UPLC-MS/MS-based metabolomic characterization and comparison of pancreatic adenocarcinoma tissues using formalin-fixed, paraffin-embedded and optimal cutting temperature-embedded materials

被引:3
|
作者
Feng, Di [1 ]
Yuan, Jing [2 ]
Liu, Qi [3 ]
Liu, Li [4 ]
Zhang, Xu [1 ]
Wu, Yali [1 ]
Qian, Yifan [1 ]
Chen, Liping [1 ]
Shi, Yan [5 ]
Gu, Mancang [1 ]
机构
[1] Zhejiang Chinese Med Univ, Coll Pharmaceut Sci, 4A119 Gaoke Rd, Hangzhou 311402, Zhejiang, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Dept Pathol, Beijing 100853, Peoples R China
[3] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21231 USA
[4] Huazhong Univ Sci & Technol, Sch Publ Hlth, Dept Epidemiol & Biostat, Minist Educ,Key Lab Environm & Hlth, Wuhan 430030, Hubei, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R China
基金
中国国家自然科学基金;
关键词
clinical metabolic profiling; FFPE tissues; OCT-embedded tissues; pancreatic cancer; UPLC-MS; metabolic pathway enrichment analysis; NUCLEAR-MAGNETIC-RESONANCE; CANCER; METABOLITES; CREATININE; CYTOSCAPE; DIAGNOSIS; SUBTYPES; PATHWAYS; PLATFORM; PROLINE;
D O I
10.3892/ijo.2019.4898
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of the present study was to compare metabolites from formalin-fixed and paraffin-embedded (FFPE) pancreatic tissue blocks with those identified in optimal cutting temperature (OCT)-embedded pancreatic tissue blocks. Thus, ultra-performance liquid chromatograph-mass spectrometry/mass spectrometry-based metabolic profiling was performed in paired frozen (n=13) and FFPE (n=13) human pancreatic adenocarcinoma tissue samples, in addition to their benign counterparts. A total of 206 metabolites were identified in both OCT-embedded and FFPE tissue samples. The method feasibility was confirmed through reproducibility and a consistency assessment. Partial least-squares discriminant analysis and heatmap analysis reliably distinguished tumor and normal tissue phenotypes. The expression of 10 compounds, including N-acetylaspartate and creatinine, was significantly different in both OCT-embedded and FFPE tumor samples. These ten compounds may be viable candidate biomarkers of malignant pancreatic tissues. The super-categories to which they belonged exhibited no significant differences between FFPE and OCT-embedded samples. Furthermore, purine, arginine and proline, and pyrimidine metabolism used a shared pathway found in both OCT-embedded and FFPE tissue samples. These results supported the notion that metabolomic data acquired from FFPE pancreatic cancer specimens are reliable for use in retrospective and clinical studies.
引用
收藏
页码:1249 / 1260
页数:12
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