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Updated: Jan 19, 2026

Proteomic Sample Preparation from Formalin Fixed and Paraffin Embedded Tissue
Published on: September 2, 2013
High-throughput proteomic analysis of FFPE tissue samples facilitates tumor stratification
Yi Zhu1,2,3, Tobias Weiss4, Qiushi Zhang1,2
1Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou, China.
This study presents a robust proteomic method for analyzing formalin-fixed, paraffin-embedded (FFPE) tissues, demonstrating their superiority over fresh-frozen samples for biomarker discovery in prostate cancer and lymphoma.
Area of Science:
- Biochemistry
- Proteomics
- Cancer Research
Background:
- Formalin-fixed, paraffin-embedded (FFPE) tissues are crucial for clinical research.
- Analyzing FFPE tissue proteomes presents unique challenges.
Purpose of the Study:
- To develop and validate a proteomic workflow for FFPE tissues.
- To compare FFPE and fresh-frozen (FF) tissue proteomes.
- To discover novel biomarkers for prostate cancer (PCa) and diffuse large B-cell lymphoma (DLBCL).
Main Methods:
- Pressure cycling technology (PCT)-SWATH mass spectrometry workflow.
- Analysis of FFPE and FF tissue samples from PCa and DLBCL cohorts.
- Assessment of proteome stability and similarity in FFPE samples.
Main Results:
- High proteome similarity between FFPE and FF PCa samples.
- Consistent protein regulation in PCa tissues confirmed.
- Temporal stability of FFPE proteome patterns demonstrated (1-15 years).
- High similarity between FFPE biopsy and section proteomes.
- Myeloperoxidase identified as a novel prognostic marker for DLBCL.
Conclusions:
- PCT-SWATH is a robust method for FFPE tissue proteomic analysis.
- FFPE tissues are practical and superior to FF tissues for proteome biomarker discovery.
- Novel biomarker candidates for PCa and DLBCL were identified.
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