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Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review)

  • Authors:
    • Jiaqi Yang
    • Yu Wang
    • Fangyuan Liu
    • Yizhong Zhang
    • Fengjuan Han
  • View Affiliations / Copyright

    Affiliations: Postgraduate School of Traditional Chinese Gynecology, Heilongjiang University of Traditional Chinese Medicine, Harbin, Heilongjiang 150040, P.R. China, Department of Gynecology, The First Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine, Harbin, Heilongjiang 150040, P.R. China
    Copyright: © Yang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 97
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    Published online on: April 28, 2025
       https://doi.org/10.3892/ijmm.2025.5538
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Abstract

Ferroptosis is a unique mode of cell death driven by iron‑dependent phospholipid peroxidation, and its mechanism primarily involves disturbances in iron metabolism, imbalances in the lipid antioxidant system and accumulation of lipid peroxides. Protein processing, modification and folding in the endoplasmic reticulum (ER) are closely related regulatory processes that determine cell function, fate and survival. The uncontrolled proliferative capacity of malignant cells generates an unfavorable microenvironment characterized by high metabolic demand, hypoxia, nutrient deprivation and acidosis, which promotes the accumulation of misfolded or unfolded proteins in the ER, leading to ER stress (ERS). Ferroptosis and ERS share common pathways in several diseases, and the two interact to affect cell survival and death. Additionally, cell death pathways are not linear signaling cascades, and different pathways of cell death may be interrelated at multiple levels. Ferroptosis and ERS in ovarian cancer (OC) have attracted increasing research interest; however, both are discussed separately regarding OC. The present review aims to summarize the associations and potential links between ferroptosis and ERS, aiming to provide research references for the development of therapeutic approaches for the management of OC.
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Copy and paste a formatted citation
Spandidos Publications style
Yang J, Wang Y, Liu F, Zhang Y and Han F: Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review). Int J Mol Med 55: 97, 2025.
APA
Yang, J., Wang, Y., Liu, F., Zhang, Y., & Han, F. (2025). Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review). International Journal of Molecular Medicine, 55, 97. https://doi.org/10.3892/ijmm.2025.5538
MLA
Yang, J., Wang, Y., Liu, F., Zhang, Y., Han, F."Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review)". International Journal of Molecular Medicine 55.6 (2025): 97.
Chicago
Yang, J., Wang, Y., Liu, F., Zhang, Y., Han, F."Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review)". International Journal of Molecular Medicine 55, no. 6 (2025): 97. https://doi.org/10.3892/ijmm.2025.5538
Copy and paste a formatted citation
x
Spandidos Publications style
Yang J, Wang Y, Liu F, Zhang Y and Han F: Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review). Int J Mol Med 55: 97, 2025.
APA
Yang, J., Wang, Y., Liu, F., Zhang, Y., & Han, F. (2025). Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review). International Journal of Molecular Medicine, 55, 97. https://doi.org/10.3892/ijmm.2025.5538
MLA
Yang, J., Wang, Y., Liu, F., Zhang, Y., Han, F."Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review)". International Journal of Molecular Medicine 55.6 (2025): 97.
Chicago
Yang, J., Wang, Y., Liu, F., Zhang, Y., Han, F."Crosstalk between ferroptosis and endoplasmic reticulum stress: A potential target for ovarian cancer therapy (Review)". International Journal of Molecular Medicine 55, no. 6 (2025): 97. https://doi.org/10.3892/ijmm.2025.5538
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