Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Jun;480(6):3455-3476.
doi: 10.1007/s11010-024-05169-9. Epub 2025 Jan 27.

Exploring ferroptosis and miRNAs: implications for cancer modulation and therapy

Affiliations
Review

Exploring ferroptosis and miRNAs: implications for cancer modulation and therapy

Mobarakeh Ajam-Hosseini et al. Mol Cell Biochem. 2025 Jun.

Abstract

Ferroptosis is a novel, iron-dependent form of non-apoptotic cell death characterized by the accumulation of lipid reactive oxygen species (ROS) and mitochondrial shrinkage. It is closely associated with the onset and progression of various diseases, especially cancer, at all stages, making it a key focus of research for developing therapeutic strategies. Numerous studies have explored the role of microRNAs (miRNAs) in regulating ferroptosis by modulating the expression of critical genes involved in iron metabolism and lipid peroxidation. Due to their diversity, unique properties, and dynamic expression patterns in diseases, exosomal miRNAs are emerging as promising biomarkers. Exosomes act as biological messengers, delivering miRNAs to target cells through specific internalization, thus influencing the ferroptosis response in recipient cells. This review summarizes the roles of miRNAs, with particular focus on exosomal miRNAs, in ferroptosis and their implications for cancer pathology. By examining the molecular mechanisms of miRNAs, we aim to provide valuable insights into potential therapeutic approaches.

Keywords: Cancer therapy; Exosome; Ferroptosis; MiRNA; Molecular mechanism.

PubMed Disclaimer

Conflict of interest statement

Declarations. Conflict of interest: The authors declare no competing interests. Ethical approval: Not applicable. Consent for publication: Not applicable.

Similar articles

Cited by

References

    1. Galluzzi L, Vitale I, Aaronson SA et al (2018) Molecular mechanisms of cell death: Recommendations of the Nomenclature Committee on Cell Death 2018. Cell Death Differ 25:486–541 - DOI - PubMed - PMC
    1. Tang D, Kang R, Vanden BT et al (2019) The molecular machinery of regulated cell death. Cell Res 29:347–364 - DOI - PubMed - PMC
    1. Cui J, Zhao S, Li Y et al (2021) Regulated cell death: discovery, features and implications for neurodegenerative diseases. Cell Commun Signal 19:1–29. https://doi.org/10.1186/s12964-021-00799-8 - DOI
    1. Deter RL, Baudhuin P, de Duve C (1967) Participation of lysosomes in cellular autophagy induced in rat liver by glucagon. J Cell Biol 35:C11. https://doi.org/10.1083/jcb.35.2.c11 - DOI - PubMed - PMC
    1. Kerr JF, Wyllie AH, Currie AR (1972) Apoptosis: a basic biological phenomenon with wideranging implications in tissue kinetics. Br J Cancer 26:239–257. https://doi.org/10.1038/bjc.1972.33 - DOI - PubMed - PMC

LinkOut - more resources