Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/139196
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Type: Journal article
Title: Advancing translational research for colorectal immuno-oncology
Author: Thomas, E.M.
Wright, J.A.
Blake, S.J.
Page, A.J.
Worthley, D.L.
Woods, S.L.
Citation: British Journal of Cancer, 2023; 129(9):1442-1450
Publisher: Springer
Issue Date: 2023
ISSN: 0007-0920
1532-1827
Statement of
Responsibility: 
Elaine M. Thomas, Josephine A. Wright, Stephen J. Blake, Amanda J. Page, Daniel L. Worthley, and Susan L. Woods
Abstract: Colorectal cancer (CRC) is a common and deadly disease. Unfortunately, immune checkpoint inhibitors (ICIs) fail to elicit effective anti-tumour responses in the vast majority of CRC patients. Patients that are most likely to respond are those with DNA mismatch repair deficient (dMMR) and microsatellite instability (MSI) disease. However, reliable predictors of ICI response are lacking, even within the dMMR/MSI subtype. This, together with identification of novel mechanisms to increase response rates and prevent resistance, are ongoing and vitally important unmet needs. To address the current challenges with translation of early research findings into effective therapeutic strategies, this review summarises the present state of preclinical testing used to inform the development of immuno-regulatory treatment strategies for CRC. The shortfalls and advantages of commonly utilised mouse models of CRC, including chemically induced, transplant and transgenic approaches are highlighted. Appropriate use of existing models, incorporation of patient-derived data and development of cutting-edge models that recapitulate important features of human disease will be key to accelerating clinically relevant research in this area.
Keywords: Cancer models; Colon cancer; Rectal cancer
Description: Published online: 10 August 2023
Rights: © The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creativecommons.org/licenses/by/4.0/.
DOI: 10.1038/s41416-023-02392-x
Grant ID: http://purl.org/au-research/grants/nhmrc/1184925
Published version: http://dx.doi.org/10.1038/s41416-023-02392-x
Appears in Collections:Molecular and Biomedical Science publications

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