Ischemia in tumors induces early and sustained phosphorylation changes in stress kinase pathways but does not affect global protein levels Journal Article


Authors: Mertins, P.; Yang, F.; Liu, T.; Mani, D. R.; Petyuk, V. A.; Gillette, M. A.; Clauser, K. R.; Qiao, J. W.; Gritsenko, M. A.; Moore, R. J.; Levine, D. A.; Townsend, R.; Erdmann-Gilmore, P.; Snider, J. E.; Davies, S. R.; Ruggles, K. V.; Fenyo, D.; Kitchens, R. T.; Li, S.; Olvera, N.; Dao, F.; Rodriguez, H.; Chan, D. W.; Liebler, D.; White, F.; Rodland, K. D.; Mills, G. B.; Smith, R. D.; Paulovich, A. G.; Ellis, M.; Carr, S. A.
Article Title: Ischemia in tumors induces early and sustained phosphorylation changes in stress kinase pathways but does not affect global protein levels
Abstract: Protein abundance and phosphorylation convey important information about pathway activity and molecular pathophysiology in diseases including cancer, providing biological insight, informing drug and diagnostic development, and guiding therapeutic intervention. Analyzed tissues are usually collected without tight regulation or documentation of ischemic time. To evaluate the impact of ischemia, we collected human ovarian tumor and breast cancer xenograft tissue without vascular interruption and performed quantitative proteomics and phosphoproteomics after defined ischemic intervals. Although the global expressed proteome and most of the >25,000 quantified phosphosites were unchanged after 60 min, rapid phosphorylation changes were observed in up to 24% of the phosphoproteome, representing activation of critical cancer pathways related to stress response, transcriptional regulation, and cell death. Both pan-tumor and tissuespecific changes were observed. The demonstrated impact of pre-analytical tissue ischemia on tumor biology mandates caution in interpreting stress-pathway activation in such samples and motivates reexamination of collection protocols for phosphoprotein analysis. © 2014 by The American Society for Biochemistry and Molecular Biology, Inc.
Journal Title: Molecular & Cellular Proteomics
Volume: 13
Issue: 7
ISSN: 1535-9476
Publisher: Amer Soc Biochemistry Molecular Biology Inc  
Date Published: 2014-07-01
Start Page: 1690
End Page: 1704
Language: English
DOI: 10.1074/mcp.M113.036392
PROVIDER: scopus
PMCID: PMC4083109
PUBMED: 24719451
DOI/URL:
Notes: Cited By (since 1996):1 -- Export Date: 1 August 2014 -- CODEN: MCPOB -- Source: Scopus
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  1. Douglas A Levine
    380 Levine
  2. Narciso Olvera
    73 Olvera
  3. Fanny Dao
    59 Dao