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The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis

Laboratory evidence of aberrant coagulation is found in the majority of patients with advanced pancreatic cancer and a clinical consequence of this is the high incidence and prevalence of vascular thromboembolic events. Other sequelae are hypothesized to be the facilitation and acceleration of mecha...

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Autores principales: Echrish, Hussein, Madden, Leigh A., Greenman, John, Maraveyas, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756361/
https://www.ncbi.nlm.nih.gov/pubmed/24212618
http://dx.doi.org/10.3390/cancers3010267
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author Echrish, Hussein
Madden, Leigh A.
Greenman, John
Maraveyas, Anthony
author_facet Echrish, Hussein
Madden, Leigh A.
Greenman, John
Maraveyas, Anthony
author_sort Echrish, Hussein
collection PubMed
description Laboratory evidence of aberrant coagulation is found in the majority of patients with advanced pancreatic cancer and a clinical consequence of this is the high incidence and prevalence of vascular thromboembolic events. Other sequelae are hypothesized to be the facilitation and acceleration of mechanisms that define the malignant phenotype, such as invasion, trafficking and anchoring, establishing the metastatic niche and inducing angiogenesis. We review the in vitro and preclinical evidence that supports the role of the coagulation apparatus in the metastatic process of pancreatic cancer, with a particular emphasis on interaction of this pathway with clinically-targeted growth factor receptor pathways. Links between hemostasis, angiogenesis and epidermal growth factor pathways and their significance as therapeutic targets are considered.
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spelling pubmed-37563612013-09-04 The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis Echrish, Hussein Madden, Leigh A. Greenman, John Maraveyas, Anthony Cancers (Basel) Review Laboratory evidence of aberrant coagulation is found in the majority of patients with advanced pancreatic cancer and a clinical consequence of this is the high incidence and prevalence of vascular thromboembolic events. Other sequelae are hypothesized to be the facilitation and acceleration of mechanisms that define the malignant phenotype, such as invasion, trafficking and anchoring, establishing the metastatic niche and inducing angiogenesis. We review the in vitro and preclinical evidence that supports the role of the coagulation apparatus in the metastatic process of pancreatic cancer, with a particular emphasis on interaction of this pathway with clinically-targeted growth factor receptor pathways. Links between hemostasis, angiogenesis and epidermal growth factor pathways and their significance as therapeutic targets are considered. Molecular Diversity Preservation International (MDPI) 2011-01-11 /pmc/articles/PMC3756361/ /pubmed/24212618 http://dx.doi.org/10.3390/cancers3010267 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Echrish, Hussein
Madden, Leigh A.
Greenman, John
Maraveyas, Anthony
The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis
title The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis
title_full The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis
title_fullStr The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis
title_full_unstemmed The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis
title_short The Hemostasis Apparatus in Pancreatic Cancer and Its Importance beyond Thrombosis
title_sort hemostasis apparatus in pancreatic cancer and its importance beyond thrombosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756361/
https://www.ncbi.nlm.nih.gov/pubmed/24212618
http://dx.doi.org/10.3390/cancers3010267
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