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Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia
Aberrant expression of long non-coding RNAs (lncRNAs) has been detected in several types of cancer, including acute lymphoblastic leukemia (ALL), but lncRNA mapped on transcribed ultraconserved regions (T-UCRs) are little explored. The T-UCRs uc.112, uc.122, uc.160 and uc.262 were evaluated by quant...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Hematologia e Hemoterapia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910170/ https://www.ncbi.nlm.nih.gov/pubmed/32014474 http://dx.doi.org/10.1016/j.htct.2019.12.003 |
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author | das Chagas, Pablo Ferreira de Sousa, Graziella Ribeiro Kodama, Márcio Hideki de Biagi Junior, Carlos Alberto Oliveira Yunes, José Andres Brandalise, Silvia Regina Calin, George Adrian Tone, Luiz Gonzaga Scrideli, Carlos Alberto de Oliveira, Jaqueline Carvalho |
author_facet | das Chagas, Pablo Ferreira de Sousa, Graziella Ribeiro Kodama, Márcio Hideki de Biagi Junior, Carlos Alberto Oliveira Yunes, José Andres Brandalise, Silvia Regina Calin, George Adrian Tone, Luiz Gonzaga Scrideli, Carlos Alberto de Oliveira, Jaqueline Carvalho |
author_sort | das Chagas, Pablo Ferreira |
collection | PubMed |
description | Aberrant expression of long non-coding RNAs (lncRNAs) has been detected in several types of cancer, including acute lymphoblastic leukemia (ALL), but lncRNA mapped on transcribed ultraconserved regions (T-UCRs) are little explored. The T-UCRs uc.112, uc.122, uc.160 and uc.262 were evaluated by quantitative real-time PCR in bone marrow samples from children with T-ALL (n = 32) and common-ALL/pre-B ALL (n = 30). In pediatric ALL, higher expression levels of uc.112 were found in patients with T-ALL, compared to patients with B-ALL. T-cells did not differ significantly from B-cells regarding uc.112 expression in non-tumor precursors from public data. Additionally, among B-ALL patients, uc.112 was also found to be increased in patients with hyperdiploidy, compared to other karyotype results. The uc.122, uc.160, and uc.262 were not associated with biological or clinical features. These findings suggest a potential role of uc.112 in pediatric ALL and emphasize the need for further investigation of T-UCR in pediatric ALL. |
format | Online Article Text |
id | pubmed-7910170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedade Brasileira de Hematologia e Hemoterapia |
record_format | MEDLINE/PubMed |
spelling | pubmed-79101702021-03-05 Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia das Chagas, Pablo Ferreira de Sousa, Graziella Ribeiro Kodama, Márcio Hideki de Biagi Junior, Carlos Alberto Oliveira Yunes, José Andres Brandalise, Silvia Regina Calin, George Adrian Tone, Luiz Gonzaga Scrideli, Carlos Alberto de Oliveira, Jaqueline Carvalho Hematol Transfus Cell Ther Original Article Aberrant expression of long non-coding RNAs (lncRNAs) has been detected in several types of cancer, including acute lymphoblastic leukemia (ALL), but lncRNA mapped on transcribed ultraconserved regions (T-UCRs) are little explored. The T-UCRs uc.112, uc.122, uc.160 and uc.262 were evaluated by quantitative real-time PCR in bone marrow samples from children with T-ALL (n = 32) and common-ALL/pre-B ALL (n = 30). In pediatric ALL, higher expression levels of uc.112 were found in patients with T-ALL, compared to patients with B-ALL. T-cells did not differ significantly from B-cells regarding uc.112 expression in non-tumor precursors from public data. Additionally, among B-ALL patients, uc.112 was also found to be increased in patients with hyperdiploidy, compared to other karyotype results. The uc.122, uc.160, and uc.262 were not associated with biological or clinical features. These findings suggest a potential role of uc.112 in pediatric ALL and emphasize the need for further investigation of T-UCR in pediatric ALL. Sociedade Brasileira de Hematologia e Hemoterapia 2021 2020-01-30 /pmc/articles/PMC7910170/ /pubmed/32014474 http://dx.doi.org/10.1016/j.htct.2019.12.003 Text en © 2020 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. http://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 Article das Chagas, Pablo Ferreira de Sousa, Graziella Ribeiro Kodama, Márcio Hideki de Biagi Junior, Carlos Alberto Oliveira Yunes, José Andres Brandalise, Silvia Regina Calin, George Adrian Tone, Luiz Gonzaga Scrideli, Carlos Alberto de Oliveira, Jaqueline Carvalho Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia |
title | Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia |
title_full | Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia |
title_fullStr | Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia |
title_full_unstemmed | Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia |
title_short | Ultraconserved long non-coding RNA uc.112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia |
title_sort | ultraconserved long non-coding rna uc.112 is highly expressed in childhood t versus b-cell acute lymphoblastic leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910170/ https://www.ncbi.nlm.nih.gov/pubmed/32014474 http://dx.doi.org/10.1016/j.htct.2019.12.003 |
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