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Noncoding RNAs As an Emerging Resistance Mechanism to Immunotherapies in Cancer: Basic Evidence and Therapeutic Implications

Overview
Journal Front Immunol
Date 2023 Sep 28
PMID 37767098
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Abstract

The increasing knowledge in the field of oncoimmunology has led to extensive research into tumor immune landscape and a plethora of clinical immunotherapy trials in cancer patients. Immunotherapy has become a clinically beneficial alternative to traditional treatments by enhancing the power of the host immune system against cancer. However, it only works for a minority of cancers. Drug resistance continues to be a major obstacle to the success of immunotherapy in cancer. A fundamental understanding of the detailed mechanisms underlying immunotherapy resistance in cancer patients will provide new potential directions for further investigations of cancer treatment. Noncoding RNAs (ncRNAs) are tightly linked with cancer initiation and development due to their critical roles in gene expression and epigenetic modulation. The clear appreciation of the role of ncRNAs in tumor immunity has opened new frontiers in cancer research and therapy. Furthermore, ncRNAs are increasingly acknowledged as a key factor influencing immunotherapeutic treatment outcomes. Here, we review the available evidence on the roles of ncRNAs in immunotherapy resistance, with an emphasis on the associated mechanisms behind ncRNA-mediated immune resistance. The clinical implications of immune-related ncRNAs are also discussed, shedding light on the potential ncRNA-based therapies to overcome the resistance to immunotherapy.

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References
1.
Iwahori K . Cytotoxic CD8 Lymphocytes in the Tumor Microenvironment. Adv Exp Med Biol. 2020; 1224:53-62. DOI: 10.1007/978-3-030-35723-8_4. View

2.
Segal M, Slack F . Challenges identifying efficacious miRNA therapeutics for cancer. Expert Opin Drug Discov. 2020; 15(9):987-992. PMC: 7415578. DOI: 10.1080/17460441.2020.1765770. View

3.
Sharma P, Hu-Lieskovan S, Wargo J, Ribas A . Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy. Cell. 2017; 168(4):707-723. PMC: 5391692. DOI: 10.1016/j.cell.2017.01.017. View

4.
Hu Z, Chen G, Zhao Y, Gao H, Li L, Yin Y . Exosome-derived circCCAR1 promotes CD8 + T-cell dysfunction and anti-PD1 resistance in hepatocellular carcinoma. Mol Cancer. 2023; 22(1):55. PMC: 10024440. DOI: 10.1186/s12943-023-01759-1. View

5.
Ge W, Chi H, Tang H, Xu J, Wang J, Cai W . Circular RNA CELF1 drives immunosuppression and anti-PD1 therapy resistance in non-small cell lung cancer via the miR-491-5p/EGFR axis. Aging (Albany NY). 2021; 13(22):24560-24579. PMC: 8660608. DOI: 10.18632/aging.203576. View