TY - JOUR
T1 - LFA-1 on leukemic cells as a target for therapy or drug delivery
AU - Phongpradist, Rungsinee
AU - Chittasupho, Chuda
AU - Okonogi, Siriporn
AU - Siahaan, Teruna
AU - Anuchapreeda, Songyot
AU - Ampasavate, Chadarat
AU - Berkland, Cory
PY - 2010
Y1 - 2010
N2 - 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.
AB - 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.
KW - HL-60 cell line
KW - Leukemia
KW - LFA-1
KW - Molt-3 cell line
KW - Molt-4 cell line
KW - Nanoparticles
KW - Peptide
KW - Targeting
KW - U937 cell line
UR - https://www.scopus.com/pages/publications/77955646154
U2 - 10.2174/138161210791920450
DO - 10.2174/138161210791920450
M3 - Review article
C2 - 20618153
AN - SCOPUS:77955646154
SN - 1381-6128
VL - 16
SP - 2321
EP - 2330
JO - Current Pharmaceutical Design
JF - Current Pharmaceutical Design
IS - 21
ER -