Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Nov;21(11):731-741.
doi: 10.1038/s41568-021-00400-x. Epub 2021 Sep 20.

Evolution and progression of Barrett's oesophagus to oesophageal cancer

Affiliations
Review

Evolution and progression of Barrett's oesophagus to oesophageal cancer

Sarah Killcoyne et al. Nat Rev Cancer. 2021 Nov.

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.

PubMed Disclaimer

References

    1. Gerstung, M. et al. The evolutionary history of 2,658 cancers. Nature 578, 122–128 (2020). This work, coming out of the largest pan-cancer analysis to date, establishes the concept of early and late mutations in the evolution of tumours, suggesting that early gene mutations might be detectable and offer the potential of earlier treatment. - PubMed - PMC - DOI
    1. Li, Y. et al. Patterns of somatic structural variation in human cancer genomes. Nature 578, 112–121 (2020). - PubMed - PMC - DOI
    1. Zack, T. I. et al. Pan-cancer patterns of somatic copy number alteration. Nat. Genet. 45, 1134–1140 (2013). - PubMed - PMC - DOI
    1. Alexandrov, L. B., Nik-Zainal, S., Wedge, D. C., Campbell, P. J. & Stratton, M. R. Deciphering signatures of mutational processes operative in human cancer. Cell Rep. 3, 246–259 (2013). - PubMed - PMC - DOI
    1. Ross-Innes, C. S. et al. Whole-genome sequencing provides new insights into the clonal architecture of Barrett’s esophagus and esophageal adenocarcinoma. Nat. Genet. 47, 1038–1046 (2015). - PubMed - PMC - DOI

Publication types