A diffusion-like process accommodates new crypts during clonal expansion in human colonic epithelium

Olpe, Cora, Khamis, Doran, Chukanova, Maria, Skoufou-Papoutsaki, Nefeli, Kemp, Richard, Marks, Kate, Tatton, Cerys, Lindskog, Cecilia, Nicholson, Anna, Brunton-Sim, Roxanne, Malhotra, Shalini, ten Hoopen, Rogier, Stanley, Rachael, Winton, Douglas J. and Morrissey, Edward (2021) A diffusion-like process accommodates new crypts during clonal expansion in human colonic epithelium. Gastroenterology, 161 (2). 548-559.e23. ISSN 0016-5085

[img]
Preview
PDF (Pre-Proof)
Available under License Creative Commons Attribution.

Download (8MB) | Preview

Abstract

Background & Aims: Colorectal cancer (CRC) is thought to arise when the cumulative mutational burden within colonic crypts exceeds a certain threshold that leads to clonal expansion and ultimately neoplastic transformation. Therefore, quantification of the fixation and subsequent expansion of somatic mutations in normal epithelium is key to understanding colorectal cancer initiation. The aim of the present study was to determine how advantaged expansions can be accommodated in the human colon.  Methods: Immunohistochemistry was used to visualize loss of the cancer driver KDM6A in formalin-fixed paraffin-embedded (FFPE) normal human colonic epithelium. Combining microscopy with neural network-based image analysis, we determined the frequencies of KDM6A-mutant crypts and fission/fusion intermediates as well as the spatial distribution of clones. Mathematical modeling then defined the dynamics of their fixation and expansion.  Results: Interpretation of the age-related behavior of KDM6A-negative clones revealed significant competitive advantage in intracrypt dynamics as well as a 5-fold increase in crypt fission rate. This was not accompanied by an increase in crypt fusion. Mathematical modeling of crypt spacing identifies evidence for a crypt diffusion process. We define the threshold fission rate at which diffusion fails to accommodate new crypts, which can be exceeded by KRAS activating mutations.  Conclusions: Advantaged gene mutations in KDM6A expand dramatically by crypt fission but not fusion. The crypt diffusion process enables accommodation of the additional crypts up to a threshold value, beyond which polyp growth may occur. The fission rate associated with KRAS mutations offers a potential explanation for KRAS-initiated polyps.

Item Type: Article
Additional Information: Sequencing data: NCBI BioProject PRJNA449344 (https://www.ncbi.nlm.nih.gov/bioproject/?term=PRJNA449344) Preprint server DOI: https://doi.org/10.1101/2020.07.10.193748
Uncontrolled Keywords: colorectal cancer initiation,crypt fission,crypt fusion,intestinal crypt,hepatology,gastroenterology,sdg 3 - good health and well-being ,/dk/atira/pure/subjectarea/asjc/2700/2721
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Related URLs:
Depositing User: LivePure Connector
Date Deposited: 06 May 2021 23:59
Last Modified: 24 Oct 2021 00:36
URI: https://ueaeprints.uea.ac.uk/id/eprint/79945
DOI: 10.1053/j.gastro.2021.04.035

Actions (login required)

View Item View Item