Protein Signature of Lung Cancer Tissues

Michael R. Mehan(SomaLogic (United States)), Deborah Ayers(SomaLogic (United States)), Derek Thirstrup(University of Washington), Wei Xiong(University of Washington), Rachel Ostroff(SomaLogic (United States)), Edward N. Brody(SomaLogic (United States)), Jeffrey J. Walker(SomaLogic (United States)), Larry Gold(SomaLogic (United States)), Thale C. Jarvis(SomaLogic (United States)), Nebojša Janjić(SomaLogic (United States)), Geoffrey S. Baird(University of Washington), Sheri K. Wilcox(SomaLogic (United States))
PLoS ONE
April 11, 2012
Cited by 90Open Access
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Abstract

Lung cancer remains the most common cause of cancer-related mortality. We applied a highly multiplexed proteomic technology (SOMAscan) to compare protein expression signatures of non small-cell lung cancer (NSCLC) tissues with healthy adjacent and distant tissues from surgical resections. In this first report of SOMAscan applied to tissues, we highlight 36 proteins that exhibit the largest expression differences between matched tumor and non-tumor tissues. The concentrations of twenty proteins increased and sixteen decreased in tumor tissue, thirteen of which are novel for NSCLC. NSCLC tissue biomarkers identified here overlap with a core set identified in a large serum-based NSCLC study with SOMAscan. We show that large-scale comparative analysis of protein expression can be used to develop novel histochemical probes. As expected, relative differences in protein expression are greater in tissues than in serum. The combined results from tissue and serum present the most extensive view to date of the complex changes in NSCLC protein expression and provide important implications for diagnosis and treatment.


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