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Ultraconserved long non-coding RNA uc 112 is highly expressed in childhood T versus B-cell acute lymphoblastic leukemia
Chagas, Pablo Ferreira das; Sousa, Graziella Ribeiro de; Kodama, Márcio Hideki; Biagi Junior, Carlos Alberto Oliveira de; Yunes, José Andres; Brandalise, Silvia Regina; Calin, George Adrian; Tone, Luiz Gonzaga; Scrideli, Carlos Alberto; Oliveira, Jaqueline Carvalho de.
  • Chagas, Pablo Ferreira das; Universidade de São Paulo - USP. Faculdade de Medicina. Ribeirão Preto. BR
  • Sousa, Graziella Ribeiro de; Universidade de São Paulo - USP. Faculdade de Medicina. Ribeirão Preto. BR
  • Kodama, Márcio Hideki; Universidade de São Paulo - USP. Faculdade de Medicina. Ribeirão Preto. BR
  • Biagi Junior, Carlos Alberto Oliveira de; Universidade de São Paulo - USP. Faculdade de Medicina. Ribeirão Preto. BR
  • Yunes, José Andres; Centro Infantil Boldrini. Campinas. BR
  • Brandalise, Silvia Regina; Centro Infantil Boldrini. Campinas. BR
  • Calin, George Adrian; MD Anderson Cancer Center. Houston. US
  • Tone, Luiz Gonzaga; Universidade de São Paulo - USP. Faculdade de Medicina. Ribeirão Preto. BR
  • Scrideli, Carlos Alberto; Universidade de São Paulo - USP. Faculdade de Medicina. Ribeirão Preto. BR
  • Oliveira, Jaqueline Carvalho de; Universidade Federal de Alfenas. Alfenas. BR
Hematol., Transfus. Cell Ther. (Impr.) ; 43(1): 28-34, Jan.-Mar. 2021. tab, graf, ilus
Article in English | LILACS | ID: biblio-1154296
ABSTRACT
ABSTRACT 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.
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Full text: Available Index: LILACS (Americas) Main subject: Diploidy / Precursor Cell Lymphoblastic Leukemia-Lymphoma / Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Limits: Female / Humans Language: English Journal: Hematol., Transfus. Cell Ther. (Impr.) Journal subject: Hematologia / TransfusÆo de Sangue Year: 2021 Type: Article Affiliation country: Brazil / United States Institution/Affiliation country: Centro Infantil Boldrini/BR / MD Anderson Cancer Center/US / Universidade Federal de Alfenas/BR / Universidade de São Paulo - USP/BR

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Full text: Available Index: LILACS (Americas) Main subject: Diploidy / Precursor Cell Lymphoblastic Leukemia-Lymphoma / Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Limits: Female / Humans Language: English Journal: Hematol., Transfus. Cell Ther. (Impr.) Journal subject: Hematologia / TransfusÆo de Sangue Year: 2021 Type: Article Affiliation country: Brazil / United States Institution/Affiliation country: Centro Infantil Boldrini/BR / MD Anderson Cancer Center/US / Universidade Federal de Alfenas/BR / Universidade de São Paulo - USP/BR