Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy

Shih-Heng Tseng,1,2 Min-Yuan Chou,2 I-Ming Chu1 1Department of Chemical Engineering, National Tsing Hua University, 2Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan Abstract: We have developed a theranostic nanoparticle, ie, cet-PEG...

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Main Authors: Tseng SH, Chou MY, Chu IM
Format: Article
Language:English
Published: Dove Medical Press 2015-05-01
Series:International Journal of Nanomedicine
Online Access:http://www.dovepress.com/cetuximab-conjugated-iron-oxide-nanoparticles-for-cancer-imaging-and-t-peer-reviewed-article-IJN
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spelling doaj-957e22a807544480b2882f0db0d869012020-11-24T21:19:52ZengDove Medical PressInternational Journal of Nanomedicine1178-20132015-05-012015default3663368521825Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapyTseng SHChou MYChu IMShih-Heng Tseng,1,2 Min-Yuan Chou,2 I-Ming Chu1 1Department of Chemical Engineering, National Tsing Hua University, 2Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan Abstract: We have developed a theranostic nanoparticle, ie, cet-PEG-dexSPIONs, by conjugation of the anti-epidermal growth factor receptor (EGFR) monoclonal antibody, cetuximab, to dextran-coated superparamagnetic iron oxide nanoparticles (SPIONs) via periodate oxidation. Approximately 31 antibody molecules were conjugated to each nanoparticle. Cet-PEG-dexSPIONs specifically bind to EGFR-expressing tumor cells and enhance image contrast on magnetic resonance imaging. Cet-PEG-dexSPION-treated A431 cells showed significant inhibition of epidermal growth factor-induced EGFR phosphorylation and enhancement of EGFR internalization and degradation. In addition, a significant increase in apoptosis was detected in EGFR-overexpressing cell lines, A431 and 32D/EGFR, after 24 hours of incubation at 37°C with cet-PEG-dexSPIONs compared with cetuximab alone. The antibody-dependent cell-mediated cytotoxicity of cetuximab was observed in cet-PEG-dexSPIONs. The results demonstrated that cet-PEG-dexSPIONs retained the therapeutic effect of cetuximab in addition to having the ability to target and image EGFR-expressing tumors. Cet-PEG-dexSPIONs represent a promising targeted magnetic probe for early detection and treatment of EGFR-expressing tumor cells. Keywords: epidermal growth factor receptor, cetuximab, superparamagnetic iron oxide nanoparticle, magnetic resonance imaging, sodium periodate, polyethylene glycolhttp://www.dovepress.com/cetuximab-conjugated-iron-oxide-nanoparticles-for-cancer-imaging-and-t-peer-reviewed-article-IJN
collection DOAJ
language English
format Article
sources DOAJ
author Tseng SH
Chou MY
Chu IM
spellingShingle Tseng SH
Chou MY
Chu IM
Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
International Journal of Nanomedicine
author_facet Tseng SH
Chou MY
Chu IM
author_sort Tseng SH
title Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
title_short Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
title_full Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
title_fullStr Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
title_full_unstemmed Cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
title_sort cetuximab-conjugated iron oxide nanoparticles for cancer imaging and therapy
publisher Dove Medical Press
series International Journal of Nanomedicine
issn 1178-2013
publishDate 2015-05-01
description Shih-Heng Tseng,1,2 Min-Yuan Chou,2 I-Ming Chu1 1Department of Chemical Engineering, National Tsing Hua University, 2Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan Abstract: We have developed a theranostic nanoparticle, ie, cet-PEG-dexSPIONs, by conjugation of the anti-epidermal growth factor receptor (EGFR) monoclonal antibody, cetuximab, to dextran-coated superparamagnetic iron oxide nanoparticles (SPIONs) via periodate oxidation. Approximately 31 antibody molecules were conjugated to each nanoparticle. Cet-PEG-dexSPIONs specifically bind to EGFR-expressing tumor cells and enhance image contrast on magnetic resonance imaging. Cet-PEG-dexSPION-treated A431 cells showed significant inhibition of epidermal growth factor-induced EGFR phosphorylation and enhancement of EGFR internalization and degradation. In addition, a significant increase in apoptosis was detected in EGFR-overexpressing cell lines, A431 and 32D/EGFR, after 24 hours of incubation at 37°C with cet-PEG-dexSPIONs compared with cetuximab alone. The antibody-dependent cell-mediated cytotoxicity of cetuximab was observed in cet-PEG-dexSPIONs. The results demonstrated that cet-PEG-dexSPIONs retained the therapeutic effect of cetuximab in addition to having the ability to target and image EGFR-expressing tumors. Cet-PEG-dexSPIONs represent a promising targeted magnetic probe for early detection and treatment of EGFR-expressing tumor cells. Keywords: epidermal growth factor receptor, cetuximab, superparamagnetic iron oxide nanoparticle, magnetic resonance imaging, sodium periodate, polyethylene glycol
url http://www.dovepress.com/cetuximab-conjugated-iron-oxide-nanoparticles-for-cancer-imaging-and-t-peer-reviewed-article-IJN
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AT chuim cetuximabconjugatedironoxidenanoparticlesforcancerimagingandtherapy
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