Endometriosis: The Role of Iron Overload and Ferroptosis

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Endometriosis may involve eutopic endometrium resistant to ferroptosis, allowing survival and implantation of shed cells, with iron overload and inflammation contributing to lesion pathophysiology.

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This paper proposes a mechanistic model of endometriosis centered on iron overload and ferroptosis resistance. It argues that an intrinsic defect in eutopic endometrium renders cells resistant to ferroptosis, enabling survival during retrograde menstruation and subsequent implantation and lesion formation, with dysregulated iron homeostasis driving localized iron overload and inflammation in established lesions. The paper also investigates an association between endometriosis and hypercholesterolemia, suggesting that the mevalonate cholesterol biosynthetic pathway may interact with ferroptosis signaling to explain how endometrial tissues evade ferroptotic pressure. The study’s key caveat is that it is largely hypothesis-driven and conceptual in nature rather than presenting detailed experimental results within the provided text. This paper is centrally about endometriosis — it frames endometriosis pathogenesis as arising from abnormal iron homeostasis and ferroptosis resistance in eutopic endometrium.

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Abstract

Iron is an essential element for cell survival, and iron deficiency is a known risk factor for many reproductive disorders. Paradoxically, such disorders are also seen more commonly under conditions of iron excess. Here, we focus on the problem of iron overload in women’s health, using endometriosis as a model system. We propose (i) that a primary defect in endometriosis is abnormal eutopic endometrium characterized by resistance to ferroptosis, a process of iron-mediated non-apoptotic programmed cell death, which allows cells spread via retrograde menstruation to survive, implant, and establish endometriotic lesions within the abdominal cavity, and (ii) that dysregulated iron homeostasis may be critical to the subsequent pathophysiology of endometriotic lesions with localized iron overload and inflammation. We further investigate the association between endometriosis and hypercholesterolemia and suggest that an interaction between the mevalonate cholesterol biosynthetic pathway and ferroptosis signaling may provide a molecular basis to explain how it is that, in some women, endometrial tissues survive and thrive under ferroptotic pressure, colonize at ectopic sites, and expand into endometriotic lesions. Similar content being viewed by others

References

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Sci. 27, 1383–1390 (2020). https://doi.org/10.1007/s43032-020-00164-z Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s43032-020-00164-z

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mesh:D004715endometriosis

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Endometriosis Endometrium Ferroptosis Iron Overload Endometriosis Endometriosis Endometrium Endometrium Female Ferroptosis Humans Iron Overload Iron Overload

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