Literature DB >> 25341932

The exploitation of Toll-like receptor 3 signaling in cancer therapy.

Tanja Matijevic Glavan, Jasminka Pavelic1.   

Abstract

Toll-like receptors (TLRs) are a group of transmembrane receptors that recognize molecular motifs of pathogen origin and activate immune response. Although TLRs were first identified in immune system cells, recent studies show they can also be expressed in tumor cells. TLR3 recognizes dsRNA or its synthetic ligand poly (I: C) and is responsible primarily for the defense against viral infections. Recent studies showed that TLR3 can trigger apoptosis in cancer cell. Furthermore, other dsRNA binding receptors (MDA5 and RIG-I), localized in cytoplasm, can also bind poly (I: C) and therefore contribute to this effect. With TLR3's capacity to induce apoptosis and activate the immune system at the same time, TLR3 ligands are an attractive therapeutic option for treatment of cancer. Novel therapies include combining poly (I: C) with other components such as chemotherapeutics, apoptosis enhancers, other TLR ligands and peptides activating the immune system. Slightly modified TLR3 agonists (Ampligen®, Hiltonol®, poly IC-LC) are already being used in clinical studies for cancer therapy as single agents or in combination with other drugs. On the other hand, latest studies forewarn that TLR3 activation can also have tumor promoting role so it is crucial to identify the terms by which TLR3 has pro-tumor/anti-tumor effect in order to safely implement TLR3 ligand based therapy into clinical trials.

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Year:  2014        PMID: 25341932     DOI: 10.2174/1381612820666140826153347

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  15 in total

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Review 2.  Intratumoural immunotherapy: activation of nucleic acid sensing pattern recognition receptors.

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Journal:  Immunooncol Technol       Date:  2019-10-16

3.  Poly(I:C) transfection induces a pro-inflammatory cascade in murine mammary carcinoma and fibrosarcoma cells.

Authors:  A Sales Conniff; G Encalada; S Patel; M Bhandary; F Al-Takrouri; L Heller
Journal:  RNA Biol       Date:  2022-01       Impact factor: 4.766

Review 4.  Immunogenic chemotherapy: Dose and schedule dependence and combination with immunotherapy.

Authors:  Junjie Wu; David J Waxman
Journal:  Cancer Lett       Date:  2018-04-10       Impact factor: 8.679

5.  Toll-like receptor 3 (TLR3) functions as a pivotal target in latent membrane protein 1 (LMP1)-mediated nasopharyngeal carcinoma cell proliferation.

Authors:  Liang Zhou; Xiaoling Hang; Lei Xie
Journal:  Int J Clin Exp Pathol       Date:  2020-02-01

6.  Combinatorial treatment with polyI:C and anti-IL6 enhances apoptosis and suppresses metastasis of lung cancer cells.

Authors:  Wai Hoe Lau; Xiphias Ge Zhu; Shamaine Wei Ting Ho; Shu Chun Chang; Jeak Ling Ding
Journal:  Oncotarget       Date:  2017-05-16

7.  Ligand dependent restoration of human TLR3 signaling and death in p53 mutant cells.

Authors:  Daniel Menendez; Julie M Lowe; Joyce Snipe; Michael A Resnick
Journal:  Oncotarget       Date:  2016-09-20

8.  RIPK3-a predictive marker for personalized immunotherapy?

Authors:  Sigrun Smola
Journal:  Oncoimmunology       Date:  2015-08-24       Impact factor: 8.110

9.  Mobilan: a recombinant adenovirus carrying Toll-like receptor 5 self-activating cassette for cancer immunotherapy.

Authors:  V Mett; E A Komarova; K Greene; I Bespalov; C Brackett; B Gillard; A S Gleiberman; I A Toshkov; S Aygün-Sunar; C Johnson; E Karasik; M Bapardekar-Nair; O V Kurnasov; A L Osterman; P S Stanhope-Baker; C Morrison; M T Moser; B A Foster; A V Gudkov
Journal:  Oncogene       Date:  2017-10-02       Impact factor: 9.867

Review 10.  TLR-mediated metabolic reprogramming in the tumor microenvironment: potential novel strategies for cancer immunotherapy.

Authors:  Lan Huang; Huaxi Xu; Guangyong Peng
Journal:  Cell Mol Immunol       Date:  2018-03-19       Impact factor: 11.530

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