Time-Course Changes in Potential Biomarkers Detected Using a Metabonomic Approach in Walker 256 Tumor-Bearing Rats

被引:15
作者
Shen, Guoqing [1 ,2 ]
Chen, Yanhua [1 ,2 ]
Sun, Jianghao [1 ,2 ]
Zhang, Ruiping [1 ,2 ]
Zhang, Yi [1 ,2 ]
He, Jiuming [1 ,2 ]
Tian, Yaping [1 ,2 ]
Song, Yongmei [3 ,4 ]
Chen, Xiaoguang [1 ,2 ]
Abliz, Zeper [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, Minist Educ, Key Lab Bioact Subst & Resource Utilizat Chinese, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
[3] Chinese Acad Med Sci, Canc Inst & Canc Hosp, State Key Lab Mol Oncol, Beijing 100021, Peoples R China
[4] Peking Union Med Coll, Beijing 100021, Peoples R China
基金
中国国家自然科学基金;
关键词
metabonomics; time-course analysis; Walker; 256; tumor; biomarkers; reversed-phase liquid chromatography; hydrophilic interaction chromatography; MAGNETIC-RESONANCE-SPECTROSCOPY; PROSTATE-CANCER PROGRESSION; MASS-SPECTROMETRY; CREATINE-KINASE; CACHECTIC RATS; L-CARNITINE; METABOLOMICS; CARCINOMA; MODELS; URINE;
D O I
10.1021/pr101198q
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A metabonomic approach based on complementary hydrophilic interaction chromatography and reversed-phase liquid chromatography combined with tandem mass spectrometry and time-course analysis of metabolites was implemented to find more reliable potential biomarkers in urine of Walker 256 tumor-bearing rats. A major challenge in metabonomics is distinguishing reliable biomarkers that are closely associated with the genesis and progression of diseases from those that are unrelated but altered significantly. In this study, these biomarkers were selected according to the change trends of discriminating metabolites during the genesis and progression of cancer. Seven consecutive batches of urine samples from preinoculation to 16 days after were collected and analyzed. Multivariate analysis revealed 87 discriminating metabolites. Time-course analysis of discriminating metabolites was used to select more reliable biomarkers with regular and reasonable change trends. Finally, 47 were found and 15 were identified including 12 carnitine derivatives, 2 amino acid derivatives, 1 nucleoside. On the basis of time-course behaviors of these potential biomarkers, we hypothesize such disruption might result from elevated cell proliferation, reduced beta-oxidation of fatty acids, and poor renal tubular reabsorption. These studies demonstrate that this method can help to find more reliable potential biomarkers and provide valuable biochemical insights into metabolic alterations in tumor-bearing biosystems.
引用
收藏
页码:1953 / 1961
页数:9
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