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High SOD and low GPX activities in RBC predict susceptibility of lung cancer patients to radiation pneumonitis

机译:红细胞中高SOD和低GPX活性预测肺癌患者易患放射性肺炎

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摘要

Radiation pneumonitis is an unpredictable complication of radiotherapy for lung cancer and a condition which can cause significant morbidity. The ability to identify patients at a high risk of developing pneumonitis is critical, since it will enable the individualization of the treatment plan. Because the cytotoxic effect of radiation is propagated through ROS and ROS-driven oxidative stress, the role of anti-oxidant defense systems in radiation pneumonitis was investigated. Using the pneumonitis-sensitive C3H/HeN mice as a model, we demonstrated that the anti-oxidant response of the lung correlated well with that of RBC. We then proceeded to test whether differences of RBC anti-oxidant response would predict the pneumonitis development in patients. SOD, GPX, CAT activities and glutathione in RBC were measured at baseline and then weekly for 6 weeks of treatment in fifteen eligible patients receiving concurrent chemo-radiotherapy for unresectable stage III NSCLC. Striking differences were found in the anti-oxidant activities of RBC with respect to the pneumonitis development. Those who developed pneumonitis showed higher SOD and lower GPX activities at baseline compared to those who did not (3.7 vs. 6.8 unit/mg for median SOD, 16.5 vs. 10.7 nmol/min/mg for median GPX). The functional imbalance of SOD and GPX was displayed consistently throughout the treatment period. The sensitivity and specificity of pneumonitis prediction were further increased when the GPX/SOD ratio was analyzed (pre-treatment P = 0.0046). Our results provide a strong rationale to monitor SOD and GPX activities of RBC to identify patients who are at risk of developing pneumonitis, and to implement a strategy of increasing the GPX/SOD ratio in order to lower the risk.
机译:放射性肺炎是肺癌放疗的不可预见的并发症,是一种可能导致重大发病的疾病。识别患肺炎高风险患者的能力至关重要,因为这将使治疗计划个性化。由于辐射的细胞毒性作用是通过ROS和ROS驱动的氧化应激传播的,因此研究了抗氧化防御系统在放射性肺炎中的作用。使用对肺炎敏感的C3H / HeN小鼠作为模型,我们证明了肺部的抗氧化反应与RBC的相关性很好。然后,我们继续测试RBC抗氧化反应的差异是否可以预测患者的肺炎发展。在基线时测量RBC中的SOD,GPX,CAT活性和谷胱甘肽,然后在15例接受同时放疗的不可切除的III期NSCLC的合格患者中,每周治疗6周。关于肺炎的发展,在RBC的抗氧化活性方面发现了惊人的差异。与未发生肺炎的人相比,发生肺炎的人在基线时表现出更高的SOD和更低的GPX活性(中值SOD为3.7 vs. 6.8单位/ mg,中值GPX为16.5 vs. 10.7 nmol / min / mg)。在整个治疗期间,SOD和GPX的功能失衡情况始终如一。当分析GPX / SOD比率时,肺炎预测的敏感性和特异性进一步提高(治疗前P = 0.0046)。我们的结果为监测RBC的SOD和GPX活性提供了有力的依据,以识别有发展为肺炎风险的患者,并实施提高GPX / SOD比值的策略以降低风险。

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