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...

Full description

Bibliographic Details
Main Authors: Muccioli, Maria, Benencia, Fabian
Format: Online
Language:English
Published: Frontiers Media S.A. 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105689/
id pubmed-4105689
recordtype oai_dc
spelling 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