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Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer
Cancer stem cells (CSCs), initially identified in leukemia in 1994, constitute a distinct subset of tumor cells characterized by surface markers such as CD133, CD44, and ALDH. Their behavior is regulated through a complex interplay of networks, including transcriptional, post-transcriptional, epigen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583419/ https://www.ncbi.nlm.nih.gov/pubmed/37853437 http://dx.doi.org/10.1186/s12943-023-01877-w |
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author | Zeng, Zhen Fu, Minyang Hu, Yuan Wei, Yuquan Wei, Xiawei Luo, Min |
author_facet | Zeng, Zhen Fu, Minyang Hu, Yuan Wei, Yuquan Wei, Xiawei Luo, Min |
author_sort | Zeng, Zhen |
collection | PubMed |
description | Cancer stem cells (CSCs), initially identified in leukemia in 1994, constitute a distinct subset of tumor cells characterized by surface markers such as CD133, CD44, and ALDH. Their behavior is regulated through a complex interplay of networks, including transcriptional, post-transcriptional, epigenetic, tumor microenvironment (TME), and epithelial-mesenchymal transition (EMT) factors. Numerous signaling pathways were found to be involved in the regulatory network of CSCs. The maintenance of CSC characteristics plays a pivotal role in driving CSC-associated tumor metastasis and conferring resistance to therapy. Consequently, CSCs have emerged as promising targets in cancer treatment. To date, researchers have developed several anticancer agents tailored to specifically target CSCs, with some of these treatment strategies currently undergoing preclinical or clinical trials. In this review, we outline the origin and biological characteristics of CSCs, explore the regulatory networks governing CSCs, discuss the signaling pathways implicated in these networks, and investigate the influential factors contributing to therapy resistance in CSCs. Finally, we offer insights into preclinical and clinical agents designed to eliminate CSCs. |
format | Online Article Text |
id | pubmed-10583419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105834192023-10-19 Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer Zeng, Zhen Fu, Minyang Hu, Yuan Wei, Yuquan Wei, Xiawei Luo, Min Mol Cancer Review Cancer stem cells (CSCs), initially identified in leukemia in 1994, constitute a distinct subset of tumor cells characterized by surface markers such as CD133, CD44, and ALDH. Their behavior is regulated through a complex interplay of networks, including transcriptional, post-transcriptional, epigenetic, tumor microenvironment (TME), and epithelial-mesenchymal transition (EMT) factors. Numerous signaling pathways were found to be involved in the regulatory network of CSCs. The maintenance of CSC characteristics plays a pivotal role in driving CSC-associated tumor metastasis and conferring resistance to therapy. Consequently, CSCs have emerged as promising targets in cancer treatment. To date, researchers have developed several anticancer agents tailored to specifically target CSCs, with some of these treatment strategies currently undergoing preclinical or clinical trials. In this review, we outline the origin and biological characteristics of CSCs, explore the regulatory networks governing CSCs, discuss the signaling pathways implicated in these networks, and investigate the influential factors contributing to therapy resistance in CSCs. Finally, we offer insights into preclinical and clinical agents designed to eliminate CSCs. BioMed Central 2023-10-18 /pmc/articles/PMC10583419/ /pubmed/37853437 http://dx.doi.org/10.1186/s12943-023-01877-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Zeng, Zhen Fu, Minyang Hu, Yuan Wei, Yuquan Wei, Xiawei Luo, Min Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
title | Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
title_full | Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
title_fullStr | Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
title_full_unstemmed | Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
title_short | Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
title_sort | regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583419/ https://www.ncbi.nlm.nih.gov/pubmed/37853437 http://dx.doi.org/10.1186/s12943-023-01877-w |
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