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Profile of soluble factors in pleural effusions predict prognosis in mesothelioma
BACKGROUND: Pleural mesothelioma is a deadly asbestos induced cancer. Less than 10% of mesothelioma patients survive 5 years post diagnosis. However survival can range from a few months to a number of years. Accurate prediction of survival is important for patients to plan for their remaining life,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925107/ https://www.ncbi.nlm.nih.gov/pubmed/34487023 http://dx.doi.org/10.3233/CBM-210280 |
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author | Dick, I.M. Lee, Y.C.G. Cheah, H.M. Miranda, A. Robinson, B.W.S. Creaney, J. |
author_facet | Dick, I.M. Lee, Y.C.G. Cheah, H.M. Miranda, A. Robinson, B.W.S. Creaney, J. |
author_sort | Dick, I.M. |
collection | PubMed |
description | BACKGROUND: Pleural mesothelioma is a deadly asbestos induced cancer. Less than 10% of mesothelioma patients survive 5 years post diagnosis. However survival can range from a few months to a number of years. Accurate prediction of survival is important for patients to plan for their remaining life, and for clinicians to determine appropriate therapy. One unusual feature of mesothelioma is that patients frequently present with tumor-associated pleural effusions early in the course of the disease. OBJECTIVE: To study whether cells and molecules present in pleural effusions provide prognostic information for mesothelioma. METHODS: We profiled the cellular constituents and concentrations of 40 cytokines, chemokines and cellular factors (collectively “soluble factors”) involved in inflammatory and immune signalling pathways in pleural effusion samples from 50 mesothelioma patients. Associations with survival were evaluated by Cox proportional hazards regression methods. Results for the two soluble factors most significantly and independently associated with survival were validated in an independent set of samples ([Formula: see text] 51) using a separate assay system. RESULTS: Survival analysis revealed that IL8, IL2Ra (CD25) and PF4 were independent determinants of a more negative prognosis in mesothelioma patients, independent of other known prognostic factors. Lipocalin2 and IL4 were associated with better prognosis. CONCLUSIONS: This study demonstrates that pleural effusions rich in a range of soluble factors are associated with poor prognosis. These findings will enhance our ability to prognosticate outcomes in mesothelioma patients. |
format | Online Article Text |
id | pubmed-8925107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89251072022-03-30 Profile of soluble factors in pleural effusions predict prognosis in mesothelioma Dick, I.M. Lee, Y.C.G. Cheah, H.M. Miranda, A. Robinson, B.W.S. Creaney, J. Cancer Biomark Research Article BACKGROUND: Pleural mesothelioma is a deadly asbestos induced cancer. Less than 10% of mesothelioma patients survive 5 years post diagnosis. However survival can range from a few months to a number of years. Accurate prediction of survival is important for patients to plan for their remaining life, and for clinicians to determine appropriate therapy. One unusual feature of mesothelioma is that patients frequently present with tumor-associated pleural effusions early in the course of the disease. OBJECTIVE: To study whether cells and molecules present in pleural effusions provide prognostic information for mesothelioma. METHODS: We profiled the cellular constituents and concentrations of 40 cytokines, chemokines and cellular factors (collectively “soluble factors”) involved in inflammatory and immune signalling pathways in pleural effusion samples from 50 mesothelioma patients. Associations with survival were evaluated by Cox proportional hazards regression methods. Results for the two soluble factors most significantly and independently associated with survival were validated in an independent set of samples ([Formula: see text] 51) using a separate assay system. RESULTS: Survival analysis revealed that IL8, IL2Ra (CD25) and PF4 were independent determinants of a more negative prognosis in mesothelioma patients, independent of other known prognostic factors. Lipocalin2 and IL4 were associated with better prognosis. CONCLUSIONS: This study demonstrates that pleural effusions rich in a range of soluble factors are associated with poor prognosis. These findings will enhance our ability to prognosticate outcomes in mesothelioma patients. IOS Press 2022-02-14 /pmc/articles/PMC8925107/ /pubmed/34487023 http://dx.doi.org/10.3233/CBM-210280 Text en © 2022 – The authors. Published by IOS Press. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Dick, I.M. Lee, Y.C.G. Cheah, H.M. Miranda, A. Robinson, B.W.S. Creaney, J. Profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
title | Profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
title_full | Profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
title_fullStr | Profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
title_full_unstemmed | Profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
title_short | Profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
title_sort | profile of soluble factors in pleural effusions predict prognosis in mesothelioma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925107/ https://www.ncbi.nlm.nih.gov/pubmed/34487023 http://dx.doi.org/10.3233/CBM-210280 |
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