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Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer
Urokinase-type plasminogen activator receptor (uPAR) is an attractive target for the treatment of cancer, because it is expressed at low levels in healthy tissues but at high levels in malignant tumours. uPAR is closely related to the invasion and metastasis of malignant tumours, plays important rol...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932206/ https://www.ncbi.nlm.nih.gov/pubmed/35303878 http://dx.doi.org/10.1186/s12967-022-03329-3 |
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author | Zhai, Bing-Tao Tian, Huan Sun, Jing Zou, Jun-Bo Zhang, Xiao-Fei Cheng, Jiang-Xue Shi, Ya-Jun Fan, Yu Guo, Dong-Yan |
author_facet | Zhai, Bing-Tao Tian, Huan Sun, Jing Zou, Jun-Bo Zhang, Xiao-Fei Cheng, Jiang-Xue Shi, Ya-Jun Fan, Yu Guo, Dong-Yan |
author_sort | Zhai, Bing-Tao |
collection | PubMed |
description | Urokinase-type plasminogen activator receptor (uPAR) is an attractive target for the treatment of cancer, because it is expressed at low levels in healthy tissues but at high levels in malignant tumours. uPAR is closely related to the invasion and metastasis of malignant tumours, plays important roles in the degradation of extracellular matrix (ECM), tumour angiogenesis, cell proliferation and apoptosis, and is associated with the multidrug resistance (MDR) of tumour cells, which has important guiding significance for the judgement of tumor malignancy and prognosis. Several uPAR-targeted antitumour therapeutic agents have been developed to suppress tumour growth, metastatic processes and drug resistance. Here, we review the recent advances in the development of uPAR-targeted antitumor therapeutic strategies, including nanoplatforms carrying therapeutic agents, photodynamic therapy (PDT)/photothermal therapy (PTT) platforms, oncolytic virotherapy, gene therapy technologies, monoclonal antibody therapy and tumour immunotherapy, to promote the translation of these therapeutic agents to clinical applications. |
format | Online Article Text |
id | pubmed-8932206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89322062022-03-23 Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer Zhai, Bing-Tao Tian, Huan Sun, Jing Zou, Jun-Bo Zhang, Xiao-Fei Cheng, Jiang-Xue Shi, Ya-Jun Fan, Yu Guo, Dong-Yan J Transl Med Review Urokinase-type plasminogen activator receptor (uPAR) is an attractive target for the treatment of cancer, because it is expressed at low levels in healthy tissues but at high levels in malignant tumours. uPAR is closely related to the invasion and metastasis of malignant tumours, plays important roles in the degradation of extracellular matrix (ECM), tumour angiogenesis, cell proliferation and apoptosis, and is associated with the multidrug resistance (MDR) of tumour cells, which has important guiding significance for the judgement of tumor malignancy and prognosis. Several uPAR-targeted antitumour therapeutic agents have been developed to suppress tumour growth, metastatic processes and drug resistance. Here, we review the recent advances in the development of uPAR-targeted antitumor therapeutic strategies, including nanoplatforms carrying therapeutic agents, photodynamic therapy (PDT)/photothermal therapy (PTT) platforms, oncolytic virotherapy, gene therapy technologies, monoclonal antibody therapy and tumour immunotherapy, to promote the translation of these therapeutic agents to clinical applications. BioMed Central 2022-03-18 /pmc/articles/PMC8932206/ /pubmed/35303878 http://dx.doi.org/10.1186/s12967-022-03329-3 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 Zhai, Bing-Tao Tian, Huan Sun, Jing Zou, Jun-Bo Zhang, Xiao-Fei Cheng, Jiang-Xue Shi, Ya-Jun Fan, Yu Guo, Dong-Yan Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer |
title | Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer |
title_full | Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer |
title_fullStr | Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer |
title_full_unstemmed | Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer |
title_short | Urokinase-type plasminogen activator receptor (uPAR) as a therapeutic target in cancer |
title_sort | urokinase-type plasminogen activator receptor (upar) as a therapeutic target in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932206/ https://www.ncbi.nlm.nih.gov/pubmed/35303878 http://dx.doi.org/10.1186/s12967-022-03329-3 |
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