Journal
JOURNAL OF PEDIATRIC SURGERY
Volume 41, Issue 1, Pages 245-251Publisher
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.jpedsurg.2005.10.048
Keywords
neuroblastoma; secretory neuropeptides; serum deprivation; oxidative stress; biomarkers
Categories
Funding
- NCI NIH HHS [CA83199, CA57350] Funding Source: Medline
- NATIONAL CANCER INSTITUTE [R01CA057350, R01CA083199] Funding Source: NIH RePORTER
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Background: Differentially expressed neuroblastoma (NB) proteins are vital for the development of new diagnostics and therapeutics. For example, secretory NB peptides (neuron-specific enolase and chromogranins) are clinically useful. We investigated polypeptide secretion by employing proteomic technologies to analyze proteins released from cultured NB cells. Methods: Neuroblastoma cell lines (SK-N-AS, SK-N-DZ, and SK--N-Fl) were grown in serum-free media. Conditioned media from each cell line was analyzed for secreted proteins by 2-dimensional polyacrylamide gel electrophoresis. Selected polypeptides were identified by liquid chromatography-linked tandem mass spectrometry. Results: We identified 5 polypeptides that were secreted or shed by NIB. Ubiquitin, beta(2)-microglobulin, insulin-like growth factor binding protein-2, superoxide dismutase (copper and zinc), and heat shock cognate 70-kd proteins were secreted from NB cells, as compared with control media. Elevated levels of these proteins have been described in serum/tissues under intracellular stress and malignancies, including NB. Conclusion: These novel secretory polypeptides may contribute to NB growth. The proteins may reveal additional tumor markers and permit putative use in the diagnosis and treatment of NB. Detection of these proteins in serum of children with NB vs controls (Using 2-dimensional polyacrylamide gel electrophoresis and mass spectrometry techniques) is currently in progress. (c) 2006 Elsevier inc. All rights reserved.
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