Effects of a Particular Heptapeptide on the IFN-α-Sensitive CML Cells

Biomed Res Int. 2015:2015:325026. doi: 10.1155/2015/325026. Epub 2015 Sep 1.

Abstract

Using the phage display biopanning technique, we have previously identified a heptapeptide KLWVIPQ which specifically binds to the surface of the IFN-α-sensitive but not the IFN-α-resistant CML cells. The effects of this heptapeptide on the IFN-α-sensitive CML cells were investigated in the present study. IFN-α-sensitive KT-1/A3 and IFN-α-resistant KT-1/A3R CML cells were transfected by pEGFP-KLWVIPQ expression vector and/or induced by IFN-α. WST-1 cell proliferation assay, flow cytometry, and western blotting were performed to determine the effects of this heptapeptide and/or IFN-α on CML cells. The viability of the KT-1/A3 cells was inhibited and apoptosis was induced by either expression of the heptapeptide KLWVIPQ or IFN-α treatment with concurrent upregulation of P53 and downregulation of P210(bcr/abl). However, these effects were not observed in the IFN-α-resistant KT-1/A3R cells. These results suggest that the heptapeptide KLWVIPQ shares a similar mechanism with IFN-α in the regulation of CML cell growth and apoptosis, implying that the heptapeptide KLWVIPQ could be a novel target to go further into mechanisms of IFN-α sensitivity and/or resistance in CML.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Gene Expression Regulation, Leukemic / drug effects
  • Genetic Vectors / metabolism
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Interferon-alpha / pharmacology*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology*
  • Molecular Sequence Data
  • Oligopeptides / chemistry
  • Oligopeptides / pharmacology*
  • Plasmids / metabolism
  • Recombination, Genetic / genetics
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Interferon-alpha
  • Oligopeptides
  • Tumor Suppressor Protein p53
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins