Translating colorectal cancer genetics into clinically useful biomarkers

被引:3
|
作者
Morley-Bunker, A. [1 ]
Walker, L. C. [1 ]
Currie, M. J. [1 ]
Pearson, J. [2 ]
Eglinton, T. [3 ]
机构
[1] Univ Otago, Mackenzie Canc Res Grp, Dept Pathol, Christchurch, New Zealand
[2] Univ Otago, Biostat & Computat Biol Unit, Christchurch, New Zealand
[3] Univ Otago, Dept Surg, Christchurch, New Zealand
关键词
CIRCULATING TUMOR-CELLS; MICROSATELLITE-INSTABILITY; COLON-CANCER; MOLECULAR-GENETICS; DNA METHYLATION; EXPRESSION; SUBTYPES; CLASSIFICATION; MUTATIONS; MARKERS;
D O I
10.1111/codi.13334
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colorectal cancer (CRC) is a major health problem worldwide accounting for over a million deaths annually. While many patients with Stage II and III CRC can be cured with combinations of surgery, radiotherapy and chemotherapy, this is morbid costly treatment and a significant proportion will suffer recurrence and eventually die of CRC. Increased understanding of the molecular pathogenesis of CRC has the potential to identify high risk patients and target therapy more appropriately. Despite increased understanding of the molecular events underlying CRC development, established molecular techniques have only produced a limited number of biomarkers suitable for use in routine clinical practice to predict risk, prognosis and response to treatment. Recent rapid technological developments, however, have made genomic sequencing of CRC more economical and efficient, creating potential for the discovery of genetic biomarkers that have greater diagnostic, prognostic and therapeutic capabilities for the management of CRC. This paper reviews the current understanding of the molecular pathogenesis of CRC, and summarizes molecular biomarkers that surgeons will encounter in current clinical use as well as those under development in clinical and preclinical trials. New molecular technologies are reviewed together with their potential impact on the understanding of the molecular pathogenesis of CRC and their potential clinical utility in classification, diagnosis, prognosis and targeting of therapy.
引用
收藏
页码:749 / 762
页数:14
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