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Identify latent chromosomal aberrations relevant to myelodysplastic syndromes
Myelodysplastic syndromes (MDS) are a group of heterogeneous hematologic malignancies. This study aims to identify latent chromosomal abnormalities relevant to MDS, which may optimize the current diagnosis of MDS. Affymetrix CytoScan 750 K microarray platform was utilized to perform a genome-wide de...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583229/ https://www.ncbi.nlm.nih.gov/pubmed/28871208 http://dx.doi.org/10.1038/s41598-017-10551-3 |
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author | Song, Qibin Chu, Yuxin Yao, Yi Peng, Min Yang, Weihong Li, Xiaoqing Huang, Shiang |
author_facet | Song, Qibin Chu, Yuxin Yao, Yi Peng, Min Yang, Weihong Li, Xiaoqing Huang, Shiang |
author_sort | Song, Qibin |
collection | PubMed |
description | Myelodysplastic syndromes (MDS) are a group of heterogeneous hematologic malignancies. This study aims to identify latent chromosomal abnormalities relevant to MDS, which may optimize the current diagnosis of MDS. Affymetrix CytoScan 750 K microarray platform was utilized to perform a genome-wide detection of chromosomal aberrations in the bone marrow cells of the patients. The findings were compared with the results from traditional karyotypic analysis and FISH to reveal latent chromosomal aberrations. Chromosomal gain, loss, and UPD, and complex karyotypes were identified in those samples. In addition to established cytogenetic aberrations detected by karyotypic analysis, CytoScan 750 K microarray also detected cryptic chromosomal lesions in MDS. Those latent defects underlying multiple gene mutations may construe the clinical variability of MDS. In Conclusion, Affymetrix CytoScan 750 K microarray is efficient in identifying latent chromosomal aberrations in MDS. |
format | Online Article Text |
id | pubmed-5583229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55832292017-09-06 Identify latent chromosomal aberrations relevant to myelodysplastic syndromes Song, Qibin Chu, Yuxin Yao, Yi Peng, Min Yang, Weihong Li, Xiaoqing Huang, Shiang Sci Rep Article Myelodysplastic syndromes (MDS) are a group of heterogeneous hematologic malignancies. This study aims to identify latent chromosomal abnormalities relevant to MDS, which may optimize the current diagnosis of MDS. Affymetrix CytoScan 750 K microarray platform was utilized to perform a genome-wide detection of chromosomal aberrations in the bone marrow cells of the patients. The findings were compared with the results from traditional karyotypic analysis and FISH to reveal latent chromosomal aberrations. Chromosomal gain, loss, and UPD, and complex karyotypes were identified in those samples. In addition to established cytogenetic aberrations detected by karyotypic analysis, CytoScan 750 K microarray also detected cryptic chromosomal lesions in MDS. Those latent defects underlying multiple gene mutations may construe the clinical variability of MDS. In Conclusion, Affymetrix CytoScan 750 K microarray is efficient in identifying latent chromosomal aberrations in MDS. Nature Publishing Group UK 2017-09-04 /pmc/articles/PMC5583229/ /pubmed/28871208 http://dx.doi.org/10.1038/s41598-017-10551-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Song, Qibin Chu, Yuxin Yao, Yi Peng, Min Yang, Weihong Li, Xiaoqing Huang, Shiang Identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
title | Identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
title_full | Identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
title_fullStr | Identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
title_full_unstemmed | Identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
title_short | Identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
title_sort | identify latent chromosomal aberrations relevant to myelodysplastic syndromes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583229/ https://www.ncbi.nlm.nih.gov/pubmed/28871208 http://dx.doi.org/10.1038/s41598-017-10551-3 |
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