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Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes

Herein, we describe the preparation of liposomes with folate-targeting properties for the encapsulation of anti-sarcosine antibodies (antisarAbs@LIP) and sarcosine (sar@LIP). The competitive inhibitory effects of exogenously added folic acid supported the role of folate targeting in liposome interna...

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Autores principales: Heger, Zbynek, Polanska, Hana, Merlos Rodrigo, Miguel Angel, Guran, Roman, Kulich, Pavel, Kopel, Pavel, Masarik, Michal, Eckschlager, Tomas, Stiborova, Marie, Kizek, Rene, Adam, Vojtech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028781/
https://www.ncbi.nlm.nih.gov/pubmed/27646588
http://dx.doi.org/10.1038/srep33379
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author Heger, Zbynek
Polanska, Hana
Merlos Rodrigo, Miguel Angel
Guran, Roman
Kulich, Pavel
Kopel, Pavel
Masarik, Michal
Eckschlager, Tomas
Stiborova, Marie
Kizek, Rene
Adam, Vojtech
author_facet Heger, Zbynek
Polanska, Hana
Merlos Rodrigo, Miguel Angel
Guran, Roman
Kulich, Pavel
Kopel, Pavel
Masarik, Michal
Eckschlager, Tomas
Stiborova, Marie
Kizek, Rene
Adam, Vojtech
author_sort Heger, Zbynek
collection PubMed
description Herein, we describe the preparation of liposomes with folate-targeting properties for the encapsulation of anti-sarcosine antibodies (antisarAbs@LIP) and sarcosine (sar@LIP). The competitive inhibitory effects of exogenously added folic acid supported the role of folate targeting in liposome internalization. We examined the effects of repeated administration on mice PC-3 xenografts. Sar@LIP treatment significantly increased tumor volume and weight compared to controls treated with empty liposomes. Moreover, antisarAbs@LIP administration exhibited a mild antitumor effect. We also identified differences in gene expression patterns post-treatment. Furthermore, Sar@LIP treatment resulted in decreased amounts of tumor zinc ions and total metallothioneins. Examination of the spatial distribution across the tumor sections revealed a sarcosine-related decline of the MT1X isoform within the marginal regions but an elevation after antisarAbs@LIP administration. Our exploratory results demonstrate the importance of sarcosine as an oncometabolite in PCa. Moreover, we have shown that sarcosine can be a potential target for anticancer strategies in management of PCa.
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spelling pubmed-50287812016-09-26 Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes Heger, Zbynek Polanska, Hana Merlos Rodrigo, Miguel Angel Guran, Roman Kulich, Pavel Kopel, Pavel Masarik, Michal Eckschlager, Tomas Stiborova, Marie Kizek, Rene Adam, Vojtech Sci Rep Article Herein, we describe the preparation of liposomes with folate-targeting properties for the encapsulation of anti-sarcosine antibodies (antisarAbs@LIP) and sarcosine (sar@LIP). The competitive inhibitory effects of exogenously added folic acid supported the role of folate targeting in liposome internalization. We examined the effects of repeated administration on mice PC-3 xenografts. Sar@LIP treatment significantly increased tumor volume and weight compared to controls treated with empty liposomes. Moreover, antisarAbs@LIP administration exhibited a mild antitumor effect. We also identified differences in gene expression patterns post-treatment. Furthermore, Sar@LIP treatment resulted in decreased amounts of tumor zinc ions and total metallothioneins. Examination of the spatial distribution across the tumor sections revealed a sarcosine-related decline of the MT1X isoform within the marginal regions but an elevation after antisarAbs@LIP administration. Our exploratory results demonstrate the importance of sarcosine as an oncometabolite in PCa. Moreover, we have shown that sarcosine can be a potential target for anticancer strategies in management of PCa. Nature Publishing Group 2016-09-20 /pmc/articles/PMC5028781/ /pubmed/27646588 http://dx.doi.org/10.1038/srep33379 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Heger, Zbynek
Polanska, Hana
Merlos Rodrigo, Miguel Angel
Guran, Roman
Kulich, Pavel
Kopel, Pavel
Masarik, Michal
Eckschlager, Tomas
Stiborova, Marie
Kizek, Rene
Adam, Vojtech
Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
title Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
title_full Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
title_fullStr Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
title_full_unstemmed Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
title_short Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
title_sort prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-targeted liposomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028781/
https://www.ncbi.nlm.nih.gov/pubmed/27646588
http://dx.doi.org/10.1038/srep33379
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