Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/111688
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Type: Journal article
Title: Oncogenic BRAF mutation induces DNA methylation changes in a murine model for human serrated colorectal neoplasia
Author: Bond, C.
Liu, C.
Kawamata, F.
McKeone, D.
Fernando, W.
Jamieson, S.
Pearson, S.
Kane, A.
Woods, S.
Lannagan, T.
Somashekar, R.
Lee, Y.
Dumenil, T.
Hartel, G.
Spring, K.
Borowsky, J.
Fennell, L.
Bettington, M.
Lee, J.
Worthley, D.
et al.
Citation: Epigenetics, 2018; 13(1):40-48
Publisher: Taylor & Francis
Issue Date: 2018
ISSN: 1559-2294
1559-2308
Statement of
Responsibility: 
Catherine E. Bond, Cheng Liu, Futoshi Kawamata, Diane M. McKeone, Winnie Fernando, Saara Jamieson, Sally-Ann Pearson, Alexandra Kane, Susan L. Woods, Tamsin R.M. Lannagan, Roshini Somashekar, Young Lee, Troy Dumenil, Gunter Hartel, Kevin J. Spring, Jennifer Borowsky, Lochlan Fennell, Mark Bettington, Jason Lee, Daniel L. Worthley, Barbara A. Leggett and Vicki L.J. Whitehall
Abstract: Colorectal cancer is a major cause of cancer death and approximately 20% arises within serrated polyps, which are under-recognized and poorly understood. Human serrated colorectal polyps frequently exhibit both oncogenic BRAF mutation and widespread DNA methylation changes, which are important in silencing genes restraining neoplastic progression. Here, we investigated whether in vivo induction of mutant Braf is sufficient to result in coordinated promoter methylation changes for multiple cancer-related genes. The BrafV637E mutation was induced in murine intestine on an FVB;C57BL/6J background and assessed for morphological and DNA methylation changes at multiple time points from 10 days to 14 months. Extensive intestinal hyperplasia developed by 10 days post-induction of the mutation. By 8 months, most mice had murine serrated adenomas with dysplasia and invasive cancer developed in 40% of mice by 14 months. From 5 months onwards, Braf mutant mice showed extensive, gene-specific increases in DNA methylation even in hyperplastic mucosa without lesions. This demonstrates that persistent oncogenic Braf signaling is sufficient to induce widespread DNA methylation changes. This occurs over an extended period of time, mimicking the long latency followed by rapid progression of human serrated neoplasia. This study establishes for the first time that DNA methylation arises slowly in direct response to prolonged oncogenic Braf signaling in serrated polyps; this finding has implications both for chemoprevention and for understanding the origin of DNA hypermethylation in cancer generally.
Keywords: BRAF; cancer biology; colorectal cancer; DNA methylation; methylation; murine model; serrated neoplasia
Rights: © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
RMID: 0030082878
DOI: 10.1080/15592294.2017.1411446
Grant ID: http://purl.org/au-research/grants/nhmrc/1050455
http://purl.org/au-research/grants/nhmrc/1063105
http://purl.org/au-research/grants/nhmrc/1110941
http://purl.org/au-research/grants/nhmrc/1081852
Published version: https://www.tandfonline.com/doi/full/10.1080/15592294.2017.1411446
Appears in Collections:Medicine publications

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