Microsatellite Instability in Colorectal Cancer

被引:95
|
作者
Boland, C. Richard
Goel, Ajay
机构
[1] Baylor Univ, Sammons Canc Ctr, GI Canc Res Lab, Div Gastroenterol,Dept Internal Med,Med Ctr, Dallas, TX 75246 USA
[2] Baylor Univ, Med Ctr, Baylor Res Inst, Dallas, TX 75246 USA
关键词
Lynch Syndrome; DNA Mismatch Repair; Hereditary Nonpolyposis Colorectal Cancer; DNA MISMATCH-REPAIR; ISLAND METHYLATOR PHENOTYPE; NONPOLYPOSIS COLON-CANCER; NITRO-N-NITROSOGUANIDINE; LYNCH-SYNDROME; CPG ISLAND; ULCERATIVE-COLITIS; ADJUVANT CHEMOTHERAPY; MUTS HOMOLOG; TUMOR-CELLS;
D O I
10.1053/j.gastro.2009.12.064
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Microsatellite instability (MSI) is a hypermutable phenotype caused by the loss of DNA mismatch repair activity. MSI is detected in about 15% of all colorectal cancers; 3% are of these are associated with Lynch syndrome and the other 12% are caused by sporadic, acquired hypermethylation of the promoter of the MLH1 gene, which occurs in tumors with the CpG island methylator phenotype. Colorectal tumors with MSI have distinctive features, including a tendency to arise in the proximal colon, lymphocytic infiltrate, and a poorly differentiated, mucinous or signet ring appearance. They have a slightly better prognosis than colorectal tumors without MSI and do not have the same response to chemotherapeutics. Discovery of MSI in colorectal tumors has increased awareness of the diversity of colorectal cancers and implications for specialized management of patients.
引用
收藏
页码:2073 / U87
页数:18
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