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Targeting the IKKβ/mTOR/VEGF Signaling Pathway as a Potential Therapeutic Strategy for Obesity-Related Breast Cancer

机译:靶向IKKβ/ mTOR的/ VEGF信号通路作为一种潜在的治疗策略与肥胖相关的乳腺癌

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摘要

Clinical correlation studies have clearly shown that obesity is associated with breast cancer risk and patient survival. Although several potential mechanisms linking obesity and cancers have been proposed, the detailed molecular mechanism of obesity-mediated breast tumorigenesis has not yet been critically evaluated. In this study, we evaluated the effects of obesity on mammary tumor initiation and progression using mice with genetic and diet-induced obesity bearing mammary tumor xenografts and mouse mammary tumor virusneu transgenic mice that were fed a high-fat diet. We show that obesity promoted mammary tumor growth and development in these animal models. Moreover, the expressions of TNFα, VEGF, IKKβ, and mTOR are upregulated in mammary tumors of obese mice, suggesting that the IKKβ/ mTOR/VEGF signaling pathway is activated by TNFα in the tumors of obese mice. More importantly, inhibitors (rapamycin, bevacizumab, and aspirin) that target members of the pathway suppressed tumorigenesis and prolonged survival more effectively in obese mice than in nonobese mice. Here, we not only identified a specific signaling pathway that contributes to mammary tumorigenesis in obese mice but also a strategy for treating obesity-mediated breast cancer.
机译:临床相关研究清楚地表明,肥胖与乳腺癌风险和患者生存率有关。尽管已经提出了几种将肥胖与癌症联系起来的潜在机制,但是肥胖介导的乳腺肿瘤发生的详细分子机制尚未得到严格的评估。在这项研究中,我们使用具有高脂饮食的遗传和饮食诱发肥胖的携带乳腺肿瘤异种移植物的小鼠和小鼠乳腺肿瘤病毒中性基因转基因小鼠,评估了肥胖对乳腺肿瘤起始和进展的影响。我们显示肥胖在这些动物模型中促进了乳腺肿瘤的生长和发育。此外,肥胖小鼠的乳腺肿瘤中TNFα,VEGF,IKKβ和mTOR的表达被上调,表明肥胖小鼠肿瘤中的IKKβ/ mTOR / VEGF信号传导途径被TNFα激活。更重要的是,与非肥胖小鼠相比,靶向该途径成员的抑制剂(雷帕霉素,贝伐单抗和阿司匹林)在肥胖小鼠中更有效地抑制了肿瘤发生并延长了生存期。在这里,我们不仅确定了导致肥胖小鼠乳腺肿瘤发生的特定信号通路,而且还提出了治疗肥胖介导的乳腺癌的策略。

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