity). Analyses of mammary carcinomas revealed that cell proliferation-associated proteins were reduced and caspase-3 activity and proapoptotic proteins were elevated by PA or RE relative to SC (P < 0.05). It was observed that these effects may be mediated, in part, by activation of AMP-activated protein kinase and down-regulation of protein kinase B and the mammalian target of rapamycin.
在能量学与癌症领域,针对旨在通过增加能量消耗或减少能量摄入来调节体重的能量平衡导向干预措施对乳腺癌发展是否具有同等效果的关注甚少。本实验的目的是确定通过在活动轮上跑步实现的体力活动(PA)或限制能量摄入(RE)对乳腺癌发生的影响。对PA组和RE组大鼠的食物摄入量进行控制,以使两组基于生长速率的净能量平衡相同,该生长速率为久坐对照组(SC)的92%。总共135只雌性Sprague-Dawley大鼠注射1-甲基-1-亚硝基脲(50 mg/kg),7天后随机分为SC组、PA组或RE组。乳腺癌发病率在SC组、RE组和PA组中分别为97.8%、88.9%和84.4%,癌症多发性分别为3.66、3.11和2.64个癌症/大鼠(SC组与PA组相比,发病率P = 0.02,多发性P = 0.03)。对乳腺癌的分析显示,相对于SC组,PA组或RE组中与细胞增殖相关的蛋白减少,半胱天冬酶-3活性和促凋亡蛋白升高(P < 0.05)。据观察,这些效应可能部分由AMP激活的蛋白激酶的激活以及蛋白激酶B和雷帕霉素哺乳动物靶点的下调介导。