Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies
In the last decade, it has become apparent that toll-like receptor (TLR) signaling can play an important role in ovarian cancer (OC) progression. Interestingly, TLR activation in immune cells can help activate an anti-tumor response, while TLR signaling in tumor cells themselves is often associated...
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2014
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pubmed-41056892014-08-06 Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies Muccioli, Maria Benencia, Fabian Immunology In the last decade, it has become apparent that toll-like receptor (TLR) signaling can play an important role in ovarian cancer (OC) progression. Interestingly, TLR activation in immune cells can help activate an anti-tumor response, while TLR signaling in tumor cells themselves is often associated with cancer-promoting inflammation. For example, it has been shown that TLR activation in dendritic cells can result in more effective antigen presentation to T cells, thereby favoring tumor eradication. However, aberrant TLR expression in OC cells is associated with more aggressive disease (likely due to recruitment of pro-tumoral leukocytes to the tumor site) and has also been implicated in resistance to mainstream chemotherapy. The delicate balance of TLR activation in the tumor microenvironment in different cell types altogether help shape the inflammatory profile and outcome of tumor growth or regression. With further studies, specific activation or repression of TLRs may be harnessed to offer novel immunotherapies or adjuvants to traditional chemotherapy for some OC patients. Herewith, we review recent literature on basic and translational research concerning therapeutic targeting of TLR pathways for the treatment of OC. Frontiers Media S.A. 2014-07-22 /pmc/articles/PMC4105689/ /pubmed/25101083 http://dx.doi.org/10.3389/fimmu.2014.00341 Text en Copyright © 2014 Muccioli and Benencia. 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. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Muccioli, Maria Benencia, Fabian |
spellingShingle |
Muccioli, Maria Benencia, Fabian Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies |
author_facet |
Muccioli, Maria Benencia, Fabian |
author_sort |
Muccioli, Maria |
title |
Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies |
title_short |
Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies |
title_full |
Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies |
title_fullStr |
Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies |
title_full_unstemmed |
Toll-like Receptors in Ovarian Cancer as Targets for Immunotherapies |
title_sort |
toll-like receptors in ovarian cancer as targets for immunotherapies |
description |
In the last decade, it has become apparent that toll-like receptor (TLR) signaling can play an important role in ovarian cancer (OC) progression. Interestingly, TLR activation in immune cells can help activate an anti-tumor response, while TLR signaling in tumor cells themselves is often associated with cancer-promoting inflammation. For example, it has been shown that TLR activation in dendritic cells can result in more effective antigen presentation to T cells, thereby favoring tumor eradication. However, aberrant TLR expression in OC cells is associated with more aggressive disease (likely due to recruitment of pro-tumoral leukocytes to the tumor site) and has also been implicated in resistance to mainstream chemotherapy. The delicate balance of TLR activation in the tumor microenvironment in different cell types altogether help shape the inflammatory profile and outcome of tumor growth or regression. With further studies, specific activation or repression of TLRs may be harnessed to offer novel immunotherapies or adjuvants to traditional chemotherapy for some OC patients. Herewith, we review recent literature on basic and translational research concerning therapeutic targeting of TLR pathways for the treatment of OC. |
publisher |
Frontiers Media S.A. |
publishDate |
2014 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105689/ |
_version_ |
1613116354330624000 |