LFA-1 on leukemic cells as a target for therapy or drug delivery

  • Rungsinee Phongpradist
  • , Chuda Chittasupho
  • , Siriporn Okonogi
  • , Teruna Siahaan
  • , Songyot Anuchapreeda
  • , Chadarat Ampasavate
  • , Cory Berkland

Research output: Contribution to journalReview articlepeer-review

23 Scopus citations

Abstract

Leukemia therapeutics are aiming for improved efficacy by targeting molecular markers differentially expressed on cancerous cells. Lymphocyte function-associated antigen-1 (LFA-1) expression on various types of leukemia has been well studied. Here, the role and expression of LFA-1 on leukemic cells and the possibility of using this integrin as a target for drug delivery is reviewed. To support this rationale, experimental results were also included where cIBR, a cyclic peptide derived from a binding site of LFA-1, was conjugated to the surface of polymeric nanoparticles and used as a targeting ligand. These studies revealed a correlation of LFA-1 expression level on leukemic cell lines and binding and internalization of cIBR-NPs suggesting a differential binding and internalization of cIBR-NPs to leukemic cells overexpressing LFA-1. Nanoparticles conjugated with a cyclic peptide against an accessible molecular marker of disease hold promise as a selective drug delivery system for leukemia treatment.

Original languageEnglish
Pages (from-to)2321-2330
Number of pages10
JournalCurrent Pharmaceutical Design
Volume16
Issue number21
DOIs
StatePublished - 2010

Keywords

  • HL-60 cell line
  • Leukemia
  • LFA-1
  • Molt-3 cell line
  • Molt-4 cell line
  • Nanoparticles
  • Peptide
  • Targeting
  • U937 cell line

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