Ontology highlight
ABSTRACT: Aim
To analyze proteomic and signal transduction alterations in irradiated melanoma cells.Methods
We combined stable isotope labeling with amino acids in cell culture (SILAC) with highly sensitive shotgun tandem mass spectrometry (MS) to create an efficient approach for protein quantification. Protein-protein interaction was used to analyze relationships among proteins.Results
Energy metabolism protein levels were significantly different in glycolysis and not significantly different in oxidative phosphorylation after irradiation. Conversely, tumor suppressor proteins related to cell growth and development were downregulated, and those related to cell death and cell cycle were upregulated in irradiated cells.Conclusion
Our results indicate that irradiation in
SUBMITTER: Yan LB
PROVIDER: S-EPMC3693007 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature