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Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer
BACKGROUND: The link between inflammation and carcinogenesis is indisputable. In trying to understand key factors at play, cancer research has developed an interest in the toll-like receptors (TLRs), which have shown signs of having prognostic value in various adenocarcinomas. We began investigating...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636725/ https://www.ncbi.nlm.nih.gov/pubmed/31314777 http://dx.doi.org/10.1371/journal.pone.0219245 |
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author | Lanki, Mira Seppänen, Hanna Mustonen, Harri Hagström, Jaana Haglund, Caj |
author_facet | Lanki, Mira Seppänen, Hanna Mustonen, Harri Hagström, Jaana Haglund, Caj |
author_sort | Lanki, Mira |
collection | PubMed |
description | BACKGROUND: The link between inflammation and carcinogenesis is indisputable. In trying to understand key factors at play, cancer research has developed an interest in the toll-like receptors (TLRs), which have shown signs of having prognostic value in various adenocarcinomas. We began investigating the expression of toll-like receptors 1, 3, 5, 7, and 9 to evaluate their prognostic value of patients with pancreatic ductal adenocarcinoma (PDAC). METHODS: We collected tumor biopsies from 154 stage I-III PDAC patients surgically treated at Helsinki University Hospital between 2002 and 2011, excluding patients undergoing neoadjuvant therapy. We used tissue microarray slides and immunohistochemistry to assess expression of TLRs 1, 3, 5, 7, and 9 in PDAC tissue. Immunopositivity scores and clinicopathological characteristics were subjected to Fisher’s exact test or the linear-by-linear association test. For the survival analysis, we applied the Kaplan-Meier method and log-rank test, and the Cox regression proportional hazard model served for univariate and multivariate analyses. RESULTS: Strong TLR1 expression was observable in 60 (39%), strong TLR3 in 48 (31%), strong TLR5 in 58 (38%), strong TLR7 in 14 (9%), and strong TLR9 in 22 (14%) patients. The multivariate analysis showed strong TLR1 expression to associate with better survival than moderate, low, or negative expression (HR = 0.68; 95% CI 0.47–0.99; p = 0.044). Additionally, those few patients with tumors negative for TLR1, TLR3, TLR7, or TLR9 fared poorly (HR = 2.41; 95% CI 1.31–4.43; p = 0.005; n = 13). CONCLUSION: Strong TLR1 expression suggested better prognosis in PDAC patients, whereas negative expression of TLR1, TLR3, TLR7, or TLR9 was a sign of poor prognosis. |
format | Online Article Text |
id | pubmed-6636725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66367252019-07-25 Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer Lanki, Mira Seppänen, Hanna Mustonen, Harri Hagström, Jaana Haglund, Caj PLoS One Research Article BACKGROUND: The link between inflammation and carcinogenesis is indisputable. In trying to understand key factors at play, cancer research has developed an interest in the toll-like receptors (TLRs), which have shown signs of having prognostic value in various adenocarcinomas. We began investigating the expression of toll-like receptors 1, 3, 5, 7, and 9 to evaluate their prognostic value of patients with pancreatic ductal adenocarcinoma (PDAC). METHODS: We collected tumor biopsies from 154 stage I-III PDAC patients surgically treated at Helsinki University Hospital between 2002 and 2011, excluding patients undergoing neoadjuvant therapy. We used tissue microarray slides and immunohistochemistry to assess expression of TLRs 1, 3, 5, 7, and 9 in PDAC tissue. Immunopositivity scores and clinicopathological characteristics were subjected to Fisher’s exact test or the linear-by-linear association test. For the survival analysis, we applied the Kaplan-Meier method and log-rank test, and the Cox regression proportional hazard model served for univariate and multivariate analyses. RESULTS: Strong TLR1 expression was observable in 60 (39%), strong TLR3 in 48 (31%), strong TLR5 in 58 (38%), strong TLR7 in 14 (9%), and strong TLR9 in 22 (14%) patients. The multivariate analysis showed strong TLR1 expression to associate with better survival than moderate, low, or negative expression (HR = 0.68; 95% CI 0.47–0.99; p = 0.044). Additionally, those few patients with tumors negative for TLR1, TLR3, TLR7, or TLR9 fared poorly (HR = 2.41; 95% CI 1.31–4.43; p = 0.005; n = 13). CONCLUSION: Strong TLR1 expression suggested better prognosis in PDAC patients, whereas negative expression of TLR1, TLR3, TLR7, or TLR9 was a sign of poor prognosis. Public Library of Science 2019-07-17 /pmc/articles/PMC6636725/ /pubmed/31314777 http://dx.doi.org/10.1371/journal.pone.0219245 Text en © 2019 Lanki et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lanki, Mira Seppänen, Hanna Mustonen, Harri Hagström, Jaana Haglund, Caj Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
title | Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
title_full | Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
title_fullStr | Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
title_full_unstemmed | Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
title_short | Toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
title_sort | toll-like receptor 1 predicts favorable prognosis in pancreatic cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636725/ https://www.ncbi.nlm.nih.gov/pubmed/31314777 http://dx.doi.org/10.1371/journal.pone.0219245 |
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