miRNAs Related to Immune Checkpoint Inhibitor Response: A Systematic Review

Author:

García-Giménez José Luis123ORCID,Saadi Wiam4,Ortega Angel L.5ORCID,Lahoz Agustin67ORCID,Suay Guillermo8ORCID,Carretero Julián5,Pereda Javier5ORCID,Fatmi Ahlam9ORCID,Pallardó Federico V.123ORCID,Mena-Molla Salvador25

Affiliation:

1. Department of Physiology, Faculty of Medicine and Dentistry, University of Valencia, 46010 Valencia, Spain

2. INCLIVA Health Research Institute, INCLIVA, 46010 Valencia, Spain

3. Consortium Center for Biomedical Network Research on Rare Diseases (CIBERER), Institute of Health Carlos III, 46010 Valencia, Spain

4. Department of Biology, Faculty of Nature, Life and Earth Sciences, University of Djillali Bounaama, Khemis Miliana 44225, Algeria

5. Department of Physiology, Faculty of Pharmacy, University of Valencia, 46100 Burjassot, Spain

6. Biomarkers and Precision Medicine Unit, Health Research Institute-Hospital La Fe, 46026 Valencia, Spain

7. Analytical Unit, Health Research Institute-Hospital La Fe, 46026 Valencia, Spain

8. Medical Oncology Department, Hospital Universitari i Politècnic La Fe, 46026 Valencia, Spain

9. Department of Microbiology & Biochemistry, Faculty of Science, University of M’sila, M’sila 28000, Algeria

Abstract

The advent of immune checkpoint inhibitors (ICIs) has represented a breakthrough in the treatment of many cancers, although a high number of patients fail to respond to ICIs, which is partially due to the ability of tumor cells to evade immune system surveillance. Non-coding microRNAs (miRNAs) have been shown to modulate the immune evasion of tumor cells, and there is thus growing interest in elucidating whether these miRNAs could be targetable or proposed as novel biomarkers for prognosis and treatment response to ICIs. We therefore performed an extensive literature analysis to evaluate the clinical utility of miRNAs with a confirmed direct relationship with treatment response to ICIs. As a result of this systematic review, we have stratified the miRNA landscape into (i) miRNAs whose levels directly modulate response to ICIs, (ii) miRNAs whose expression is modulated by ICIs, and (iii) miRNAs that directly elicit toxic effects or participate in immune-related adverse events (irAEs) caused by ICIs.

Funder

UV-La Fe 2022 Programa PROYECTOS DE INNOVACIÓN

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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