Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Hematologia e Hemoterapia 2021
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
_version_ 1783656074711138304
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
work_keys_str_mv AT daschagaspabloferreira ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT desousagraziellaribeiro ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT kodamamarciohideki ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT debiagijuniorcarlosalbertooliveira ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT yunesjoseandres ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT brandalisesilviaregina ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT calingeorgeadrian ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT toneluizgonzaga ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT scridelicarlosalberto ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia
AT deoliveirajaquelinecarvalho ultraconservedlongnoncodingrnauc112ishighlyexpressedinchildhoodtversusbcellacutelymphoblasticleukemia