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EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC
Overexpression of epidermal growth factor receptor (EGFR) is closely associated with a poor prognosis in non-small cell lung cancer (NSCLC), thus making it a promising biomarker for NSCLC diagnosis. Here, we conjugated a single-chain antibody (scFv) targeting EGFR with Fe(3)O(4)/Au nanoparticles to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902179/ https://www.ncbi.nlm.nih.gov/pubmed/33624188 http://dx.doi.org/10.1007/s10334-021-00916-1 |
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author | Lu, Yuan Huang, Jing Li, Fakai Wang, Yuan Ding, Ming Zhang, Jian Yin, Hong Zhang, Rui Ren, Xinling |
author_facet | Lu, Yuan Huang, Jing Li, Fakai Wang, Yuan Ding, Ming Zhang, Jian Yin, Hong Zhang, Rui Ren, Xinling |
author_sort | Lu, Yuan |
collection | PubMed |
description | Overexpression of epidermal growth factor receptor (EGFR) is closely associated with a poor prognosis in non-small cell lung cancer (NSCLC), thus making it a promising biomarker for NSCLC diagnosis. Here, we conjugated a single-chain antibody (scFv) targeting EGFR with Fe(3)O(4)/Au nanoparticles to form an EGFR-specific molecular MRI bioprobe (scFv@Fe(3)O(4)/Au) to better detect EGFR-positive NSCLC tumors in vivo. In vitro, we demonstrated that the EGFR-specific scFv could specifically deliver Fe(3)O(4)/Au to EGFR-positive NSCLC cells. In vivo experiments showed that the accumulation of scFv@Fe(3)O(4)/Au in tumor tissue was detectable by magnetic resonance imaging (MRI) at the indicated time points after systemic injection. The T2W signal-to-noise ratio (SNR) of EGFR-positive SPC-A1 tumors was significantly decreased after scFv@Fe(3)O(4)/Au injection, which was not observed in the tumors of mice injected with BSA@Fe(3)O(4)/Au. Furthermore, transmission electron microscopy (TEM) analysis showed the specific localization of scFv@Fe(3)O(4)/Au in the SPC-A1 tumor cell cytoplasm. Collectively, the results of our study demonstrated that scFv@Fe(3)O(4)/Au might be a useful probe for the noninvasive diagnosis of EGFP-positive NSCLC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10334-021-00916-1. |
format | Online Article Text |
id | pubmed-7902179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-79021792021-02-24 EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC Lu, Yuan Huang, Jing Li, Fakai Wang, Yuan Ding, Ming Zhang, Jian Yin, Hong Zhang, Rui Ren, Xinling MAGMA Research Article Overexpression of epidermal growth factor receptor (EGFR) is closely associated with a poor prognosis in non-small cell lung cancer (NSCLC), thus making it a promising biomarker for NSCLC diagnosis. Here, we conjugated a single-chain antibody (scFv) targeting EGFR with Fe(3)O(4)/Au nanoparticles to form an EGFR-specific molecular MRI bioprobe (scFv@Fe(3)O(4)/Au) to better detect EGFR-positive NSCLC tumors in vivo. In vitro, we demonstrated that the EGFR-specific scFv could specifically deliver Fe(3)O(4)/Au to EGFR-positive NSCLC cells. In vivo experiments showed that the accumulation of scFv@Fe(3)O(4)/Au in tumor tissue was detectable by magnetic resonance imaging (MRI) at the indicated time points after systemic injection. The T2W signal-to-noise ratio (SNR) of EGFR-positive SPC-A1 tumors was significantly decreased after scFv@Fe(3)O(4)/Au injection, which was not observed in the tumors of mice injected with BSA@Fe(3)O(4)/Au. Furthermore, transmission electron microscopy (TEM) analysis showed the specific localization of scFv@Fe(3)O(4)/Au in the SPC-A1 tumor cell cytoplasm. Collectively, the results of our study demonstrated that scFv@Fe(3)O(4)/Au might be a useful probe for the noninvasive diagnosis of EGFP-positive NSCLC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10334-021-00916-1. Springer International Publishing 2021-02-24 2021 /pmc/articles/PMC7902179/ /pubmed/33624188 http://dx.doi.org/10.1007/s10334-021-00916-1 Text en © European Society for Magnetic Resonance in Medicine and Biology (ESMRMB) 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Research Article Lu, Yuan Huang, Jing Li, Fakai Wang, Yuan Ding, Ming Zhang, Jian Yin, Hong Zhang, Rui Ren, Xinling EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC |
title | EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC |
title_full | EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC |
title_fullStr | EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC |
title_full_unstemmed | EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC |
title_short | EGFR-specific single-chain variable fragment antibody-conjugated Fe(3)O(4)/Au nanoparticles as an active MRI contrast agent for NSCLC |
title_sort | egfr-specific single-chain variable fragment antibody-conjugated fe(3)o(4)/au nanoparticles as an active mri contrast agent for nsclc |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902179/ https://www.ncbi.nlm.nih.gov/pubmed/33624188 http://dx.doi.org/10.1007/s10334-021-00916-1 |
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