HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Anticancer peptide CIGB-300 binds to nucleophosmin/B23, impairs its CK2-mediated phosphorylation, and leads to apoptosis through its nucleolar disassembly activity.

Abstract
CIGB-300, formerly known as P15-tat, is a proapoptotic peptide with established antiproliferative activity in vitro and antitumoral activity in vivo. This hypothesis-driven peptide was initially selected for its ability to impair the in vitro CK2-mediated phosphorylation in one of its substrates through direct binding to the conserved acidic phosphoaceptor domain. However, the actual in vivo target(s) on human cancer cells among the hundreds of CK2 substrates as well as the subsequent events that lead to apoptosis on tumor cells remains to be determined. In this work, we identified the multifunctional oncoprotein nucleophosmin/B23 as a major target for CIGB-300. In vivo, the CIGB-300-B23 interaction was shown by pull-down experiments and confirmed by the early in situ colocalization of both molecules in the cell nucleolus. Moreover, CIGB-300 inhibits the CK2-mediated phosphorylation of B23 in a dose-dependent fashion both in vitro and in vivo as shown using the recombinant GST fusion protein and the metabolic labeling approach, respectively. Such phosphorylation impairment was correlated with the ability of CIGB-300 to induce nucleolar disassembly as documented by the use of established markers for nucleolar structure. Finally, we showed that such a sequence of events leads to the rapid and massive onset of apoptosis both at the molecular and cellular levels. Collectively, these findings provide important clues by which the CIGB-300 peptide exerts its proapoptotic effect on tumor cells and highlights the suitability of the B23/CK2 pathway for cancer-targeted therapy.
AuthorsYasser Perera, Hernán G Farina, Jeovanis Gil, Arielis Rodriguez, Fernando Benavent, Lila Castellanos, Roberto E Gómez, Boris E Acevedo, Daniel F Alonso, Silvio E Perea
JournalMolecular cancer therapeutics (Mol Cancer Ther) Vol. 8 Issue 5 Pg. 1189-96 (May 2009) ISSN: 1538-8514 [Electronic] United States
PMID19417160 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Biomarkers, Tumor
  • NPM1 protein, human
  • Nuclear Proteins
  • Peptides, Cyclic
  • Phosphoproteins
  • phosphoprotein C23
  • Nucleophosmin
  • Casein Kinase II
  • CIGB-300
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Biomarkers, Tumor
  • Casein Kinase II (metabolism)
  • Cell Line, Tumor
  • Cell Nucleolus (metabolism)
  • Humans
  • Intracellular Space
  • Molecular Targeted Therapy
  • Nuclear Proteins (metabolism)
  • Nucleophosmin
  • Peptides, Cyclic (chemical synthesis, metabolism, pharmacology)
  • Phosphoproteins (metabolism)
  • Phosphorylation (drug effects)
  • Protein Binding
  • Protein Transport
  • Small Cell Lung Carcinoma (pathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: