Serrated colorectal cancer: preclinical models and molecular pathways

被引:16
作者
Aiderus, Aziz [1 ]
Barker, Nick [2 ,3 ]
Tergaonkar, Vinay [1 ,4 ]
机构
[1] ASTAR, Inst Mol & Cell Biol IMCB, Lab NFκB Signalling, 61 Biopolis Dr, Singapore 138673, Singapore
[2] Natl Univ Singapore NUS, Yong Loo Lin Sch Med, Dept Physiol, 2 Med Dr,MD9, Singapore 117593, Singapore
[3] ASTAR, Inst Mol & Cell Biol IMCB, 61 Biopolis Dr, Singapore 138673, Singapore
[4] Natl Univ Singapore NUS, Yong Loo Lin Sch Med, Dept Biochem, 8 Med Dr,MD7, Singapore 117596, Singapore
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
ISLAND METHYLATOR PHENOTYPE; MICROSATELLITE INSTABILITY; BRAF MUTATION; DNA METHYLATION; TUMOR PROGRESSION; STEM-CELLS; POLYPS; ADENOMAS; TUMORIGENESIS; KRAS;
D O I
10.1016/j.trecan.2023.09.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Serrated lesions are histologically heterogeneous, and detection can be challenging as these lesions have subtle features that may be missed by endoscopy. Furthermore, while approximately 30% of colorectal cancers (CRCs) arise from serrated lesions, only 8-10% of invasive serrated CRCs exhibit serrated morphology at presentation, suggesting potential loss of apparent characteristics with increased malignancy. Thus, understanding the genetic basis driving serrated CRC initiation and progression is critical to improve diagnosis and identify therapeutic biomarkers and targets to guide disease management. This review discusses the preclinical models of serrated CRCs reported to date and how these systems have been used to provide mechanistic insights into tumor initiation, progression, and novel treatment targets.
引用
收藏
页码:76 / 91
页数:16
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