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Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene

Acute lymphoblastic leukemia (ALL) in children or adults is characterized by structural and numeric aberrations in chromosomes; these anomalies strongly correlate with prognosis and clinical outcome. Therefore, this work aimed to identify the genes present in chromosomal gain regions found more freq...

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Autores principales: Zapata-García, Jessica Alejandra, Riveros-Magaña, Alma Rocío, Ortiz-Lazareno, Pablo Cesar, Hernández-Flores, Georgina, Jave-Suárez, Luis Felipe, Aguilar-Lemarroy, Adriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689318/
https://www.ncbi.nlm.nih.gov/pubmed/36428851
http://dx.doi.org/10.3390/diagnostics12112788
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author Zapata-García, Jessica Alejandra
Riveros-Magaña, Alma Rocío
Ortiz-Lazareno, Pablo Cesar
Hernández-Flores, Georgina
Jave-Suárez, Luis Felipe
Aguilar-Lemarroy, Adriana
author_facet Zapata-García, Jessica Alejandra
Riveros-Magaña, Alma Rocío
Ortiz-Lazareno, Pablo Cesar
Hernández-Flores, Georgina
Jave-Suárez, Luis Felipe
Aguilar-Lemarroy, Adriana
author_sort Zapata-García, Jessica Alejandra
collection PubMed
description Acute lymphoblastic leukemia (ALL) in children or adults is characterized by structural and numeric aberrations in chromosomes; these anomalies strongly correlate with prognosis and clinical outcome. Therefore, this work aimed to identify the genes present in chromosomal gain regions found more frequently in patients with acute lymphoblastic leukemia (ALL) and ALL-derived cell lines using comparative genomic hybridization (CGH). In addition, validation of the genes found in these regions was performed utilizing RNAseq from JURKAT, CEM, and SUP-B15 cell lines, as well as expression microarrays derived from a MILE study. Chromosomes with common gain zones that were maintained in six or more samples were 14, 17, and 22, in which a total of 22 genes were identified. From them, NT5C3B, CNP, ACLY, and GNB1L maintained overexpression at the mRNA level in the cell lines and in patients with ALL. It is noteworthy that SALL2 showed very high expression in T-ALL, while JUP was highly expressed in B-ALL lineages. Interestingly, the latter correlated with worse survival in patients. This provided evidence that the measurement of these genes has high potential for clinical utility; however, their expressions should first be evaluated with a sensitive test in a more significant number of patients.
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spelling pubmed-96893182022-11-25 Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene Zapata-García, Jessica Alejandra Riveros-Magaña, Alma Rocío Ortiz-Lazareno, Pablo Cesar Hernández-Flores, Georgina Jave-Suárez, Luis Felipe Aguilar-Lemarroy, Adriana Diagnostics (Basel) Article Acute lymphoblastic leukemia (ALL) in children or adults is characterized by structural and numeric aberrations in chromosomes; these anomalies strongly correlate with prognosis and clinical outcome. Therefore, this work aimed to identify the genes present in chromosomal gain regions found more frequently in patients with acute lymphoblastic leukemia (ALL) and ALL-derived cell lines using comparative genomic hybridization (CGH). In addition, validation of the genes found in these regions was performed utilizing RNAseq from JURKAT, CEM, and SUP-B15 cell lines, as well as expression microarrays derived from a MILE study. Chromosomes with common gain zones that were maintained in six or more samples were 14, 17, and 22, in which a total of 22 genes were identified. From them, NT5C3B, CNP, ACLY, and GNB1L maintained overexpression at the mRNA level in the cell lines and in patients with ALL. It is noteworthy that SALL2 showed very high expression in T-ALL, while JUP was highly expressed in B-ALL lineages. Interestingly, the latter correlated with worse survival in patients. This provided evidence that the measurement of these genes has high potential for clinical utility; however, their expressions should first be evaluated with a sensitive test in a more significant number of patients. MDPI 2022-11-14 /pmc/articles/PMC9689318/ /pubmed/36428851 http://dx.doi.org/10.3390/diagnostics12112788 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zapata-García, Jessica Alejandra
Riveros-Magaña, Alma Rocío
Ortiz-Lazareno, Pablo Cesar
Hernández-Flores, Georgina
Jave-Suárez, Luis Felipe
Aguilar-Lemarroy, Adriana
Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene
title Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene
title_full Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene
title_fullStr Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene
title_full_unstemmed Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene
title_short Comparative Genomic Hybridization and Transcriptome Sequencing Reveal Genes with Gain in Acute Lymphoblastic Leukemia: JUP Expression Emerges as a Survival-Related Gene
title_sort comparative genomic hybridization and transcriptome sequencing reveal genes with gain in acute lymphoblastic leukemia: jup expression emerges as a survival-related gene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689318/
https://www.ncbi.nlm.nih.gov/pubmed/36428851
http://dx.doi.org/10.3390/diagnostics12112788
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