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Development of a clinical microarray system for genetic analysis screening
OBJECTIVES: Research on the relationship between diseases and genes and the advancement of genetic analysis technologies have made genetic testing in medical care possible. There are various methods for genetic testing, including PCR-based methods and next-generation sequencing; however, screening t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803787/ https://www.ncbi.nlm.nih.gov/pubmed/36593945 http://dx.doi.org/10.1016/j.plabm.2022.e00306 |
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author | Okamura, Hiroshi Yamano, Hirofumi Tsuda, Toshiya Morihiro, Junichi Hirayama, Koichi Nagano, Hiroaki |
author_facet | Okamura, Hiroshi Yamano, Hirofumi Tsuda, Toshiya Morihiro, Junichi Hirayama, Koichi Nagano, Hiroaki |
author_sort | Okamura, Hiroshi |
collection | PubMed |
description | OBJECTIVES: Research on the relationship between diseases and genes and the advancement of genetic analysis technologies have made genetic testing in medical care possible. There are various methods for genetic testing, including PCR-based methods and next-generation sequencing; however, screening tests in clinical laboratories are becoming more diverse; therefore, novel measurement systems and equipment are required to meet the needs of each situation. In this study, we aimed to develop a novel microarray-based genetic analysis system that uses a Peltier element to overcome the issues of conventional microarrays, such as the long measurement time and high cost. METHODS: We constructed a microarray system to detect the UDP-glucuronosyltransferase gene polymorphisms UGT1A1*6 and UGT1A1*28 in patients eligible for irinotecan hydrochloride treatment for use in clinical laboratories. To evaluate the performance of the system, the hybridization temperature and reaction time were determined, and the results were compared with those obtained using a conventional hybridization oven. RESULTS: The hybridization temperature reached its target in 1/27th of the time required by the conventional system. We assessed 111 human clinical samples and found that our results agreed with those obtained using existing methods. The total time for the newly developed device was reduced by 85 min compared to that for existing methods, as the automated DNA microarray eliminates the time that existing methods spend on manual operation. CONCLUSIONS: The surface treatment technology used in our system enables high-density and strong DNA fixation, allowing the construction of a measurement system suitable for clinical applications. |
format | Online Article Text |
id | pubmed-9803787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98037872023-01-01 Development of a clinical microarray system for genetic analysis screening Okamura, Hiroshi Yamano, Hirofumi Tsuda, Toshiya Morihiro, Junichi Hirayama, Koichi Nagano, Hiroaki Pract Lab Med Original Research Article OBJECTIVES: Research on the relationship between diseases and genes and the advancement of genetic analysis technologies have made genetic testing in medical care possible. There are various methods for genetic testing, including PCR-based methods and next-generation sequencing; however, screening tests in clinical laboratories are becoming more diverse; therefore, novel measurement systems and equipment are required to meet the needs of each situation. In this study, we aimed to develop a novel microarray-based genetic analysis system that uses a Peltier element to overcome the issues of conventional microarrays, such as the long measurement time and high cost. METHODS: We constructed a microarray system to detect the UDP-glucuronosyltransferase gene polymorphisms UGT1A1*6 and UGT1A1*28 in patients eligible for irinotecan hydrochloride treatment for use in clinical laboratories. To evaluate the performance of the system, the hybridization temperature and reaction time were determined, and the results were compared with those obtained using a conventional hybridization oven. RESULTS: The hybridization temperature reached its target in 1/27th of the time required by the conventional system. We assessed 111 human clinical samples and found that our results agreed with those obtained using existing methods. The total time for the newly developed device was reduced by 85 min compared to that for existing methods, as the automated DNA microarray eliminates the time that existing methods spend on manual operation. CONCLUSIONS: The surface treatment technology used in our system enables high-density and strong DNA fixation, allowing the construction of a measurement system suitable for clinical applications. Elsevier 2022-12-23 /pmc/articles/PMC9803787/ /pubmed/36593945 http://dx.doi.org/10.1016/j.plabm.2022.e00306 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Article Okamura, Hiroshi Yamano, Hirofumi Tsuda, Toshiya Morihiro, Junichi Hirayama, Koichi Nagano, Hiroaki Development of a clinical microarray system for genetic analysis screening |
title | Development of a clinical microarray system for genetic analysis screening |
title_full | Development of a clinical microarray system for genetic analysis screening |
title_fullStr | Development of a clinical microarray system for genetic analysis screening |
title_full_unstemmed | Development of a clinical microarray system for genetic analysis screening |
title_short | Development of a clinical microarray system for genetic analysis screening |
title_sort | development of a clinical microarray system for genetic analysis screening |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803787/ https://www.ncbi.nlm.nih.gov/pubmed/36593945 http://dx.doi.org/10.1016/j.plabm.2022.e00306 |
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