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Peptide aptamer identified by molecular docking targeting translationally controlled tumor protein in leukemia cells.

Abstract
Bioinformatics screening and molecular docking analyses were utilized to select high affinity peptides targeting translationally controlled tumor protein (TCTP). Selected peptide aptamers were tested towards cancer cell lines with different levels of TCTP expression. One peptide (WGQWPYHC) revealed specific cytotoxicity according to the TCTP expression in tumor cells without affecting normal cells. Western blot analysis showed peptide-induced down-regulation of TCTP as primary target as well as of cell-cycle related downstream proteins (CDK2, CDK6, Cyclin D3) in MOLT-4 leukemia cells. "WGQWPYHC" deserves further analysis for targeted therapy of TCTP-expressing tumor cells. Graphical abstract Molecular docking on TCTP, cytotoxicity toward MOLT-4 leukemia cell line and downregulation of CDK2, CDK6, CyclinD3 and TCTP proteins.
AuthorsOnat Kadioglu, Thomas Efferth
JournalInvestigational new drugs (Invest New Drugs) Vol. 34 Issue 4 Pg. 515-21 (08 2016) ISSN: 1573-0646 [Electronic] United States
PMID26972431 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Aptamers, Peptide
  • Biomarkers, Tumor
  • RNA, Small Interfering
  • TPT1 protein, human
  • Tumor Protein, Translationally-Controlled 1
Topics
  • Antineoplastic Agents (pharmacology)
  • Aptamers, Peptide (pharmacology)
  • Biomarkers, Tumor (genetics, metabolism)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Humans
  • Leukemia (drug therapy, metabolism)
  • Molecular Docking Simulation
  • RNA, Small Interfering
  • Tumor Protein, Translationally-Controlled 1

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