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Comparison of mouse urinary metabolic profiles after exposure to the inflammatory stressors γ radiation and lipopolysaccharide.比较γ射线和脂多糖刺激后小鼠尿液代谢谱的变化。
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UPLC-MS-based urine metabolomics reveals indole-3-lactic acid and phenyllactic acid as conserved biomarkers for alcohol-induced liver disease in the Ppara-null mouse model.基于 UPLC-MS 的尿液代谢组学研究揭示了吲哚-3-乳酸和苯乳酸作为 Ppara 基因敲除小鼠模型酒精性肝病的保守生物标志物。
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基于质谱的代谢组学鉴定出可预测辐射诱发癌症的纵向尿液代谢物谱。

Mass Spectrometry-Based Metabolomics Identifies Longitudinal Urinary Metabolite Profiles Predictive of Radiation-Induced Cancer.

作者信息

Cook John A, Chandramouli Gadisetti V R, Anver Miriam R, Sowers Anastasia L, Thetford Angela, Krausz Kristopher W, Gonzalez Frank J, Mitchell James B, Patterson Andrew D

机构信息

Radiation Biology Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Pathology/Histotechnology Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland.

出版信息

Cancer Res. 2016 Mar 15;76(6):1569-77. doi: 10.1158/0008-5472.CAN-15-2416. Epub 2016 Feb 15.

DOI:10.1158/0008-5472.CAN-15-2416
PMID:26880804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4794383/
Abstract

Nonlethal exposure to ionizing radiation (IR) is a public concern due to its known carcinogenic effects. Although latency periods for IR-induced neoplasms are relatively long, the ability to detect cancer as early as possible is highly advantageous for effective therapeutic intervention. Therefore, we hypothesized that metabolites in the urine from mice exposed to total body radiation (TBI) would predict for the presence of cancer before a palpable mass was detected. In this study, we exposed mice to 0 or 5.4 Gy TBI, collected urine samples periodically over 1 year, and assayed urine metabolites by using mass spectrometry. Longitudinal data analysis within the first year post-TBI revealed that cancers, including hematopoietic, solid, and benign neoplasms, could be distinguished by unique urinary signatures as early as 3 months post-TBI. Furthermore, a distinction among different types of malignancies could be clearly delineated as early as 3 months post-TBI for hematopoietic neoplasms, 6 months for solid neoplasms, and by 1 year for benign neoplasms. Moreover, the feature profile for radiation-exposed mice 6 months post-TBI was found to be similar to nonirradiated control mice at 18 months, suggesting that TBI accelerates aging. These results demonstrate that urine feature profiles following TBI can identify cancers in mice prior to macroscopic detection, with important implications for the early diagnosis and treatment.

摘要

由于已知电离辐射(IR)具有致癌作用,非致死性暴露于电离辐射成为一个公众关注的问题。尽管IR诱发肿瘤的潜伏期相对较长,但尽早检测出癌症对于有效的治疗干预极为有利。因此,我们推测,全身辐射(TBI)小鼠尿液中的代谢产物能够在可触及肿块被检测到之前预测癌症的存在。在本研究中,我们将小鼠暴露于0或5.4 Gy的TBI,在1年的时间里定期收集尿液样本,并使用质谱法分析尿液代谢产物。TBI后第一年的纵向数据分析显示,早在TBI后3个月,包括造血、实体和良性肿瘤在内的癌症就可以通过独特的尿液特征进行区分。此外,早在TBI后3个月对于造血肿瘤、6个月对于实体肿瘤以及1年后对于良性肿瘤,就可以清晰地划分不同类型恶性肿瘤之间的差异。而且,发现TBI后6个月的辐射暴露小鼠的特征谱与18个月的未受辐射对照小鼠相似,这表明TBI会加速衰老。这些结果表明,TBI后的尿液特征谱能够在宏观检测之前识别小鼠中的癌症,这对于早期诊断和治疗具有重要意义。