Direct quantification of gene expression in homogenates of formalin-fixed, paraffin-embedded tissues. (April 2006)

• Record Type: Journal Article
• Authors: Yang, Wen; Maqsodi, Botoul; Ma, Yunqing; Bui, Son; Crawford, Kimberly L.; McMaster, Gary K.; Witney, Frank; Luo, Yuling
• Is Part Of: Biotechniques. Volume 40:Number 4(2006)
• Page Start: 481
• Page End: 486
• Publication Date: 2006-04
• Subjects: Biology, Experimental -- Periodicals; Molecular biology -- Periodicals; Medical technology -- Periodicals; Biology, Experimental; Medical technology; Molecular biology; Clinical Laboratory Techniques -- Periodicals; Research -- Periodicals; Medical Laboratory Science -- Periodicals; Periodicals; Electronic journals; 570
• DOI: 10.2144/000112133
• Languages: English
• ISSNs: 0736-6205

Abstract

Formalin-fixed, paraffin-embedded (FFPE) tissues represent an important source of archival materials for gene expression profiling. We report here the development of a modified branch DNA assay that allows direct quantification of messenger RNA (mRNA) transcripts in homogenates from FFPE tissue sections without the need for RNA isolation and reverse transcription into cDNA. Formalin fixation essentially has no effect on the branch DNA assay, and RNA degradation only marginally reduces the signal by 2- to 3-fold. Under the same conditions, formalin fixation and RNA degradation greatly reduces real-time reverse transcription PCR (RT-PCR) efficiency, reducing signals by as much as 15- and 1400-fold, respectively. Although both technologies can generate biologically meaningful expression profiles from FFPE human lung tumor specimens, the branch DNA assay is more sensitive than real-time RT-PCR under the conditions tested. Our results therefore suggest that the branch DNA assay is an ideal tool for retrospective analysis of gene expression in archival tissues.