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巴雷特食管发展为食管癌。

Evolution and progression of Barrett's oesophagus to oesophageal cancer.

机构信息

Medical Research Council Cancer Unit, Hutchison/Medical Research Council Research Centre, University of Cambridge, Cambridge, UK.

European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.

出版信息

Nat Rev Cancer. 2021 Nov;21(11):731-741. doi: 10.1038/s41568-021-00400-x. Epub 2021 Sep 20.

Abstract

Cancer cells are shaped through an evolutionary process of DNA mutation, cell selection and population expansion. Early steps in this process are driven by a set of mutated driver genes and structural alterations to the genome through copy number gains or losses. Oesophageal adenocarcinoma (EAC) and the pre-invasive tissue, Barrett's oesophagus (BE), provide an ideal example in which to observe and study this evolution. BE displays early genomic instability, specifically in copy number changes that may later be observed in EAC. Furthermore, these early changes result in patterns of progression (that is, 'born bad', gradual or catastrophic) that may help to describe the evolution of EAC. As only a small proportion of patients with BE will go on to develop cancer, a better understanding of these patterns and the resulting genomic changes should improve early detection in EAC and may provide clues for the evolution of cancer more broadly.

摘要

癌细胞是通过 DNA 突变、细胞选择和种群扩张的进化过程形成的。这个过程的早期步骤是由一组突变的驱动基因和基因组通过拷贝数增加或减少引起的结构改变驱动的。食管腺癌(EAC)和前侵袭性组织巴雷特食管(BE)为观察和研究这种进化提供了一个理想的范例。BE 表现出早期的基因组不稳定性,特别是在拷贝数变化方面,这些变化以后可能会在 EAC 中观察到。此外,这些早期变化导致了进展模式(即“天生不良”、渐进或灾难性),这可能有助于描述 EAC 的进化。由于只有一小部分 BE 患者会发展为癌症,因此更好地了解这些模式和由此产生的基因组变化应该可以提高 EAC 的早期检测,并且可能为更广泛的癌症进化提供线索。

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