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表观遗传学在子宫内膜异位症中的作用:一项综合评估。

Epigenetics' responsibility in endometriosis: A comprehensive assessment.

作者信息

Akano Oyedayo Phillips, Amos Victor Oluwaloseyi, Fawole Israel Opeyemi, Oyindamola Adewole Christianah, Ajayi Ayodeji Folorunsho

机构信息

Department of Physiology, Olabisi Onabanjo University, Ago-Iwoye, Ogun State, Nigeria.

Department of Physiology, Ladoke Akintola University of Technology, Ogbomoso, Oyo State, Nigeria.

出版信息

J Steroid Biochem Mol Biol. 2025 Oct;253:106814. doi: 10.1016/j.jsbmb.2025.106814. Epub 2025 Jun 11.

Abstract

Endometriosis is a chronic inflammatory disease characterized by the presence of endometrial-like tissue outside the uterus, affecting women of reproductive age. Despite extensive research, its pathophysiology remains unclear, with genetic, hormonal, and environmental factors playing interconnected roles. Epigenetic processes, including non-coding RNAs, histone modifications, and DNA methylation, have been implicated in the genesis and progression of endometriosis. These modifications impact physiological functions such as inflammation, cell division, apoptosis, and hormone sensitivity. Recent findings on epigenetic alterations in endometriosis highlight their role in the abnormal behavior of ectopic endometrial-like cells. Aberrant DNA methylation patterns in genes related to immunological control and oestrogen metabolism contribute to the invasiveness and durability of lesions. Histone modifications, such as methylation and acetylation, regulate gene expression by altering chromatin structure. Non-coding RNAs, particularly microRNAs, influence tissue remodeling and inflammation. Given the reversible nature of epigenetic modifications, they present promising therapeutic targets for innovative treatment strategies. Epigenetic-based therapies aim to reverse pathological gene expression patterns, offering hope for more personalized and effective management of endometriosis. Further research is needed to fully utilize epigenetic processes in treating this debilitating disease.

摘要

子宫内膜异位症是一种慢性炎症性疾病,其特征是子宫外存在类似子宫内膜的组织,影响育龄女性。尽管进行了广泛研究,但其病理生理学仍不清楚,遗传、激素和环境因素相互关联地发挥作用。表观遗传过程,包括非编码RNA、组蛋白修饰和DNA甲基化,与子宫内膜异位症的发生和发展有关。这些修饰影响诸如炎症、细胞分裂、细胞凋亡和激素敏感性等生理功能。最近关于子宫内膜异位症表观遗传改变的研究结果突出了它们在异位类似子宫内膜细胞异常行为中的作用。与免疫控制和雌激素代谢相关基因中的异常DNA甲基化模式导致病变的侵袭性和持续性。组蛋白修饰,如甲基化和乙酰化,通过改变染色质结构来调节基因表达。非编码RNA,特别是微小RNA,影响组织重塑和炎症。鉴于表观遗传修饰的可逆性,它们为创新治疗策略提供了有前景的治疗靶点。基于表观遗传的疗法旨在逆转病理基因表达模式,为更个性化、有效地管理子宫内膜异位症带来希望。需要进一步研究以充分利用表观遗传过程来治疗这种使人衰弱的疾病。

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