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Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations

The early and specific detection of tumors remains a barrier in oncology, especially in cases such as the triple-negative breast cancer (TNBC). To address this gap, aptamers have found an important application in the recognition of tumor biomarkers such as mucin 1 (MUC1). However, there are still so...

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Autores principales: Santos do Carmo, Fagner, Ricci-Junior, Eduardo, Cerqueira-Coutinho, Cristal, Albernaz, Marta de Souza, Bernardes, Emerson Soares, Missailidis, Sotiris, Santos-Oliveira, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5191850/
https://www.ncbi.nlm.nih.gov/pubmed/28053523
http://dx.doi.org/10.2147/IJN.S118482
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author Santos do Carmo, Fagner
Ricci-Junior, Eduardo
Cerqueira-Coutinho, Cristal
Albernaz, Marta de Souza
Bernardes, Emerson Soares
Missailidis, Sotiris
Santos-Oliveira, Ralph
author_facet Santos do Carmo, Fagner
Ricci-Junior, Eduardo
Cerqueira-Coutinho, Cristal
Albernaz, Marta de Souza
Bernardes, Emerson Soares
Missailidis, Sotiris
Santos-Oliveira, Ralph
author_sort Santos do Carmo, Fagner
collection PubMed
description The early and specific detection of tumors remains a barrier in oncology, especially in cases such as the triple-negative breast cancer (TNBC). To address this gap, aptamers have found an important application in the recognition of tumor biomarkers such as mucin 1 (MUC1). However, there are still some difficulties in the use of aptamer, as their rapid biological clearance makes their use as drugs limited. In this study, the anti-MUC1 aptamer was used as a drug delivery system (DDS) for a radioactive polymeric nanoparticle (NP) in the imaging of TNBCs. Thus, poly(lactic-co-glycolic acid) NPs loaded with the anti-MUC1 aptamer and labeled with technetium-99m were used for a biodistribution study and imaging of TNBC. The results confirmed that the NP was successfully obtained, with a mean size of 262 nm, according to the dynamic light scattering data. The biodistribution assay in induced animal models with TNBC showed that although there was a high capture by intestine (>30%), the DDS developed had a high tumor uptake (5%) and with great in vivo imaging properties, corroborating the possibility of use of this DDS as an imaging drug for TNBC.
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spelling pubmed-51918502017-01-04 Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations Santos do Carmo, Fagner Ricci-Junior, Eduardo Cerqueira-Coutinho, Cristal Albernaz, Marta de Souza Bernardes, Emerson Soares Missailidis, Sotiris Santos-Oliveira, Ralph Int J Nanomedicine Original Research The early and specific detection of tumors remains a barrier in oncology, especially in cases such as the triple-negative breast cancer (TNBC). To address this gap, aptamers have found an important application in the recognition of tumor biomarkers such as mucin 1 (MUC1). However, there are still some difficulties in the use of aptamer, as their rapid biological clearance makes their use as drugs limited. In this study, the anti-MUC1 aptamer was used as a drug delivery system (DDS) for a radioactive polymeric nanoparticle (NP) in the imaging of TNBCs. Thus, poly(lactic-co-glycolic acid) NPs loaded with the anti-MUC1 aptamer and labeled with technetium-99m were used for a biodistribution study and imaging of TNBC. The results confirmed that the NP was successfully obtained, with a mean size of 262 nm, according to the dynamic light scattering data. The biodistribution assay in induced animal models with TNBC showed that although there was a high capture by intestine (>30%), the DDS developed had a high tumor uptake (5%) and with great in vivo imaging properties, corroborating the possibility of use of this DDS as an imaging drug for TNBC. Dove Medical Press 2016-12-19 /pmc/articles/PMC5191850/ /pubmed/28053523 http://dx.doi.org/10.2147/IJN.S118482 Text en © 2017 do Carmo et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Santos do Carmo, Fagner
Ricci-Junior, Eduardo
Cerqueira-Coutinho, Cristal
Albernaz, Marta de Souza
Bernardes, Emerson Soares
Missailidis, Sotiris
Santos-Oliveira, Ralph
Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
title Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
title_full Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
title_fullStr Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
title_full_unstemmed Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
title_short Anti-MUC1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
title_sort anti-muc1 nano-aptamers for triple-negative breast cancer imaging by single-photon emission computed tomography in inducted animals: initial considerations
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5191850/
https://www.ncbi.nlm.nih.gov/pubmed/28053523
http://dx.doi.org/10.2147/IJN.S118482
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