Use este identificador para citar ou linkar para este item: http://repositorio.ufc.br/handle/riufc/61922
Tipo: Artigo de Periódico
Título: Telomerase (hTERT) Overexpression Reveals a Promising Prognostic Biomarker and Therapeutical Target in Different Clinical Subtypes of Pediatric Acute Lymphoblastic Leukaemia
Autor(es): Nogueira, Beatriz Maria Dias
Pantoja, Laudreísa da Costa
Silva, Emerson Lucena da
Mello Júnior, Fernando Augusto Rodrigues
Teixeira, Eliel Barbosa
Wanderley, Alayde Vieira
Maués, Jersey Heitor da Silva
Moraes Filho, Manoel Odorico de
Moraes, Maria Elisabete Amaral de
Montenegro, Raquel Carvalho
Khayat, André Salim
Nunes, Caroline Aquino Moreira
Palavras-chave: Acute Lymphoblastic Leukemia;Leucemia Linfoblástica;Gene Expression;Expressão Gênica;Telomerase
Data do documento: 2021
Instituição/Editor/Publicador: Genes
Citação: Nogueira, B. M. D. et al. Telomerase (hTERT) Overexpression Reveals a Promising Prognostic Biomarker and Therapeutical Target in Different Clinical Subtypes of Pediatric Acute Lymphoblastic Leukaemia. Genes, 12, 1632, 2021. Disponível em: https://doi.org/10.3390/genes12101632 Acesso em: 08/11/2021
Abstract: Acute Lymphoblastic Leukemia (ALL) is a neoplasm of the hematopoietic system defined as a clonal expansion of an abnormal lymphoid precursor cell. It mostly affects children under five years of age and is the most common tumor to afflict pediatric patients. The expression of the human telomerase gene (hTERT) in patients with ALL has been studied as a biomarker and could become a new therapeutic target. We evaluate the role of hTERT gene expression in ALL pediatric patients, through quantitative real-time PCR technique, and the possible correlation between hTERT expression and clinical variables: gender, age, white blood cells (WBC), gene fusions, and immunophenotyping. The analysis between healthy controls and ALL patients (N = 244) was statistically significant (p < 0.001), demonstrating hTERT overexpression in these patients. In comparison with the usual set of clinical variables, the data were not statistically significant (p > 0.05), indicating that hTERT is equally overexpressed among patients regardless of gender, age, gene fusions, and immunophenotyping. Moreover, patients who presented a higher hTERT expression level had a significant (p < 0.0001) lower overall survival rate. In summary, hTERT expression emerges as an important molecular pathway in leukemogenesis regardless patient’s clinical variables, thus, the data here presented pointed it as a valuable biomarker in pediatric acute lymphoblastic leukemia and a promising target for new therapeutic and prognostic measures.
URI: http://www.repositorio.ufc.br/handle/riufc/61922
ISSN: 2073-4425
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