摘要:在乳腺癌小鼠模型中,热量限制和垂直袖胃切除术后肿瘤生长的代谢内分泌和炎症相关

Tori L. McFarlane, Kristina K Camp, Elaine M Glenny, Erika T Rezeli, Michael F. Coleman, S. Hursting
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引用次数: 0

摘要

乳腺癌是美国女性癌症相关死亡的第二大原因,而肥胖是公认的乳腺癌风险和进展因素。因此,确定有效打破肥胖与癌症之间联系的干预措施非常重要。本临床前项目旨在比较饮食和手术减肥后肥胖小鼠的循环细胞因子和代谢内分泌激素水平,以确定可能影响肿瘤质量结果的血清标志物。在整个研究过程中,20只对照雌性C57BL/6小鼠保持10 kcal%脂肪饮食。所有其他小鼠被放置在60千卡%的饮食中15周,以促进饮食诱导肥胖(DIO),然后随机接受:a)垂直袖胃切除术(VSG)同时切换到对照饮食(16只小鼠);b)假手术和继续DIO方案(18只小鼠);c)假手术转换为慢性卡路里限制(CCR);每日热量减少30%)方案(16只小鼠);d)假手术,改用间歇性卡路里限制(ICR);每周5天卡路里减少14%,每周2天卡路里减少70%)方案(19只小鼠)。在减肥干预10周后,收集禁食动物的血清,分析葡萄糖(通过血糖仪)、细胞因子(通过BioRad小鼠细胞因子23-plex面板在BioRad MAGPIX仪器上)和激素(BioRad小鼠糖尿病8-plex面板),以表征E0771乳腺癌细胞原位移植前的全身代谢内分泌和炎症环境。与DIO小鼠相比,手术或饮食减肥降低了典型由肥胖引起的血清细胞因子,包括白细胞介素6 (IL-6)、白细胞介素2 (IL-2)和肿瘤坏死因子α (tnf - α)。与VSG小鼠相比,CCR和ICR小鼠血清中只有循环趋化因子配体13 (CXCL13)显著降低。此外,与VSG小鼠相比,CCR和ICR小鼠的空腹血糖水平和循环纤溶酶原激活物抑制剂-1 (PAI-1)均显著降低。因此,这些数据表明,降低循环CXCL13、PAI-1和/或降低空腹血糖可能有助于CCR和ICR优于VSG的抗肿瘤作用。本研究得到了R35CA197627 to S. Hursting的支持。引文格式:Tori L. McFarlane, Kristina Kalevas Camp, Elaine M. Glenny, Erika Rezeli, Michael F. Coleman, Stephen D. Hursting。在乳腺癌小鼠模型中,热量限制和垂直袖胃切除术后肿瘤生长的代谢内分泌和炎症相关性[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):2577。
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Abstract 2577: Metaboendocrine and inflammatory correlates of tumor growth following caloric restriction and vertical sleeve gastrectomy in a mouse model of breast cancer
Breast cancer is the second leading cause of cancer-related deaths in women living in the United States, and obesity is a well-established breast cancer risk and progression factor. Identifying interventions that effectively break the obesity-cancer link is therefore of great importance. This preclinical project aims to compare circulating cytokine and metaboendocrine hormone levels in formerly obese mice following dietary and surgical weight loss to identify serum markers potentially contributing to differential tumor mass outcomes. 20 control female C57BL/6 mice were maintained on a 10 kcal% fat diet throughout the study. All other mice were placed on a 60 kcal% diet for 15 weeks to promote diet-induced obesity (DIO), then randomized to receive either: a) vertical sleeve gastrectomy (VSG) with concurrent switch to control diet (16 mice); b) sham surgery and continuation of DIO regimen (18 mice); c) sham surgery with switch to a chronic calorie restricted (CCR; 30% daily calorie reduction) regimen (16 mice); or d) sham surgery with switch to an intermittent calorie restricted (ICR; 14% calorie reduction 5 days per week, 70% calorie reduction 2 non-consecutive days per week) regimen (19 mice). Following 10 weeks of weight loss interventions, serum from fasted animals was collected, and glucose (by glucometer), cytokines (by BioRad Mouse Cytokine 23-plex panel on a BioRad MAGPIX Instrument), and hormones (BioRad Mouse Diabetes 8-plex panel) were analyzed to characterize the systemic metaboendocrine and inflammatory environment immediately prior to orthotopic transplantation of E0771 mammary cancer cells. Surgical or dietary weight loss reduced serum cytokines that are classically induced by obesity, including interleukin 6 (IL-6), interleukin 2 (IL-2), and tumor necrosis factor alpha (TNFα), compared with DIO mice. Compared with VSG mice, only circulating chemokine ligand 13 (CXCL13) was significantly lower in serum from both CCR and ICR mice. Moreover, CCR and ICR mice displayed significantly lower fasting blood glucose levels and circulating plasminogen activator inhibitor-1 (PAI-1) compared with VSG mice. Therefore, these data suggest that decreased circulating CXCL13, PAI-1 and/or decreased fasted blood glucose may contribute to the superior antitumor effects of CCR and ICR versus VSG. This research was supported by R35CA197627 to S. Hursting. Citation Format: Tori L. McFarlane, Kristina Kalevas Camp, Elaine M. Glenny, Erika Rezeli, Michael F. Coleman, Stephen D. Hursting. Metaboendocrine and inflammatory correlates of tumor growth following caloric restriction and vertical sleeve gastrectomy in a mouse model of breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2577.
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