High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine

被引:101
|
作者
Gatalica, Zoran [1 ]
Vranic, Semir [2 ]
Xiu, Joanne [1 ]
Swensen, Jeffrey [1 ]
Reddy, Sandeep [1 ]
机构
[1] Caris Life Sci, 4610 South,44th Pl, Phoenix, AZ 85040 USA
[2] Univ Clin Ctr Sarajevo, Dept Pathol, Sarajevo, Bosnia & Herceg
关键词
Colorectal cancer; Microsatellite instability; Lynch syndrome; Biomarkers; Conventional chemotherapy; Targeted therapy; GENE COPY NUMBERS; MISMATCH-REPAIR; THYMIDYLATE SYNTHASE; LYNCH-SYNDROME; ADJUVANT CHEMOTHERAPY; PD-1; BLOCKADE; CANCER; METHYLATION; ASSOCIATION; MUTATIONS;
D O I
10.1007/s10689-016-9884-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Approximately 15 % of colorectal carcinomas (CRC) display high level microsatellite instability (MSI-H) due to either a germline mutation in one of the genes responsible for DNA mismatch repair (Lynch syndrome, 3 %) or somatic inactivation of the same pathway, most commonly through hypermethylation of the MLH1 gene (sporadic MSI-H, 12 %). Although heterogeneous, MSI-H colorectal carcinomas as a group show some distinct biologic characteristics when compared to CRC with stable or low level microsatellite instability. In the present review we will highlight therapeutically relevant characteristics of MSI-H tumors which could lead to specific responses to some conventional chemotherapy or novel targeted therapy agents.
引用
收藏
页码:405 / 412
页数:8
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