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
. 2024 Aug;172(4):547-565.
doi: 10.1111/imm.13789. Epub 2024 Apr 2.

A review on comprehending immunotherapeutic approaches inducing ferroptosis: Managing tumour immunity

Affiliations
Free article
Review

A review on comprehending immunotherapeutic approaches inducing ferroptosis: Managing tumour immunity

Soumyadeep Chattopadhyay et al. Immunology. 2024 Aug.
Free article

Abstract

Ferroptosis, a necrotic, iron-dependent controlled cell death mechanism, is distinguished by the development of lipid peroxides to fatal proportions. Malignant tumours, influenced by iron to promote fast development, are vulnerable to ferroptosis. Based upon mounting evidence it has been observed that ferroptosis may be immunogenic and hence may complement immunotherapies. A new approach includes iron oxide-loaded nano-vaccines (IONVs), having supremacy for the traits of the tumour microenvironment (TME) to deliver specific antigens through improving the immunostimulatory capacity by molecular disintegration and reversible covalent bonds that target the tumour cells and induce ferroptosis. Apart from IONVs, another newer approach to induce ferroptosis in tumour cells is through oncolytic virus (OVs). One such oncolytic virus is the Newcastle Disease Virus (NDV), which can only multiply in cancer cells through the p53-SLC7A11-GPX4 pathway that leads to elevated levels of lipid peroxide and intracellular reactive oxygen species leading to the induction of ferroptosis that induce ferritinophagy.

Keywords: ferritinophagy; ferroptosis; immunostimulatory; immunotherapy; regulated cell death; tumour microenvironment (TME).

PubMed Disclaimer

References

REFERENCES

    1. Dixon SJ, Lemberg KM, Lamprecht MR, Skouta R, Zaitsev EM, Gleason CE, et al. Ferroptosis: an iron‐dependent form of nonapoptotic cell death. Cell. 2012;149(5):1060–1072. https://doi.org/10.1016/j.cell.2012.03.042
    1. Wu P, Zhang X, Duan D, Zhao L. Organelle‐specific mechanisms in crosstalk between apoptosis and ferroptosis. Oxid Med Cell Longev. 2023;2023:1–14. [cited 2023 Dec 04]. Available from: https://www.hindawi.com/journals/omcl/2023/3400147/
    1. Gao M, Yi J, Zhu J, Minikes AM, Monian P, Thompson CB, et al. Role of mitochondria in ferroptosis. Mol Cell. 2019;73(2):354–363.e3. [cited 2023 Dec 04]. Available from: https://pubmed.ncbi.nlm.nih.gov/30581146/
    1. Dolma S, Lessnick SL, Hahn WC, Stockwell BR. Identification of genotype‐selective antitumor agents using synthetic lethal chemical screening in engineered human tumor cells. Cancer Cell. 2003;3(3):285–296. [cited 2023 Dec 04]. Available from: https://pubmed.ncbi.nlm.nih.gov/12676586/
    1. Zhang S, Hu R, Geng Y, Chen K, Wang L, Imam MU. The regulatory effects and the signalling pathways of natural bioactive compounds on ferroptosis. Foods. 2021;10(12):2952. [cited 2023 Dec 05]. Available from: https://www.mdpi.com/2304-8158/10/12/2952. https://www.sciencedirect.com/science/article/pii/S258900422030691X