Publications by authors named "Thayana da Conceicao Barbosa"

Article Synopsis
  • Acute lymphoblastic leukemia (ALL) is the most common cancer in children, with B-cell ALL (B-ALL) being the predominant subtype; recent advancements in genomic sequencing have enhanced our understanding of its genetic basis.
  • A study was conducted on 126 B-ALL patients in Rio de Janeiro to analyze the frequency of specific genetic variants (SNPs) in the IKZF1 and CDKN2A/2B genes and compare these with the general population.
  • The study found that certain SNPs (rs3731217, rs4132601, rs11978267) were more common in B-ALL patients, which could lead to improved personalized therapies and better treatment outcomes for affected children.
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Introduction: Acute lymphoblastic leukemia (ALL) presents a poor prognosis in adults. The adoption of pediatric protocols has been changing this scenario, especially for adolescents and young adults (AYA).

Objective And Method: We aimed to evaluate a consecutive series of patients treated at the State Institute of Hematology of Rio de Janeiro between 2012 and 2020, focusing on the AYA subgroup.

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Cytokine Receptor-Like Factor 2 (CRLF2) overexpression occurs in 5-15% of B-cell precursor acute lymphoblastic leukaemia (B-ALL). In ∼50% of these cases, the mechanisms underlying this dysregulation are unknown. IKAROS Family Zinc Finger 1 (IKZF1) is a possible candidate to play a role in this dysregulation since it binds to the CRLF2 promoter region and suppresses its expression.

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Chronic myeloid leukemia (CML) is a rare disease in children. Different from that in adults, childhood CML involves transformative events occurring over a short time period. CML transformation to lymphoid blast phase (BP) is associated with copy number abnormalities, characteristic of BCR-ABL1 positive acute lymphoblastic leukemia, but not of CML in the chronic phase.

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Intragenic amplification defines a novel, relapse-prone subtype of B-cell precursor acute lymphoblastic leukemia with a poor outcome.

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