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Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways

Malignant cancers employ diverse and intricate immune evasion strategies, which lead to inadequately effective responses of many clinical cancer therapies. However, emerging data suggest that activation of the tolerant innate immune system in cancer patients is able, at least partially, to counterac...

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Detalles Bibliográficos
Autores principales: Li, Kai, Qu, Shuai, Chen, Xi, Wu, Qiong, Shi, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343938/
https://www.ncbi.nlm.nih.gov/pubmed/28216575
http://dx.doi.org/10.3390/ijms18020404
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author Li, Kai
Qu, Shuai
Chen, Xi
Wu, Qiong
Shi, Ming
author_facet Li, Kai
Qu, Shuai
Chen, Xi
Wu, Qiong
Shi, Ming
author_sort Li, Kai
collection PubMed
description Malignant cancers employ diverse and intricate immune evasion strategies, which lead to inadequately effective responses of many clinical cancer therapies. However, emerging data suggest that activation of the tolerant innate immune system in cancer patients is able, at least partially, to counteract tumor-induced immunosuppression, which indicates triggering of the innate immune response as a novel immunotherapeutic strategy may result in improved therapeutic outcomes for cancer patients. The promising innate immune targets include Toll-like Receptors (TLRs), RIG-I-like Receptors (RLRs), and Stimulator of Interferon Genes (STING). This review discusses the antitumor properties of TLRs, RLRs, and STING-mediated innate immune pathways, as well as the promising innate immune targets for potential application in cancer immunotherapy.
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spelling pubmed-53439382017-03-16 Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways Li, Kai Qu, Shuai Chen, Xi Wu, Qiong Shi, Ming Int J Mol Sci Review Malignant cancers employ diverse and intricate immune evasion strategies, which lead to inadequately effective responses of many clinical cancer therapies. However, emerging data suggest that activation of the tolerant innate immune system in cancer patients is able, at least partially, to counteract tumor-induced immunosuppression, which indicates triggering of the innate immune response as a novel immunotherapeutic strategy may result in improved therapeutic outcomes for cancer patients. The promising innate immune targets include Toll-like Receptors (TLRs), RIG-I-like Receptors (RLRs), and Stimulator of Interferon Genes (STING). This review discusses the antitumor properties of TLRs, RLRs, and STING-mediated innate immune pathways, as well as the promising innate immune targets for potential application in cancer immunotherapy. MDPI 2017-02-14 /pmc/articles/PMC5343938/ /pubmed/28216575 http://dx.doi.org/10.3390/ijms18020404 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Li, Kai
Qu, Shuai
Chen, Xi
Wu, Qiong
Shi, Ming
Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
title Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
title_full Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
title_fullStr Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
title_full_unstemmed Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
title_short Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
title_sort promising targets for cancer immunotherapy: tlrs, rlrs, and sting-mediated innate immune pathways
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343938/
https://www.ncbi.nlm.nih.gov/pubmed/28216575
http://dx.doi.org/10.3390/ijms18020404
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