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作为癌症因果关系和遗传性的机制,宪法外遗传改变?

Constitutional epimutation as a mechanism for cancer causality and heritability?

机构信息

Department of Medicine (Oncology), Stanford Cancer Institute, Stanford University, Grant Building S169, 1291 Welch Road, Stanford, California 94305, USA.

出版信息

Nat Rev Cancer. 2015 Oct;15(10):625-34. doi: 10.1038/nrc4001. Epub 2015 Sep 18.

Abstract

Constitutional epimutation, which is an aberration in gene expression due to an altered epigenotype that is widely distributed in normal tissues (albeit frequently mosaic), provides an alternative mechanism to genetic mutation for cancer predisposition. Observational studies in cancer-affected families have revealed intergenerational inheritance of constitutional epimutation, providing unique insights into the heritability of epigenetic traits in humans. In this Opinion article, the potential contribution of constitutional epimutation to the 'missing' causality and heritability of cancer is explored.

摘要

由于表观基因型的改变导致基因表达异常的结构性表观突变广泛存在于正常组织中(尽管通常是嵌合体),这为癌症易感性提供了一种不同于基因突变的机制。在受癌症影响的家族中进行的观察性研究揭示了结构性表观突变的跨代遗传,为人类表观遗传特征的遗传性提供了独特的见解。在这篇观点文章中,探讨了结构性表观突变对癌症“缺失”因果关系和遗传性的潜在贡献。

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