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Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies

Poor targeting of therapeutics leading to severe adverse effects on normal tissues is considered one of the obstacles in cancer therapy. To help overcome this, nanoscale drug delivery systems have provided an alternative avenue for improving the therapeutic potential of various agents and bioactive...

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Autores principales: Tian, Hailong, Zhang, Tingting, Qin, Siyuan, Huang, Zhao, Zhou, Li, Shi, Jiayan, Nice, Edouard C., Xie, Na, Huang, Canhua, Shen, Zhisen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469622/
https://www.ncbi.nlm.nih.gov/pubmed/36096856
http://dx.doi.org/10.1186/s13045-022-01320-5
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author Tian, Hailong
Zhang, Tingting
Qin, Siyuan
Huang, Zhao
Zhou, Li
Shi, Jiayan
Nice, Edouard C.
Xie, Na
Huang, Canhua
Shen, Zhisen
author_facet Tian, Hailong
Zhang, Tingting
Qin, Siyuan
Huang, Zhao
Zhou, Li
Shi, Jiayan
Nice, Edouard C.
Xie, Na
Huang, Canhua
Shen, Zhisen
author_sort Tian, Hailong
collection PubMed
description Poor targeting of therapeutics leading to severe adverse effects on normal tissues is considered one of the obstacles in cancer therapy. To help overcome this, nanoscale drug delivery systems have provided an alternative avenue for improving the therapeutic potential of various agents and bioactive molecules through the enhanced permeability and retention (EPR) effect. Nanosystems with cancer-targeted ligands can achieve effective delivery to the tumor cells utilizing cell surface-specific receptors, the tumor vasculature and antigens with high accuracy and affinity. Additionally, stimuli-responsive nanoplatforms have also been considered as a promising and effective targeting strategy against tumors, as these nanoplatforms maintain their stealth feature under normal conditions, but upon homing in on cancerous lesions or their microenvironment, are responsive and release their cargoes. In this review, we comprehensively summarize the field of active targeting drug delivery systems and a number of stimuli-responsive release studies in the context of emerging nanoplatform development, and also discuss how this knowledge can contribute to further improvements in clinical practice.
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spelling pubmed-94696222022-09-14 Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies Tian, Hailong Zhang, Tingting Qin, Siyuan Huang, Zhao Zhou, Li Shi, Jiayan Nice, Edouard C. Xie, Na Huang, Canhua Shen, Zhisen J Hematol Oncol Review Poor targeting of therapeutics leading to severe adverse effects on normal tissues is considered one of the obstacles in cancer therapy. To help overcome this, nanoscale drug delivery systems have provided an alternative avenue for improving the therapeutic potential of various agents and bioactive molecules through the enhanced permeability and retention (EPR) effect. Nanosystems with cancer-targeted ligands can achieve effective delivery to the tumor cells utilizing cell surface-specific receptors, the tumor vasculature and antigens with high accuracy and affinity. Additionally, stimuli-responsive nanoplatforms have also been considered as a promising and effective targeting strategy against tumors, as these nanoplatforms maintain their stealth feature under normal conditions, but upon homing in on cancerous lesions or their microenvironment, are responsive and release their cargoes. In this review, we comprehensively summarize the field of active targeting drug delivery systems and a number of stimuli-responsive release studies in the context of emerging nanoplatform development, and also discuss how this knowledge can contribute to further improvements in clinical practice. BioMed Central 2022-09-12 /pmc/articles/PMC9469622/ /pubmed/36096856 http://dx.doi.org/10.1186/s13045-022-01320-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Tian, Hailong
Zhang, Tingting
Qin, Siyuan
Huang, Zhao
Zhou, Li
Shi, Jiayan
Nice, Edouard C.
Xie, Na
Huang, Canhua
Shen, Zhisen
Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
title Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
title_full Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
title_fullStr Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
title_full_unstemmed Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
title_short Enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
title_sort enhancing the therapeutic efficacy of nanoparticles for cancer treatment using versatile targeted strategies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469622/
https://www.ncbi.nlm.nih.gov/pubmed/36096856
http://dx.doi.org/10.1186/s13045-022-01320-5
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