The anticancer functions of RIG-I-like receptors, RIG-I and MDA5, and their applications in cancer therapy
- PMID: 28917654
- DOI: 10.1016/j.trsl.2017.08.004
The anticancer functions of RIG-I-like receptors, RIG-I and MDA5, and their applications in cancer therapy
Abstract
Cancer is a major cause of death worldwide, and its incidence and mortality continuously increase in China. Nowadays, cancer heavily influences our health and constitutes enormous burden on society and families. Although there are many tools for cancer treatment, but the overall therapeutic effect is poor. In addition, cancer cells often develop resistance to therapy due to defective cell death or immune escape mechanisms. Therefore, it is a promising way for cancer treatment to effectively activate apoptosis and conquer immunosuppression. RIG-I-like receptors (RLRs) belong to RNA-sensing pattern recognition receptors (PRRs), one of the major subsets of PRRs, and play a critical role in sensing RNA viruses and initiate host antiviral responses such as the production of type I interferons (IFNs), proinflammatory cytokines, and other immune response molecules. Recent studies have demonstrated that tumor cells could mimic viral infection to activate viral recognition of immune system and the activation of interferon response pathway. RIG-I and MDA5, two members of RLRs family, could induce growth inhibition or apoptosis of multiple types of cancer cells on the activation by RNA ligands in IFN-dependent or IFN-independent approach. Previous studies have reviewed PRRs as promising immunotherapy targets for colorectal cancer and pancreatic cancer. However, until now, a comprehensive review on the role of RLRs in the development and treatment of various cancers is still lacking. In this article, we reviewed the latest studies on the roles as well as the mechanisms of RIG-I and MDA5 in the development of various cancers and therapeutic potentials of targeting RIG-I and MDA5 for cancer treatment.
Copyright © 2017 Elsevier Inc. All rights reserved.
Similar articles
-
An arms race between 5'ppp-RNA virus and its alternative recognition receptor MDA5 in RIG-I-lost teleost fish.Elife. 2024 Sep 30;13:RP94898. doi: 10.7554/eLife.94898. Elife. 2024. PMID: 39347580 Free PMC article.
-
Analysis of Porcine RIG-I Like Receptors Revealed the Positive Regulation of RIG-I and MDA5 by LGP2.Front Immunol. 2021 May 18;12:609543. doi: 10.3389/fimmu.2021.609543. eCollection 2021. Front Immunol. 2021. PMID: 34093517 Free PMC article.
-
LGP2 binds to PACT to regulate RIG-I- and MDA5-mediated antiviral responses.Sci Signal. 2019 Oct 1;12(601):eaar3993. doi: 10.1126/scisignal.aar3993. Sci Signal. 2019. PMID: 31575732
-
Structures of RIG-I-Like Receptors and Insights into Viral RNA Sensing.Adv Exp Med Biol. 2019;1172:157-188. doi: 10.1007/978-981-13-9367-9_8. Adv Exp Med Biol. 2019. PMID: 31628656 Review.
-
Comparative Structure and Function Analysis of the RIG-I-Like Receptors: RIG-I and MDA5.Front Immunol. 2019 Jul 17;10:1586. doi: 10.3389/fimmu.2019.01586. eCollection 2019. Front Immunol. 2019. PMID: 31379819 Free PMC article. Review.
Cited by
-
RIG-I-like Receptor Regulation of Immune Cell Function and Therapeutic Implications.J Immunol. 2022 Sep 1;209(5):845-854. doi: 10.4049/jimmunol.2200395. J Immunol. 2022. PMID: 36130131 Free PMC article. Review.
-
The molecular mechanism of RIG-I activation and signaling.Immunol Rev. 2021 Nov;304(1):154-168. doi: 10.1111/imr.13022. Epub 2021 Sep 12. Immunol Rev. 2021. PMID: 34514601 Free PMC article. Review.
-
Death-associated protein 3 in cancer-discrepant roles of DAP3 in tumours and molecular mechanisms.Front Oncol. 2024 Jan 30;13:1323751. doi: 10.3389/fonc.2023.1323751. eCollection 2023. Front Oncol. 2024. PMID: 38352299 Free PMC article. Review.
-
Bacterial Translocation in Gastrointestinal Cancers and Cancer Treatment.Biomedicines. 2022 Feb 4;10(2):380. doi: 10.3390/biomedicines10020380. Biomedicines. 2022. PMID: 35203589 Free PMC article. Review.
-
Poly(I:C) transfection induces a pro-inflammatory cascade in murine mammary carcinoma and fibrosarcoma cells.RNA Biol. 2022 Jan;19(1):841-851. doi: 10.1080/15476286.2022.2084861. RNA Biol. 2022. PMID: 35737804 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources