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Proteomic profile regulated by the anticancer peptide CIGB-300 in non-small cell lung cancer (NSCLC) cells.

Abstract
CIGB-300 is a proapoptotic peptide-based drug that abrogates the CK2-mediated phosphorylation. This peptide has antineoplastic effect on lung cancer cells in vitro and in vivo. To understand the mechanisms involved on such anticancer activity, the NCI-H125 cell line proteomic profile after short-term incubation (45 min) with CIGB-300 was investigated. As determined by 2-DE or 2D-LC-MS/MS, 137 proteins changed their abundances more than 2-fold in response to the CIGB-300 treatment. The expression levels of proteins related to ribosome biogenesis, metastasis, cell survival and proliferation, apoptosis, and drug resistance were significantly modulated by the presence of CIGB-300. The protein translation process was the most affected (23% of the identified proteins). From the proteome analysis of the NCI-H125 cell line, novel potentialities for CIGB-300 as anticancer agent were evidenced.
AuthorsArielis Rodríguez-Ulloa, Yassel Ramos, Jeovanis Gil, Yasser Perera, Lila Castellanos-Serra, Yairet García, Lázaro Betancourt, Vladimir Besada, Luis J González, Jorge Fernández-de-Cossio, Aniel Sanchez, Joem M Serrano, Hernán Farina, Daniel F Alonso, Boris E Acevedo, Gabriel Padrón, Alexis Musacchio, Silvio E Perea
JournalJournal of proteome research (J Proteome Res) Vol. 9 Issue 10 Pg. 5473-83 (Oct 01 2010) ISSN: 1535-3907 [Electronic] United States
PMID20804217 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Peptides, Cyclic
  • Proteome
  • CIGB-300
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Carcinoma, Non-Small-Cell Lung (metabolism, pathology)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Cell Survival (drug effects)
  • Chromatography, Liquid
  • Cluster Analysis
  • Electrophoresis, Gel, Two-Dimensional
  • Humans
  • Lung Neoplasms (metabolism, pathology)
  • Mass Spectrometry
  • Peptides, Cyclic (pharmacology)
  • Protein Biosynthesis (drug effects)
  • Proteome (analysis, classification)
  • Proteomics (methods)

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