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Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis?
BACKGROUND: Cancer-related venous thromboembolism (VTE) heralds a poor prognosis, especially in pancreatic adenocarcinoma (PAC). Tissue factor (TF) is implicated as one of the main culprits in PAC-associated VTE and disease progression. METHODS: In a prospective cohort study of 79 PAC patients, we m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973148/ https://www.ncbi.nlm.nih.gov/pubmed/27404454 http://dx.doi.org/10.1038/bjc.2016.170 |
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author | Woei-A-Jin, F J Sherida H Tesselaar, Margot E T Garcia Rodriguez, Patrica Romijn, Fred P H T M Bertina, Rogier M Osanto, Susanne |
author_facet | Woei-A-Jin, F J Sherida H Tesselaar, Margot E T Garcia Rodriguez, Patrica Romijn, Fred P H T M Bertina, Rogier M Osanto, Susanne |
author_sort | Woei-A-Jin, F J Sherida H |
collection | PubMed |
description | BACKGROUND: Cancer-related venous thromboembolism (VTE) heralds a poor prognosis, especially in pancreatic adenocarcinoma (PAC). Tissue factor (TF) is implicated as one of the main culprits in PAC-associated VTE and disease progression. METHODS: In a prospective cohort study of 79 PAC patients, we measured plasma CA19–9 and microparticle-associated TF activity (MP-TF activity). In addition, we enumerated TF(+)MPs and MUC1(+)MPs in plasma (n=55), and studied the expression of TF, MUC1, CD31 and CD68 in tumour tissue (n=44). RESULTS: Plasma MP-TF activity was markedly elevated in PAC patients with VTE compared with those without (median: 1925 vs 113 fM Xa min(−1); P<0.001) and correlated with the extent of thromboembolic events, metastatic disease and short survival. Similar results were found for CA19–9. Patients with massively progressing thrombosis and cerebral embolisms despite anticoagulant therapy (n=3) had the highest MP-TF activities (12 118–40 188 fM Xa min(−1)) and CA19–9 (40 730–197 000 kU l(−1)). All tumours expressed MUC1 and TF. MP-TF activity did not correlate with intensity of TF expression in adenocarcinoma cells, but corresponded with numbers of TF(+) macrophages in the surrounding stroma. CONCLUSIONS: Circulating TF(+)MPs and mucins may concertedly aggravate coagulopathy in PAC. Understanding of underlying mechanisms may result in new treatment strategies for VTE prevention and improvement of survival. |
format | Online Article Text |
id | pubmed-4973148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49731482017-07-26 Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? Woei-A-Jin, F J Sherida H Tesselaar, Margot E T Garcia Rodriguez, Patrica Romijn, Fred P H T M Bertina, Rogier M Osanto, Susanne Br J Cancer Molecular Diagnostics BACKGROUND: Cancer-related venous thromboembolism (VTE) heralds a poor prognosis, especially in pancreatic adenocarcinoma (PAC). Tissue factor (TF) is implicated as one of the main culprits in PAC-associated VTE and disease progression. METHODS: In a prospective cohort study of 79 PAC patients, we measured plasma CA19–9 and microparticle-associated TF activity (MP-TF activity). In addition, we enumerated TF(+)MPs and MUC1(+)MPs in plasma (n=55), and studied the expression of TF, MUC1, CD31 and CD68 in tumour tissue (n=44). RESULTS: Plasma MP-TF activity was markedly elevated in PAC patients with VTE compared with those without (median: 1925 vs 113 fM Xa min(−1); P<0.001) and correlated with the extent of thromboembolic events, metastatic disease and short survival. Similar results were found for CA19–9. Patients with massively progressing thrombosis and cerebral embolisms despite anticoagulant therapy (n=3) had the highest MP-TF activities (12 118–40 188 fM Xa min(−1)) and CA19–9 (40 730–197 000 kU l(−1)). All tumours expressed MUC1 and TF. MP-TF activity did not correlate with intensity of TF expression in adenocarcinoma cells, but corresponded with numbers of TF(+) macrophages in the surrounding stroma. CONCLUSIONS: Circulating TF(+)MPs and mucins may concertedly aggravate coagulopathy in PAC. Understanding of underlying mechanisms may result in new treatment strategies for VTE prevention and improvement of survival. Nature Publishing Group 2016-07-26 2016-07-12 /pmc/articles/PMC4973148/ /pubmed/27404454 http://dx.doi.org/10.1038/bjc.2016.170 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Molecular Diagnostics Woei-A-Jin, F J Sherida H Tesselaar, Margot E T Garcia Rodriguez, Patrica Romijn, Fred P H T M Bertina, Rogier M Osanto, Susanne Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? |
title | Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? |
title_full | Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? |
title_fullStr | Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? |
title_full_unstemmed | Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? |
title_short | Tissue factor-bearing microparticles and CA19.9: two players in pancreatic cancer-associated thrombosis? |
title_sort | tissue factor-bearing microparticles and ca19.9: two players in pancreatic cancer-associated thrombosis? |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973148/ https://www.ncbi.nlm.nih.gov/pubmed/27404454 http://dx.doi.org/10.1038/bjc.2016.170 |
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