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Housing temperature-induced stress drives therapeutic resistance in murine tumour models through β2-adrenergic receptor activation

机译:外壳温度诱导的应激通过β2-肾上腺素能受体的活化驱动鼠类肿瘤模型的治疗抗性

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摘要

Cancer research relies heavily on murine models for evaluating the anti-tumour efficacy of therapies. Here we show that the sensitivity of several pancreatic tumour models to cytotoxic therapies is significantly increased when mice are housed at a thermoneutral ambient temperature of 30 °C compared with the standard temperature of 22 °C. Further, we find that baseline levels of norepinephrine as well as the levels of several anti-apoptotic molecules are elevated in tumours from mice housed at 22 °C. The sensitivity of tumours to cytotoxic therapies is also enhanced by administering a β-adrenergic receptor antagonist to mice housed at 22 °C. These data demonstrate that standard housing causes a degree of cold stress sufficient to impact the signalling pathways related to tumour-cell survival and affect the outcome of pre-clinical experiments. Furthermore, these data highlight the significant role of host physiological factors in regulating the sensitivity of tumours to therapy.
机译:癌症研究严重依赖鼠类模型来评估治疗方法的抗肿瘤功效。在这里,我们显示,当小鼠被放置在30°C的热中性环境温度下时,与标准温度22°C相比,几种胰腺肿瘤模型对细胞毒性疗法的敏感性显着提高。此外,我们发现在22°C饲养的小鼠的肿瘤中,去甲肾上腺素的基线水平以及几种抗凋亡分子的水平均升高。通过对22℃下饲养的小鼠施用β-肾上腺素能受体拮抗剂,还可以增强肿瘤对细胞毒性疗法的敏感性。这些数据表明,标准外壳会引起一定程度的冷应激,足以影响与肿瘤细胞存活相关的信号传导途径,并影响临床前实验的结果。此外,这些数据突出了宿主生理因素在调节肿瘤对治疗敏感性中的重要作用。

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