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Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages

The tumor microenvironment (TME) is the internal environment that tumors depend on for survival and development. Tumor-associated macrophages (TAMs), as an important part of the tumor microenvironment, which plays a crucial role in the occurrence, development, invasion and metastasis of various mali...

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Autores principales: Miao, Yingying, Wang, Shuang, Zhang, Butian, Liu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186348/
https://www.ncbi.nlm.nih.gov/pubmed/37205099
http://dx.doi.org/10.3389/fimmu.2023.1133238
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author Miao, Yingying
Wang, Shuang
Zhang, Butian
Liu, Lin
author_facet Miao, Yingying
Wang, Shuang
Zhang, Butian
Liu, Lin
author_sort Miao, Yingying
collection PubMed
description The tumor microenvironment (TME) is the internal environment that tumors depend on for survival and development. Tumor-associated macrophages (TAMs), as an important part of the tumor microenvironment, which plays a crucial role in the occurrence, development, invasion and metastasis of various malignant tumors and has immunosuppressant ability. With the development of immunotherapy, eradicating cancer cells by activating the innate immune system has yielded encouraging results, however only a minority of patients show a lasting response. Therefore, in vivo imaging of dynamic TAMs is crucial in patient-tailored immunotherapy to identify patients who will benefit from immunotherapy, monitor efficacy after treatment, and identify alternative strategies for non-responders. Meanwhile, developing nanomedicines based on TAMs-related antitumor mechanisms to effectively inhibit tumor growth is expected to become a promising research field. Carbon dots (CDs), as an emerging member of the carbon material family, exhibit unexpected superiority in fluorescence imaging/sensing, such as near infrared imaging, photostability, biocompatibility and low toxicity. Their characteristics naturally integrate therapy and diagnosis, and when CDs are combined with targeted chemical/genetic/photodynamic/photothermal therapeutic moieties, they are good candidates for targeting TAMs. We concentrate our discussion on the current learn of TAMs and describe recent examples of macrophage modulation based on carbon dot-associated nanoparticles, emphasizing the advantages of their multifunctional platform and their potential for TAMs theranostics.
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spelling pubmed-101863482023-05-17 Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages Miao, Yingying Wang, Shuang Zhang, Butian Liu, Lin Front Immunol Immunology The tumor microenvironment (TME) is the internal environment that tumors depend on for survival and development. Tumor-associated macrophages (TAMs), as an important part of the tumor microenvironment, which plays a crucial role in the occurrence, development, invasion and metastasis of various malignant tumors and has immunosuppressant ability. With the development of immunotherapy, eradicating cancer cells by activating the innate immune system has yielded encouraging results, however only a minority of patients show a lasting response. Therefore, in vivo imaging of dynamic TAMs is crucial in patient-tailored immunotherapy to identify patients who will benefit from immunotherapy, monitor efficacy after treatment, and identify alternative strategies for non-responders. Meanwhile, developing nanomedicines based on TAMs-related antitumor mechanisms to effectively inhibit tumor growth is expected to become a promising research field. Carbon dots (CDs), as an emerging member of the carbon material family, exhibit unexpected superiority in fluorescence imaging/sensing, such as near infrared imaging, photostability, biocompatibility and low toxicity. Their characteristics naturally integrate therapy and diagnosis, and when CDs are combined with targeted chemical/genetic/photodynamic/photothermal therapeutic moieties, they are good candidates for targeting TAMs. We concentrate our discussion on the current learn of TAMs and describe recent examples of macrophage modulation based on carbon dot-associated nanoparticles, emphasizing the advantages of their multifunctional platform and their potential for TAMs theranostics. Frontiers Media S.A. 2023-05-02 /pmc/articles/PMC10186348/ /pubmed/37205099 http://dx.doi.org/10.3389/fimmu.2023.1133238 Text en Copyright © 2023 Miao, Wang, Zhang and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Miao, Yingying
Wang, Shuang
Zhang, Butian
Liu, Lin
Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
title Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
title_full Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
title_fullStr Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
title_full_unstemmed Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
title_short Carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
title_sort carbon dot-based nanomaterials: a promising future nano-platform for targeting tumor-associated macrophages
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186348/
https://www.ncbi.nlm.nih.gov/pubmed/37205099
http://dx.doi.org/10.3389/fimmu.2023.1133238
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AT wangshuang carbondotbasednanomaterialsapromisingfuturenanoplatformfortargetingtumorassociatedmacrophages
AT zhangbutian carbondotbasednanomaterialsapromisingfuturenanoplatformfortargetingtumorassociatedmacrophages
AT liulin carbondotbasednanomaterialsapromisingfuturenanoplatformfortargetingtumorassociatedmacrophages