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
相关论文
共 50 条
  • [31] MLH1 and MSH2 mutations in Colombian families with hereditary nonpolyposis colorectal cancer (Lynch syndrome) -: description of four novel mutations
    Giraldo, A
    Gómez, A
    Salguero, G
    García, H
    Aristizábal, F
    Gutiérrez, O
    Angel, LA
    Padrón, J
    Martínez, C
    Martínez, H
    Malaver, O
    Flórez, L
    Barvo, R
    FAMILIAL CANCER, 2005, 4 (04) : 285 - 290
  • [32] MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations
    Alejandro Giraldo
    Andrea Gómez
    Gustavo Salguero
    Herbert García
    Fabio Aristizábal
    Óscar Gutiérrez
    Luis Alberto Ángel
    Jorge Padrón
    Carlos Martínez
    Humberto Martínez
    Omar Malaver
    Luis Flórez
    Rosa Barvo
    Familial Cancer, 2005, 4 : 285 - 290
  • [33] A Comprehensive Analysis of the Phenotypic Manifestations of Mismatch Repair Gene Mutations: Comparing MSH6 with MLH1 and MSH2 Mutation Carriers
    Kastrinos, Fay
    Steyerberg, Ewout W.
    Balmana, Judith
    Syngal, Sapna
    GASTROENTEROLOGY, 2009, 136 (05) : A449 - A450
  • [34] Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability
    Herfarth, KKF
    Kodner, IJ
    Whelan, AJ
    Ivanovich, JL
    Bracamontes, JR
    Wells, SA
    Goodfellow, PJ
    GENES CHROMOSOMES & CANCER, 1997, 18 (01): : 42 - 49
  • [35] Identify the human homologue of DNA mismatch repair genes (MSH2 and MLH1) from Dictyostelium
    Xu, XS
    Zhang, Y
    Wang, G
    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2004, 44 (03) : 238 - 238
  • [36] Immunohistochemical detection of MLH1 and MSH2 in renal cell tumors
    Lin, F
    Yang, XJ
    Brown, RE
    Zhang, PL
    LABORATORY INVESTIGATION, 2005, 85 : 153A - 153A
  • [37] Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX
    Mac Partlin, M
    Homer, E
    Robinson, H
    McCormick, CJ
    Crouch, DH
    Durant, ST
    Matheson, EC
    Hall, AG
    Gillespie, DAF
    Brown, R
    ONCOGENE, 2003, 22 (06) : 819 - 825
  • [38] Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX
    Mary Mac Partlin
    Elizabeth Homer
    Helen Robinson
    Carol J McCormick
    Dorothy H Crouch
    Stephen T Durant
    Elizabeth C Matheson
    Andrew G Hall
    David AF Gillespie
    Robert Brown
    Oncogene, 2003, 22 : 819 - 825
  • [39] Immunohistochemical detection of MLH1 and MSH2 in renal cell tumors
    Lin, F
    Yang, XJ
    Brown, RE
    Zhang, PL
    MODERN PATHOLOGY, 2005, 18 : 153A - 153A
  • [40] Rare single-nucleotide variants of MLH1 and MSH2 genes in patients with Lynch syndrome
    Mirabdolhosseini, Seyed Mohsen
    Taleghani, Mohammad Yaghoob
    Rejali, Leili
    Sadeghi, Hossein
    Fatemi, Nayeralsadat
    Tavallaei, Mehdi
    Meyari, Amin Famil
    Saeidi, Narges
    Moghadam, Pardis Ketabi
    Sadeghi, Amir
    Aghdaei, Hamid Asadzadeh
    Zali, Mohammad Reza
    Mojarad, Ehsan Nazemalhosseini
    CANCER REPORTS, 2024, 7 (01)