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首页> 外文期刊>Integrative cancer therapies. >Effects of Steady Low-Intensity Exercise on High-Fat Diet Stimulated Breast Cancer Progression Via the Alteration of Macrophage Polarization
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Effects of Steady Low-Intensity Exercise on High-Fat Diet Stimulated Breast Cancer Progression Via the Alteration of Macrophage Polarization

机译:通过巨噬细胞极化的改变,稳定低强度运动对高脂饮食刺激乳腺癌进展的影响

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Physical inactivity and high-fat diet, especially high saturated fat containing diet are established risk factors for breast cancer that are amenable to intervention. High-fat diet has been shown to induce tumor growth and metastasis by alteration of inflammation but steady exercise has anti-tumorigenic effects. However, the mechanisms underlying the effects of physical activity on high-fat diet stimulated breast cancer initiation and progression are currently unclear. In this study, we examined how the intensity of physical activity influences high fat diet-stimulated breast cancer latency and progression outcomes, and the possible mechanisms behind these effects. Five-week-old female Balb/c mice were fed either a control diet or a high-fat diet for 8?weeks, and then 4T1 mouse mammary tumor cells were inoculated into the mammary fat pads. Exercise training occurred before tumor cell injection, and tumor latency and tumor volume were measured. Mice with a high-fat diet and low-intensity exercise (HFLE) had a longer tumor latency period, slower tumor growth, and smaller tumor volume in the final tumor assessment compared with the control, high-fat diet control (HFDC), and high-fat diet with moderate-intensity exercise (HFME) groups. Steady low- and moderate-intensity exercise had no effect on cell proliferation but induced apoptosis by activating caspase-3 through the alteration of Bcl-2, Bcl-xL, and Bax expression. Furthermore, steady exercise reduced M2 macrophage polarization in breast tumor tissue, which has been linked to tumor growth. The myokine, myostatin, reduced M2 macrophage polarization through the inhibition of the JAK-STAT signaling pathway. These results suggest that steady low-intensity exercise could delay breast cancer initiation and growth and reduce tumor volume through the induction of tumor cell apoptosis and the suppression of M2 macrophage polarization.
机译:物理不活跃和高脂饮食,尤其是含有高饱和脂肪的饮食,是患有干预的乳腺癌的危险因素。已经显示高脂饮食通过改变炎症,但稳定的运动具有抗致瘤效果。然而,目前尚不清楚身体活动对高脂饮食刺激乳腺癌发起和进展的影响。在这项研究中,我们研究了身体活性强度如何影响高脂肪饮食刺激的乳腺癌潜伏期和进展结果,以及这些效果背后的可能机制。将五周龄雌性BALB / C小鼠喂食控制饮食或高脂饮食8?周,然后将4T1小鼠乳腺肿瘤细胞接种到乳腺脂肪垫中。在肿瘤细胞注射之前发生运动训练,并测量肿瘤潜伏期和肿瘤体积。具有高脂饮食和低强度运动(HFLE)的小鼠具有更长的肿瘤潜伏期,肿瘤生长较慢,并且与对照,高脂饮食(HFDC)相比,最终肿瘤评估中的肿瘤增长较慢,肿瘤体积较小高脂饮食,具有中等强度运动(HFME)组。稳定的低和中等强度运动对细胞增殖没有影响,但通过通过Bcl-2,Bcl-XL和Bax表达的改变激活Caspase-3诱导细胞凋亡。此外,稳定运动减少了乳腺肿瘤组织中的M2巨噬细胞极化,与肿瘤生长有关。 Myokine,Myostatin,通过抑制Jak-Stat信号通路来减少M2巨噬细胞极化。这些结果表明,稳定的低强度运动可以通过诱导肿瘤细胞凋亡和抑制M2巨噬细胞极化来延迟乳腺癌引发和生长并降低肿瘤量。

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