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...
Main Authors: | , , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2021-03-01
|
Series: | Molecular Cancer |
Online Access: | https://doi.org/10.1186/s12943-021-01347-1 |
id |
doaj-6c9b855579b040d7a4a07c53dfa5ef3f |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT markpward plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT lauraekane plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT lucyanorris plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT bashirmmohamed plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT tanyakelly plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT markbates plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT andresclarke plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT nathanbrady plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT carammartin plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT robertdbrooks plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT dougabrooks plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT stavrosselemidis plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT seanhanniffy plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT ericpdixon plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT sharonaotoole plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell AT johnjoleary plateletsimmunecellsandthecoagulationcascadefriendorfoeofthecirculatingtumourcell |
_version_ |
1721542735954968576 |