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Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors
BACKGROUND: To screen tumors with microsatellite instability (MSI) arising due to DNA mismatch repair deficiency (dMMR), a panel of five quasi-monomorphic mononucleotide-repeat markers amplified in a multiplex PCR (Pentaplex) are commonly used. In spite of its several strengths, the pentaplex assay...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767035/ https://www.ncbi.nlm.nih.gov/pubmed/29329588 http://dx.doi.org/10.1186/s12967-017-1376-4 |
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author | Takehara, Yuko Nagasaka, Takeshi Nyuya, Akihiro Haruma, Tomoko Haraga, Junko Mori, Yoshiko Nakamura, Keiichiro Fujiwara, Toshiyoshi Boland, C. Richard Goel, Ajay |
author_facet | Takehara, Yuko Nagasaka, Takeshi Nyuya, Akihiro Haruma, Tomoko Haraga, Junko Mori, Yoshiko Nakamura, Keiichiro Fujiwara, Toshiyoshi Boland, C. Richard Goel, Ajay |
author_sort | Takehara, Yuko |
collection | PubMed |
description | BACKGROUND: To screen tumors with microsatellite instability (MSI) arising due to DNA mismatch repair deficiency (dMMR), a panel of five quasi-monomorphic mononucleotide-repeat markers amplified in a multiplex PCR (Pentaplex) are commonly used. In spite of its several strengths, the pentaplex assay is not robust at detecting the loss of MSH6-deficiency (dMSH6). In order to overcome this challenge, we designed this study to develop and optimize a panel of four quasi-monomorphic mononucleotide-repeat markers (Tetraplex) for identifying solid tumors with dMMR, especially dMSH6. METHODS: To improve the sensitivity for tumors with dMMR, we established a quasi-monomorphic variant range (QMVR) of 3–4 bp for the four Tetraplex markers. Thereafter, to confirm the accuracy of this assay, we examined 317 colorectal cancer (CRC) specimens, comprising of 105 dMMR [45 MutL homolog (MLH)1-deficient, 45 MutS protein homolog (MSH)2-deficient, and 15 MSH6-deficient tumors] and 212 MMR-proficient (pMMR) tumors as a test set. In addition, we analyzed a cohort of 138 endometrial cancers (EC) by immunohistochemistry to determine MMR protein expression and validation of our new MSI assay. RESULTS: Using the criteria of ≥ 1 unstable markers as MSI-positive tumor, our assay resulted in a sensitivity of 97.1% [95% confidence interval (CI) = 91.9–99.0%] for dMMR, and a specificity of 95.3% (95% CI = 91.5–97.4%) for pMMR CRC specimens. Among the 138 EC specimens, 41 were dMMR according to immunohistochemistry. Herein, our Tetraplex assay detected dMMR tumors with a sensitivity of 92.7% (95% CI = 80.6–97.5%) and a specificity of 97.9% (95% CI = 92.8–99.4%) for pMMR tumors. With respect to tumors with dMSH6, in the CRC-validation set, Tetraplex detected dMSH6 tumors with a sensitivity of 86.7% (13 of 15 dMSH6 CRCs), which was subsequently validated in the EC test set as well (sensitivity, 75.0%; 6 of 8 dMSH6 ECs). CONCLUSIONS: Our newly optimized Tetraplex system will help offer a robust and highly sensitive assay for the identification of dMMR in solid tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-017-1376-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5767035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57670352018-01-17 Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors Takehara, Yuko Nagasaka, Takeshi Nyuya, Akihiro Haruma, Tomoko Haraga, Junko Mori, Yoshiko Nakamura, Keiichiro Fujiwara, Toshiyoshi Boland, C. Richard Goel, Ajay J Transl Med Research BACKGROUND: To screen tumors with microsatellite instability (MSI) arising due to DNA mismatch repair deficiency (dMMR), a panel of five quasi-monomorphic mononucleotide-repeat markers amplified in a multiplex PCR (Pentaplex) are commonly used. In spite of its several strengths, the pentaplex assay is not robust at detecting the loss of MSH6-deficiency (dMSH6). In order to overcome this challenge, we designed this study to develop and optimize a panel of four quasi-monomorphic mononucleotide-repeat markers (Tetraplex) for identifying solid tumors with dMMR, especially dMSH6. METHODS: To improve the sensitivity for tumors with dMMR, we established a quasi-monomorphic variant range (QMVR) of 3–4 bp for the four Tetraplex markers. Thereafter, to confirm the accuracy of this assay, we examined 317 colorectal cancer (CRC) specimens, comprising of 105 dMMR [45 MutL homolog (MLH)1-deficient, 45 MutS protein homolog (MSH)2-deficient, and 15 MSH6-deficient tumors] and 212 MMR-proficient (pMMR) tumors as a test set. In addition, we analyzed a cohort of 138 endometrial cancers (EC) by immunohistochemistry to determine MMR protein expression and validation of our new MSI assay. RESULTS: Using the criteria of ≥ 1 unstable markers as MSI-positive tumor, our assay resulted in a sensitivity of 97.1% [95% confidence interval (CI) = 91.9–99.0%] for dMMR, and a specificity of 95.3% (95% CI = 91.5–97.4%) for pMMR CRC specimens. Among the 138 EC specimens, 41 were dMMR according to immunohistochemistry. Herein, our Tetraplex assay detected dMMR tumors with a sensitivity of 92.7% (95% CI = 80.6–97.5%) and a specificity of 97.9% (95% CI = 92.8–99.4%) for pMMR tumors. With respect to tumors with dMSH6, in the CRC-validation set, Tetraplex detected dMSH6 tumors with a sensitivity of 86.7% (13 of 15 dMSH6 CRCs), which was subsequently validated in the EC test set as well (sensitivity, 75.0%; 6 of 8 dMSH6 ECs). CONCLUSIONS: Our newly optimized Tetraplex system will help offer a robust and highly sensitive assay for the identification of dMMR in solid tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-017-1376-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-12 /pmc/articles/PMC5767035/ /pubmed/29329588 http://dx.doi.org/10.1186/s12967-017-1376-4 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Takehara, Yuko Nagasaka, Takeshi Nyuya, Akihiro Haruma, Tomoko Haraga, Junko Mori, Yoshiko Nakamura, Keiichiro Fujiwara, Toshiyoshi Boland, C. Richard Goel, Ajay Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
title | Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
title_full | Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
title_fullStr | Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
title_full_unstemmed | Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
title_short | Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
title_sort | accuracy of four mononucleotide-repeat markers for the identification of dna mismatch-repair deficiency in solid tumors |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767035/ https://www.ncbi.nlm.nih.gov/pubmed/29329588 http://dx.doi.org/10.1186/s12967-017-1376-4 |
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