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Hypoxia-targeted gold nanorods for cancer photothermal therapy

Tumor hypoxia is a well-recognized driver of resistance to traditional cancer therapies such as chemotherapy and radiation therapy. We describe development of a new nanoconstruct composed of gold nanorods (GNRs) conjugated to carbonic anhydrase IX (CAIX) antibody that specifically binds to CAIX, a b...

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Autores principales: Chen, Yuan, Bian, Xiaomei, Aliru, Maureen, Deorukhkar, Amit A., Ekpenyong, Oscar, Liang, Su, John, Jyothy, Ma, Jing, Gao, Xiuqing, Schwartz, Jon, Singh, Pankaj, Ye, Yuanqing, Krishnan, Sunil, Xie, Huan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995181/
https://www.ncbi.nlm.nih.gov/pubmed/29899876
http://dx.doi.org/10.18632/oncotarget.25492
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author Chen, Yuan
Bian, Xiaomei
Aliru, Maureen
Deorukhkar, Amit A.
Ekpenyong, Oscar
Liang, Su
John, Jyothy
Ma, Jing
Gao, Xiuqing
Schwartz, Jon
Singh, Pankaj
Ye, Yuanqing
Krishnan, Sunil
Xie, Huan
author_facet Chen, Yuan
Bian, Xiaomei
Aliru, Maureen
Deorukhkar, Amit A.
Ekpenyong, Oscar
Liang, Su
John, Jyothy
Ma, Jing
Gao, Xiuqing
Schwartz, Jon
Singh, Pankaj
Ye, Yuanqing
Krishnan, Sunil
Xie, Huan
author_sort Chen, Yuan
collection PubMed
description Tumor hypoxia is a well-recognized driver of resistance to traditional cancer therapies such as chemotherapy and radiation therapy. We describe development of a new nanoconstruct composed of gold nanorods (GNRs) conjugated to carbonic anhydrase IX (CAIX) antibody that specifically binds to CAIX, a biomarker of hypoxia, to facilitate targeting tumor hypoxic areas for focused photothermal ablation. Physicochemical characterization studies confirmed the size, shape, monodispersity, surface charge, and serum stability of the GNRs. Enzyme-linked immunosorbent assays and cellular binding and uptake studies confirmed successful conjugation of antibody to the GNRs and specificity for CAIX. Near-infrared irradiation of CAIX-overexpressing cells treated with GNR/anti-CAIX resulted in significantly higher cell death than cells treated with control GNRs. In vivo biodistribution studies using hyperspectral imaging and inductively coupled plasma mass spectrometry confirmed intravenous administration results not only in greater accumulation of GNR/anti-CAIX in tumors than control GNRs but also greater penetration into hypoxic areas of tumors. Near-infrared ablation of these tumors showed no tumor regression in the sham-treated group, regression but recurrence in the non-targeted-GNR group, and complete tumor regression in the targeted-GNR group. GNR/anti-CAIX nanoconstructs show promise as hypoxia targeting and photothermal ablation agents for cancer treatment.
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spelling pubmed-59951812018-06-13 Hypoxia-targeted gold nanorods for cancer photothermal therapy Chen, Yuan Bian, Xiaomei Aliru, Maureen Deorukhkar, Amit A. Ekpenyong, Oscar Liang, Su John, Jyothy Ma, Jing Gao, Xiuqing Schwartz, Jon Singh, Pankaj Ye, Yuanqing Krishnan, Sunil Xie, Huan Oncotarget Research Paper Tumor hypoxia is a well-recognized driver of resistance to traditional cancer therapies such as chemotherapy and radiation therapy. We describe development of a new nanoconstruct composed of gold nanorods (GNRs) conjugated to carbonic anhydrase IX (CAIX) antibody that specifically binds to CAIX, a biomarker of hypoxia, to facilitate targeting tumor hypoxic areas for focused photothermal ablation. Physicochemical characterization studies confirmed the size, shape, monodispersity, surface charge, and serum stability of the GNRs. Enzyme-linked immunosorbent assays and cellular binding and uptake studies confirmed successful conjugation of antibody to the GNRs and specificity for CAIX. Near-infrared irradiation of CAIX-overexpressing cells treated with GNR/anti-CAIX resulted in significantly higher cell death than cells treated with control GNRs. In vivo biodistribution studies using hyperspectral imaging and inductively coupled plasma mass spectrometry confirmed intravenous administration results not only in greater accumulation of GNR/anti-CAIX in tumors than control GNRs but also greater penetration into hypoxic areas of tumors. Near-infrared ablation of these tumors showed no tumor regression in the sham-treated group, regression but recurrence in the non-targeted-GNR group, and complete tumor regression in the targeted-GNR group. GNR/anti-CAIX nanoconstructs show promise as hypoxia targeting and photothermal ablation agents for cancer treatment. Impact Journals LLC 2018-05-29 /pmc/articles/PMC5995181/ /pubmed/29899876 http://dx.doi.org/10.18632/oncotarget.25492 Text en Copyright: © 2018 Chen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Yuan
Bian, Xiaomei
Aliru, Maureen
Deorukhkar, Amit A.
Ekpenyong, Oscar
Liang, Su
John, Jyothy
Ma, Jing
Gao, Xiuqing
Schwartz, Jon
Singh, Pankaj
Ye, Yuanqing
Krishnan, Sunil
Xie, Huan
Hypoxia-targeted gold nanorods for cancer photothermal therapy
title Hypoxia-targeted gold nanorods for cancer photothermal therapy
title_full Hypoxia-targeted gold nanorods for cancer photothermal therapy
title_fullStr Hypoxia-targeted gold nanorods for cancer photothermal therapy
title_full_unstemmed Hypoxia-targeted gold nanorods for cancer photothermal therapy
title_short Hypoxia-targeted gold nanorods for cancer photothermal therapy
title_sort hypoxia-targeted gold nanorods for cancer photothermal therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995181/
https://www.ncbi.nlm.nih.gov/pubmed/29899876
http://dx.doi.org/10.18632/oncotarget.25492
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