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First case of AML with rare chromosome translocations: a case report of twins
BACKGROUND: Leukemia is different from solid tumor by harboring genetic rearrangements that predict prognosis and guide treatment strategy. PML-RARA, RUNX1-RUNX1T1, and KMT2A-rearrangement are common genetic rearrangements that drive the development of acute myeloid leukemia (AML). By contrast, rare...
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/PMC5913884/ https://www.ncbi.nlm.nih.gov/pubmed/29688850 http://dx.doi.org/10.1186/s12885-018-4396-4 |
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author | Wang, Lin Sun, Yanhua Sun, Yanli Meng, Lingbin Xu, Xin |
author_facet | Wang, Lin Sun, Yanhua Sun, Yanli Meng, Lingbin Xu, Xin |
author_sort | Wang, Lin |
collection | PubMed |
description | BACKGROUND: Leukemia is different from solid tumor by harboring genetic rearrangements that predict prognosis and guide treatment strategy. PML-RARA, RUNX1-RUNX1T1, and KMT2A-rearrangement are common genetic rearrangements that drive the development of acute myeloid leukemia (AML). By contrast, rare genetic rearrangements may also contribute to leukemogenesis but are less summarized. CASE PRESENTATION: Here we reported rare fusion genes ZNF717-ZNF37A, ZNF273-DGKA, and ZDHHC2-TTTY15 in a 47-year-old AML-M4 patient with FLT3 internal tandem duplication (ITD) discovered by whole genome sequencing (WGS) using the patient’s healthy sibling as a sequencing control. CONCLUSION: This is, to our knowledge, the first case of AML with fusion gene ZNF717-ZNF37A, ZNF273-DGKA, and ZDHHC2-TTTY15. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4396-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5913884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59138842018-04-30 First case of AML with rare chromosome translocations: a case report of twins Wang, Lin Sun, Yanhua Sun, Yanli Meng, Lingbin Xu, Xin BMC Cancer Case Report BACKGROUND: Leukemia is different from solid tumor by harboring genetic rearrangements that predict prognosis and guide treatment strategy. PML-RARA, RUNX1-RUNX1T1, and KMT2A-rearrangement are common genetic rearrangements that drive the development of acute myeloid leukemia (AML). By contrast, rare genetic rearrangements may also contribute to leukemogenesis but are less summarized. CASE PRESENTATION: Here we reported rare fusion genes ZNF717-ZNF37A, ZNF273-DGKA, and ZDHHC2-TTTY15 in a 47-year-old AML-M4 patient with FLT3 internal tandem duplication (ITD) discovered by whole genome sequencing (WGS) using the patient’s healthy sibling as a sequencing control. CONCLUSION: This is, to our knowledge, the first case of AML with fusion gene ZNF717-ZNF37A, ZNF273-DGKA, and ZDHHC2-TTTY15. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4396-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-23 /pmc/articles/PMC5913884/ /pubmed/29688850 http://dx.doi.org/10.1186/s12885-018-4396-4 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 | Case Report Wang, Lin Sun, Yanhua Sun, Yanli Meng, Lingbin Xu, Xin First case of AML with rare chromosome translocations: a case report of twins |
title | First case of AML with rare chromosome translocations: a case report of twins |
title_full | First case of AML with rare chromosome translocations: a case report of twins |
title_fullStr | First case of AML with rare chromosome translocations: a case report of twins |
title_full_unstemmed | First case of AML with rare chromosome translocations: a case report of twins |
title_short | First case of AML with rare chromosome translocations: a case report of twins |
title_sort | first case of aml with rare chromosome translocations: a case report of twins |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913884/ https://www.ncbi.nlm.nih.gov/pubmed/29688850 http://dx.doi.org/10.1186/s12885-018-4396-4 |
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