Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?

Abstract Cancer cells that transit from primary tumours into the circulatory system are known as circulating tumour cells (CTCs). These cancer cells have unique phenotypic and genotypic characteristics which allow them to survive within the circulation, subsequently extravasate and metastasise. CTCs...

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Main Authors: Mark P. Ward, Laura E. Kane, Lucy A. Norris, Bashir M. Mohamed, Tanya Kelly, Mark Bates, Andres Clarke, Nathan Brady, Cara M. Martin, Robert D. Brooks, Doug A. Brooks, Stavros Selemidis, Sean Hanniffy, Eric P. Dixon, Sharon A. O’Toole, John J. O’Leary
Format: Article
Language:English
Published: BMC 2021-03-01
Series:Molecular Cancer
Online Access:https://doi.org/10.1186/s12943-021-01347-1
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spelling doaj-6c9b855579b040d7a4a07c53dfa5ef3f2021-04-04T11:28:03ZengBMCMolecular Cancer1476-45982021-03-0120111710.1186/s12943-021-01347-1Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?Mark P. Ward0Laura E. Kane1Lucy A. Norris2Bashir M. Mohamed3Tanya Kelly4Mark Bates5Andres Clarke6Nathan Brady7Cara M. Martin8Robert D. Brooks9Doug A. Brooks10Stavros Selemidis11Sean Hanniffy12Eric P. Dixon13Sharon A. O’Toole14John J. O’Leary15Department of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinTrinity St. James’s Cancer Institute, St James’s HospitalDepartment of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinCancer Research Institute, University of South AustraliaCancer Research Institute, University of South AustraliaSchool of Health and Biomedical Sciences, RMIT UniversityBD Research Centre IrelandBD Technologies and Innovation, Research Triangle ParkDepartment of Histopathology and Morbid Anatomy, Trinity College DublinDepartment of Histopathology and Morbid Anatomy, Trinity College DublinAbstract Cancer cells that transit from primary tumours into the circulatory system are known as circulating tumour cells (CTCs). These cancer cells have unique phenotypic and genotypic characteristics which allow them to survive within the circulation, subsequently extravasate and metastasise. CTCs have emerged as a useful diagnostic tool using “liquid biopsies” to report on the metastatic potential of cancers. However, CTCs by their nature interact with components of the blood circulatory system on a constant basis, influencing both their physical and morphological characteristics as well as metastatic capabilities. These properties and the associated molecular profile may provide critical diagnostic and prognostic capabilities in the clinic. Platelets interact with CTCs within minutes of their dissemination and are crucial in the formation of the initial metastatic niche. Platelets and coagulation proteins also alter the fate of a CTC by influencing EMT, promoting pro-survival signalling and aiding in evading immune cell destruction. CTCs have the capacity to directly hijack immune cells and utilise them to aid in CTC metastatic seeding processes. The disruption of CTC clusters may also offer a strategy for the treatment of advance staged cancers. Therapeutic disruption of these heterotypical interactions as well as direct CTC targeting hold great promise, especially with the advent of new immunotherapies and personalised medicines. Understanding the molecular role that platelets, immune cells and the coagulation cascade play in CTC biology will allow us to identify and characterise the most clinically relevant CTCs from patients. This will subsequently advance the clinical utility of CTCs in cancer diagnosis/prognosis.https://doi.org/10.1186/s12943-021-01347-1
collection DOAJ
language English
format Article
sources DOAJ
author Mark P. Ward
Laura E. Kane
Lucy A. Norris
Bashir M. Mohamed
Tanya Kelly
Mark Bates
Andres Clarke
Nathan Brady
Cara M. Martin
Robert D. Brooks
Doug A. Brooks
Stavros Selemidis
Sean Hanniffy
Eric P. Dixon
Sharon A. O’Toole
John J. O’Leary
spellingShingle Mark P. Ward
Laura E. Kane
Lucy A. Norris
Bashir M. Mohamed
Tanya Kelly
Mark Bates
Andres Clarke
Nathan Brady
Cara M. Martin
Robert D. Brooks
Doug A. Brooks
Stavros Selemidis
Sean Hanniffy
Eric P. Dixon
Sharon A. O’Toole
John J. O’Leary
Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
Molecular Cancer
author_facet Mark P. Ward
Laura E. Kane
Lucy A. Norris
Bashir M. Mohamed
Tanya Kelly
Mark Bates
Andres Clarke
Nathan Brady
Cara M. Martin
Robert D. Brooks
Doug A. Brooks
Stavros Selemidis
Sean Hanniffy
Eric P. Dixon
Sharon A. O’Toole
John J. O’Leary
author_sort Mark P. Ward
title Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
title_short Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
title_full Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
title_fullStr Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
title_full_unstemmed Platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
title_sort platelets, immune cells and the coagulation cascade; friend or foe of the circulating tumour cell?
publisher BMC
series Molecular Cancer
issn 1476-4598
publishDate 2021-03-01
description Abstract Cancer cells that transit from primary tumours into the circulatory system are known as circulating tumour cells (CTCs). These cancer cells have unique phenotypic and genotypic characteristics which allow them to survive within the circulation, subsequently extravasate and metastasise. CTCs have emerged as a useful diagnostic tool using “liquid biopsies” to report on the metastatic potential of cancers. However, CTCs by their nature interact with components of the blood circulatory system on a constant basis, influencing both their physical and morphological characteristics as well as metastatic capabilities. These properties and the associated molecular profile may provide critical diagnostic and prognostic capabilities in the clinic. Platelets interact with CTCs within minutes of their dissemination and are crucial in the formation of the initial metastatic niche. Platelets and coagulation proteins also alter the fate of a CTC by influencing EMT, promoting pro-survival signalling and aiding in evading immune cell destruction. CTCs have the capacity to directly hijack immune cells and utilise them to aid in CTC metastatic seeding processes. The disruption of CTC clusters may also offer a strategy for the treatment of advance staged cancers. Therapeutic disruption of these heterotypical interactions as well as direct CTC targeting hold great promise, especially with the advent of new immunotherapies and personalised medicines. Understanding the molecular role that platelets, immune cells and the coagulation cascade play in CTC biology will allow us to identify and characterise the most clinically relevant CTCs from patients. This will subsequently advance the clinical utility of CTCs in cancer diagnosis/prognosis.
url https://doi.org/10.1186/s12943-021-01347-1
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