Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

被引:260
|
作者
Mensenkamp, Arjen R. [1 ]
Vogelaar, Ingrid P. [1 ]
van Zelst-Stams, Wendy A. G. [1 ]
Goossens, Monique [2 ]
Ouchene, Hicham [1 ]
Hendriks-Cornelissen, Sandra J. B. [2 ]
Kwint, Michael P. [2 ]
Hoogerbrugge, Nicoline [1 ]
Nagtegaal, Iris D. [2 ]
Ligtenberg, Marjolijn J. L. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Pathol, NL-6500 HB Nijmegen, Netherlands
关键词
Genetic; Colorectal Cancer; Mismatch Repair Deficiency; Lynch-Like Syndrome; VARIANT CLASSIFICATION; FUNCTIONAL-ANALYSIS; CANCER; GENE; RISK; RNA; RECOMMENDATIONS; BIOINFORMATICS; METHYLATION; AVOIDANCE;
D O I
10.1053/j.gastro.2013.12.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Lynch syndrome is caused by germline mutations in the mismatch repair (MMR) genes. Tumors are characterized by microsatellite instability (MSI). However, a considerable number of MSI-positive tumors have no known molecular mechanism of development. By using Sanger and ion semiconductor sequencing, 25 MSI-positive tumors were screened for somatic mutations and loss of heterozygosity in mutL homolog 1 (MLH1) and mutS homolog 2 (MSH2). In 13 of 25 tumors (8 MLH1-deficient and 5 MSH2-deficient tumors), we identified 2 somatic mutations in these genes. We conclude that 2 acquired events explain the MMR-deficiency in more than 50% of the MMR-deficient tumors without causal germline mutations or promoter methylation.
引用
收藏
页码:643 / +
页数:12
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