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肿瘤学中的精准表观遗传疗法。

Precision epigenetic therapies in oncology.

作者信息

Chaudhary Arundhati, Orchard Kayleigh J A, Salani Francesca, Partsou Theodora, Eccleston Mark, Bocci Guido, Italiano Antoine, Crea Francesco

机构信息

Cancer Research Group, School of Life, Health and Chemical Sciences, The Open University, Walton Hall, Milton Keynes, MK7 6AA, UK.

Sant' Anna School of Advanced Studies, Institute of Life Sciences, Piazza Martiri della Liberta 33, Pisa, 56124, Italy.

出版信息

Cancer Metastasis Rev. 2025 Sep 19;44(4):71. doi: 10.1007/s10555-025-10288-w.

Abstract

Phenotypic plasticity is a key mechanism of metastatic progression and cancer therapy resistance. This hallmark of human malignancies is enabled by highly conserved epigenetic mechanisms that control gene expression. Functional alterations in DNA methylation and histone post-translational modifications have been extensively described as drivers of metastatic dissemination and therapy resistance. Pharmacological inhibitors of epigenetic enzymes can revert these alterations, thereby stopping cancer progression and counteracting the emergence of resistant clones. Despite promising pre-clinical evidence, the clinical implementation of epigenetic therapies in solid cancers has led to disappointing results. Several factors can explain these challenges, including the lack of rational combinations. Notably, response to epigenetic treatments can be heterogeneous and short-lived. A liquid biopsy technology that allows the measure of specific epigenetic alterations enables patient selection and therapy monitoring, leading to the development of precision epigenetic therapies. In this review, we discuss the state of the art of this emerging treatment modality, and we identify key challenges that need to be overcome to reach the full potential of this new therapeutic concept.

摘要

表型可塑性是转移进展和癌症治疗耐药性的关键机制。人类恶性肿瘤的这一特征是由控制基因表达的高度保守的表观遗传机制实现的。DNA甲基化和组蛋白翻译后修饰的功能改变已被广泛描述为转移扩散和治疗耐药性的驱动因素。表观遗传酶的药理抑制剂可以逆转这些改变,从而阻止癌症进展并对抗耐药克隆的出现。尽管临床前证据很有前景,但表观遗传疗法在实体癌中的临床应用却导致了令人失望的结果。几个因素可以解释这些挑战,包括缺乏合理的联合用药。值得注意的是,对表观遗传治疗的反应可能是异质性的且短暂的。一种能够测量特定表观遗传改变的液体活检技术有助于患者选择和治疗监测,从而推动精准表观遗传疗法的发展。在这篇综述中,我们讨论了这种新兴治疗方式的现状,并确定了要充分发挥这一新治疗概念的潜力需要克服的关键挑战。

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