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Toll-Like Receptor 9 in Breast Cancer

Toll-like receptor 9 (TLR9) is a cellular DNA receptor of the innate immune system. DNA recognition via TLR9 results in an inflammatory reaction, which eventually also activates a Th1-biased adaptive immune attack. In addition to cells of the immune system, TLR9 mRNA and protein are also widely expr...

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Detalles Bibliográficos
Autores principales: Sandholm, Jouko, Selander, Katri S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105583/
https://www.ncbi.nlm.nih.gov/pubmed/25101078
http://dx.doi.org/10.3389/fimmu.2014.00330
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author Sandholm, Jouko
Selander, Katri S.
author_facet Sandholm, Jouko
Selander, Katri S.
author_sort Sandholm, Jouko
collection PubMed
description Toll-like receptor 9 (TLR9) is a cellular DNA receptor of the innate immune system. DNA recognition via TLR9 results in an inflammatory reaction, which eventually also activates a Th1-biased adaptive immune attack. In addition to cells of the immune system, TLR9 mRNA and protein are also widely expressed in breast cancer cell lines and in clinical breast cancer specimens. Although synthetic TLR9-ligands induce cancer cell invasion in vitro, the role of TLR9 in cancer pathophysiology has remained unclear. In the studies conducted so far, tumor TLR9 expression has been shown to have prognostic significance only in patients that have triple-negative breast cancer (TNBC). Specifically, high tumor TLR9 expression predicts good prognosis among TNBC patients. Pre-clinical studies suggest that TLR9 expression may affect tumor immunophenotype and contribute to the immunogenic benefit of chemotherapy. In this review, we discuss the possible contribution of tumor TLR9 to the pathogenesis and treatment responses in breast cancer.
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spelling pubmed-41055832014-08-06 Toll-Like Receptor 9 in Breast Cancer Sandholm, Jouko Selander, Katri S. Front Immunol Immunology Toll-like receptor 9 (TLR9) is a cellular DNA receptor of the innate immune system. DNA recognition via TLR9 results in an inflammatory reaction, which eventually also activates a Th1-biased adaptive immune attack. In addition to cells of the immune system, TLR9 mRNA and protein are also widely expressed in breast cancer cell lines and in clinical breast cancer specimens. Although synthetic TLR9-ligands induce cancer cell invasion in vitro, the role of TLR9 in cancer pathophysiology has remained unclear. In the studies conducted so far, tumor TLR9 expression has been shown to have prognostic significance only in patients that have triple-negative breast cancer (TNBC). Specifically, high tumor TLR9 expression predicts good prognosis among TNBC patients. Pre-clinical studies suggest that TLR9 expression may affect tumor immunophenotype and contribute to the immunogenic benefit of chemotherapy. In this review, we discuss the possible contribution of tumor TLR9 to the pathogenesis and treatment responses in breast cancer. Frontiers Media S.A. 2014-07-22 /pmc/articles/PMC4105583/ /pubmed/25101078 http://dx.doi.org/10.3389/fimmu.2014.00330 Text en Copyright © 2014 Sandholm and Selander. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sandholm, Jouko
Selander, Katri S.
Toll-Like Receptor 9 in Breast Cancer
title Toll-Like Receptor 9 in Breast Cancer
title_full Toll-Like Receptor 9 in Breast Cancer
title_fullStr Toll-Like Receptor 9 in Breast Cancer
title_full_unstemmed Toll-Like Receptor 9 in Breast Cancer
title_short Toll-Like Receptor 9 in Breast Cancer
title_sort toll-like receptor 9 in breast cancer
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105583/
https://www.ncbi.nlm.nih.gov/pubmed/25101078
http://dx.doi.org/10.3389/fimmu.2014.00330
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