共 12 条
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.
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页码:1249 / 1260
页数:12
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