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Proteomics of dedifferentiation of SK-N-BE2 neuroblastoma cells

Authors :
Claire da Silva Santos
Serhiy Souchelnytskyi
Justyna Kolakowska
Keiko Funa
Sanaz Attarha
Ravi Kanth Rao Saini
Source :
Repositório Institucional da UFBA, Universidade Federal da Bahia (UFBA), instacron:UFBA
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

Texto completo: acesso restrito. p.202–209 Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2015-03-25T14:53:45Z No. of bitstreams: 1 Ravi Kanth Rao Saini.pdf: 2117613 bytes, checksum: 95cbb30ce4af03fc5ef8925bde8aeb65 (MD5) Approved for entry into archive by Delba Rosa (delba@ufba.br) on 2015-03-30T11:56:06Z (GMT) No. of bitstreams: 1 Ravi Kanth Rao Saini.pdf: 2117613 bytes, checksum: 95cbb30ce4af03fc5ef8925bde8aeb65 (MD5) Made available in DSpace on 2015-03-30T11:56:06Z (GMT). No. of bitstreams: 1 Ravi Kanth Rao Saini.pdf: 2117613 bytes, checksum: 95cbb30ce4af03fc5ef8925bde8aeb65 (MD5) Previous issue date: 2014 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.

Details

ISSN :
0006291X
Volume :
454
Database :
OpenAIRE
Journal :
Biochemical and Biophysical Research Communications
Accession number :
edsair.doi.dedup.....d27ee8db6aa398e03cb3ac242a026eb2
Full Text :
https://doi.org/10.1016/j.bbrc.2014.10.065