Abstract
We show that immunohistochemistry for hMSH2 and hMLH1 is an easy and reproducible routine procedure. The interpretation of the staining results is unequivocal and investigator-independent. It is now necessary to validate the specificity and sensitivity of the method in a multicenter study with tumors of known mutations. As a consequence perhaps MIN testing may be replaced by immunohistochemistry as a first-line pretesting for HNPCC, reducing cost and time required.
MeSH terms
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Adaptor Proteins, Signal Transducing
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Adult
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Carrier Proteins
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DNA-Binding Proteins*
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Female
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Genetic Testing*
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Humans
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Immunoenzyme Techniques
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Male
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MutL Protein Homolog 1
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MutS Homolog 2 Protein
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Neoplasm Proteins / genetics*
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Nuclear Proteins
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Proto-Oncogene Proteins / genetics*
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Sensitivity and Specificity
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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Proto-Oncogene Proteins
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MSH2 protein, human
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MutL Protein Homolog 1
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MutS Homolog 2 Protein