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A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours

Salmonella enterica serotype Typhimurium is a food-borne pathogen that also selectively grows in tumours and functionally decreases P-glycoprotein (P-gp), a multidrug resistance transporter. Here we report that the Salmonella type III secretion effector, SipA, is responsible for P-gp modulation thro...

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Autores principales: Mercado-Lubo, Regino, Zhang, Yuanwei, Zhao, Liang, Rossi, Kyle, Wu, Xiang, Zou, Yekui, Castillo, Antonio, Leonard, Jack, Bortell, Rita, Greiner, Dale L., Shultz, Leonard D., Han, Gang, McCormick, Beth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512628/
https://www.ncbi.nlm.nih.gov/pubmed/27452236
http://dx.doi.org/10.1038/ncomms12225
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author Mercado-Lubo, Regino
Zhang, Yuanwei
Zhao, Liang
Rossi, Kyle
Wu, Xiang
Zou, Yekui
Castillo, Antonio
Leonard, Jack
Bortell, Rita
Greiner, Dale L.
Shultz, Leonard D.
Han, Gang
McCormick, Beth A.
author_facet Mercado-Lubo, Regino
Zhang, Yuanwei
Zhao, Liang
Rossi, Kyle
Wu, Xiang
Zou, Yekui
Castillo, Antonio
Leonard, Jack
Bortell, Rita
Greiner, Dale L.
Shultz, Leonard D.
Han, Gang
McCormick, Beth A.
author_sort Mercado-Lubo, Regino
collection PubMed
description Salmonella enterica serotype Typhimurium is a food-borne pathogen that also selectively grows in tumours and functionally decreases P-glycoprotein (P-gp), a multidrug resistance transporter. Here we report that the Salmonella type III secretion effector, SipA, is responsible for P-gp modulation through a pathway involving caspase-3. Mimicking the ability of Salmonella to reverse multidrug resistance, we constructed a gold nanoparticle system packaged with a SipA corona, and found this bacterial mimic not only accumulates in tumours but also reduces P-gp at a SipA dose significantly lower than free SipA. Moreover, the Salmonella nanoparticle mimic suppresses tumour growth with a concomitant reduction in P-gp when used with an existing chemotherapeutic drug (that is, doxorubicin). On the basis of our finding that the SipA Salmonella effector is fundamental for functionally decreasing P-gp, we engineered a nanoparticle mimic that both overcomes multidrug resistance in cancer cells and increases tumour sensitivity to conventional chemotherapeutics.
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spelling pubmed-55126282017-07-19 A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours Mercado-Lubo, Regino Zhang, Yuanwei Zhao, Liang Rossi, Kyle Wu, Xiang Zou, Yekui Castillo, Antonio Leonard, Jack Bortell, Rita Greiner, Dale L. Shultz, Leonard D. Han, Gang McCormick, Beth A. Nat Commun Article Salmonella enterica serotype Typhimurium is a food-borne pathogen that also selectively grows in tumours and functionally decreases P-glycoprotein (P-gp), a multidrug resistance transporter. Here we report that the Salmonella type III secretion effector, SipA, is responsible for P-gp modulation through a pathway involving caspase-3. Mimicking the ability of Salmonella to reverse multidrug resistance, we constructed a gold nanoparticle system packaged with a SipA corona, and found this bacterial mimic not only accumulates in tumours but also reduces P-gp at a SipA dose significantly lower than free SipA. Moreover, the Salmonella nanoparticle mimic suppresses tumour growth with a concomitant reduction in P-gp when used with an existing chemotherapeutic drug (that is, doxorubicin). On the basis of our finding that the SipA Salmonella effector is fundamental for functionally decreasing P-gp, we engineered a nanoparticle mimic that both overcomes multidrug resistance in cancer cells and increases tumour sensitivity to conventional chemotherapeutics. Nature Publishing Group 2016-07-25 /pmc/articles/PMC5512628/ /pubmed/27452236 http://dx.doi.org/10.1038/ncomms12225 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Mercado-Lubo, Regino
Zhang, Yuanwei
Zhao, Liang
Rossi, Kyle
Wu, Xiang
Zou, Yekui
Castillo, Antonio
Leonard, Jack
Bortell, Rita
Greiner, Dale L.
Shultz, Leonard D.
Han, Gang
McCormick, Beth A.
A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours
title A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours
title_full A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours
title_fullStr A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours
title_full_unstemmed A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours
title_short A Salmonella nanoparticle mimic overcomes multidrug resistance in tumours
title_sort salmonella nanoparticle mimic overcomes multidrug resistance in tumours
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512628/
https://www.ncbi.nlm.nih.gov/pubmed/27452236
http://dx.doi.org/10.1038/ncomms12225
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