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BMC Genomics. 2008 May 23;9:246. doi: 10.1186/1471-2164-9-246.

Correlation of mRNA and protein levels: cell type-specific gene expression of cluster designation antigens in the prostate.

Author information

1
Department of Urology, University of Washington, Seattle WA 98195, USA. lpascal@systemsbiology.org

Abstract

BACKGROUND:

: Expression levels of mRNA and protein by cell types exhibit a range of correlations for different genes. In this study, we compared levels of mRNA abundance for several cluster designation (CD) genes determined by gene arrays using magnetic sorted and laser-capture microdissected human prostate cells with levels of expression of the respective CD proteins determined by immunohistochemical staining in the major cell types of the prostate - basal epithelial, luminal epithelial, stromal fibromuscular, and endothelial - and for prostate precursor/stem cells and prostate carcinoma cells. Immunohistochemical stains of prostate tissues from more than 50 patients were scored for informative CD antigen expression and compared with cell-type specific transcriptomes.

RESULTS:

: Concordance between gene and protein expression findings based on 'present' vs. 'absent' calls ranged from 46 to 68%. Correlation of expression levels was poor to moderate (Pearson correlations ranged from 0 to 0.63). Divergence between the two data types was most frequently seen for genes whose array signals exceeded background (> 50) but lacked immunoreactivity by immunostaining. This could be due to multiple factors, e.g. low levels of protein expression, technological sensitivities, sample processing, probe set definition or anatomical origin of tissue and actual biological differences between transcript and protein abundance.

CONCLUSION:

: Agreement between these two very different methodologies has great implications for their respective use in both molecular studies and clinical trials employing molecular biomarkers.

PMID:
18501003
PMCID:
PMC2413246
DOI:
10.1186/1471-2164-9-246
[Indexed for MEDLINE]
Free PMC Article
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