Advancing translational research for colorectal immuno-oncology

被引:14
作者
Thomas, Elaine M. [1 ]
Wright, Josephine A. [2 ]
Blake, Stephen J. [2 ]
Page, Amanda J. [3 ,4 ]
Worthley, Daniel L. [2 ]
Woods, Susan L. [1 ,2 ]
机构
[1] Univ Adelaide, Adelaide Med Sch, Adelaide, SA, Australia
[2] South Australian Hlth & Med Res Inst, Precis Canc Med Theme, Adelaide, SA, Australia
[3] Univ Adelaide, Sch Biomed, Adelaide, SA, Australia
[4] South Australian Hlth & Med Res Inst, Lifelong Hlth Theme, Adelaide, SA, Australia
基金
英国医学研究理事会;
关键词
MISMATCH REPAIR DEFICIENCY; MOUSE MODELS; COLON-CANCER; MICROSATELLITE INSTABILITY; LYNCH SYNDROME; T-CELL; INTESTINAL ADENOMAS; MICE; PD-1; TUMORIGENESIS;
D O I
10.1038/s41416-023-02392-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1442 / 1450
页数:9
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