Abstract
Hereditary nonpolyposis colorectal cancer (HNPCC) is inherited as a dominant disorder caused by germline defects in one of at least four mismatch repair (MMR) genes. Two of these genes, hMSH2 and hMLH1, account for the vast majority of the germline mutations in HNPCC kindreds, whereas hPMS1 and hPMS2 are mutated in only few families. MMR genes also are susceptible to somatic mutations in sporadic tumors. The mutational spectrum of the MMR genes shows no predominant type of mutation. Furthermore, the mutations are spread throughout the length of the genes, with no significant hot spots. Identification of MMR genes as the cause of HNPCC made presymptomatic diagnosis a reality. However, the presence of multiple genes and the heterogeneity of mutations present challenges to the development of diagnostic tests for this disease.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Adaptor Proteins, Signal Transducing
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Adenosine Triphosphatases*
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Carrier Proteins
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Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis
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Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
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DNA Repair / genetics*
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DNA Repair Enzymes*
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DNA-Binding Proteins*
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Forecasting
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Genes
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Germ-Line Mutation
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Humans
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Mismatch Repair Endonuclease PMS2
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MutL Protein Homolog 1
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MutL Proteins
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MutS Homolog 2 Protein
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Mutation*
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Neoplasm Proteins / genetics
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Nuclear Proteins
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Proto-Oncogene Proteins / genetics
Substances
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Adaptor Proteins, Signal Transducing
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Carrier Proteins
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DNA-Binding Proteins
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MLH1 protein, human
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Neoplasm Proteins
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Nuclear Proteins
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PMS1 protein, human
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Proto-Oncogene Proteins
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Adenosine Triphosphatases
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PMS2 protein, human
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MSH2 protein, human
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Mismatch Repair Endonuclease PMS2
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MutL Protein Homolog 1
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MutL Proteins
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MutS Homolog 2 Protein
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DNA Repair Enzymes