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ABSTRACT: Purpose
The aim of this study was to evaluate whether upfront cellular enrichment via laser capture microdissection (LCM) is necessary for accurately quantifying predictive biomarkers in nonsmall cell lung cancer tumors.Experimental design
Fifteen snap frozen surgical biopsies were analyzed. Whole tissue lysate and matched highly enriched tumor epithelium via LCM were obtained for each patient. The expression and activation/phosphorylation levels of 26 proteins were measured by reverse phase protein microarray. Differences in signaling architecture of dissected and undissected matched pairs were visualized using unsupervised clustering analysis, bar graphs, and scatter plots.Results
Overall patient matched LCM and undissected material displayed very distinct and dif
SUBMITTER: Baldelli E
PROVIDER: S-EPMC4547918 | biostudies-literature | 2015 Oct
REPOSITORIES: biostudies-literature