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Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types

SIMPLE SUMMARY: Cancer-associated thrombosis is the first cause of death in cancer after cancer-progression itself; however, thrombotic risk is not the same in all cancer types. Here, we exemplified cancer-cell interactions with platelets in tumor microenvironments and their effect on overall thromb...

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Autores principales: Palacios-Acedo, Ana-Luisa, Langiu, Mélanie, Crescence, Lydie, Mège, Diane, Dubois, Christophe, Panicot-Dubois, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833365/
https://www.ncbi.nlm.nih.gov/pubmed/35159000
http://dx.doi.org/10.3390/cancers14030730
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author Palacios-Acedo, Ana-Luisa
Langiu, Mélanie
Crescence, Lydie
Mège, Diane
Dubois, Christophe
Panicot-Dubois, Laurence
author_facet Palacios-Acedo, Ana-Luisa
Langiu, Mélanie
Crescence, Lydie
Mège, Diane
Dubois, Christophe
Panicot-Dubois, Laurence
author_sort Palacios-Acedo, Ana-Luisa
collection PubMed
description SIMPLE SUMMARY: Cancer-associated thrombosis is the first cause of death in cancer after cancer-progression itself; however, thrombotic risk is not the same in all cancer types. Here, we exemplified cancer-cell interactions with platelets in tumor microenvironments and their effect on overall thrombotic risk. We chose three distinct cancer types with varying thrombotic risks: oral cancer (low risk), colorectal cancer (medium risk) and pancreatic cancer (high risk). Understanding these interactions and their consequences is crucial for deepening researcher’s and clinician’s knowledge of cancer-associated thrombosis and finding innovative biomarkers and therapeutic targets. ABSTRACT: The first cause of death in cancer patients, after tumoral progression itself, is thrombo-embolic disease. This cancer-associated hypercoagulability state is known as Trousseau’s syndrome, and the risk for developing thrombotic events differs according to cancer type and stage, as well as within patients. Massive platelet activation by tumor cells is the key mediator of thrombus formation in Trousseau’s syndrome. In this literature review, we aimed to compare the interactions between cancer cells and platelets in three different cancer types, with low, medium and high thrombotic risk. We chose oral squamous cell carcinoma for the low-thrombotic-risk, colorectal adenocarcinoma for the medium-thrombotic-risk, and pancreatic carcinoma for the high-thrombotic-risk cancer type. We showcase that understanding these interactions is of the highest importance to find new biomarkers and therapeutic targets for cancer-associated thrombosis.
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spelling pubmed-88333652022-02-12 Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types Palacios-Acedo, Ana-Luisa Langiu, Mélanie Crescence, Lydie Mège, Diane Dubois, Christophe Panicot-Dubois, Laurence Cancers (Basel) Review SIMPLE SUMMARY: Cancer-associated thrombosis is the first cause of death in cancer after cancer-progression itself; however, thrombotic risk is not the same in all cancer types. Here, we exemplified cancer-cell interactions with platelets in tumor microenvironments and their effect on overall thrombotic risk. We chose three distinct cancer types with varying thrombotic risks: oral cancer (low risk), colorectal cancer (medium risk) and pancreatic cancer (high risk). Understanding these interactions and their consequences is crucial for deepening researcher’s and clinician’s knowledge of cancer-associated thrombosis and finding innovative biomarkers and therapeutic targets. ABSTRACT: The first cause of death in cancer patients, after tumoral progression itself, is thrombo-embolic disease. This cancer-associated hypercoagulability state is known as Trousseau’s syndrome, and the risk for developing thrombotic events differs according to cancer type and stage, as well as within patients. Massive platelet activation by tumor cells is the key mediator of thrombus formation in Trousseau’s syndrome. In this literature review, we aimed to compare the interactions between cancer cells and platelets in three different cancer types, with low, medium and high thrombotic risk. We chose oral squamous cell carcinoma for the low-thrombotic-risk, colorectal adenocarcinoma for the medium-thrombotic-risk, and pancreatic carcinoma for the high-thrombotic-risk cancer type. We showcase that understanding these interactions is of the highest importance to find new biomarkers and therapeutic targets for cancer-associated thrombosis. MDPI 2022-01-30 /pmc/articles/PMC8833365/ /pubmed/35159000 http://dx.doi.org/10.3390/cancers14030730 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
Palacios-Acedo, Ana-Luisa
Langiu, Mélanie
Crescence, Lydie
Mège, Diane
Dubois, Christophe
Panicot-Dubois, Laurence
Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types
title Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types
title_full Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types
title_fullStr Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types
title_full_unstemmed Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types
title_short Platelet and Cancer-Cell Interactions Modulate Cancer-Associated Thrombosis Risk in Different Cancer Types
title_sort platelet and cancer-cell interactions modulate cancer-associated thrombosis risk in different cancer types
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833365/
https://www.ncbi.nlm.nih.gov/pubmed/35159000
http://dx.doi.org/10.3390/cancers14030730
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