Proteomics of dedifferentiation of SK-N-BE2 neuroblastoma cells
Proteomics
0301 basic medicine
Proteome
Nuclear Proteins
Nerve Tissue Proteins
DNA-Activated Protein Kinase
Cell Dedifferentiation
Mass Spectrometry
Neoplasm Proteins
3. Good health
Neuroblastoma
03 medical and health sciences
Neural Stem Cells
Tissue Array Analysis
Cell Line, Tumor
Spheroids, Cellular
Biomarkers, Tumor
Neoplastic Stem Cells
Humans
Protein Interaction Maps
DOI:
10.1016/j.bbrc.2014.10.065
Publication Date:
2014-10-18T05:47:53Z
AUTHORS (6)
ABSTRACT
Neuroblastoma develops through processes which include cellular dedifferentiation. Ability of tumors to form spheroids is one of the manifestations of dedifferentiation and carcinogenic transformation. To study mechanisms of dedifferentiation of neuroblastoma cells, we generated spheroids and performed a proteomics study to compare the spheroids with parental SK-N-BE2 cells. We observed that dedifferentiation induced extensive changes in the proteome profiles of the cells, which affected more than 30% of detected cellular proteins. Using mass spectrometry, we identified 239 proteins affected by dedifferentiation into spheroids as compared to the parental cells. These proteins represented such regulatory processes as transcription, cell cycle regulation, apoptosis, cell adhesion, metabolism, intracellular transport, stress response, and angiogenesis. A number of potent regulators of stemness, differentiation and cancer were detected as subnetworks formed by the identified proteins. Our validation tissue microarray study of 30 neuroblastoma cases confirmed that two of the identified proteins, DISC1 and DNA-PKcs, had their expression increased in advanced malignancies. Thus, our report unveiled extensive changes of the cellular proteome upon dedifferentiation of neuroblastoma cells, indicated top subnetworks and clusters of molecular mechanisms involved in dedifferentiation, and provided candidate biomarkers for clinical studies.
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CITATIONS (4)
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