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Review
. 2022 Jan 26:12:834681.
doi: 10.3389/fonc.2022.834681. eCollection 2022.

Ferroptosis: Redox Imbalance and Hematological Tumorigenesis

Affiliations
Review

Ferroptosis: Redox Imbalance and Hematological Tumorigenesis

Hongying Lan et al. Front Oncol. .

Abstract

Ferroptosis is a novel characterized form of cell death featured with iron-dependent lipid peroxidation, which is distinct from any known programmed cell death in the biological processes and morphological characteristics. Recent evidence points out that ferroptosis is correlated with numerous metabolic pathways, including iron homeostasis, lipid metabolism, and redox homeostasis, associating with the occurrence and treatment of hematological malignancies, such as multiple myeloma, leukemia, and lymphoma. Nowadays, utilizing ferroptosis as the target to prevent and treat hematological malignancies has become an active and challenging topic of research, and the regulatory network and physiological function of ferroptosis also need to be further elucidated. This review will summarize the recent progress in the molecular regulation of ferroptosis and the physiological roles and therapeutic potential of ferroptosis as the target in hematological malignancies.

Keywords: ferroptosis; hematologic malignancies; iron homeostasis; lipid metabolism; redox.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Morphological Features of different programmed cell death.
Figure 2
Figure 2
Regulatory pathways of ferroptosis. The proteins in yellow are key defense systems; the red line represents inhibiting effect (as in Figure 4 ).
Figure 3
Figure 3
Regulation of iron transport in vivo.
Figure 4
Figure 4
Metabolic regulation associated with ferroptosis.

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References

    1. Szabó C. Mechanisms of Cell Necrosis. Crit Care Med (2005) 33(12):4–5. doi: 10.1097/01.CCM.0000187002.88999.CF - DOI - PubMed
    1. Padanilam BJ. Cell Death Induced by Acute Renal Injury: A Perspective on the Contributions of Apoptosis and Necrosis. Am J Physiol-Renal Physiol (2003) 284(4):F608–F27. doi: 10.1152/ajprenal.00284.2002 - DOI - PubMed
    1. Ranganath RM, Rao Nagashree N. Role of Programmed Cell Death in Development. Int Rev Cytol (2001) 202:159–242. Academic Press. doi: 10.1016/S0074-7696(01)02005-8 - DOI - PubMed
    1. Hirschhorn T, Stockwell BR. The Development of the Concept of Ferroptosis. Free Radical Biol Med (2019) 133:130–43. doi: 10.1016/j.freeradbiomed.2018.09.043 - DOI - PMC - PubMed
    1. Sen S. Programmed Cell Death: Concept, Mechanism and Control. Biol Rev (1992) 67(3):287–319. doi: 10.1111/j.1469-185X.1992.tb00727.x - DOI - PubMed

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