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Dissecting Target Toxic Tissue and Tissue Specific Responses of Irinotecan in Rats Using Metabolomics Approach

机译:用代谢组学方法解剖大鼠伊利替康的目标毒性组织和组织特异性反应

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摘要

As an anticancer agent, irinotecan (CPT-11) has been widely applied in clinical, especially in the treatment of colorectal cancer. However, its clinical use has long been limited by the side effects and potential tissue toxicity. To discriminate the target toxic tissues and dissect the specific response of target tissues after CPT-11 administration in rats, untargeted metabolomic study was conducted. First, differential metabolites between CPT-11 treated group and control group in each tissue were screened out. Then, based on fold changes of these differential metabolites, principal component analysis and hierarchical cluster analysis were performed to visualize the degree and specificity of the influences of CPT-11 on the metabolic profiles of nine tissues. Using this step-wise method, ileum, jejunum, and liver were finally recognized as target toxic tissues. Furthermore, tissue specific responses of liver, ileum, and jejunum to CPT-11 were dissected and specific differential metabolites were screened out. Perturbations in Krebs cycle, amino acid, purine and bile acid metabolism were observed in target toxic tissues. In conclusion, our study put forward a new approach to dissect target toxic tissues and tissue specific responses of CPT-11 using metabolomics.
机译:伊立替康(CPT-11)作为抗癌剂已广泛应用于临床,特别是在结直肠癌的治疗中。但是,其临床应用长期以来一直受到副作用和潜在的组织毒性的限制。为了区分目标毒性组织并解剖大鼠CPT-11后的靶组织特异性反应,进行了非目标代谢组学研究。首先,筛选出各组织中CPT-11治疗组和对照组之间的差异代谢产物。然后,根据这些差异代谢产物的倍数变化,进行主成分分析和层次聚类分析,以可视化CPT-11对9种组织代谢谱的影响程度和特异性。使用这种逐步方法,回肠,空肠和肝脏最终被识别为目标毒性组织。此外,解剖了肝脏,回肠和空肠对CPT-11的组织特异性反应,并筛选出特定的差异代谢物。在靶毒性组织中观察到克雷布斯循环,氨基酸,嘌呤和胆汁酸代谢的扰动。总之,我们的研究提出了一种新的方法来利用代谢组学研究靶标毒性组织和CPT-11的组织特异性反应。

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