Abstract
Lynch syndrome is an inherited disease caused by a germline mutation in one of four DNA mismatch repair (MMR) genes. The clinical manifestations can be somewhat variable depending upon which gene is involved, and where the mutation occurs. Moreover, the approach to the diagnosis of Lynch syndrome is becoming more complex as more is learned about the disease, and one needs to understand how the DNA MMR proteins function, and what makes them malfunction, to have an optimal appreciation of how to interpret diagnostic studies such as microsatellite instability and immunohistochemistry of the DNA MMR proteins. Finally, an understanding of the role of the DNA MMR system in regulation of the cell cycle and the response to DNA damage helps illuminate the differences in natural history and response to chemotherapeutic agents seen in Lynch syndrome.
MeSH terms
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Adaptor Proteins, Signal Transducing / genetics
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Adenosine Triphosphatases / genetics
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Cell Line, Tumor
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Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis*
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Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
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Colorectal Neoplasms, Hereditary Nonpolyposis / pathology
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DNA Mismatch Repair*
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DNA Repair Enzymes / genetics
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DNA-Binding Proteins / genetics
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Genetic Research
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Genotype
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Humans
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Microsatellite Instability*
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Mismatch Repair Endonuclease PMS2
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MutL Protein Homolog 1
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MutS Homolog 2 Protein / genetics
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Mutation
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Nuclear Proteins / genetics
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Phenotype
Substances
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Adaptor Proteins, Signal Transducing
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DNA-Binding Proteins
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G-T mismatch-binding protein
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MLH1 protein, human
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Nuclear 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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MutS Homolog 2 Protein
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DNA Repair Enzymes