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Anti-tumor Activity of Toll-Like Receptor 7 Agonists

Toll-like receptors (TLRs) are a class of pattern recognition receptors that play a bridging role in innate immunity and adaptive immunity. The activated TLRs not only induce inflammatory responses, but also elicit the development of antigen specific immunity. TLR7, a member of TLR family, is an int...

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Autores principales: Chi, Huju, Li, Chunman, Zhao, Flora Sha, Zhang, Li, Ng, Tzi Bun, Jin, Guangyi, Sha, Ou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450331/
https://www.ncbi.nlm.nih.gov/pubmed/28620298
http://dx.doi.org/10.3389/fphar.2017.00304
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author Chi, Huju
Li, Chunman
Zhao, Flora Sha
Zhang, Li
Ng, Tzi Bun
Jin, Guangyi
Sha, Ou
author_facet Chi, Huju
Li, Chunman
Zhao, Flora Sha
Zhang, Li
Ng, Tzi Bun
Jin, Guangyi
Sha, Ou
author_sort Chi, Huju
collection PubMed
description Toll-like receptors (TLRs) are a class of pattern recognition receptors that play a bridging role in innate immunity and adaptive immunity. The activated TLRs not only induce inflammatory responses, but also elicit the development of antigen specific immunity. TLR7, a member of TLR family, is an intracellular receptor expressed on the membrane of endosomes. TLR7 can be triggered not only by ssRNA during viral infections, but also by immune modifiers that share a similar structure to nucleosides. Its powerful immune stimulatory action can be potentially used in the anti-tumor therapy. This article reviewed the anti-tumor activity and mechanism of TLR7 agonists that are frequently applied in preclinical and clinical investigations, and mainly focused on small synthetic molecules, including imiquimod, resiquimod, gardiquimod, and 852A, etc.
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spelling pubmed-54503312017-06-15 Anti-tumor Activity of Toll-Like Receptor 7 Agonists Chi, Huju Li, Chunman Zhao, Flora Sha Zhang, Li Ng, Tzi Bun Jin, Guangyi Sha, Ou Front Pharmacol Pharmacology Toll-like receptors (TLRs) are a class of pattern recognition receptors that play a bridging role in innate immunity and adaptive immunity. The activated TLRs not only induce inflammatory responses, but also elicit the development of antigen specific immunity. TLR7, a member of TLR family, is an intracellular receptor expressed on the membrane of endosomes. TLR7 can be triggered not only by ssRNA during viral infections, but also by immune modifiers that share a similar structure to nucleosides. Its powerful immune stimulatory action can be potentially used in the anti-tumor therapy. This article reviewed the anti-tumor activity and mechanism of TLR7 agonists that are frequently applied in preclinical and clinical investigations, and mainly focused on small synthetic molecules, including imiquimod, resiquimod, gardiquimod, and 852A, etc. Frontiers Media S.A. 2017-05-31 /pmc/articles/PMC5450331/ /pubmed/28620298 http://dx.doi.org/10.3389/fphar.2017.00304 Text en Copyright © 2017 Chi, Li, Zhao, Zhang, Ng, Jin and Sha. http://creativecommons.org/licenses/by/4.0/ 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 Pharmacology
Chi, Huju
Li, Chunman
Zhao, Flora Sha
Zhang, Li
Ng, Tzi Bun
Jin, Guangyi
Sha, Ou
Anti-tumor Activity of Toll-Like Receptor 7 Agonists
title Anti-tumor Activity of Toll-Like Receptor 7 Agonists
title_full Anti-tumor Activity of Toll-Like Receptor 7 Agonists
title_fullStr Anti-tumor Activity of Toll-Like Receptor 7 Agonists
title_full_unstemmed Anti-tumor Activity of Toll-Like Receptor 7 Agonists
title_short Anti-tumor Activity of Toll-Like Receptor 7 Agonists
title_sort anti-tumor activity of toll-like receptor 7 agonists
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450331/
https://www.ncbi.nlm.nih.gov/pubmed/28620298
http://dx.doi.org/10.3389/fphar.2017.00304
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