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Briefings in Functional Genomics Advance Access originally published online on May 10, 2006
Briefings in Functional Genomics 2006 5(2):169-175; doi:10.1093/bfgp/ell017
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© The Author 2006. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

Technique Review

Unravelling the proteome of formalin-fixed paraffin-embedded tissue

Brian L. Hood, Thomas P. Conrads and Timothy D. Veenstra

Corresponding author. Timothy D. Veenstra, Laboratory of Proteomics and Analytical Technologies, National Cancer Institute at Frederick, SAIC-Frederick, Inc., PO. Box B, Frederick, MD 21702, USA. E-mail: veenstra{at}ncifcrf.gov

Biofluid detectable biomarkers that originate at the site of diseased tissues would be advantageous, in that, they may provide mechanistic information concerning the manifestation and progression of the disease. Unfortunately, tissue biopsies are precious samples that can generally be acquired in small amounts due to the invasive nature of the sample collection. One of the foundations of pathological diagnosis for decades has been from formalin-fixed paraffin-embedded (FFPE) tissues, of which a vast archive exists worldwide. These tissues have also been widely used for immunohistochemistry and in situ hybridization studies examining for expression of specific proteins or transcripts. Unfortunately, the ability to analyse FFPE tissues using mass spectrometry (MS) has been essentially non-existent until recently. In this review, methods that allow the extraction of peptides from FFPE tissues and their proteomic analysis using MS are described. The ability to identify the proteins extracted from FFPE tissues allows comparative analyses that enable the potential discovery of novel biomarkers at the site of the diseased tissue.

Keywords: biomarker discovery, formalin-fixed paraffin-embedded tissue, laser-capture microdissection, mass spectrometry, proteomics


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