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The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance
The ever-growing perception of cancer stem cells (CSCs) as a plastic state rather than a hardwired defined entity has evolved our understanding of the functional and biological plasticity of these elusive components in malignancies. Pancreatic cancer (PC), based on its biological features and clinic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556195/ https://www.ncbi.nlm.nih.gov/pubmed/34453639 http://dx.doi.org/10.1007/s10555-021-09979-x |
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author | Patil, Kalyani Khan, Farheen B. Akhtar, Sabah Ahmad, Aamir Uddin, Shahab |
author_facet | Patil, Kalyani Khan, Farheen B. Akhtar, Sabah Ahmad, Aamir Uddin, Shahab |
author_sort | Patil, Kalyani |
collection | PubMed |
description | The ever-growing perception of cancer stem cells (CSCs) as a plastic state rather than a hardwired defined entity has evolved our understanding of the functional and biological plasticity of these elusive components in malignancies. Pancreatic cancer (PC), based on its biological features and clinical evolution, is a prototypical example of a CSC-driven disease. Since the discovery of pancreatic CSCs (PCSCs) in 2007, evidence has unraveled their control over many facets of the natural history of PC, including primary tumor growth, metastatic progression, disease recurrence, and acquired drug resistance. Consequently, the current near-ubiquitous treatment regimens for PC using aggressive cytotoxic agents, aimed at ‘‘tumor debulking’’ rather than eradication of CSCs, have proven ineffective in providing clinically convincing improvements in patients with this dreadful disease. Herein, we review the key hallmarks as well as the intrinsic and extrinsic resistance mechanisms of CSCs that mediate treatment failure in PC and enlist the potential CSC-targeting ‘natural agents’ that are gaining popularity in recent years. A better understanding of the molecular and functional landscape of PCSC-intrinsic evasion of chemotherapeutic drugs offers a facile opportunity for treating PC, an intractable cancer with a grim prognosis and in dire need of effective therapeutic advances. |
format | Online Article Text |
id | pubmed-8556195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-85561952021-11-04 The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance Patil, Kalyani Khan, Farheen B. Akhtar, Sabah Ahmad, Aamir Uddin, Shahab Cancer Metastasis Rev Article The ever-growing perception of cancer stem cells (CSCs) as a plastic state rather than a hardwired defined entity has evolved our understanding of the functional and biological plasticity of these elusive components in malignancies. Pancreatic cancer (PC), based on its biological features and clinical evolution, is a prototypical example of a CSC-driven disease. Since the discovery of pancreatic CSCs (PCSCs) in 2007, evidence has unraveled their control over many facets of the natural history of PC, including primary tumor growth, metastatic progression, disease recurrence, and acquired drug resistance. Consequently, the current near-ubiquitous treatment regimens for PC using aggressive cytotoxic agents, aimed at ‘‘tumor debulking’’ rather than eradication of CSCs, have proven ineffective in providing clinically convincing improvements in patients with this dreadful disease. Herein, we review the key hallmarks as well as the intrinsic and extrinsic resistance mechanisms of CSCs that mediate treatment failure in PC and enlist the potential CSC-targeting ‘natural agents’ that are gaining popularity in recent years. A better understanding of the molecular and functional landscape of PCSC-intrinsic evasion of chemotherapeutic drugs offers a facile opportunity for treating PC, an intractable cancer with a grim prognosis and in dire need of effective therapeutic advances. Springer US 2021-08-28 2021 /pmc/articles/PMC8556195/ /pubmed/34453639 http://dx.doi.org/10.1007/s10555-021-09979-x Text en © The Author(s) 2021 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/) . |
spellingShingle | Article Patil, Kalyani Khan, Farheen B. Akhtar, Sabah Ahmad, Aamir Uddin, Shahab The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
title | The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
title_full | The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
title_fullStr | The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
title_full_unstemmed | The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
title_short | The plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
title_sort | plasticity of pancreatic cancer stem cells: implications in therapeutic resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556195/ https://www.ncbi.nlm.nih.gov/pubmed/34453639 http://dx.doi.org/10.1007/s10555-021-09979-x |
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