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Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer

Targeted delivery of drugs to tumor cells, which circumvent resistance mechanisms and induce cell killing, is a lingering challenge that requires innovative solutions. Here, we provide two bioengineered strategies in which nanotechnology is blended with cancer medicine to preferentially target disti...

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Autores principales: Saha, Tanmoy, Mondal, Jayanta, Khiste, Sachin, Lusic, Hrvoje, Hu, Zhang-Wei, Jayabalan, Ruparoshni, Hodgetts, Kevin J., Jang, HaeLin, Sengupta, Shiladitya, Lee, Somin Eunice, Park, Younggeun, Lee, Luke P., Goldman, Aaron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478290/
https://www.ncbi.nlm.nih.gov/pubmed/34589378
http://dx.doi.org/10.1515/nanoph-2021-0142
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author Saha, Tanmoy
Mondal, Jayanta
Khiste, Sachin
Lusic, Hrvoje
Hu, Zhang-Wei
Jayabalan, Ruparoshni
Hodgetts, Kevin J.
Jang, HaeLin
Sengupta, Shiladitya
Lee, Somin Eunice
Park, Younggeun
Lee, Luke P.
Goldman, Aaron
author_facet Saha, Tanmoy
Mondal, Jayanta
Khiste, Sachin
Lusic, Hrvoje
Hu, Zhang-Wei
Jayabalan, Ruparoshni
Hodgetts, Kevin J.
Jang, HaeLin
Sengupta, Shiladitya
Lee, Somin Eunice
Park, Younggeun
Lee, Luke P.
Goldman, Aaron
author_sort Saha, Tanmoy
collection PubMed
description Targeted delivery of drugs to tumor cells, which circumvent resistance mechanisms and induce cell killing, is a lingering challenge that requires innovative solutions. Here, we provide two bioengineered strategies in which nanotechnology is blended with cancer medicine to preferentially target distinct mechanisms of drug resistance. In the first ‘case study’, we demonstrate the use of lipid–drug conjugates that target molecular signaling pathways, which result from taxane-induced drug tolerance via cell surface lipid raft accumulations. Through a small molecule drug screen, we identify a kinase inhibitor that optimally destroys drug tolerant cancer cells and conjugate it to a rationally-chosen lipid scaffold, which enhances anticancer efficacy in vitro and in vivo. In the second ‘case study’, we address resistance mechanisms that can occur through exocytosis of nanomedicines. Using adenocarcinoma HeLa and MCF-7 cells, we describe the use of gold nanorod and nanoporous vehicles integrated with an optical antenna for on-demand, photoactivation at ∼650 nm enabling release of payloads into cells including cytotoxic anthracyclines. Together, these provide two approaches, which exploit engineering strategies capable of circumventing distinct resistance barriers and induce killing by multimodal, including nanophotonic mechanisms.
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spelling pubmed-84782902021-09-28 Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer Saha, Tanmoy Mondal, Jayanta Khiste, Sachin Lusic, Hrvoje Hu, Zhang-Wei Jayabalan, Ruparoshni Hodgetts, Kevin J. Jang, HaeLin Sengupta, Shiladitya Lee, Somin Eunice Park, Younggeun Lee, Luke P. Goldman, Aaron Nanophotonics Research Article Targeted delivery of drugs to tumor cells, which circumvent resistance mechanisms and induce cell killing, is a lingering challenge that requires innovative solutions. Here, we provide two bioengineered strategies in which nanotechnology is blended with cancer medicine to preferentially target distinct mechanisms of drug resistance. In the first ‘case study’, we demonstrate the use of lipid–drug conjugates that target molecular signaling pathways, which result from taxane-induced drug tolerance via cell surface lipid raft accumulations. Through a small molecule drug screen, we identify a kinase inhibitor that optimally destroys drug tolerant cancer cells and conjugate it to a rationally-chosen lipid scaffold, which enhances anticancer efficacy in vitro and in vivo. In the second ‘case study’, we address resistance mechanisms that can occur through exocytosis of nanomedicines. Using adenocarcinoma HeLa and MCF-7 cells, we describe the use of gold nanorod and nanoporous vehicles integrated with an optical antenna for on-demand, photoactivation at ∼650 nm enabling release of payloads into cells including cytotoxic anthracyclines. Together, these provide two approaches, which exploit engineering strategies capable of circumventing distinct resistance barriers and induce killing by multimodal, including nanophotonic mechanisms. De Gruyter 2021-06-25 /pmc/articles/PMC8478290/ /pubmed/34589378 http://dx.doi.org/10.1515/nanoph-2021-0142 Text en © 2021 Tanmoy Saha et al., published by De Gruyter, Berlin/Boston https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Saha, Tanmoy
Mondal, Jayanta
Khiste, Sachin
Lusic, Hrvoje
Hu, Zhang-Wei
Jayabalan, Ruparoshni
Hodgetts, Kevin J.
Jang, HaeLin
Sengupta, Shiladitya
Lee, Somin Eunice
Park, Younggeun
Lee, Luke P.
Goldman, Aaron
Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
title Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
title_full Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
title_fullStr Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
title_full_unstemmed Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
title_short Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
title_sort nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478290/
https://www.ncbi.nlm.nih.gov/pubmed/34589378
http://dx.doi.org/10.1515/nanoph-2021-0142
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