Cargando…
The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC
SIMPLE SUMMARY: This review takes the extracellular matrix (ECM) as the starting point, and describes its influence and related mechanisms on the biological behavior of pancreatic ductal carcinoma (PDAC). It focuses on how the ECM regulates cancer stem cells and thus affects the metastasis and drug...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406497/ https://www.ncbi.nlm.nih.gov/pubmed/36010993 http://dx.doi.org/10.3390/cancers14163998 |
_version_ | 1784774135589634048 |
---|---|
author | Wang, Dan Li, Yuqiang Ge, Heming Ghadban, Tarik Reeh, Matthias Güngör, Cenap |
author_facet | Wang, Dan Li, Yuqiang Ge, Heming Ghadban, Tarik Reeh, Matthias Güngör, Cenap |
author_sort | Wang, Dan |
collection | PubMed |
description | SIMPLE SUMMARY: This review takes the extracellular matrix (ECM) as the starting point, and describes its influence and related mechanisms on the biological behavior of pancreatic ductal carcinoma (PDAC). It focuses on how the ECM regulates cancer stem cells and thus affects the metastasis and drug resistance of PDAC. Finally, current and ongoing treatment strategies for ECM are presented. ECM-related factors and mechanisms are both the focus and difficulty of current therapeutic strategy research, but further exploration is crucial for effectively eradicating the disease and improving patient survival. ABSTRACT: Pancreatic ductal adenocarcinoma (PDAC) is rich in dense fibrotic stroma that are composed of extracellular matrix (ECM) proteins. A disruption of the balance between ECM synthesis and secretion and the altered expression of matrix remodeling enzymes lead to abnormal ECM dynamics in PDAC. This pathological ECM promotes cancer growth, survival, invasion, and alters the behavior of fibroblasts and immune cells leading to metastasis formation and chemotherapy resistance, which contribute to the high lethality of PDAC. Additionally, recent evidence highlights that ECM, as a major structural component of the tumor microenvironment, is a highly dynamic structure in which ECM proteins establish a physical and biochemical niche for cancer stem cells (CSCs). CSCs are characterized by self-renewal, tumor initiation, and resistance to chemotherapeutics. In this review, we will discuss the effects of the ECM on tumor biological behavior and its molecular impact on the fundamental signaling pathways in PDAC. We will also provide an overview of how the different ECM components are able to modulate CSCs properties and finally discuss the current and ongoing therapeutic strategies targeting the ECM. Given the many challenges facing current targeted therapies for PDAC, a better understanding of molecular events involving the interplay of ECM and CSC will be key in identifying more effective therapeutic strategies to eliminate CSCs and ultimately to improve survival in patients that are suffering from this deadly disease. |
format | Online Article Text |
id | pubmed-9406497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94064972022-08-26 The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC Wang, Dan Li, Yuqiang Ge, Heming Ghadban, Tarik Reeh, Matthias Güngör, Cenap Cancers (Basel) Review SIMPLE SUMMARY: This review takes the extracellular matrix (ECM) as the starting point, and describes its influence and related mechanisms on the biological behavior of pancreatic ductal carcinoma (PDAC). It focuses on how the ECM regulates cancer stem cells and thus affects the metastasis and drug resistance of PDAC. Finally, current and ongoing treatment strategies for ECM are presented. ECM-related factors and mechanisms are both the focus and difficulty of current therapeutic strategy research, but further exploration is crucial for effectively eradicating the disease and improving patient survival. ABSTRACT: Pancreatic ductal adenocarcinoma (PDAC) is rich in dense fibrotic stroma that are composed of extracellular matrix (ECM) proteins. A disruption of the balance between ECM synthesis and secretion and the altered expression of matrix remodeling enzymes lead to abnormal ECM dynamics in PDAC. This pathological ECM promotes cancer growth, survival, invasion, and alters the behavior of fibroblasts and immune cells leading to metastasis formation and chemotherapy resistance, which contribute to the high lethality of PDAC. Additionally, recent evidence highlights that ECM, as a major structural component of the tumor microenvironment, is a highly dynamic structure in which ECM proteins establish a physical and biochemical niche for cancer stem cells (CSCs). CSCs are characterized by self-renewal, tumor initiation, and resistance to chemotherapeutics. In this review, we will discuss the effects of the ECM on tumor biological behavior and its molecular impact on the fundamental signaling pathways in PDAC. We will also provide an overview of how the different ECM components are able to modulate CSCs properties and finally discuss the current and ongoing therapeutic strategies targeting the ECM. Given the many challenges facing current targeted therapies for PDAC, a better understanding of molecular events involving the interplay of ECM and CSC will be key in identifying more effective therapeutic strategies to eliminate CSCs and ultimately to improve survival in patients that are suffering from this deadly disease. MDPI 2022-08-18 /pmc/articles/PMC9406497/ /pubmed/36010993 http://dx.doi.org/10.3390/cancers14163998 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Wang, Dan Li, Yuqiang Ge, Heming Ghadban, Tarik Reeh, Matthias Güngör, Cenap The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC |
title | The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC |
title_full | The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC |
title_fullStr | The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC |
title_full_unstemmed | The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC |
title_short | The Extracellular Matrix: A Key Accomplice of Cancer Stem Cell Migration, Metastasis Formation, and Drug Resistance in PDAC |
title_sort | extracellular matrix: a key accomplice of cancer stem cell migration, metastasis formation, and drug resistance in pdac |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406497/ https://www.ncbi.nlm.nih.gov/pubmed/36010993 http://dx.doi.org/10.3390/cancers14163998 |
work_keys_str_mv | AT wangdan theextracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT liyuqiang theextracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT geheming theextracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT ghadbantarik theextracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT reehmatthias theextracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT gungorcenap theextracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT wangdan extracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT liyuqiang extracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT geheming extracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT ghadbantarik extracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT reehmatthias extracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac AT gungorcenap extracellularmatrixakeyaccompliceofcancerstemcellmigrationmetastasisformationanddrugresistanceinpdac |